vaccine lawsuit

[Guest guest]

Hi,

This may be old news to some of you. I found out that there is a large

fund for vaccine injuries that the govt has. I also found out that you

have 3 years from the onset of autism spectrum or whatever damages to

file a case. I accidentally ran across this info, only about 4 months

from the statute of limitations. I am filing a case for my daughter

who became very constipated and then went on the autism spectrum after

her MMR-1 yr shots. I have an attorney that does cases all over the

USA. He seems OK, but he has not done much yet since i just started

this. If anyone is interested, I will forward on the attorney's

website. I would hate for anyone on this list or anywhere to not know

about this fund and not know that there are attorneys waiting to "help"

us get to this fund - and then find out that 3 years is the statute of

limitations. (That is another thing that gets me going, sometimes it

takes more than 3 yeras to piece this crazy puzzle together)

Angi

jeanie ward wrote:

,

What a horrific story..................Again,

never let anyone give anything to you or your child without knowing

what the ingredients are................It needs to be in his

chart that he is allergic or had a negative reaction to PEG, so this

doesn't happen again................they could have used

phosphate soda, or mag citrate.............How do we know that the

previous Miralax didn't cause the nerve damage and this is why the

children become worse with the soiling issues? Wasn't your child tested

for this before? What was the theroy then?

It also goes under the name of Movicol in the UK.......................

http://www.ecommunity.com/medications/d01023A1.aspx?medicationID=23895

From:

Jennie <mykidshisgift>

Subject: Update on hospital stay!A scare!

To: miralax

Date: Saturday, November 1, 2008, 10:33 AM

I left almost 2 wks ago because my son had to be

admitted into

hospital for more testing. I blocked my group mails so I wouldnt come

back to to much so I have not been up on the groups! Anyways he was

admitted and they wanted to do a IV cleanout for the needed tests. I

noticed within a few hours he started with stomach swelling and

questioned what they was using? They told me it was something new

(miralax isnt new so didnt worry to much) and works great, it is

called "Go lightly". Well through out the night into the next day the

swelling continued. I was really starting to worry and no poo into

the next day. They even said he should have already. Into the next

night the nurse left the containor in the room of go lightly and I

got up and looked at the ingredients. I was freeked out to see it was

PEG!! I told them it doesnt work that great for him and causes severe

swelling/issues. Around 2am I called the nurse in because the

swelling was so severe he looked deformed/veins bulging ect. This

scared me and I told them something wasnt write. They looked at him

and ordered STAT exrays thinking he had blockage. Well no blockage! I

told them it was the PEG and has to be off of it. The doc pulled him

write off that morning. He said most would have evacuated by the next

morning and we was on the second morning! I told him that is what it

does to him swelling, but this was the worst i had ever seen(it was

going into him IV around the clock). The worst is yet to come, his

blood work came back and he had a dramatic drop in potassium and

started having heart fluxuations he ended up in ICU. The PEG when

sits in the body to long this can deplete the potassium and cause

heart issues(this is something new to me on miralax/PEG) . Also I

wasnt told tell after the fact that infusing potassium back in to get

the levels needed can also be dangerous on the heart and this is why

he went into ICU! Well his levels went back to normal and heart

fluxuations stopped. They monitered him for a while and ended up

doing his biopsy in ICU instead of the norm room for precautions.

They was an excellent staff and so is our doctor, he had the best

care ever. But wanted to let those who dont know about the postassium

drops and diurectics(sp) staying in the body to long- Potassium

drops/dangerous on heart! This makes me wonder also about when he was

on miralax and nothing coming out for a few days and this happening

at home(heart/potassiu m)! I well never touch that stuff again no

matter how needed it may seem. Well they did the deeper biobsy for

nerve testing and we havent gotten the results back yet. He breifly

suggested and showed us the biopsy/scope pics, suspects the intrance

beginning with the anus may be missing the nerves. If this is it,

this explains why my son no matter how loose/even watery the stools

are still cant move(motility) ! It stops about 5/6 inches befor the

anus opening due to no nerve contractions. Eventually he gets so full

and loose it just pushes out. This is what I have been suspecting for

about 2yrs or so now. If hirschsprungs he would have been born with

this, but this is not official diagnoses as of yet, may be something

else. The thing that is even more flustrating to me is if it is

hirschsprungs then why did he get 10 times worse after his vaccine

allergic reaction almost 4yrs ago(I discovered through research that

vaccines and any allergic reaction to anything can damage the

intestinal nerve cells)I suspect that instead of admitting vaccines

does this they diagnose many with hirschprungs etc!? He only had

occaissional constipation befor that day and then after severe gi

issues, I know the allergic reaction to vaccines caused this severe

issue but yet this was possibly something he was born with. I have

researched this to death and cant get to much info on enviromental

triggers or makes worse on hirschrungs and allergic reactions. Im

stumped, I do recall coming accross some info in past on hirsprungs

can be enviromentaly triggered in a certain nurmber of people but for

the life of me I cant find it now. I guess at this point I need to

quit trying to figure this out until we get his test results most

likely monday or so! I hope all is well with everyone!

Jennie<><

[Guest guest]

We mayed it by 4 days!! Autism is the hard one when it comes to the compensation program! I think there is a vac attorney in texas that is taking on the autism cases! Our sons reaction to his vaccines was immediate/ended in hospital and they are still fighting us the vaccines didnt hurt him and it was so obvious. They have made the injury table so difficult. I have watched it dwendle down to nothing. We finally made it to hearing stage! I sure hope you get somewhere, we are having troubles due to my son already had many medical issues! But at least we filed. I also heard if you file through the comp program and get denied, then you can go after the manufactours, but only if you filed comp first. Best of luck!! Jennie<><

From: Jennie <mykidshisgift@ yahoo.com>Subject: Update on hospital stay!A scare!To: miralax@yahoogroups .comDate: Saturday, November 1, 2008, 10:33 AM

I left almost 2 wks ago because my son had to be admitted into hospital for more testing. I blocked my group mails so I wouldnt come back to to much so I have not been up on the groups! Anyways he was admitted and they wanted to do a IV cleanout for the needed tests. I noticed within a few hours he started with stomach swelling and questioned what they was using? They told me it was something new(miralax isnt new so didnt worry to much) and works great, it is called "Go lightly". Well through out the night into the next day the swelling continued. I was really starting to worry and no poo into the next day. They even said he should have already. Into the next night the nurse left the containor in the room of go lightly and I got up and looked at the ingredients. I was freeked out to see it was PEG!! I told them it doesnt work that great for him and causes severe swelling/issues. Around 2am I called

the nurse in because the swelling was so severe he looked deformed/veins bulging ect. This scared me and I told them something wasnt write. They looked at him and ordered STAT exrays thinking he had blockage. Well no blockage! I told them it was the PEG and has to be off of it. The doc pulled him write off that morning. He said most would have evacuated by the next morning and we was on the second morning! I told him that is what it does to him swelling, but this was the worst i had ever seen(it was going into him IV around the clock). The worst is yet to come, his blood work came back and he had a dramatic drop in potassium and started having heart fluxuations he ended up in ICU. The PEG when sits in the body to long this can deplete the potassium and cause heart issues(this is something new to me on miralax/PEG) . Also I wasnt told tell after the fact that infusing potassium back in to get the

levels needed can also be dangerous on the heart and this is why he went into ICU! Well his levels went back to normal and heart fluxuations stopped. They monitered him for a while and ended up doing his biopsy in ICU instead of the norm room for precautions. They was an excellent staff and so is our doctor, he had the best care ever. But wanted to let those who dont know about the postassium drops and diurectics(sp) staying in the body to long- Potassium drops/dangerous on heart! This makes me wonder also about when he was on miralax and nothing coming out for a few days and this happening at home(heart/potassiu m)! I well never touch that stuff again no matter how needed it may seem. Well they did the deeper biobsy for nerve testing and we havent gotten the results back yet. He breifly suggested and showed us the biopsy/scope pics, suspects the intrance beginning with the anus may be missing the

nerves. If this is it, this explains why my son no matter how loose/even watery the stools are still cant move(motility) ! It stops about 5/6 inches befor the anus opening due to no nerve contractions. Eventually he gets so full and loose it just pushes out. This is what I have been suspecting for about 2yrs or so now. If hirschsprungs he would have been born with this, but this is not official diagnoses as of yet, may be something else. The thing that is even more flustrating to me is if it is hirschsprungs then why did he get 10 times worse after his vaccine allergic reaction almost 4yrs ago(I discovered through research that vaccines and any allergic reaction to anything can damage the intestinal nerve cells)I suspect that instead of admitting vaccines does this they diagnose many with hirschprungs etc!? He only had occaissional constipation befor that day and then after severe gi issues, I know

the allergic reaction to vaccines caused this severe issue but yet this was possibly something he was born with. I have researched this to death and cant get to much info on enviromental triggers or makes worse on hirschrungs and allergic reactions. Im stumped, I do recall coming accross some info in past on hirsprungs can be enviromentaly triggered in a certain nurmber of people but for the life of me I cant find it now. I guess at this point I need to quit trying to figure this out until we get his test results most likely monday or so! I hope all is well with everyone! Jennie<><