These are the
daily updates that were posted to the website while Garrett was sick:
Services for
Garrett
Garrett's Memorial Service will be held
on Saturday, July 8th, 2006
Memorial Service Details:
When: 10:00 - 11:30 am
Location: St Eugene’s
Cathedral
2323 Montgomery Drive, Santa Rosa CA 95405
Burial/Interment:
When: Noon - 2:00 pm
Location: Calvary Catholic
Cemetery
2930 Bennett Valley Road, Santa Rosa CA 95405
The family requests that any contributions in Garrett's memory be made to the
Garrett Fogg Memorial Trust Fund (currently being
established, more information to follow).
Comments (2 total)
My thoughts and prayers are with you all. I cringe when I read
an obituary in the paper of a young child, and it ultimately brings many a tear
to mine eyes. God Bless you, Garrett, and may you rest easy; you're a true
angel now.
--Suzie Campiglio<
<mailto:campi21@prodigy.net>
2006-07-06
I am so sorry for the loss of your son and brother. I just
learned of this through the Tuscaloosa News Paper in
--Stacy Shaw
<mailto:stshaw@halek12.org>
2006-10-27
Sadly, Garrett passed away this
morning. Greg, Lisa and Leanne thank you all for your caring
concern and support throughout these difficult past weeks. Services are
still being planned, and more information will be posted here as soon as it is
available.
2006-07-01
Comments (72 total)
Our family is mourning along with many,
many others today for Garrett. I am so sorry and wish that there was something
I could say to comfort you, but I know no words can do that. We are all better
for knowing him. Our thoughts and prayers are with you.
Shellie, Zac and Taylor
--The Olson Family
<mailto:sztolson@sbcglobal.net>
2006-07-01
God be with you and your family. This
has got to breaking your hearts. I didn't know Garrett
or his family, but I'll be praying for you all. God Bless.
--Diana
2006-07-02
Dear Greg, Lisa, and Leanne,
You might not remember me - but my name is Carolyn and I know that you've met
my husband Mark in he PICU.
We've seen one another in the waiting room of the PICU a few times.
I have been praying for Garrett every night. Mark and I have his blog on our computer and we are deeply touched by your
grace and strength in this most trying chapter of your life.
Our love and prayers are with your forever.
You are an inspiration.
--Carolyn Reibel
2006-07-02
Hello, i didnt know your son, but i fell
for you and your family.
I think it is amazing that you made this website, and it touches me that you
have been getting so much support.
Stay strong, GARRET's memory will help you get
through this!
--Felicia Strope
2006-07-02
Garrett touched all of our lives, and we
will never forget him. Our prayers are with you and your family. Our deepest
sympathy......
--Victoria Garcia & Family
<mailto:Victorialee55@hotmail.com>
2006-07-02
We are so sorry. Garrett was a wonderful
person and a strong athlete. We were lucky to have known him even though it has
only been since we moved here 1-1/2 years ago. Greg, Lisa and Leanne, we wish
you all the best through this very trying time. We will continue to keep you in
our prayers. Sincerely, Cindy, Pat & Jane Halahan
2006-07-02
My heart is breaking for all of you. You
are always in my thoughts and prayers. I love you guys.
God's peace to you all,
Samantha
--Samantha Durham
2006-07-02
Dear Fogg
Family,
I did not know Garrett well, but I had a couple of conversations with him a few
years ago. He was sweet,and
I even had a slight crush on him when I was in 10th grade. I will be graduating
with Leanne next year, and I am sorry that I do not know her well either. Last
school year she and I shared Spanish and History class together. She is a very
talented girl in many ways as was your son Garrett. Nobody will ever forget his
sweet, happy smile, or his personality. I only pray for you all to get better
soon. Leanne and Garrett loved each other a lot, and he was always happy. I
hope to get to know Leanne better next year, and I will always wish I knew
Garrett better. I am sorry he was taken away from this earth at such a young
age, but it is good to know he is no longer suffering from his illness. My
prayers go out to the whole Fogg family, and everyone
suffering.
<3 samantha Roatch
2006-07-02
Dear Greg, Lisa and Leanne,
I am really at a loss for words having followed Garrett's battle for all these
weeks. The only words that come to me - is that I am so sorry.
Matt, Cristina and the girls in
--The Fonseca Family
2006-07-02
Hello Foggs. I
knew Garrett from school. He was a great kid. The best thing that I can
remember him by was by his smile and his skater hair :).
I miss him alot. When I heard the news, it blew me
away. I just want you to know that I am praying for you. Its
hard when we dont understand why these kinds of
things happen. I pray that you will get through this. I wish you the best in
everything. I will never forget Garrett or his wonderful smile.
Sincerely,
Katie Slater
--Katie Slater
<mailto:englandceleb1@comcast.net>
2006-07-02
I am not sure what to say other then I'm
so sorry for all the agony you must have been feeling for the past few weeks. I
know it's never clear on what words to use in a situation such as this, but I
am so sorry for your loss. I am sure he is in a much better place but it is still
never easy to accept for a parent. I never met Garrett, however he wrestled
with my little brother and I remember seeing him at the meets and telling my
mom that he was my favorite of all of them and I just wanted to squeeze his
cheeks! he was precious and I'm sure he is quite the
perfect angel watching over you through these hard times. Please know that your
family is in my thoughts and prayers.
God bless,
Jamie Lew
2006-07-02
Dear fogg
family I pray for your family and i will continue to
do so.Garrett is in a great place now. god bless
--sam bishop
2006-07-02
Im very sorry to hear
about Garrett. I
didn't know him but he sounded like a very nice kid. He's in a better place now.Also ignore those dumb people who posted the rude Comments they probably dont even go to carrillo(this has been going through myspace
and probably got to them). They are probably just really bored and have nothing
better to do. I will keep your family and him in my prayers. God bless.
--Anonymous
2006-07-02
I am very sorry. Garrett was a great
person. He is in a better place now. Your family and Garrett himself will be in
my prayers. It was wonderful of you all to be so strong.
God Bless you all.
--Addie Lewis
2006-07-02
Greg, Lisa and Leanne: As so many others
have expressed, we are deeply saddened by your loss. We wish you comfort and
peace. You have been embraced by so many people that care for your family and
hopefully we will be able to help you as your needs arise. Take care -Randy,
Julie and Alex Hartz
--The Hartz Familyy
2006-07-02
Dear Fogg
Family,
I'm so sorry to hear about Garrett. I didn't know him to well, but I knew that
he was an amazing person and I only wish I had gotten to know him more. You
guys have been in my prayers from the beginning and you will continue to be in
my prayers. I hope that you get through this period smoothly and with as little
pain as possible. Just remember that Garrett is in a better place now and pain
free. God Bless.
-Whitney
2006-07-02
Oh My.. Im sooo sorry for your Son's loss. He will be greatly
missed by those that loved him and his friends. Just remember that he is in
God's hands and Jesus loves him and will take great care of him. I will be
praying for you and your family.
Take Care
God Bless
Nicole
2006-07-02
Garrett was in my Spanish class and I
was one of the only two freshmen in my class. I was very nervous, as many freshman are, to meet new people. Garrett made it easy for
me to feel comfortable in the upper classmen class. He was always smiling and
making jokes he got along great with everyone. I really looked up to his easy
going ways, he will surely be missed by many. I will
not only mourn his death but celebrate the wonderful things he did and the
great life he lived.
Sorry for you loss
Your in my prayers ~jess
--Jessica Sallee
2006-07-02
I am so sorry to hear of your news!
Losing a loved one is never easy and it is even more difficult when it involves
such a young life. Garrett sounds like an amazing young man and I can tell his
life definately influenced everyone around him in a
positive way. I will keep your family in my thoughts and prayers and please
know that there is love out there for you during this difficult time! He has
been taken into Gods hands, a place more serene and peaceful than any of us can
imagine. My mom is in heaven too (I'm 23) and I will ask her to watch over him
as well :) Have comfort in knowing that you miss him because there was so much
love for him in your hearts..and
there always will be. God Bless and keep strong. :)
--
2006-07-02
Greg and Lisa,
We are so saddened and sorry to hear about Garrett's passing. Our prayers are
with you, and have been since first meeting you. We are both thinking of you
guys, and pray that you and your daughter will be blessed in so many ways. Your
love will continue to keep Garrett with you forever. We never really loose anyone, we just don't see them for awhile. So don't say
good-bye, you'll all be together again someday.
God's healing and blessings to you all.
Jamie & Danny
Buchanan
--Jamie Buchanan
<mailto:IamJamieB@aol.com>
2006-07-02
I am so truly sorry for your loss.
Garrett really fought the fight well. I thought that he would recover. Please
know that so many people are there for you at this tragic time. Lean on each
other and use your faith to carry you through. Garrett is lucky to have had all
of you in his life and he will continue to watch over you. God Bless,
Christine Prothero
2006-07-02
I didn't know your son, but I know the
pain of losing someone so suddenly to something so unexpected. Life must carry
on but he can never be forgotten. Your family is in my thoughts during this
rough time!
2006-07-02
I did not know your son but I wanted you
to know I am thinking of all of you in your time of need. God Bless, you all.
--Desiree Condon
2006-07-02
R.I.P. Garrett Fogg
2006-07-02
Greg- I was devastated by the news of
Garrett's passing. I had been holding out hope and cannot even imagine what you
and your family are going through. Garrett is where he is meant to be.
I feel that we were able to bond in the hospital and the sharing of our stories
helped me through some rough nites there in PICU.
When things settle down, please give me a call.
I want you to come meet my daughter - Rosalie. I know the Hospital is probably
the last place you would want to visit, but it might help you to see her
inspirational fight.
(www.rosaliereibel.blogspot.com).
She and Garrett shared shared time in the PICU
together. As I am sure you remember, she is 2 and was diagnosed with Brain
Cancer which is being treated. She is fighting through her post operative
syndrome and second round of chemo now.
You and your family are in my thoughts and prayers!
Regards,
Mark Reibel
415-652-6488
2006-07-02
RIP GARRETT FOGG
2006-07-02
hey i just
want to tell you guys how sorry i am and how he was
an amazing boy...he was smart and had everything going for him.....i wish you guys the best and i
hope everything works out for you....please let me know when the services are
being held i would like to attend them..my e-mail address is compchick2001@netscape.net...my
name is kayla i attended
school with your daughter leanne and i knew your son..he
was wonderful and i am sorry for your loss.....best
wishes!!!
Kayla
2006-07-02
Dear Greg, Lisa, and Leanne,
We are so very sad to hear of your loss. Our son Tyler has many great memories
of playing baseball with Garrett on the Mets and enjoyed even more at MCHS.
Our thoughts are with you at this difficult time, The Brownlee Family
Rod, Karen, Tyler & Taylor
--Brownlee Family
2006-07-02
Dear Fogg
Family
I didn't know Garrett very well, but he seemed like a great person. During the
school year, wrestling and basketball practices often ended at the same time,
and when he was done with wrestling and was walking through the gym, all of us
basketball players would always stop practicing and wave to him. He was always
a good sport and would wave back and yell hello to us. He seemed like a truly
sweet kid, and we all have fond memories of him. Your whole family is in our
thoughts and prayers. Leanne, i know this must be
especially difficult for you but just know that we are all thinking of you.
Best wishes and thoughts to the whole family
2006-07-02
Dear Lisa,Gregg, and Leanne,
We are so terribly sorry to hear of Garrett's passing, will continue to keep
you in prayer and thought. Much love and peace to you all.
Kendall Galvez and Family
2006-07-02
23:21:31 GMT
dear fogg family,
i am terribly sorry for the lost of your son Garrett.
he meant alot to us and your
family. you can be sad, but he wants you to be happy
because he is now in a state of peace and in a painless situation. i would gladly come to his service
would be a honor because he was a bright and brave boy fighting a sickness. bless you very much.
--jolenne aplin
and
<mailto:irelandrocks222@hotmail.com>
2006-07-03
00:12:12 GMT
Greg, Lisa and Leanne --
I am a colleague of Uncle Will Pakutka, who I work
with in the sports department of the New York Daily News.
I obviously never have met any of you, but let me just say how ... how sad I am
... and how much love came through in your posts about Garrett ... and how I'm sure
he could feel that love.
My heart goes out to you ...
JG
--john gruber
<mailto:jgruber@nydailynews.com>
2006-07-03
I knew Garrett from school, and I am so
terribly sorry. i have been
thinking about your family a lot and I can only imagine what you are going
through. Garrett was an amazing person, and he will never be forgotten.
--Carla Curle
<mailto:vballgrl777@yahoo.com>
2006-07-03
Dear Greg Lisa & Leanne,
We are all in a state of shock with Garrets passing. Our hearts go out to you.
All of us feel blessed for knowing Garrett and the time we were able to spend
with him. He will always be in a special place in our hearts.
We know he is now in a better place.
Our hearts go out to you.
The Kunde Family.
--The Kunde Familyy
2006-07-03
Dear Foggs,
I was very sorry to hear about Garrett. I know I will always remember him. All
the track memories, and wrestling memories, and biology w/ Mrs. Mojtahedi (I'm sure you heard about her). He will always be
remembered by the people that knew him, and judging by this website, it seems
he will be remembered by people who didn't know him. I'm sorry for your loss.
Mark Robinson and family
2006-07-03
Fogg family,
i am very sorry for your loss. Garrett is in a better
place in heaven now. God bless you. R.I.P. Garrett <3
2006-07-03
Dear Foggs,
I love all of you and I am deeply saddened about the loss of Garrett. I will
never forget spending time with him on the pole vault pits with all the kids.
He was always a trooper and I was privileged to know him. He was just like his
dad in that he could make friends wherever he went. He felt like a little
brother to me, yet he was an example for me. My heart goes
out to you and know that you've got all of our support. You're in my
prayers.
Ty Olson
2006-07-03
Dear Fogg
Family - I am so sorry to hear of Garrett's passing. I was introduced to your
website through a Weight Watchers group and have been following your story
since May. Please accept our deepest condolences. Your family is in our
thoughts and our prayers.
Sincerely,
The Christian Family
--Megan Christian
<mailto:whscoachmeg@comcast.net>
2006-07-03
Dearest Fogg
Family,
We're deeply sorry about the news of Garrett's passing. Please accept our
sincerest condolances. Our thoughts and prayers are
with and for you.
Love,
Ben, Elsa, Katrina, and Annie Alonso
--Alonso Family
<mailto:f3istykid@sbcglobal.net>
2006-07-03
Dear Fogg
Family,
We are so sorry to hear of your loss. Our sons played together on the Mets and
I will always remember his terrific attitude no matter what the odds, his smile
and a terrific curve ball.
You are in our prayers.
The Vlahandreas Family
2006-07-03
Dear Fogg
Family,
I was shocked when i heard the news. I was praying
for him every night. I thought he was going to pull through and it would just
take him some time. When i heard of Garrett's passing
i didn't move a muscle. I just sat there thinking of
the last time i saw him outside the hospital and how
cheerful he was. That is how i am going to remember
him and i am sure others as well. If you need
anything, do not hesitate to ask me and my family. We are here for you no
matter what you may need.
Garrett will always be in my heart.
Ross Tucker
--Ross Tucker
<mailto:Tuck234@aol.com>
2006-07-03
Dear Fogg
Family--
We were so sad to hear of Garrett's passing. Not a moment has gone by since
Saturday that you are not in our hearts. Garrett is such a beautiful name (we
have a Garrett as well) and he was such a sweet spirit, with a sweet smile, and
we will remember him always. We hope his memory will help you to get thru such
a difficult time as this and we are thinking of you.
Cindy and Mark Tucker, (ross's parents)
--Cindy and ,Mark TTucker
2006-07-03
Hey guys. I strongly admire and
appreciate this website, it has honestly helped me
cope with all this. I hope that in some way it has helped you as well.
I have learned over recent years that not only is it important to mourn the
loss of someone so dear, it's just as important and crucial to celebrate and
honor that someone, and there's a lot to celebrate and honor about Garrett.
There's no doubt that you'll be seeing my family, frends,
and I at the services.
- Aubree Jacobsen,,
neighbor and friend from 2 doors down
--Aubree
<mailto:irishbabe707@hotmail.com>
2006-07-03
Dear Greg, Lisa & Leanne,
Garrett is a champion. His spirit lives on in our hearts.
--Pat & Lee Elaine Nobriga
2006-07-03
Dear Greg, Lisa & Leanne,
Garrett is a champion. His spirit lives on in our hearts.
--Pat & Lee Elaine Nobriga
2006-07-03
HE WILL ALWAYS BE
IN OUR HEARTS AND ALL I COULD SAY IS HE IS A GREAT PERSON AND WE WILL ALWAYS
REMEMBER HIM!!! WELL STAY STRONG AND I KNOW IT IS REALLY DIFFICULT!!!
2006-07-03
Dear Greg ,Lisa
and Leanne, We are so sorry about Garrett. I know your hearts are broken but
always know what great parents and sister you are. You are in our prayers.
--Mary,,Jerry and David
Wellman
2006-07-03
Dear Greg, Lisa, and Leanne,
We are so sorry for your loss. Sam and Leanne have had a number of classes
together and every year we could count on seeing Greg and Garrett at the Little
League field. Our hearts go out to you at this very sad time.
--Carol, Bill, and Sam Adams
2006-07-03
Dear Lisa, Greg and Leanne,
We are so sorry for your loss. Words cannot express it. Even though Garrett
wasn't in the same grade as our kids, he touched our lives. He was in track
with all three, Ben, Stefan and Megan, at different times. Ben and Stefan
enjoyed playing soccer with him on the blacktop during elementary shcool.
Our thoughts and prayers are with you,
Kathy, Mike, Stefan, Ben, and Megan
2006-07-03
I didn't know Garrett very well, but
Leanne and Greg, I've known you guys for two years and I am so sorry for your
family's loss. Garrett was everything you could have wished for in a son and
brother: smart, athletic, and kind. He will be in our hearts forever.
My thoughts are with you,
Maddy Titone
2006-07-03
Dear Fogg
Family,
I've never met you, but my husband Vinnie knew you
well. We have and continue to keep you and your family in our prayers and are
so pained by your loss. What is so amazing to me through all of this, you have
continued to think about others and provide these daily updates. We continue to
pray for peace and joy in these days to come as you remember Garretts life.
God Bless,
Cindy Lamica
--Cindy Lamica
>
<mailto:wrntygrl@comcast.net>
2006-07-03
Lisa and Family
I can't tell how much sadness we are feeling about your loss. Lisa - you had
such a tremendous influence on so many young people at
--conniie giuliano
<mailto:connie.giuliano@kp.org>
2006-07-03
Im am so sorry for your loss. This is just
so sad. My thoughts are with you during this difficult time. May time help heal
your pain.
--Gabi>
2006-07-03
I know there are not words to lessen any
of your grief, but please know so many are thinking of Garrett, you and your
family. You have conducted this struggle with grace and courage. THank you for sharing your story.
--The Klein family
<mailto:lkkrn@comcast,net>
2006-07-03
This must be terible,
im am so sorry. I remember Garrett from middle school, and a summer school class awhile back. He was sweet
kid, and really nice to everybody. I hope that he as happy now, as he was when
he was still alive
jeny
--Jeny
2006-07-03
i am soo
terribly sorry and sad for your loss. all my memories
of garrett are those of happieness
and fun. your family is in my prayers
stay strong
2006-07-03
I didn't really know Garrett, although
he went to my school and was in my grade. It's amazing that something like this
can happen. I mean, you assume that things happen to other people at other
schools, and then WHAM- wow, someone that i probably
bumped into in the hallways is gone. I'm very sorry for your loss, as well as
for Garrett. He would have gone far.
~ Allie
2006-07-03
I am vary sorry
for your loss. i new Garrett from Rincon Valley
Middle School he was always smiling and laughing when ever i
would walk by him.I never once saw him with a frown
on his face.He will be missed but never forgotten.
~Brandi Dunbar
2006-07-04
i didnt really
know Garret.
but saw him around rincon vally middle all the time.
he would ALWAYS be smiling and not caring about wut
other people thought even if he was a crazy kid :]
i remember seeing him in the halls and i was really upset and crying cuz
my brother has died.
and he came up to me and sat. and
talked.
i didnt
even know him.
hes such a caring and
wonderful guy.
R.I.P.
i will see you soon
<3
Brittany Rose
--Brittany Rose
2006-07-04
i am siting
here mourning your loss. my son has a shunt after
suffering a brain injury and has been cared for by many of the professionals at
ucsf children's whom you continuously thank. we also live in
--amy evans
<mailto:amyellenevans@yahoo.com>
2006-07-04
I'm so sorry to hear of your loss. Mrs. Fogg was a teacher of mine for a few years, so I had the
pleasure of listening to her light up as she spoke of her children. My prayers
are with the entire Fogg family.
--Hillary Smith
2006-07-04
Our thoughts are with you.....
2006-07-04
I'm so sorry to hear of your loss. Your in our hearts, thoughts and prayers. May Garrett rest
in peace.
The Torliatt Family in
--BB Torliatt
<mailto:jbtorliatt@comcast.net>
2006-07-04
Greg and Lisa, I was so shocked and
saddened when I read the paper this morning. Pugs played soccer with Garrett
and I can remember the days of carpooling to practice. Your family is in our
thoughts and prayers.
--The Brown family
Cheryl, Matt, Thomas and Pugs
2006-07-04
I cannot imagine what your family is
going through, but it is amazing to see how strong you are. I have two sons
(one being my only biological child), and I will always make sure to cherish
every moment with them as one never knows when it may be the last.
2006-07-04
I didn't know Garrett but being a parent
myself I couldn't even imagine losing a child. It's not right children should
never go before their parents. I know people always say that the person is
resting in a better place and we as the parents want to say he/she should be
resting here at home where they belong. But alas that is not
to be but what we can say is that he is no longer suffering or in pain.
My prayers go out to your family and may he rest in peace. He is now on some
playing field running around having so much fun with the biggest smile on his
face.. Just remember his smile and hear his laugh and
hopefully that will help make some of the pain go away... Go in peace Garrett..
--Corinne Inong
2006-07-04
18:26:20 GMT
You may not remember me, but I'm one of
the residents from the PICU in May. I'm so sorry for your loss. I wish that
there was something more that we could have done for your son. Your friends and
family are incredibly supportive and amazing people.
My thoughts and prayers are with you and your family.
--Alison
<mailto:gehlea@peds.ucsf.edu>
2006-07-05
05:39:52 GMT
I'll never forget how Garrett was always
smiling. I am terribly sorry for your loss and pray that you all get through
this.
-Suzie McDonald
2006-07-05
06:19:31 GMT
I am saddened by this and I want you to
know me and my family are here for you.
--Matt Johnson
2006-07-06
03:45:44 GMT
Hello this is jessica and Kelli u
probably dont no us but we are friends of kolton and kari Odle. We are both extremely sorry of your loss.We will continue praying for your family and friends
to help them through this very hard times.
2006-07-06
04:13:21 GMT
I have been following Garrett's
situation and updates since the beginning. You're in the arms of an angel now,
and a wonderful angel he is. Somehow, I hope knowing that can help soothe your
pain. Your family is a courageous bunch. God bless and I'm so sorry for your
huge loss.
2006-07-06
16:59:08 GMT
I have been following Garrett's
situation and updates since the beginning. You're in the arms of an angel now,
and a wonderful angel he is. Somehow, I hope knowing that can help soothe your
pain. Your family is a courageous bunch. God bless and I'm so sorry for your
huge loss.
2006-07-06
16:59:11 GMT
Wednesday &
Garrett had a
rough night on Wednesday, storming and running a fever. His nurse and doctors
calmed him with medications to let him rest. The strategy for Garrett now it to
make him comfortable these next days due to the damage to his brain that was
revealed in the last scan. Doctors can no longer fix or change what has
happened and we are extremely heart broken. His drain was not putting out much
fluid and a decision was made to close it. He was put on a few medicines so
that he does not feel pain or anxiety, but can rest and be surrounded by his
family and close friends. We have been with him throughout the day and night,
with someone always holding his hand and talking to him. His Ipod played in the background, showing what a wide variety
of music and comedy tastes he has developed. The television plays his favorite
movies and TV shows and we share stories about what an incredible person he is.
We will continue to update the web page as time allows.
Thank you to
all of the staff that stop by to see Garrett. The care here at UCSF's Children's Hospital has been amazing and individuals
are too numerous to mention and thank at this time - to Villa Romana for the delicious pizzas Thursday night - to Mike
and David Livingston, JD, Vinnie, John Borba and
family, Sharon and Mikayla Baer, Colin, Beth, Danny,
Ricky, Tony, Connie, Vicki, Jake, Natalie, and Tina for visiting and being
available day and/or night and to everyone of Garrett's friends and supporters
for your prayers and thoughts.
2006-06-30
Comments (11 total)
I am at a loss of words. I love you guys. I have checked this
site everyday since I heard about Garrett. I have kept you in my thoughts. Each
and every time I hug my sweet Eliana I think of you.
The whole Lee side has you in their hearts.
--Monica Plisskin<
<mailto:monicapl@yahoo.com>
2006-06-30 20:47:33 GMT
Garrett has touched us all. Not a day has gone by, without one
of my children asking, "How is Garrett today"? Stay strong, and know
that so many people have fallen in love with your son, and that he has taught
my children to cherish every moment of every day. Out prayers and thoughts
continue, you are such wonderful parents, and he is so lucky to have you.
--Victoria Garcia
<mailto:Victorialee55@hotmail.com>
2006-06-30 23:35:43 GMT
Dear Greg and Family,
I am so sorry to hear about Garrett and what he, and you are all going through.
We'll keep Garrett and you in our prayers.
Scott Laube
PS Garrett - Pole vaulters rule!!!
--Scott Laube
<mailto:slaube@comcast.com>
2006-06-30 23:50:12 GMT
I talk with Collins tonight, my heart is with you and Garrett.. I can't even try to count how many Marines are thinking
about this young over the last few months.. Chesty
Puller will look over this young man, ooohhhhrrrraaaaaaaaa
Martin Hohengger
--Martin (ex-Makita rep)annd Marine
<mailto:mhohenegger@prodigy.net>
2006-07-01 02:35:16 GMT
I talk with Collins tonight, my heart is with you and Garrett.. I can't even try to count how many Marines are thinking
about this young man over the last few months.. Chesty
Puller (God Father of the United States Marine Corps) will look over this young
man, ooohhhhrrrraaaaaaaaa
Martin Hohengger
--(ex-Makita rep)and Marine
<mailto:mhohenegger@prodigy.net>
2006-07-01 02:38:05 GMT
I talk with Collins tonight, my heart is with you and Garrett.. I can't even try to count how many Marines are thinking
about this young man over the last few months.. Chesty
Puller (God Father of the United States Marine Corps) will look over this young
man, ooohhhhrrrraaaaaaaaa
Martin Hohengger
--(ex-Makita rep)and Marine
<mailto:mhohenegger@prodigy.net>
2006-07-01 02:39:56 GMT
Dear Greg and Family,
Our thoughts and prayers are with Garrett, and you, his loving and courageous
family.
- David Root and Marilyn Wolf
-
2006-07-01 04:39:43 GMT
i love you garrett.
and to the fogg's you have
shown tremendous strength in the face of such hardship. i wish i could be there to
do something to help.
--Ben Stone
2006-07-01 14:53:21 GMT
Lisa, Greg, and family,
We are so very sorry to hear that Garrett has gone to join the Lord. His
wonderful smile and spirit will stay with all of us. Our prayers and warmest
embrace are with you.
The Garrison Family
--Doug Garrison
<http://familygforcelobal.net>
2006-07-01 22:24:25 GMT
We are so shocked and heart broken to hear about Garrett. God
must really need more angels in heaven because there doesn't seem to be any
other reason. It is so impossible to know the pain that your family feels and
can only say you will survive even if at times you think you might not want to.
Thank god for all your wonderful time together and know you will meet in heaven
once again. May peace find you on earth one day again!! with
huge love.the farrells
--The Farrells
2006-07-03 05:26:07 GMT
Your strength and courage as a family is truly inspirational.
2006-07-04 08:41:45 GMT
Garrett
finished all of his antibiotic medications and was only on food and fluids with
occasional meds for blood pressure and fever. Not having seen signs of response
as before surgery, we were worried about this change. The CT-scan revealed a
new and significant area of injury/bleeding to the right side of Garrett's
brain and created a difficult situation to face. We met with a large staff of
doctors, neurologists, neuro surgeons, nurses, and
other support personnel to decide as a team as how to approach this new
development. No surgery will be able to improve his condition and his state of
consciousness may remain as he is right now and potentially
worsen. Right now, the plan is to provide as much care for
Garrett as possible so he can remain comfortable as we work through this
phase. Garrett's strength and will to fight continues to
impress everyone.
Special thanks
to his nurses, Erika and Shauna, to Robin of Compass Care, and to our
Social Worker, Maria. We appreciated all of the staff that made extra efforts
to attend the meeting, and especially to Dr. Li who came back after hours to
talk with us and reflect on the past weeks. To John Borba who stayed up much of
the night with Garrett as he struggled through his fever and storming, and to
Uncle Marty who did the same. Thank you also to all of you who continually
check for updates and send messages. We have made it through this tough time
because of the support, encouragement, hope, expertise, and prayers of so many.
2006-06-28
Comments (6 total)
Lisa, Greg and Leanne,
My heart is with all of you. Many a tears have been shed in your behalf as I
have read each day of the love and care you have given to Garrett. You are all
amazing! Your family continues to be in my prayers and in my thoughts as I
check numerous times a day for updates on Garrett. A hug is being sent your
way. Love, Rachel Allred
2006-06-29
I feel compelled to write and express my thoughts with you all.
I got Garrett's name from a Weight Watchers chat room and I have been following
his progress for about a month now. I continue to offer prayers and good
thoughts towards Garrett and your family. You all are such pillars of strength
and I have belief that Garrett will thrive. Thank you for your daily updates, I
check a few times a day to see how he is doing. God bless you all...Christine Prothero
2006-06-29
Dear Greg, Lisa, Leanne and Garrett,
It meant a great deal to me that I was able to come and spend time with all of
you on Garrett's last days. You're an incredibly strong-willed, courageous
family. Greg and Lisa, you two are wonderful parents, you did what has been the
best for Garrett, there was nothing more you could
have done. Don't second guess your actions, what is happening is the way that
God intended it to be, please keep faith and stay strong, Garrett needs your
strength the find that happier place, and as you both said, he feels no pain.
Love and best wishes are continually being sent your way from all over. Your
family has been a personal insteration to me and no
matter what Garrett will always be with me, nothing can change my love for him,
and his strength and memory will always remain with me. His heart-warming smile
and contagious laugh will be one of my fondest memories. I love all of you,
more than words can explain; thank you for your continual support, I hope to
return the strength. I hope these next couple of days will be peaceful for all
and I hope Garrett with remain comfortable and will find happiness.
With all the love in my heart,
Natalie Pearce
--Natalie
<mailto:cheerleadinchiq@sbcglobal.net>
2006-06-29
As a PICU nurse in
--Tiffany Lord
<mailto:TLord@att.net>
2006-06-30
Dear Greg, Lisa, and Leanne, I have tried to type something for
the past 15 minutes and cannot find any words to offer the 4 of you any
comfort. You have endured more in the past month and a half than I could ever
endure. Garrett continues to fight valiantly despite an infection that won't
leave him alone. I could only wish peace and comfort for your family. You are
in my prayers constantly. I hope that Garrett is in no pain. Much love to you
all. Debbie Fladseth
2006-06-30
Do you think Garrett's meningitis may have been caused by
injury? I feel this may be more common then they know. I am so sorry for your
loss. My prayers are with you.
--Thia
<mailto:clsund@cox.net>
2006-07-04
This day went
much the same as the one before with Garrett showing some signs of wakefulness
while he slept most of the day. He would open his eyes wide but did not appear
to focus on someone for very long or respond to stimuli like before the last
surgery. Physical Therapy happened in the morning with movements to his
shoulders - he didn't like it and stiffened up. Slower movements to the arms
and wrists, feet and legs did work well on loosening him and getting him to
relax. Later in the day another CT scan was taken to look at some questionable
areas around the right ventricle that showed up on the last sonogram on Sunday.
The scan revealed that more bleeding had occurred on the right side a few days
prior, most likely because the original infection had weakened vessels. With
this new information it was agreed that we would meet as a team on Tuesday to
discuss changes in treatment and what this means for Garrett's chances of
recovery.
Thank you to his nurses: Erika and Sheila. It was good to see Uncle Marty and
John Borba visit us and stay the night. More family from out-of-state are due to arrive this week.
2006-06-28 04:35:30 GMT
Saturday, June 24 &
Garrett
continued to calm down after the impact of the surgery that left him storming,
with a fever, and awake for long periods of time. This weekend he did manage to
sleep and by Monday morning showed more signs of being awake on his own. His
awareness of us has diminished somewhat and we are hoping that it is only a
temporary setback because of the event. Although his fevers continued, there
were no signs of infection, which is good. The drain was lowered to work more
aggressively and keep his pressures down. That device is to be used for a few
weeks before re-evaluating it's need and either remove
it or put in a permanent shunt - either has to be done before leaving ICU. The
swelling in his face and head increased over the weekend and is now slowly
lessening. An ultrasound was done to check on the size of his ventricles -
noting that they were not increasing in size, but are still large. A CT Scan is
scheduled for Monday or early in the week to get a more complete view and
better understanding of fluid inside his head. Greg has been working on setting
up visits for rehab facilities that we hope Garrett can be admitted to in the
next month or so, and remain for two to six months. One facility, specializing
in neurological injuries has already visited the hospital and is
looking into admitting him for care as soon as he is released from ICU and
medically stable. Garrett's Uncle Marty from New Jersey arrives on Monday
and Uncle Chris and his family are planning on driving out from Texas to visit
very soon.
Thanks to his
nurses: Hannah, Amy, and Robyn as well as Keith, John, and other nurses who
helped throughout the weekend. Also - to the Neuro
Surgeons (Drs. Gupta and Dr. Sanai) and staff for
continuing to follow and treat Garrett in hopes that he can recover and regain
as much functioning as possible.
2006-06-26 19:53:04 GMT
Comments (2 total)
Tell Garrett that I know he will pull through, because he is one
of the strongest guys I know. I know rehab will be really hard, but I know you
will get through it.
Your friend Jordan
--Jordan Kunde
>
<mailto:jordan14jk@yahoo.com>
2006-06-27 02:17:40 GMT
moo.
--bob<
2006-07-03 06:23:27 GMT
Garrett
continued to recover from the sedation used during the Thursday surgery.
His storming went on but in a much less intense form. He remained awake for
most of the night and day, resting and sleeping for only short periods of
time. While waiting for the placement of another feeding tube he went
several more hours without nourishment, except for fluids. As the sedation was
wearing off and he was returning more to how he was before surgery, we noticed
that he had not been coughing which caused secretions to build up in the back
of his throat. The evening nurse needed to suction him and pay special
attention to his airway that was also being blocked at times by his tongue. By
early Saturday morning, he began small coughs again, which we hope will
continue so that he can maintain his own breathing and keep a safe airway. The
drain helped to keep his pressures at a safe level, and the G-tube has been
used for medicines, not yet for food. An
ultrasound was done to check the size of his ventricles and x-rays were taken
in the evening to verify proper placement of his feeding tube. Nurses
began using the feeding tube early Saturday morning. Leanne and Mikayla stopped by to see him and spent extra time with
Greg, enjoying the stores and having lunch together on Irving Street.
Thanks again to
his nurses: Winnie and Erika and to all the staff that helped him throughout
the day. Also - we do read your messages and appreciate your taking time to let
us and Garrett know that you are following his story, caring about him, and
hoping for his best recovery. Good luck to Garrett's friends, the decathletes:
Paul, Chris, and Jake who are competing at the US Track and
Field National Outdoor Championships Friday and Saturday.
2006-06-24 20:50:46 GMT
Comments (1 total)
There isn't a day goes by, that we don't check on Garrett's
progress. He is a part of "Our Family" now. My children ask daily how
Garrett is doing, and we look forward to hearing from you, and praying each day
that he is improving. Looks like are prayers are being answered, and we all
continue to pray for Garrett and his family. Since the early days of his
illness, just look at how far he has come ! What a
handsome young man he is !! I realize it has been a
long journey, but the outcome will be all that we hoped for and more !
--Victoria Garcia
<mailto:Victorialee55@hotmail.com>
2006-06-25 14:50:05 GMT
The morning before surgery Garrett was again showing some
improvement in his abilities to respond - he would look and turn toward the
person speaking, moving his arm when propted and
reacting appropriately to stimuli. The operations: to put in a G-tube for
feeding and to put in a drain for his left ventricle which was holding fluid, went well. They had to place Garrett under sedation
and set him up on the respirator once more. When he returned, he was breathing
on his own and still slightly groggy. A few hours later he began reacting to
the sedation from anesthesia and started his storming episodes. Although this
was expected, we were unaware that he would go through the same type of
"rewiring" activity that he had done coming off of the sedation weeks
ago. Garrett was not hurting himself, but for staff and parents it was difficult
to see him struggle. His heart rate, breathing rate, body temperature, and
blood pressure would rise, and he would tighten up
until the storming episode was finished, then he would be able to calm
down and return to normal. For several hours throughout the day and into the
night it continued and by morning it was less intense. The tube that was put in
is already in use for medicines. The drain is working to relieve pressure in
his head and will hopefully give Garrett time to get back on track and maintain
his own pressures without help, or the need for a shunt. We hope to see Garrett
continue to respond and improve after this short "pause."
Special thanks to his nurses: Kali and Winnie as well as Dr. Tina (who stayed
with us through the storming) and all the staff that helped out yesterday.
Thanks too to Dr. Conrad Epting for his
professionalism, expertise, genuine kindness, and natural ability to remain
calm during stressful situations. We appreciate everyone.
2006-06-24
Comments (1 total)
Lisa and family, just wanted to let you know that I'm checking
site regularly and sending many healing thoughts for all of you. Wish I could
do more!
--Shirley Spina
A few new things happened today - Garrett's feeding tube was in
place to be used for both medicines and foods. He had a visit from the Physical
Therapist who moved his legs really well and worked on flexing his feet,
ankles, knees, and hips. He had a visit from the Occupational Therapist who
moved his arms - hands, wrists, elbows, and shoulders. You could tell that the
moves with his shoulders were uncomfortable because he appeared very distressed
and moaned loudly. The orthopaedist came and put new
splints on his feet which will work on his achilles tendons to stretch them back to normal. The
rehab doctor came and had him respond to some quick tests - he seems to be
making slow progress, but is improving, showing signs that he can follow simple
directions, remain awake and alert for longer periods of time, and look at
people that are talking to him. He is still very confused and slow to react,
but we will take the small gains. His breathing continued to
improve and at night he even slept more calmly, needing to do very
little to manage his secretions. He is adjusting well to things, and we hope
that he reacts and adjusts quickly after surgery on Thursday. Thank you to his
nurses: Shauna, Alex, and Jen and to the PT, OT and Ortho staff who worked well
with him and taught us how to help him too. Again, we appreciate your Comments,
photos, and checking up on Garrett. He is a fighter and continues to impress us
all.
2006-06-22
Comments (3 total)
Hi Lisa and Greg, The pictures are truly wonderful. I am so glad
that he is getting stronger and is ready to begin therapy. Are the therapists
teaching you how to do the ROM exercises and achilles' stretches? I hope so, but remember to
approach the therapy slowly so as not to overwhelm him. He has been through
quite a bit the last 5 months. Kristin and Doug are taking the boat out this
weekend and would like Leanne to join them. So proud of
Garrett. Love, Debbie and Doug Fladseth
2006-06-23
We are so glad to read of Garrett's progress. Please be mindful
that rehab requires much patience and faith...often it seems like two steps
forward, one step back. Remember we are all still praying for you and Garrett.
He will make great progress, we're sure! Love from NJ.
The Regan clan
--The Regan Clan
<mailto:cor52@aol.com>
2006-06-23
The journey begins...Polly H
2006-06-24
We moved along
this day with Garrett continuing to "manage his fluids" by doing a
lot of coughing and swallowing as he was getting used to breathing. Without the
suctioning happening, he is more calm and you can see
a more relaxed look in his face. Supportive oxygen was cut back and disconinued early Wednesday morning. On this day we met
with several staff members in the ICU to decide on a daily schedule of events
(physical therapy, occupational therapy, cleaning - body and teeth, breaks, fun
time - movie or music, visits, sleep, etc.) and a routine for visitors and
people to follow when they talk to or help Garrett to recall information,
events, familiar faces... Things moved ahead with Thursday's surgery plan for
the G-tube and now to put in a drain on the left side of his head to control
fluid in his ventricle. At this time we are not planning on the trache as he keeps breathing well without support. He takes
rest periods, but is doing well being awake ! for lon ger
spans of time. And - he has become less critical, not needing one-on-one care.
Now his nurses have two patients. Thank you to his nurses: Adrian and Fatin. Thanks also for the Comments and emails regarding rehab and long-term care for patients
in his condition. We are still focusing on getting him the best possible
therapy and chances to reach his potential of recovery and every idea helps. It
is so nice to read your messages and see your photos - they keep us going when
times get rough.
See Below for
the caption to the following pictures! And thanks for checking in!
2006-06-21
Comments (1 total)
Wow. What a thrill for all! I have never seen a look more
intense. And loving.
Bob Thompson - ProgramParentUntied
--Bob Thompson
<mailto:grtmd@aol.com>
Great Job
Garrett!
Pictures!
Here are pictures of Garrett
taken by the UCSF nursing staff during his most recent success of removing his
breathing tubes just yesterday. Garrett was scared at first, but
"locked-in" eye contact with Mom/Dad to help comfort him through this
process and really impressed the whole UCSF staff by breathing on his own for
the first time in 5 weeks! -Way to go Garrett!!!
2006-06-21
Comments (7 total)
Dear Greg & Lisa...I check into this
website every day to see how Garrett is doing. It is so inspiring to see the
strength, determination and courage ALL of you show to all of us who are
rooting for Garrett's recovery. I am very proud of all 4 of you and am proud your are my step-brother. I pray every day for all of you
and hope that Garrett continues his amazing progress.
To all of the Fogg Family friends...what a blessing
you are to this wonderful family. Way to go.
--Marci
<mailto:mvonfeld@sonomacourt.org>
2006-06-21
Greg and Lisa: Was great to see Garrett.
We are keeping all of you in our thoughts and prayers. Thanks for the daily
updates. Take Care-The Hartz Family
2006-06-21
This is such good news!
I check the site everyday to see how Garrett is doing. I am looking forward to
the time that he can receive visitors :)
Please let me know if you need any help with anything at all!
--Monica Plisskin<
<mailto:monicapl@yahoo.com>
2006-06-21
Garrett looks amazing! Thank you for
sharing these wonderful pictures. You can see the tremendous amount of love
between you. He is a great person with a huge heart and you are an amazing
family. You are always in my thoughts-
Shellie, Zac and Taylor
--The Olson Family
<mailto:sztolson@sbcglobal.net>
2006-06-21
Lisa and family,
Thank you for the updates. Our thoughts and prayers are with you. Ken and Marcy
Collins
2006-06-21
YAY! Garrett im
so proud of you! you have been in my thoughts and
prayers everyday and will continue to be! i
miss you and love you buddy!
love,Kelley
2006-06-22
It is so good to see Garrett looking at you.I am so proud to call you guys
family.
Love, Diana
Garrett
continued to breathe on his own and after the first few hours, began to take
short naps and waking to clear his mouth and throat. We watched all his vital
signs during the evening and it seemed as if he was a lot more
calm and comfortable, breathing rate was normal, and oxygen uptake too.
A blood pressure medicine was removed as he showed he no longer needed it;
storming has not occurred in a while; he was able to look at us for longer
periods of time, especially when he was breathing on his own again, and seemed
to recognize our voices; he still needs to improve his purposeful responses
though, as they are minimal at best, and inconsistent. Even though he moves his
arms and legs somewhat, he is not ready to purposely move or show us that he
understands. We are working with him and hoping that this will improve over
time. We are looking for rehab facilities that take children or young adults
his age, who will intensely move him forward if
he does not meet requirements/qualifications for hospital rehab. In the later
evening, a new feeding tube was put in and used for some medications, but will
need to be removed and put back again due to its placement. In all, Garrett had
a great day - really triumphed over questions as to what he could handle and
may now be able to avoid the trache on Thursday.
Thanks to his nurses: Kali, Carole, and Sheila...to Dr. Li and Dr. Epting for believing in him...to the RTs
who made sure he was OK throughout the whole transition, and to the crowd of
staff who watched and cheered his big accomplishment. He looks so good. Thanks
again to the Baer family for taking care of Leanne and helping her with college
paperwork and everything else she needs.
This morning,
Garrett was still resting when doctors again tested his cough and gag. It
was difficult to see him go through the testing, but he did well and was later
put on oxygen, and off of the ventilator. Blood gasses tested fine and the plan
went ahead to remove the breathing tube, allowing him to breathe on his own for
the first time in over 5 weeks. A pretty intense and scary few moments after
the tube was taken out were followed by some mouth suctioning, coughing, and
finally noisily breathing on his own. As I write this
he has been doing well for the first 30 minutes and it is an emotional pleasure
to see his mouth and little face again. Greg has been there, holding his hand
and we have both been talking to him, reminding him that he knows how to do
this, how proud we are of him, and how handsome he is. Still needing to wait
and see, we are hoping that Garrett continues to manage his mouth fluids ,
stays calm, and can breathe on his own from now on.
2006-06-19
Comments (3 total)
hey, it angelo domitri-
tell garrett when you gett
the chance that he is my hero, and always will be. he
is a fighter, and i wish i
could be as strong as he is.
2006-06-20
Hey you guys.
It sounds like Garrett's improved a lot. I'm really glad to hear that. He'll be
fine in no time. I have faith in that. Even though I'm not religious myself, I
still think about Garrett before I go to bed and hope that his condition
improves more and more. I also wanted to wish Mr. Fogg
a belated Happy Father's Day =]
--Hannah Escallier>
<mailto:proud2bashorty14@yahoo.com>
2006-06-20
Dear Lisa and Family,
I'm so glad that Garrett is breathing on his own. That is a really joyful
thing. I continue to keep you all in my thoughts and wish for peace in your
lives.
Love,
Mauri
--Mauri Fox
<mailto:edfox@pacific.net>
With Saturday
having so much activity, Garrett decided to take most of the day and night to
rest and sleep. He has adjusted well to all the lessening of interventions, and
today showed doctors that he had a decent gag reflex. More coughing has been occuring with the breathing tube, and suctioning has become
more frequent and irritating to him, causing him to tear up at times. We are
looking into giving Garrett the chance to breathe on his own before going
through with the trache tube surgery. Also on this
day, the Borba family stopped by and gave him a gift so that he could play his Ipod music in the room. Familiar voices, sounds, faces, and
movies are part of the days now so that Garrett can begin to remember as much
as possible. Jake and his mom Amy came down to talk to him and before leaving,
were able to see him with his eyes open, looking around. Leanne drove down to
the hospital for Father's Day to spend some time with her dad. Later in the day
we went to dinner at Villa Romana on
The day began
relatively quietly with Garrett calm and focusing more on people talking to
him. He showed slight movements in his arms, legs, shoulders, and neck that
continued off and on throughout the day. Other support (Foley) was removed and
he took a little while, but again, adjusted well even though some concerns were
raised about his ability to do without it, considering his neurological state.
He had another IV line removed from his hand since he is
needing less and less medication. At some points in the day he
became agitated, but the episodes were short. He is doing less shaking, and
when stiffening up, can relax with gentle touching and moving of his joints -
this brings down his blood pressure too. The breathing tube is still in place
even though he is breathing without it; the suctioning required at times is
very irritating, gets him mad, and in response, he will sometimes bite his
tongue; he has a good cough. W! ith
the drain being clamped early in the day, a CT scan was scheduled for Sunday to
check on the left ventricle area and be sure he is draining fluids properly.
After viewing that, we will be able to compare areas of injury to prior scans,
see how he is progressing, and either make changes to or continue the plan for
his recovery. It was nice to see Grandma and Grandpa Fogg-Vonfeldt
who came by later in the afternoon - Garrett looked in their direction when
they talked to him.
Thank you and
good luck to the National/District Elementary Physical Education Teachers of
the Year (Krista, Gwen, Holly, Carol, and Sue) for the gift, and who will be
presenting at the annual TOY workshop in
2006-06-18
Comments (2 total)
Lisa,
You, Garrett, Greg and Leanne are in my thoughts and prayers. May the road to
recovery be filled with more "good" days than "bad".
Take care, Susan
--Susan Clark
<mailto:clarksusan55@yahoo.com>
2006-06-19
HI Lisa and Greg,
we are glad to hear of so many improvements. Doug is giving John Borba some See's candy to give to the nurses. They are true angels and
we wanted to give them something from Garrett's friends. Kristin is working
full time during the week, but is available on weekends and weeknights for
Leanne. Does Leanne need rides down to see Garrett? We are available. OUr continued love, support and prayers for you. Love, debbie
--Debbie Fladseth<
This was one busy day. Garrett had a lot of
attention, beginning with some deep suctioning of his breathing tube - it took
out a lot of junk and helped him to breathe easier throughout the night and
into the next morning. He needed two units of blood; had a special x-ray to
view his stomach before the g-tube surgery next week (this required ingesting a
white fluid); had two ultrasounds - one to check on his kidneys and the other
to look at the size of his ventricles in his brain (to be sure they were not
getting bigger since raising the drain level to 15 and expecting his body to
regulate fluid levels). He began running a fever that went up to 104 before it
abruptly came down to normal within an hour or so. It went up again slightly
during the night, returning to near normal once again. As far as responses - he
is still able to do very little on command; we know this is an incredibly slow
process, but at this time, Garrett would not qual! ify for rehab programs according
to guidelines and in this condition. We work with him all day long and notice
small improvements and new movements at times. His storming episodes have
pretty much ended. Only short bursts of aggravation occur (like when getting
suctioned) that cause trembling and his blood pressure to rise. We appreciate
the help and guidance of the neurologist and neuro
surgeon teams who evaluate him each day and give us information about how to
test his progress and understand his current condition. Again, we are focusing
on helping Garrett to improve his abilities to respond, interact, and reach a
level of brain activity that will allow him professional rehab opportunities.
Thanks to his nurses for the day: Robyn and
Sheila, and to Irene Borba, who came down and helped out watching Garrett
during the night.
2006-06-18
Things continued to progress
as Garrett is to become less dependent on medications and interventions on his
road to recovery. He is getting more stable, but is still in critical condition
and needing a lot of attention and tests. He had a relatively quiet morning, a
small period of storming, and a pretty quiet night. His neuro
doctors moved up his drain to see if he could manage his fluid (doing well
after slight swelling); He continues to be fed through the tube although their
are some concerns about his "absorbing" enough calories and nutrients;
Responses are there, but still very slight and depending on his mood; His fever
is becoming more under control. The plan now is to keep pressures in check
through weaning medicines and monitoring; to keep him on the ventilator, but
just for spontaneous support (he is pretty much on his own); and to keep track
of improvements that allow him off of ventilation - coughing, gaging, and and breathing on his
own (this is very close too). He is also trying to swallow. The surgeries next
week will be to insert the trache tube and g-tube and
he is being prepared for that. We are talking about pediatric rehab centers and
will start our research as soon as possible. Lots going
on...each day is busy.
Thanks to his nurses: Robyn and Sheila, to Dr.
Li (who is always patient, thorough, and professional), to Carolyn (neuro nurse practitioner) who stops by daily to check and
walk us through the process, and to the entire staff here for their willingness
to "never give up" and do whatever it takes for Garrett.
Today Garrett
continued on in the same way, showing small signs of recognizing voices and/or
faces of his dad, mom, and sister. He is still not moving his arms or legs
intentionally, just while shaking or tensing during the episodes of storming
which have become more tolerable. He looks around when his eyes are open, but
does not seem to focus attention. His blood pressure is being treated
throughout the day. He is nearly off all sedation medication, and is tolerating
breathing with almost no assistance from the ventilator (although with the
lessening of sedation, you can tell his frustration with the breathing tube).
The feeding tube became blocked again and a new one had to be inserted - right
now it is working fine. Since Garrett's current condition seems to have
stabilized, plans are to do a trache and G-tube (for
feeding) next Thursday, to allow for ease of care, and to look into
the best possible long term care programs and rehab for children in his
condition. We are still very hopeful Garrett's condition will improve
significantly in the rehab phase of his care.
Thanks to his
nurses: Winnie, Jen, Hannah, and Rachel, and to Jake (2006 NCAA Decathlon
Champion), Tom, and mom Kit Arnold, Tony (who brought Garrett's yearbook), and
Connie - our best neighbor.
2006-06-15 23:21:19 GMT
Comments (1 total)
Hello, Lisa, just wanted to send love
and support, from one mom to another. You have our continued prayers, thoughts and caring.
--Carole Regan and family
<mailto:cor52@aol.com>
Garrett began
his day with short periods of storming even though he was amazingly tired from
being awake all night. He showed a great ability to gag when he vomited up the
food that was sent to his stomach through the feeding tube. Greg was right
there and nurses quickly took care of him - cleaning out his mouth and throat,
inserting a new tube, and slowly re-introducing food. His fevers continued
although not peaking as high as before. The ventilator was adjusted to give Garrett
more of a workout and expect him to breathe more on his own - he did well. He
senses our being there, calms down with soft touch, and will let you know when
he is irritated. Our afternoon meeting was thorough, and covered aspects of
Garrett's scan and injuries, answered many questions, provided insights into
his progress and responses so far, and informed us of his long term care,
comfort, and needs. The entire team of specialists, doctors, nurses, and other
hospital personnel from the many areas were impressive, professional, and
supportive. We admire their wealth of knowledge and appreciated their time and
willingness to continue to do whatever they can to help Garrett improve.
Special thanks
to today's nurses: Alex, Winnie, and Hannah for taking care of all three
patients (Garrett, and mom and dad). Leanne came down to spend a few days with
us all - thanks to John and Irene Borba for driving and being around during the
difficult time.
2006-06-15
Garrett took a
pretty good nap today, resting for long periods in the morning and throughout
the afternoon. By early evening though, he was up, and stayed up the whole
night - not really storming, just wide-eyed and awake with short bursts of
activity. Some of his medications continued to drop while others were added to
prevent withdrawal effects, muscle fatigue, and other infections. His blood
pressure is more under control; fever still spikes at times; he moves very
little; he shows small signs that he recognizes voices. The plan is to continue
treatment and allow Garrett to move forward, progressing and improving as
far as he can in spite of his injuries and current condition. His nursing staff
was wonderful today- Elizabeth and Shauna.
Special thanks
to Nurse Shauna who has to be one of the most considerate and caring people in
the world - going out of her way to make us (Lisa and Greg) feel
important and special. It was nice to see work friends, Vinnie,
Dan, and JD last evening and hang out for a while.
2006-06-14
This was
another day, with Garrett transitioning through times of quiet and sleep, to
moments of storming. It seems as if he is able to sleep for longer periods of
uninterrupted time while struggling/storming episodes, although intense and
still with a high fever, were shorter in duration. The doctors have adjusted
his medications to keep blood pressure down and at the same time, lowering
his dosages of pain and anxiety drugs each day. Garrett is now
completely on the feeding tube and has adjusted well; is breathing on both the
ventilator and on his own; is still receiving antibiotics to deal with
infections. Concerns still surround the results of his last CT scan which
indicated injury not only to the left side of his brain, but also to the right,
because of the initial infection and it's spreading. We will meet again
with the team on Tuesday to decide on changes in treatment (if any), and to
review signs of improvem ent, stability, or damage. Thanks to his nurses:
Elizabeth, Fatin, and Shannon.
Thank you to
all of the students at Washington School who made cards: to Mrs. Schwan's class for the lovely book (that was incredible to
read), to Mrs. Romain's class for their letters, and
to the staff at Jefferson School, for their generosity. We read your web
page Comments each day and it
helps to keep us upbeat, feeling cared for, and hopeful.
2006-06-13
Today had its
ups and downs, but was relatively a better day for Garrett. Early hours were
more difficult as he went into storming again and spiking a fever (104+). The
rest of the day was much calmer, allowing him more rest and less stressful
periods of activity. For Garrett now, the plan is to continue to lower his
dosages of medications and monitor his ability to wake up and recover from the
initial injury/infection. Another meeting is planned, with the Neuro Surgeon team, doctors, and Neurologists, for
Tuesday - to evaluate his progress and make any necessary changes. Only a few
IV bags remain; he is fully on the feeding tube (which gives him better
nutrition and protein, and allows his body to maintain its strength and work
more efficiently); he is getting Tylenol and Motrin for his fever; his tremors
have developed more of a pattern and he is being left to rest during his
quieter times. A nursing "team" has been estab!
lished and specific
guidelines for taking care of and monitoring Garrett are in place. Thanks to
his wonderful nurses: Alex and Shauna. We appreciated the time the entire staff
spent in the meeting, going over his progress, answering questions, and
planning for the days ahead.
Special thanks
to Mike Livingston for posting pictures of the MCHS graduation - we were sorry
to miss it, but felt like we were there. And to Mrs. Gebb and her class for the heartfelt cards and gifts.
Garrett had a
relatively calm day, beginning to open his eyes more and yawn, (nurse Kali
was really looking out for him and made sure he remained
stable) up until early evening when he began to "storm" - high
blood pressure, elevated heart rate, breathing rate, and increased swelling and
body temperature. It lasted a few hours with the nurses doing their best to
protect him by administering medicines to calm his pressure and fever. His ICP,
pressure in his head, was again maintained to safe levels. For most of the late
evening he was calm and rested. Shannon (his nurse) did everything to keep
the room quiet and Garrett comfortable. Early in the morning Saturday, another
storming episode happened, lasting for hours. The CT scan revealed that there
were no more new pockets of infection, that swelling is occuring
because of this "weaning" process, and that some damage has been
noticed on the right side, due to t he prior infection area. Doctors are aware
of his condition and communicated that he will have ups and downs as he
continues to use less and less sedation and medication. His brain is now
reacting to the initial trauma that happened four weeks ago. Uncle Curt, from
Jersey, arrived Friday night and will be here for several days.
Thank you for
checking up on Garrett, for all the cards and help, and prayers. He is fighting
through this tough time. Special thanks to the band,
2006-06-10
Comments (2 total)
Dear Lisa and family,
Thanks for the daily updates. As I start my summer vacation I will have more
time to think and pray for Garrett. I'm here if you need anything.
Love and Peace,
Mauri
--Mauri Fox
<mailto:edfox@pacific.net>
2006-06-11
Lots of love and prayers from the Farrell Family: Mick, Streeta,Max and Shane. We were
shocked to hear the news from
This was a busy
day. Garrett continued to adjust to the lessening of medications with tremors
and fever. Blood pressure, heart rate, breathing rate all increased while his
ICP (pressures inside his head) were fine. It remains difficult to see him
struggle, but he must go through this in order to wake up and show us his
ability to recover. He now has a feeding tube and is moving slowly from IV
feedings to a better source of nutrition that involve his stomach and
intestines (which are in good working order now). Things take time and he is
improving in his need for medications - the IV bags are being taken away and/or
lightened in dose. Some additional medication are
being given for his fever and high blood pressure to help him while he is on
this bumpy road to recovery. Tomorrow we have another CT scan to check on fluid
collections and areas where changes may have ocurred.
Thanks to his nurses that went above and beyond: Elizabeth, Rachel, and Joe and
to the entire nursing staff for the extra care and consideration that Garrett
is receiving during this time.
Best of luck to
all the graduates! Enjoy your accomplishments and be sure to celebrate with
safety in mind. Never Smoke.
We think the neuro surgeon here was able to best put it into words: It
is difficult when you move from the dark into the light. Garrett continued
to wake up from his sedation and was agitated, spiked a fever, and had many
tremors. Although his heart rate, breathing rate, and blood pressure rose with
each incident, the pressure inside his head remained low/safe. We noticed
different stages of this process and that each one has its own characteristics.
Still with a fever and on less medication for sedation, he is going through a kindof rough period to allow his brain to
"re-wire." This can take several days and may move through more
phases. He is being monitored and taken care of by so many people, and we truly
appreciate their unending care and concern. Thanks to Conrad for his calm and
upbeat way of looking at and handling stressful situations, to Garrett's
nurses, Joe and Robyn, Neuro Nurse Caroline (for
answering so many questions in a comforting way), and to all the staff that
worked with him yesterday. Thanks also to Alex Lepf
for covering at
2006-06-08
Comments (1 total)
Hi Lisa and family. We haven't forgotten all of you for one
moment. Best wishes and prayers continue to flow west. Take care of everyone.
Hope everything continues to improve. Fingers are crossed.
--Holly Gansz
Today began the
lessening of heavy sedation medication. One third was removed from Garrett's
amount. Within a few hours you could notice his eyes starting to flicker and
some muscle trembling. This continued throughout the day and as the second
third of medicine was taken off, he became even more active - fluttering his
eyes, moving legs and hands, and again, trembling. We were up during the
evening trying to calm him since he tried to breathe over the ventilator too
much and even seemed to get a little scared. Wednesday the final third dose
will be removed and we should see some different behaviors. Garrett started a slight
fever overnight and the staff are trying to figure out
why by testing several samples of his fluids. Thanks to his nurses: Keith, Fatin, and Sheila as well as Maureen and Robyn from the day
before.
2006-06-08
Comments (1 total)
Lisa and Greg,
It must be exciting and scary to watch Garrett come off the sedation. I hope
that it goes as smooth as it possibly can. Thanks for the updates. I can see a
little improvement each day. Am praying for more rapid
recovery so that you can feel at peace when Garrett wakes up. The
waiting is certainly the hardest part. Garrett's spirit will help him in his
recovery. That joyful mischievous boy is just raring to come out of sedation. Love and prayers to you and the family. Love, Debbie Fladseth
Garrett had
another quiet day with no increase in pressures. He stayed calm and cool (no fever) and did well when the NaCl
drip was weaned. Tomorrow, staff will begin lowering his heavy sedation and
check to make sure that he is ready to slowly wake up. Removing one medicine at
a time is a long process and we are anxious to move along.
We wanted to
thank our employers: Washington School of Cloverdale Unified
2006-06-06
Comments (4 total)
We met your family while we were in PICU with our Daughter
Rosalie. Greg and I have talked numerous times in the hallways and Cafe. I have
been searching for this blog and am now glad I will
be able to keep up on Garrett's progress without bothering you. We know how it
is.
Our thoughts and prayers are with you!
Stay Strong!
Mark and Carolyn Reibel
--Mark Reibel
<mailto:reibelm@gmail.com>
2006-06-07
I've been checking in on Garrets condition everyday, and it
sounds so encouraging ! Our prayers are working ! Thanks so much for the updates.....
--Victoria Garcia
<mailto:Victorialee55@hotmail.com>
2006-06-07
Hey Mrs. Fogg!! It stinks that your
not here with us these last couple days of school, but we would rather you be
with your son most definatly right now. My family and
I are keeping him in our prayers. Hope to see you next year! ~ Alysia Ramirez
--Alysia Ramirez
2006-06-07
I got this web address from Michelle Larson and just wanted to
tell you that I am thinking of your family and wishing you all the very best
outcomes.
--Bobbee Valentinee
<mailto:BobbeeV@Comcast.net>
Garrett had a
good day with low pressures and no fever. He had another thorough cleaning,
tolerating it well, and without signs of skin breakdown. The plan is still in
place to begin weaning him from his heavy sedation throughout the week,
beginning Monday. Swelling in his arms and torso has begun to subside slightly
and the staff are paying attention to everything. He
is getting compliments on the strength of his heart, lungs, and kidney
functions. Sister Leanne and special "Substitute Mom" Sharon
Baer stopped by yesterday to visit. We appreciate his nurses for the day:
Jennifer, Winnie, and Shelia as well as all the PICU staff who take such good
care of him.
2006-06-05
Comments (1 total)
I am so glad that he is doing so good.
I check here everyday. As soon as he is ready I would love to come visit. I want so badly to give you guys a great big
hug!!!
--Monica
<mailto:monicapl@yahoo.com>
This
first day following the surgery Garrett did really well. His pressures were maintained and even
dropped slightly as the day went on - no fever as well, as he remained nice and
cool. Swelling was noticed around his face, in his arms, and around his body.
The staff helped him through that with an additional medication to help him
release the extra fluid build up from the surgery. He responded nicely and
continues to be monitored for any changes. The plan is to keep him quiet and
calm another day and begin lightening up on his sedation on Monday. That
process of "waking him up" will take another three to four days.
Thanks to his nurses for the day, Veronica and Shelia and again to all the
staff and support at UCSF's Children's Hospital.
Good luck to
Vivian Hernandez, an ICU nurse who is carrying Garrett's photo as she completes
the AIDS bike ride from
2006-06-04
Comments (6 total)
Hello Greg, I am very sorry to hear of Garrett's illness. Our
thoughts and prayers are with you and your family and we pray for Garrett's
full recovery.
--John Haskin
2006-06-05
All of us in the Kunde family are
saying prayers for Garrett every day.All our best ...
and let us know of anything you need.
--Jeff Kunde
<mailto:jeff@kunde.com>
2006-06-05
Dear Fogs, Hello it is Greg Murphy from down in Morro bay. Colin has been keeping me posted on your
situation. I am so sorry you guys are being subjected to this sort of terrible
experience. My heart has been heavy and Susanne and I are constantly talking
about your family and hoping that things will improve. We wish our best and...I
don't know. My thoughts are with you.
Greg Murphy
--Greg Murphy
<mailto:Gmurphy789@aol.com>
2006-06-05
Dear Lisa and family, I think about you
every day. I'm praying for Garrett's recovery and your family's continued
strength. You are amazing. Please let me know if there is something I can do.
Don't worry about school.
Love, Claudia
--Claudia Rosatti<
<mailto:rosattic@admin.cusd.org>
2006-06-05
You are in our thoughts and prayers
everyday. Thank you for generously keeping everyone updated during this
unimaginable time for your family.
-The Olson family
--Shellie Olson
<mailto:sztolson@sbcglobal.net>
2006-06-05
Greg and Lisa,
WE got your message yesterday. WE think of all of you daily. Kristin comes home
Tuesday night and we talked to her today. She said that she will do anything
for you and Leanne. She is welcome to stay with us any time and for any length
of time. Kristin will start a job next week, but is available days till then
and evenings. She will call Leanne when she gets home. WE are amazed at your family';s strength. Garrett is
amazingly strong and his extra fit and young body will fight its way through
this very challenging time. We are here for anything you need. Just ask. love, the Fladseths
Early this
morning, the nurses made sure Garrett was ready for surgery. He was stable and
comfortable. The anesthesiologists came by to take him (Dr. Cheesbro
and staff) safely to the OR. Neuro Surgeon, Dr. Perry
reported that the surgery went as expected with no surprises. He had been able
to remove pockets of infection fluid (that so far revealed the bacteria was not
even visible) and noticed swelling on the right side of his brain was somewhat
significant, agreeing that it was a good choice to operate when we did, in an
effort to prevent damage. Garrett remained stable and comfortable throughout
the night and maintained his pressures. The next 24-72 hours he needs his rest
and quiet so that he can avoid any complications or increases in pressures.
Thanks to the whole team of Operating Room doctors and personnel, his nurses:
Veronica and Shannon, and the entire PICU staff for their continued dedication
and care. Aunt Jenni went back to
2006-06-03
Comments (1 total)
it sounds so encouraging that there is no fever for several
days now- i'm always impressed and grateful for how
nurturing, dedicated, and educated medical staff are... i'm
also glad that you getting so much support lisa.
--candaace
Today was busy,
getting Garrett ready for his up-coming surgery. He was given medicines and
additional blood factors to help him clot as needed on Friday. Four of us
worked together to get him cleaned up from head to toe and check for any areas
of infection on his skin. He looks good; no fever; swelling is going down in
his arms; and a rash he developed appears under control. Throughout the night
his pressures remained stable. Occasional tremors were due to his sedation
levels. All staff continue to monitor him and care
about his condition. We want to thank his nurses: Shannon and Winnie for their
hard work, dedication, and expertise when caring for Garrett.
2006-06-03
Garrett continued to remain stable with his pressures. He is
still very sedated and tolerating his condition really
well and without a fever. A group meeting went over the MRI that showed how
areas of infection were removed from the left side of his brain, while some
still remained on the right. Another surgery is scheduled for Friday morning to
remove the two areas where there are fluid collections. Thursday will be a day
of rest and preparation for the surgery. Thanks to his "team" of
doctors/specialsts/PICU staff - Dr. Soifert, Dr. Perry, Dr. Collins, and his nurses: Jennifer,
John, Alex, as well as everyone who visits to check on him and cares for him
throughout the day. Keep Garrett in your thoughts and prayers for a successful
surgery and recovery.
Special
Appreciation for Kristen Frizzell Kerns, of Hinton, Cochran, and Borba, for taking time to create and update the webpage for
Garrett.
Still in stable
condition, it was decided that Garrett would be able to handle an MRI. Although
the procedure required a lot of preparation and more time than a scan, things
went well. He tolerated the trip and test really well, returning with good
pressure numbers and again, without a fever. Throughout the night, he
maintained somewhat lower pressures and renewed our sense of confidence that he
is recovering slowly. By Wednesday, after looking at the MRI and speaking with
specialists, we will see the extent of his injuries and the challenges that he
may face. His nurses today did an amazing job caring for him: Winnie, Jennifer,
and Shelia. Thanks also to the neuro surgeons,
neurologists, Caroline (their nurse), the PICU staff, Infectious disease
specialists, and radiology team for their tremendous amount of work and care
every day. We truly appreciate the Borba family for their great
support and the Baer family (and friends!)
for taking such good care of Leanne during this uneasy time.
Again, visits
would be better left on hold for a while. Garrett is still heavily sedated and
being observed for signs of improvement. We will have a chance to better
welcome friends in the next days ahead. Thanks for staying posted.
2006-05-31
Comments (1 total)
Hey Garrett and the rest of the family-
I really hope Garrett gets better soon. I had science and Spanish classes with
him last year and he was really nice. He's a good kid and a really good
athlete. Garrett and the rest of the family, I'm thinking about you guys often
and hoping for the best. Get well soon, Garrett!!
-- Hannah Escallier
--Hannah Escallier> (The Canadian)
<mailto:proud2bashorty14@yahoo.com>
Throughout the
entire day Garrett remained stable with his pressures on the higher end of
normal and without running a fever. He continued to be under heavy sedation,
tolerating things well. An MRI will be done in a day or so to check on his
areas of injury, collections of infection, and to see if any medications can be
modified or added so that he can begin the "waking up" process which
was put off for an extra day. His nurses: Kali, John, and Kristen gave Garrett
special attention and care.
Thank you for
all the cards mailed to our home and the many "Get Well" wishes from
the students at
Thanks,
Lisa
2006-05-31
Comments (2 total)
If I know garrett
he'll be "running up"
2006-05-31 05:18:27 GMT
Hi Mrs.Fogg this is ashley, I hope you guys are doing
well and I hope Garrett gets better. We all miss you at school. We all want
Garrett to get better. Thanks for all you've done at school!
--Ashley Rilea
Garrett's
pressures were maintained all night and into the next day. They went up
slightly during an x-ray procedure and remained there throughout the day and
evening. He stayed cool (no fever) and was very stable although his
numbers were on the higher end. Everyone has been monitoring him and taking
great care of his needs. The plan is to keep him under sedation another day or
so, and then see what he can handle. His nurses: Erika, Amy, and John were
wonderful. Thanks also to Shannon for her expertise and help, and to all the
doctors, respiratory specialists, and staff that continually check on him.
Keep Garrett in your thoughts and prayers. He is staying strong.
2006-05-29 21:36:47 GMT
Comments (4 total)
Fogg family:
Garrett is in our family's prayers night and day. I gotta
tell you, when you got Dallin praying for you, good
things happen - he is a boy of incredible faith and God listens to him. Be
still and know that God is.
All our love and kindest thoughts,
The Lowder Family
PS...LeeAnne was the BOMB saturday. We're very proud of her. We love you guys.
--Brad Lowder
<mailto:bradley.lowder@gte.net>
2006-05-30 00:58:38 GMT
Amen to everything said by Brad. Much love
--davidd
<mailto:dliving@sbcglobal.net>
2006-05-30 06:39:31 GMT
Greg, Lisa, Leanne & Garrett...stay strong. You have a lot
of people who love you thinking about you and praying for you. We love you
all...Aunt Marci & Ciara
--Marci VonFeldt
2006-05-30 18:32:32 GMT
Great to hear!
--Dr. Eman
<mailto:drparenteau@hotmail.com>
Garrett needed
to be very quiet and still after surgery to allow his body to recover and to
keep his pressures down. He did very well throughout the day - was stable and
had no fever. The next few days ahead are still very important for his
recovery. As pressures stay low and manageable, he can be slowly weaned from the
sedation; if they rise, it becomes more difficult. He received special
attention from all the doctors that checked in on him, and his nurses: Vivian,
Julie, and Amy. We appreciate all the love and care he is receiving
from everyone on staff.
Leanne did well
in her race - had a PR in the 3200m, 11:10 and finished fifth.
Thank you to
the staff at Cloverdale High and CUSD for your kindness, generosity, and
thoughts. To everyone, we love reading the Comments
on the website and enjoy the photos. Garrett will really appreciate them when
he gets the chance.
Lisa
2006-05-29 04:23:15 GMT
Comments (2 total)
I hope you feel better garret, i am thinking about you alot
lately, get well soon!
-Jake D.
2006-05-29
04:27:51 GMT
We thank you so much for finding time to
post these daily updates. I know that my mom and my sisters check this site
every morning. We are here for you should you need
anything at all.
--Monica P.
<mailto:mom2eliana@hotmail.com>
Garrett's
pressures and temperature improved all night. He was given medicines to prepare
him for a surgery that he underwent that afternoon. A significant amount of
infection fluid was removed and additional drains were put in to help manage
the pressure. He returned from surgery looking handsome and relaxed. We would
really like to thank all the UCSF staff that helped him including: Neuro Surgeons, Dr. Perry and Dr. Sanai,
Anesthesiologist, Dr. Graves, his nurses throughout the day: Joe, Winnie, and
Jennifer, as well as all the PICU support staff/residents, led by Dr. Lee and
Dr. Soifer.
It would still
be best to call ahead before stopping by these next couple of days. Garrett is
recovering and needs lots of quiet time.
2006-05-27
Comments (1 total)
Hey, i am soooooooooooooo
glad to hear that Garret is doin better! i was getting kinda
worried! Anyway, i am still praying for him every
night before i go to bed. I hope you feel better
garret!
Garrett had a
CT scan today and it showed how he was healing and how the infection was still
in certain areas. Because his condition is so sensitive, we would like to ask
friends/family to put visits on hold for a few days. We will still send daily
updates. Keep Garrett in your thoughts and prayers.
Throughout the
early morning hours Garrett stayed calm and with low pressures. Near to
Thank you for
the messages, photo attachments, and your generosity. To the staff at
2006-05-25
Garrett began
the day, again with a fever and some larger numbers in his pressure (ICP). No
scan was done, and the plan is to do it on Wednesday instead. His nurse today
(Elizabeth) worked throughout her shift to get his signs under control and
eventually was able to leave knowing that his fever was cooled and pressure
signs were better. He is again under heavy sedation to allow the antibiotics to
do their best at finding his infection, to let him rest, and to let his IC
Pressure stay down. Visitors today included Uncle Eric from New Jersey, Grandma
and Grandpa Fogg-Vonfeldt, Uncle Jeff, and Zack Reitzel. John Borba had stayed overnight and left in the
morning. Thanks again for all your best wishes for Garrett. I know he
will appreciate them when he wakes up.
2006-05-24
Throughout the
night Garrett again needed some help with the pressure. His fever remained up.
In the morning it was decided to do another CT scan to see what was going on
"inside." The picture showed us information about an area where we
believe the infection is still remaining, and that the inflamation
inside was still a concern, but may be lessening. Another similar, but
stronger antiobiotic will be used by tonight to
better attack his infection. His fever was brought down to normal with a
cooling blanket and a lot of TLC from Rick, his nurse for the day. Garrett's
pressure inside his head also improved and remained low with the medicines they
are giving him to help. We are hopeful. Visitors today included: John Borba and
Colin Davidson (Aunt Denise goes back to New Jersey tomorrow morning and
his Uncle Eric will arrive shortly there after.)
2006-05-23
Garrett ran a
high fever all day Sunday and his pressures were difficult to maintain, but the
wonderful staff worked throughout the day to monitor his conditon,
adjust medicines to keep him stable, and figure out his best possible treatment.
His heart, lungs, and muscles are very strong and healthy and we know
he will fight through this tough time. Visitors included: Garrett's friends -
Ricky, Natalie, Ross, Teresa (Ricky's mom), Juan, Evan, and Jake. Also: Barry
and Amy Chapman, Rich Parchman, Vince Gearing and
Laura Capinas.
Thank you for
all your wonderful messages to Garrett - it is very comforting to see so much
support and love for him. I liked how Max attached a picture of Garrett while
they were on the snowboarding trip. So Coooool!
(Lisa)
2006-05-23
Garrett had a
great day with signs of improvement in his tests. He remained very stable under
his sedation throughout the day. We had many visitors: The Borba Family, Calvin
Trampleasure, David and Mike Livingston, Tye Olson, Colin and Beth
Davidson, and Michael Brew. Leanne (Garrett's sister) ran in her North Coast
Sectional Track Meet, finishing second in the 1600m with a PR of 5:06. Later in
the day she WON the 3200m with another PR of 11:10. Amazing! During the
evening/early morning, Garrett started a slight fever. Medicines were adjusted
to help him through it, and many tests were done to find out why. (He has the
BEST people taking care of him at UCSF Children's Hospital, and we are so
grateful.)
Garrett has
been on medicines to keep him extremely sedated so that his brain and body can
rest. The treatment has been working to keep his brain pressure low and safe. A
meeting with the neurology staff and surgeon gave a clearer picture of
long-term effects on his brain and potential levels of recovery. We want the
staff to continue to all they can to let Garrett recover - an MRI at a later
date will give us more information about how the illness affected his brain.
Garrett had a good night with signs of improvement.
2006-05-21
Garrett has
been stable most of the day but had a few physical reactions while his
sedatives were low and his vitals spiked (he was swinging his arm aggressively
and Mom had to constrain him) plus he blinked after a Nurse asked him to today
(she was cute; we think he was flirting). UCSF care staff are
concerned he is not getting quality recovery time/recommends putting him in a
deeper medically induced state for 48-72 hours to help reduce the
swelling. Full dose kicked in by evening time he was in a deep
resting state with all key vitals showing improvement; except his heart rate
increased a bit. Most of the facial swelling from surgery has gone
down and Garrett is looking more like himself again; he still has good color
and shivers sometimes when the room temperature gets too cold. -No
Visitors today.
2006-05-19
Completed
cat-scan today; showing good signs. Plan was to prep Garrett for an MRI
(Magnetic Resonance Image) to get a better image of what's going on in
Garrett's head, but at the end of the day, the UCSF staff decided this was more
risky than beneficial and opted to delay this process for a few more days. Rest
of the day vitals signs were stable. -Visitors during the day included: Grandma
Karen, Grandpa Bob, Sister Leanne, Michelle Rege and
John/Irene Borba. Noticed Garret was breathing above the respirator
today; Nurse commented all breathing, heart, kidney functions are working great
and Garrett seems like a "real healthy kid" which should greatly help
his recovery.
2006-05-19
Garrett's vital
numbers were steady today with primary concern = keeping ICP steady and
low. BP (Blood Pressure) still is and has been higher than normal for
some time. UCSF staff now confidently identified the infection as a
strep bacterial (non-contagious) strain. -Visitors today included Aunt Denise
(from Joisy) staying for 1 week and Rich Parchman.
2006-05-19
Long night as
Garrett completed two surgeries: left frontoparietal hemicraniectomy surgery, plus installing cathodes to drain
his front sinus cavities then had to be rushed back due to excessive swelling
just after post-op to remove excess fluids + install a "bolt" that
helps measure/monitor pressure via an ICP (inter-cranial pressure) reading.
-Visitors later this evening included ";Uncle" John Borba and Ron Pili.
Transported
Garrett from Sutter/Santa
2006-05-19
Follow-up
2006-05-19
After complaining
about "pain above his eyebrows and on the top of his head," over the
past day or so, Garrett developed a 102 fever and seemed to be getting worse.
We took Garrett back into his Pediatric care office (his first visit was on
Wednesday, May 10th); then after examination was admitted to Sutter Emergency.
After completing several tests including a spinal tap,
was diagnosed with Viral Meningeal Encephalitis and
released to go home under close care, frequent wakings,
and taking Tylenol w/codeine. Garrett had a great night and looked and felt
better.