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Love & Prayers 4 Nathen
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Home | About Nathen | Neuroblastoma & Other Links | Guestbook, Slideshow & Photos | Flyers / Blood Drive / Donations | Contact Amanda, Chris or Nathen | Happy Thoughts Only
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L O V E & P R A Y E R S 4 N A T H E N
"Nathen" October 2007
Our little man has already been through 4 chemo's.


Heart Wishes for Nathen!
"This is my wish for you: Comfort on difficult days, smiles when sadness intrudes,
rainbows to follow the clouds, laughter to kiss your lips, sunsets to warm your heart, hugs when spirits sag, beauty
for your eyes to see, friendships to brighten your being, faith so that you can believe, confidence for when you doubt, courage
to know yourself, patience to accept the truth, Love to complete your life."
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| L o v e & P r a y e r s 4 N a t h e n |
This weblog is our online journal of our little boy Nathen, that you can call "Nathen's
Journey". You'll find personal information that is being logged as often as possible since finding out about our son's
illness, neuroblastoma. There will be links to articles and items of interest on the web that you
may find interesting on the subject.
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2007.10.01
2007.09.01
2007.08.01
2007.07.01

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Wednesday, October 24, 2007
October 24th
Well another post with some not so great news.. Over the past couple of days Nathens has had more problems with his feeding
tube. Monday Night around midnight the tube came completely out of his stomache. It was very painful for him and there were
still stitches on it, which were used to keep it attched to the J-junum(lower intstine) They held him down and put it back
in and said that it would be ok. Then the next morning(Tuesday) The surgery team came in and shut off his feeds and told me
to not let anyone put anything through it til they could do an Xray with contrast to make sure it is in where it needed to
be. Basicly he had his feeds shut off for most of the day. Then around 1 they finally took the Xrays and gave us the go ahead
to turn them back on. But unfotunately they wanted to up his rate and when we did that evening he threw up about an hour later(first
time in about 3 or 4 days) and out came the tube again. SO PEAT AND REPEAT.. Turned off feeds They held him down re-inserted
the tube into his sore infected belly and told us not to put anything through til they did another Xray.. and then about 10pm
they gave us the go ahead again and the doctor left orders to turn him up 5ml by the end of the night and I told them no way..
out of the question... not til the docs came in in the morning and I could talk to them and get a set plan in writing for
everyone to understand and follow. Im not going to sit back and watch my baby suffer more than he has to for no good reason.
If they cant understand he has to go up slowly then I will have to tell them to just put him back on TPN( IV nutrients) and
stop the feeds that are making him throw up and get sick. I will keep you all informed on how things go over the next few
days. His chemo is due Friday October 26th but his counts have to be high enough to start so time will tell.
I want to Thank My mom and My two younger brothers Brad and Bobby for taking up money to set aside for our trip
to New York. I know they were not able to raise as much as they would of liked to of raised, but every bit helps
and they did a great job! Thanks you guys, I LOVE YOU. I also want to thank everyone who donated money, We really appreciate
your help. I hope to find out in the next couple of days about the trip to New York, as of right now I am waiting to hear
from the insurance so I can coordinate the trip and plan it all out. Thanks every one so much. Please pray for his counts
to recover and his next bone marrow to be clean.
Amanda
3:00 am cdt
Monday, October 22, 2007
Quick update
Just a quick note to everyone. Nathen has been feeling pretty bad over the past week or so. He has had alot of pain in
his tummy where they put the feeding tube in and he started having some blood and fluid draining out of it last night. They
changed his antibiotics to a very strong one and said he has an infection in it. His morphine dose has also been doubled to
help him be more comfortable. Over the weekend the surgeons stopped by and we discussed all the problems Nathen has been having
with the feeding tube and the surgeon said that if they cant resolveall of his issuses with the tube they may end up
just taking it out and going from there to figure out about nutrition for him.. so this next week will tell alot about what
they plan to do and Chemo starts again on Friday. Another thing, just want everyone to know that we dont have alot of space
on here to put up photos so I have added them to my myspace page so that everyone can go look at them for now til I can figure
out how else to get them added on here. The URL to my page is www.myspace.com/mandypootoyou . Let me know if you have any problems getting to the pictures
and I will try to rush on getting a photo host or something. Thanks to everyone for all of your continued support through
this rough journey. Keep praying for mommies little turkey...
Amanda
10:20 am cdt
Monday, October 15, 2007
NEW UPDATE ON NATERS 10/15
I want to appologize to everyone for not posting in so long, We have been having a rocky time over the past month.Last
I posted Nathen was about to start his third round of chemo and he was doing fairly well. He had gotten to where he had taken
a few steps here and there for mommy and daddy and when his sissy and bubba (Nicole and Zach) came to visit him he walked
all the way from the family area to our room. He also was licking on foods and chewing the flavor out and spitting it back
out. Then we started his third round of chemo which was 5 days long and he got sick all over again. he stopped walking stopped
showing interest in food and also started running fevers again. After his counts came back up and the fevers stopped we got
to come home for a few days. We came home on 9/27 which was a Thursday. Thursday night Nathen would not stay put, did not
want to be inside.. he wanted to go go go, so I bundled him up and we went. We drove around for a while and around midnight
we went to grandmas house and visited with grandma and grandpa, even though it was late they were both excited to see Nathen
up and feeling so much better. After about 2 hours at grandmas house Nathen was pointing at the door again and was ready to
go go go again. So we went, and we drove some more. When we got home we sat in dads recliner til about 4am when he finally
passed out.On friday I mentioned to dad that I wanted for us to take Nathen down to Lawton to visit his family and to get
nathen OUT while he can. dad and I both agreed that, going down would be a great idea as long as everyone knew that if they
had been sick or have been around someone that has been sick to not come visit for Nathens sake. I called Aunt Kathy and told
her what we wanted to do and I could hear in her voice that she was excited about us coming down with Nathen. Friday night
Nathen once again wanted to go go go.. so I once again drove drove drove..We drove around for a bit then stopped by grandmas
again but Nathen started to point at the door again wanting to go.. so we drove around for a while more and then I decided
to go to walmart and walk around with him to save on gas and maybe get him to pick some food out that he would want to eat.
Dad called us around 3:30 to make sure we were ok and to see how come we were not home yet.. told him that when I asked Nathen
if he wanted to go home he shook his head no. After walmart we went home and Nathen finally passed out about 4:30am. On Saturday
we went to see everyone in Lawton , when we got to Aunt Kathy's house she came out to greet us and Nathen was excited and
smiling but as soon as she opened the door to get him out he started crying and realized we were not going bye bye anymore..
We went inside and Nathen was not happy with anything.. I took him back into little Roberts room to try to get him in playing
and he was shaking his head no.. then Robert started playing peek a boo with him and he started to smile... Then Robert started
beating his toys up and Nathen was belly laughing at him.
We came home around 6pm on Saturday and that night Nathen actually wanted to go to bed with mommy and daddy instead of
sleeping in the recliner (wheew). The recliner is comfortable but Nathen has had tubes coming out of him and I was affraid
of pulling out the tube or hurting him so needless to say I sleep very uncomfortable in the recliner. Sunday we cooked dinner
and Nathen sat at teh table with us and tried to eat with us, he was very interested in dinner which was a great sign. After
dinner we loaded up to go back to the hospital to get all his pre op stuff taken care for surgery Monday morning. Nathen screamed
for like 3 hours straight wanting to leave and not be here at the hospital. Finally the doctor caved in and gave him something
to help relax him but it wore off after an hour and then he started again. I called Chris and he came back up here and we
walked around with Nathen til he fell asleep. I was sooo glad that dad came back to help us. I was a mess watching my little
man cry and not be able to help him and calm him down. Monday Morning 10/1 he had his surgery and when he came out of surgery
he was in the recovery room when dad and I came in he was crying mamma mamma. I went over and grabbed him and calmed him down
the best I could. Then I handed him to dad to hold so I could go prepare his bed and room for him since we had moved to a
new room while he was in surgery. The next day they started his feeds through his J-tube and the doctor wanted him up to 35ml
an hour by that night, which is not alot but when you have not processed anything through your digestive track in over three
months it is alot. By that night when they got him up to the 35 ml he was puking and puking and had diarhea. I tried to tell
the doc the next morning that it was too much too fast but she ignored me and told them she wanted him up to 45 ml by that
night.. Well for the next several days Nathen was as sick as can be and was throwing up and pooping on average 12-15 time
per day of each. I was at my wits ends with these doctors not listening to me and me watching my baby be so sick knowing that
it could be stopped if they would listen.We started his forth round of chemo on Friday the 5th which did not help matters
any. Finally The GI doc came up and asked me about what was going on and she said I was right it was too much too fast and
they had to stop. She told them to stop the feeds and give his gut a break and do the TPN( IV form of nutrition) for a few
days and then we would slowly start him back on the feeds. Well as soon as they stopped the feeds he quit throwing up and
quit the diarhea.. IMAGINE THAT.. Just like I had tried to tell them it was the feeds making him sick, so basicly he was getting
sick over and over for almost a whole week for nothing... Then on Friday they started his feeds back at 10ml an hour and he
started gting sick again.. no where near as much but he was getting sick so on Sunday the GI doc came in and told them to
stop the feeds again and we would do some test when his counts come up again. So for now he is neutropoenic and is running
fevers again... last night Sunday the 14th is when he started the fevers and it got up to 103.7 so now that he is not sick
from the feeds he is sick from the chemo. Keep praying for him and praying for us to make it to New York where the doctors
are that specialize in his kind of cancer. In the mean time I am getting with everyone I know to try to figure out a way to
get money raised to help us get there and set up living arrangements for Him and I. If anyone is interested in helping us
out with finances they can contact my mom or myself through nathens email address or my email address. Amanda.camp@yahoo.com
or Nathen's email nathentrueblood@verizon.net. Thank you to everyone for your support in this very trying time that Myself,
Nathen and our family are going through.
Amanda
11:23 am cdt
Thursday, September 13, 2007
Update on my little man 9-13-07
Nathen has been doing alot better,last week we had several test done to see where the cancer stands... over the past
three weeks we had cat scans done that the doctors had told us that his head scan showed that it was normal again and the
one of his stomache showed that the lymph nodes that were all cancerous in his belly were gone and the tumor had calcified
some.. Then last week they did the MIBG scan(neuroblastoma scan) and the doctor came and told me they were wrong all of it
was still there.. his head, and his belly.. they said that it has shrunk some but there are no clear areas yet. they did a
bone marrow test as well, when we first came in his bone marrow was 80% neuroblastoma cells and the bone marrow test from
last week showed that one side had 20% neuoblastoma cells and that the other side had 30% Neuroblastoma cells..so the bone
marrow has gotten alot better, we are hoping that by the end of this round of chemo that we started yesterday his bone marrow
will be clear so we can harvest stem cells for his stem cell transplant at the end of the chemo and surgery. We have 5 days
of chemo this time and we will be here for the whole 5 days and if he handles it ok we may get to go home. If he does the
same as the last two times we will have to stay here til he gets better from the chemo which has been about 1 or 2 after
the last rounds of chemo. I am hoping we will get to go home this time though, he and I both need to get out of here for a
while.. it is taking a huge toll on us both. once again thanks to everyone....
Amanda
1:59 pm cdt
Sunday, September 2, 2007
GREAT NEWS!
Friday August 31st we had another cat scan of Nathens head. That afternoon the doctor stopped me
in the hall to tell me the results. I had Nahen in one arm and his IV pole in the other hand, then the doc says, Hey I just
got the results back from his cat scan.. I was like ok... kinda scared but then she said the radiologist told her that the
cat scan was completely normal. I asked what does that mean and she says that there was not any cancer left on his head. She
says that it did not show any lit ups spots that are cancerous.. This is great news since he had a large lesion that went
from the front of his skull to the back of his skull and also one on his bottom jaw.She said that when we get the Neuroblastoma
scan next week that it may show some signs of it still there but it would be very little if any because if it was the same
it would have shown up on the cat scan. needless to say I was crying my eyes out in joy and we proceeded to walk down the
hall and I was jumping up and down and hugging and kissing Nathen all over. He looked at me like I was crazy and was trying
to figure out what Mom was doing. We get a kidney scan, bone scan, cat scan of the rest of his body, bone marrow test and
the neuroblastoma scan(MIBG) This coming week. I am very anxious to find out all the results to see how much the chemo has
affected the cancer in my little mans body. I will keep you all posted... thank you and please keep praying, I am convinced
that it is working.
Amanda
3:35 pm cdt
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I'll make changes to this site on a regular basis, sharing news, views, experiences, photos...whatever occurs
to me. Check back often!
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