HBOT Question

[Guest guest]

I have been following this group for quite a long time. I am wondering

if anyone has used HBOT to treat CFS or ME. I was dx'd with CFSME back

in 2006 and got so bad I was put on Temp Disability. I was desparate and

after all the meds and accupuncture and ND's did not work, I tried HBOT

and it seemed to work for me. Although I recovered too slowly I was back

to work in three months. It has been 5 years now and I still have some

sleep issues but I am so glad not to be so sick anymore. We have formed

a COOP program here in Wisconsin that offers the lowest cost for HBOT in

the country - 40 treatments with lodging included for $2600. Although it

was

originally designed for Cerebral Palsy children, if you are interested

please send me an email. More info on the program is located at

http://www.o2clinics.com/Group_HBOT_COOP.pdf

<http://www.o2clinics.com/Group_HBOT_COOP.pdf>

<http://www.o2clinics.com/Group_HBOT_COOP.pdf

<http://www.o2clinics.com/Group_HBOT_COOP.pdf> > . Please email me if

you

have any experience with HBOT and CFS, ME, Lymes, etc...

My best to you all.

Thanks,

Kent MacLaughlin