thanks to DianaA for telling me about her experiences. i called canada and talked to them back in May 2009. it will cost about $4000 for 40 dives in 20 days and that includes staying there. so a $1000 plane ticket will bring it to about 5 grand to try HBOT. i have been waiting til this fall or winter when i am at my worst so i can see exactly what HBOT can do for me.

If any of you can wait til winter and want to try HBOT, maybe we can plan a trip together so we can keep each other company (pass the time etc).

Mike

Mike,
You will find the staff at the camp, just an amazing caring group of people. You will also see mothers of children with CP, that feel blessed by each and every improvement they see in their child. You will see an amazing amount of love between mother and child. Also everyone their will be on the same mission....healing! I'm sure you will be touched.
I truly hope you gain benefit from the treatment and pay special attention to improvement even weeks after the treatment. It takes time for new micro vascular systems to grow. Try and do all 40 dives.
When I was there there was a parent who had an ear infection and couldn't take her child in, so I took the child into the multiplace chamber with me. Go with an open heart and mind. I think it would be amazing if someone else could do this with you. Regardless, you will leave with life long friends.
There are usually people there with cars that will offer you trips into town and dinners out on weekends, or for grocery shopping. I'll give you hints on the restaurants later. Try "Chez Piggy" if you get the opportunity, fantastic. If Dots Taxi can pick you up at the airport, ( I think I still have her number) that will be the icing on the cake. She is amazing! Call and let me know your schedule if you can. Also, I believe that the HBOT has kept me mobile, on much less medication and has prevented atrophy. I wish you the best.
Blessing....di

Anyone knows about HBOT facility for kids in houston?
I am planning to get this for my 6 months old daughter who is found with severe PVL in brain. Any idea for treatment for such a young baby. Does it cause any side effects?