I would love and appreciate response, and emails concerning whether you followed the exact timeline of dosage and application of the Rxs according to http://www.davidwheldon.co.uk/ms-treatment1.html
Also, did the "ADJUNCTS" section of vitamins, etc prove beneficial ??? (she is on alot of them already)
I am desperate to start this, but feel I am so unqualified to be the one mediating with a GP on it on my mom's behalf. PLEASE- ADISE ME. I'm 26, and the only one left to fend for her future. Her neurologists are timid on experimental treatments, and will not advise or support this. (i see, always the case)
I started this account so I can work to research on my mother's behalf. She is 58, and has moved on from relapse/remit onto progressive. She has had symptoms since 1992, diagnosed in 2003. 3 years ago, her baclofen spinal pump malfunctioned, skyrocketing her into a winter of delirious, debilitating near death withdrawals from the drug. She semi-recovered after 5 months of that old Rx balancing dance. For these 3 years, she is powerchair bound, zero use of legs (although spasms and pain persist), her arms are now very weak, and she is recently showing signs of Alzhiemers (hence, my panic to find a REAL treatment and not just the Rxs she takes for all the symptoms, as I am losing her mentally, and very rapidly). She is on the full regmine of Copaxone (for several years), etc.