Re: Re: Question about Hyperbaric Oxygen Therapy for MCS.

[Guest guest]

--- yukon_paula <yukon_paula@...> wrote:

Hi a,

If you need more data, research my toxicologist's

name, Dr. Gunnar Heuser. He's in Agoura Hills, CA. He

believes that there is an increasing amount of

evidence demonstrating that low pressure hyperbaric

treatment induces permanent changes in a damaged

brain. When I went into the tank for treatment I saw

several brain scans above the tank showing significant

changes in the brain after several treatments. I do

remember also that I paid initially for treatment but

then submitted it to my insurance and they did

reimburse me partially. Hope you can try it.

Christi

> Thanks Christi,

>

> From what I have read, HOT is used more frequently

> in the US than

> Canada. Several clinics are opening up across the

> country at this

> time, and this will certainly make treatment more

> readily available.

>

> I am going to ask my physicians to consider a trial

> of therapy but

> could certainly use data & research, as well as user

> satisfaction to

> support my case.

>

> Thank you for your speedy response,

>

> a

>

> > Hi a,

> > My toxicologist uses hyperbaric oxygen as his

> primary

> > treatment for mold patients. He believes it really

> > does detox the body. He says it helps patients to

> > sweat more effectively and thus get the toxins

> out.

> > I've done it once in a zippered tank for an hour.

> It

> > felt great at the end of the session, and the

> feeling

> > lasted a week or so but like everything else...the

> > symptoms come back.

> > I wish I could do it more often but it is an

> expensive

> > treatment that often isn't covered by insurance.

> Some

> > chiropractic offices offer it as well but I think

> you

> > have to give them your doctor's request for

> treatment.

> > I can give you a couple of places in southern CA

> if

> > you want to try it.

> > Christi

> > > Greetings all,

> > >

> > > I am new to the group and have not had a chance

> to

> > > go through all of

> > > the posts, but I am hoping that someone might

> have

> > > information for me.

> > >

> > > I developed MCS following a severe mould

> exposure in

> > > 2000.

> > >

> > > From reading about the SPECT scans and changes

> due

> > > to 'perfume'

> > > triggers, I am wondering if anyone has pursued

> > > hyperbaric oxygen

> > > therapy.

> > >

> > > I use oxygen regularly for headaches; pain;

> joint

> > > aches; chest pain;

> > > etc. when triggered, and find that it is most

> > > useful.

> > >

> > > Thanks for any advice,

> > >

> > > a

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> >

> >

> > __________________________________________________

> >