His neurologist has sent him home with the message that there is no protocol to help him, that he will be in wheelchair within 2 years if he makes it that far.
From XMas onwards he will go on sick leave for 3 months after which he will retire officially from the work force... he is only 63, not a nice Xmas present to be given.
I have been googling for this condition, and it appears it can be hereditary but also as result of being infected by the HTLV-I virus (Human T-lymphotropic virus type I). This appears to be a retrovirus.. and right now I am on steep learning curve to learn as much as possible about this . There appear to be 3 other forms of this HTLV virus (II, III, and IV).
Anyhow, I hope to talk to him soon and I'd like to have some more info as to a possible alternative protocol. Is any of the members on the list familiar with this condition (PSP) or the HTLV-I virus. If so, do you have any details of a possible protocol .
My immediate thought was the BE unit (blood electrifier), CS and Vit C..
I am only at the very beginning of researching this condition and the retrovirus but would appreciate all and any input from those who have knowledge and experience with a possible protocol regarding this.
Thanks all in advance
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