by Nancy W » Sat Dec 12, 2015 10:23 pm
David, I have had an interesting Fall. Clearly exacerbating symptoms of myo-neural damage over the summer. Sleep became next to impossible due to all the muscle fasciculations. My naturyopath provided me with a prescription for CBD/THC, which helps, tremendously. I traveled twice in this period of time, each journey about 10 days, and I did each trip without bringing marijuana, since marijuana is illegal in Texas (where my kids and grandkids are) and in Mexico (where you go immediately to jail if they find pot). Both trips were nightmares for me. Almost no sleep, which ultimately produced mind-blowing anxiety. Home again, I realized I was becoming weaker and weaker. Dragging my right foot. Tripping over it. Poor grip strength. Dr. G. encouraged me to get a diagnostic work-up, which has been easier said than done. But, system complications aside, I am scheduled to see Seattle's top ALS neurologist this coming Friday.
I have been doing a lot of reading. Of course I have read the articles written by Dr. Graveline and the other docs on this site. With the symptom set I have (pretty much the entire symptom set for ALS), I have also been on the ALS site reading. I have been looking over the "Deanna Protocol," a mostly nutritional and supplemental approach to lessening the effects for the statin damage. Somewhere I stumbled upon four books written by Hannah Yoseph, MD and her husband, James Yoseph, who is affected by statin-damage, I believe. One is called "Statin-Induced Neuropathy and Myopathy, and the newest one is titled "Conquering Lou Gehrig's Disease: The ALS Diet." I just finished reading that one...it has a lot of the same info as the other one I referred to. Much of the discussion relates to the damage by mycotoxins, which are statins. Also other very interesting information about CWD's and about infections within the cells. I haven't read the other two books yet, one called "Serial Killers." And the other called "Poisoned." She is taking a different approach than I have read about elsewhere. The "diet" she proposes is not the same as the (expensive) Deanna Protocol for ALS.
Wondered if you have read any of their books, or if anyone else reading this post has??? Any thoughts?
Which leads me to my question to you about LBD and apoptosis. Can you post the link again? I have reread your posts. How much Benadryl do you take? What changes did you notice and in what time frame?
I am glad that I am going to see Dr. Elliott...Figure he can well diagnose ALS. And if he is worth his reputation, then he must be aware of the connection with statin/mycotoxicity. He is about to leave the ALS clinic he is in and go to a different hospital locally, so this visit will probably not include the full diagnostics, but will be more of an initial consult. I want to be as well-informed about options and ideas as I can.
Will report back in about a week...Nancy