Here is a series of emails we received from our client Mr. W.E. Myasthenia Gravis is an ‘incurable’ disease according to medical establishment.
Loss of muscle control is the result, for example one looses control of eye muscles and cannot control eyes, facial muscles, and in fact all muscle in the body deteriorates slowly.
15th Sept 22
Hello Marten, W. here !
Most blizzard, our email thread completely disappeared from my email, somewhere in the belly of the beast !
On my side, Me making steady progress, but always when things go really fine, one does exaggerate and finds himself in the need of recovery time. (So much, however to catch up on life activities...) So it's ebb and flow here, But general direction is on the plus side !
All the best to you and yours,
W.
3rd Oct. 22
Hello Marten ! W. here 🙂👍
Hope you are all good!
Over here, just progress to report. My "MG" is fading slowly into the background, more days seem to be quite "normal", and I have the need to exercise again. lifting weight, resistance training actually, very good...still way to go but very very encouraging.
And again, all the best to you and yours !
W.
21st Oct 22
Good evening Marten !
My oh my, time flies ! Sorry for the sparing reports, I am pretty actif these days, (too much, I am afraid !), need once in a while to slow down, and recuperate energy, so far so good, feel almost pretty normal !
Best to you, have a beautiful weekend !
W.
Hi W… happy new year :)
How have you been?
Hi Marten, happy new year to you too :)
So far so good! I am feeling fine most of the time, sometimes still a bit wobble , need to stay away from sugar and alcohol (not that i am drinking (almost never), but the end of the year was of course an exception , and my body did not appreciate 😐
My neurologist says I am still rebuilding my nerve connections, and that takes time, so patience if course...
I follow you on your newsletter, great stuff you have been up to ! Wish you all the best in all your new endeavors !
Best regards
W.
Wonderful news!
Did your neurologist comment on your progress?
Hey good evening Marten !
Actually, since the beginning of this illness, I am sort of a head scratcher for all the specialistes who checked me. The neurologist said from the beginning, that this is an "atypical" case of MG. I had a major MG crisis when admitted to the hospital, diagnostic very pessimistic but somehow managed to recuperate to basic functionality within 3-4 days . The fact that my blood test revealed antibodies regarding the covid "spike Protein" but nothing else from the virus was intriguing (I am not vaccinated) as well.
My progress is certainly regarded as spectacular, but no comments.
I cannot speak about alternate treatments within the "official" Swiss medical establishment, for insurance reasons as well.
SO well , very happy to be on my best way to complete stability!
Regards
W.