Hey guys!
My mother has been diagnosed with SCA3. For the past 5 years I have been looking aggressively to improve her quality of life.
My new hope is a treatment with oxygen.
Has anyone done this?
Thanks.
Hey guys!
My mother has been diagnosed with SCA3. For the past 5 years I have been looking aggressively to improve her quality of life.
My new hope is a treatment with oxygen.
Has anyone done this?
Thanks.
I’ve seen this question asked on other ataxia support groups, only one person had tried it. For him, some troubling symptoms were relieved (quality of life), but it was in no way a cure 🙂 xB
Hi I go to some MS groups, as their symptoms seem almost identical to the symptoms I have, lots of MS suffers have oxygen therapy and I’ve heard it can really help. I would love to have it but when I looked into it my nearest place is very hard to get to and they said you need it almost every week to see effects. If you join some online MS group you could get lots of information from them. A lot of the MS people also have vitB12 injections and take vit D supplements. I don’t know medically how close MS is to ataxia but I do know 2 sisters one has MS and the other has ataxia .
hi i have tried it and it helped me while i was doing it but its not a cure its more a relief of symptoms. But what has really helped me is following Anthony Williams protocol. I am a raw food vegan. Now i feel i treat the underlying cause.
I have used it at Chrioprator office he gave me exercises etc oxygen I was up and going but was gettting very expensive so I quit. It was called brain based therapy amazing