I was suggesting this site to someone I recently discovered has M.S. when I realized I hadn't actually been here in a while.
The biggest recent development on the M.S. front is that my neurologist, who has been skeptical of the CAP treatment, ordered an MRI (I guess so she could point out progression that just HAD to be there).
My oldest MRI that has the results in digital format is from 2010. I provided copies of all of my MRIs for which I have digital results to the hospital for comparison. The radiologist compared my latest MRI with the prior ones and said he could find no change since the 2010 one.
My neurologist still doesn't accept the CAP, but she does acknowledge going from having exacerbations every 90-120 days to no exacerbations for more than a dozen years at the same time I did the CAP is a coincidence she can't explain.
13 Nov 2022 04:23 pm
30 Nov 2022 11:01 pm
HDWhit - SO good to hear…
HDWhit - SO good to hear from you. And SO good to hear your update. Still living 'off the grid'?
The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi
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Hello hdwhit, long time no…
Hello hdwhit, long time no see. It is now nearly the end of 2022, so getting on for twenty years since David and Chuck Stratton first found the best antibiotics to cure chlamydia pneumoniae. Then David gave me the same antibiotics and found that they also cured my multiple sclerosis.
I think that I can say that now since my last relapse is getting on for twenty years ago. I just wish that David was still here so that we could both enjoy life together.
Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent. Still improving bit by bit and no relapses since finishing treatment.