Myasthenia Gravis Support Group
Myasthenia gravis (MG) is a neuromuscular disease leading to fluctuating muscle weakness and fatiguability. The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Although myasthenia gravis may affect any voluntary muscle, muscles that control eye and eyelid movement, facial expression, and...
Not really sure why you ask the questions - we're not masters of our destiny. That is in someone else's hands - for better or worse, it might sometimes seem...
i know that you dont like what is going on with your body and mg. unfortunatly this is a very commun happening with all of us and mg.
as i mentioned before , you acn be at the minimum of both meds and do ok.
i am takem the minimum required of mestidone #30 mgs, daily and prednisone 1 every other day, some time i let go couple of days .
mestidone is specificly to control mg,, prednisone a corticoid steriods dedicated for the inmune system, but remember that prednisone gives the body a minimum amount of cortisol, the natural substance that out body produce about 5 mgs, daily
which actualy it is used also to control all infections in the body.
i know you are very set-up in the ways you want to control the meds, and i agree entirely with you
you just have to find the balance of actions and reactions of your body, actualy you will be able to get it right.
the only things that i can suggest to help is, control of stress and emotions, excersises , sports and all others activities, all to be done with mesure, and stop when you fell tired, take a break and maybe laydown 1/2 hr, this will set you up properly.
best of luck
Currently, I am still on 5mg Prednisone but had to up the Mestinon, following a bit of a relapse last year, I went through the cycle of increasing Prednisone up to about 40mg each day and back down again. Mestinon went to maybe 5x 60mg in a day, I'm currently down to an average of 3x 60mg and feeling pretty good - so it will gently reduce even further. I'm still on long-term Azathioprine and suspect that I always will be, warts an' all! All by the way, under the supervision of my Neurologist - the only thing I ever vary myself being Mestinon.