The following information is NOT intended to endorse drugs or recommend therapy. While these reviews might be helpful, they are not a substitute for the expertise, skill, knowledge and judgement of healthcare practitioners in patient care.
pyridostigmine for Dysautonomia: Has been very helpful for both my dysautonomia and related gastroparesis symptoms. I feel stronger too, but the effect doesn't last long. I have to take it at least 4 x daily.
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Mestinon (pyridostigmine) for Myasthenia Gravis: I've taken Mestinon for 3 years, since I was first diagnosed with Generalized MG/Optical MG. There has been a great improvement in my weakness. I'm able to keep my eyes open, I don't lose my balance nearly as much, fall less often. I take it every 3 hours and if I miss a dose, the weakness increases. It's quite like taking a pain reliever for a severe headache in that it lessens the symptoms, but they will return as it wears off.
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pyridostigmine for Myasthenia Gravis: I WAS PUT ON THIS MEDICATION IN FEB OF 08 WHEN I WAS DIAGNOSED WITH MYASTHENIA GRAVIS. IT TOOK ABOUT A MONTH OR TWO TO GET THE DOSING RIGHT, BUT ONCE I DID IT WAS FABULOUS WITH MINIMAL SIDE AFFECTS. I LOVE THIS DRUG. IT HAS WORKED WONDERS TO KEEP MY SYMPTOMS AT A MINIMUM.
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Bashe said: 
