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File - Roll Call-Check In   Message List  
Reply | Forward Message #1810 of 2355 |
Re: [cerebralpalsy] File - Roll Call-Check In


Faith,

Thanks so much for reiterating what I have been trying to say all this time.  It helps to hear it from another mom.  I am just about going out of my mind with this.

Jan


-----Original Message-----
From: Faith Mills <tmrcj@...>
To: cerebralpalsy@yahoogroups.com
Sent: Thu, 1 Nov 2007 8:53 am
Subject: Re: [cerebralpalsy] File - Roll Call-Check In

They need to get in there and FIGURE it out.  If they have to do exploratory surgery then so be it.  That child should NOT have to be in so much pain.  If his fundo has come undone then he could be refluxing, plus there is probably scar tissue etc..that needs to be addressed.  Tell them if they don't do something and SOON you are going to go to a new doctor or hospital get another opinion and if something happens to your son they will be sued from here to eternity for NOT addressing it.  Kids with CP know what pain is. THey live with it every day.  If its debilitating him to the point where he cries and doesn't want to go to school then there is a major issue going on and they might have to OPEN HIM UP to see what the problem is.  I hope you get some answers .  Go to the ER and refuse to leave that hospital until they agree to do surgery.  1.5 years is long enough to figure out that he's not getting better on his own. I'm not a big pro advocate of surgery unless really needed but here seems to be a pretty obvious case of something extra needing to be done.

Faith


JnDysn@... wrote:

Hi I am new to the group and am having some very difficult times with my son right now.  Jacob is 10 years old and has CP, he is in a wheelchair and is starting to walk a little bit more and more in his walker.  The problems that we are having is medical issues with a constant pain in his stomach,   This abdominal pain has been going on and off for a 1 1/2 years now, but the last 6 weeks has been the worst which has caused Jacob to not want to eat, sleep or go to school.  He wants Mom with him all the time, even to sleep at night. 

We had several scans and tests run and here is what they know so far, they know that when he eats food gets hung up in the esophagus then when it finally breaks through, the stomach isn't emptying properly, and that he has a Hiatal (?) Hernia, also the fundlyplication surgery that they did when he was 2 has come on done.  The Radiologist who did the scans said that his recommendation was surgery to correct all of that.  Jacob's pediatric gastrointerologist and pediatric surgeon both say that they feel that there must be something more going on and they are hesitant to operate because they feel there must be something more going on.  The amount of pain Jacob says he is in doesn't equate to what they see.  And they seem to be splitting hairs over whether Jacob is really in the amount of pain that he says he is in or not.  Jacob at first was saying it was a 3-4 pain, but the last 6 weeks has been saying it is a level 8 pain.  I know my son and he has had so many surgeries and hospital stays and he knows pain and never has complained like this.

We were in the hospital for 4 days 2 weeks ago and thought that they were going to do surgery on that Friday, but they said they wanted a couple of other specialist to look at Jacob, the specialist they brought in were a Hypnotists and a child psychiatrist.  The hypnotists asked Jacob if he would like to walk and if he would like to be free from pain, and what if he told Jacob he could hypnotize him and make that happen.  I looked at him and asked him if he thought he was God or something, because Jacob has CP and brain damage the part of the brain that is damaged is the part that controls the muscles.  I told him that we have been praying for 10 years for Jacob to walk and he has been through 10 years of aggressive therapy to walk and he thought he could just hypnotize Jacob and say rise up and walk and that would happen.  I would kiss the ground that he walks on and his feet if that could happen, but I don't think he is God.

The other Dr. they sent us to was a CP Dr. who said that this was she thought all from the gastric problems.  And that the surgeon needed to do something.  They remembered when Jacob was little and had problems like this with not eating the stomach not emptying and that they hesitated to do surgery then and once they did he was like a new child.  I had been trying to tell them that all along.  She also said she felt something that felt like maybe a tear or pulling away of the stomach, maybe another hernia right where Jacob points to the pain which is above the belly button.

The surgeon mean while is on vacation for 2 weeks and my son is suffering.  I am wondering if any other parents have dealt with anything like this?  Or have any ideas. A lady that I work with said she went thought the exact same thing with a hernia and Dr.'s telling her it wasn't big enough to cause all of that pain and yet when they finally agreed to operate they found that the scans had only picked up the top part of the hernia and the rest of it rather large in size had spidered underneath other organs. 

I have been fighting this battle as I said for 1 1/2 years, Jacob will get really bad and de_hydrated and end up in the hospital for a few days, start feeling a little better and then a month or so we are back in the hospital.  This time he has been in the hospital twice for several days and hasn't wanted to leave the hospital, he keeps saying "Mom why don't they do something this hurts really bad, why don't they just operate and get it over with so I can feel better? Now he is starting to get very depressed.  He cries a lot and says that he is feeling really sad and doesn't want to feel sad, but he can't help it.

I am so torn up over all of this and feel so helpless.  I am trying to stay strong for him.  This week his Dad told him that he had missed to much school he had to start going back to school, because he has missed almost 2 months of school, and that he would have to miss school when and if they do operate.  So every morning this week it is the same thing, Jacob crying and saying " Why are you making me go to school?  You are only making me cause dad says so.  Can't you see I am in so much pain"  He is very smart cognitively and he loves school.  When I took him to school Monday morning, there were 65 kids there to great him, clapping and cheering, Yeah Jacob is back, Yeah Jacob is back.  He had a big old smile on his face, and yet still fights us on going because of the pain.

I am trying to work full-time and take care of everything else at home with 2 other older boys. 

I am sorry this is so lengthy, any thoughts are help would be so greatly appreciated.

Thanks and God Bless,
Jan







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Thu Nov 1, 2007 1:48 pm

jndysn
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They need to get in there and FIGURE it out. If they have to do exploratory surgery then so be it. That child should NOT have to be in so much pain. If his...
Faith Mills
tmrcj
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Nov 1, 2007
12:53 pm

Faith, Thanks so much for reiterating what I have been trying to say all this time.? It helps to hear it from another mom.? I am just about going out of my...
JnDysn@...
jndysn
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Nov 1, 2007
1:50 pm

My godson still had constant pain after his fundo. ( At the time he was a student of mine, he became my godson a year later). Reason, he stomach wasn't...
Debra Marasco-McNulty
debraphp
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Nov 1, 2007
5:12 pm

Jan, I am so sorry you are having such a time with doctors!! Please get a second and 3rd opinion...and not from a doctor that the original docs refer you...
Castle
castletowery
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Nov 4, 2007
4:11 pm

HI everyone! Ethan is doing well. He started preschool this fall and he is doing awesome! He is in a class with children who all have speech delays and...
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suecassy
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Nov 2, 2007
3:49 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
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Dec 1, 2007
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Hi ALl well I hope 2008 takes a turn for the better as Daire has started this year being really sick, we thought at one stage we were loosing him. GP perplexed...
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Hi all, We have been very busy these last few months. I finally had a baby last August and i am just now up to speed physically and hormonally. I forgot that...
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pajak4
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Feb 2, 2008
11:41 am

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Mar 1, 2008
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Hello, My name is Lisa and my son Joshua is 4 yrs old and has CP, Hydrocephalus w VP shunt, CVI, and profound cognitive delays. He goes to a special needs...
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Mar 7, 2008
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Hi, My name is Lisa and my son Joshua is 4 1/2 yrs old and has CP, Hydrocephalus, CVI, and profound cognitive delays. We have been working on strengthening his...
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May 1, 2008
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May 11, 2008
2:17 pm

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Jun 1, 2008
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Happy June!!! I have not been very active....winter was hard....my son Jordan was sick all the time and hospitalized for a 5 day stay for pneumonia. Now that...
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Jul 1, 2008
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WOW we have been busy!!! Cayden is starting intensive therapy next...she will be getting suit therapy 3 hours a day 5 days a week for the next 3 weeks ...
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castletowery
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Jul 1, 2008
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Castle, Please let me know how IMOT goes for Cayden...I have been wanting to try it with Aubrey but I'm not thrilled with the (only) center in town that offers...
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Jul 2, 2008
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Hi Castle, yes, my guess is that the irritability is from the diazapam.  it is valium and she may be working through the dependence.  Matt was on it too for...
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pajak4
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Jul 2, 2008
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Castle, I remember when my daughter was little and she went off Phenobarbital she wouldn't sleep as much and was cranky to say the least. I also know as they...
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Aug 5, 2008
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We're spending the summer in Las Vegas, NV and Dream Therapies is here. But we do therapeutic riding at Stepping Stone Stables in Pikeville, NC back home. It...
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Nov 1, 2008
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