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Help about pedi-neuros

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Hello,

I just joined, so I don't know if you (anyone) can help on this subject.

My 3mo old g'daughter (Ally) has mild/moderate(?)HIE. I've been

researching HBOT for about 2 wks in hope that there would be a benefit

for her. Ally's parents have approached she medical team (thru the

pediatrician)as to their position re: HBOT. Her pediatric neurologist

just responded with a resounding NO!! He stated that, of the 900

members in his association, none of them support the use of HBOT.

There is a recent article in their newsletter that evidently sites

" numerous " problems, including seizures while undergoing treatment

(and not being able to provide aid until decompression is complete).

He stated that he has (2) of his patients that have gone thru the

treatments (@ the same facility that would provide treatment to ALLY)

& haven't shown ANY benefits.

Unfortunately, I feel like I'm putting my son-in-law in the middle, as

I'm not in direct contact w/the Dr. I've suggested that, since the

assoc & this Dr. are pointing out that there is no research supporting

the " benefits " and are using these examples (seizures,etc) as

potential " risks " , would be kind enough to give me the links

supporting these risks?

Can anyone offer some support (documents/links, etc), so I can feel

confident in pursuing HBOT for ALLY? Ultimatsly, it isn't my call to

make. I just want my kids to be as informed as they can be when they

decide.

Thank you,

Terry Miner

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