Hello folks, am glad to find you here today because i have suffered for over 3 years without finding anybody to talk to about MG. I was diagnosed with MG in 2014 just after my graduation from college. Before the diagnosis my symptoms were severe but after i started using mestinon and prednisone tablets, i felt better though the weakness will always come upon any lengthy physical exercise even now. I took the drugs for about five months and i coun't afford them anymore coz here in Kenya they are expensive and rare. Up to date i still feel like am normal although i can't run or lift heavy items. I don't know what might be cooking since i stopped the drugs almost 3 years ago.I really need your advice if you've got this experience. Currently am 31 years old.
Hi, I know it’s normal for diarrhea to be extreme with taking pyridostigmine, but has anyone ever experienced the opposite? My father has had diarrhea since having colon surgery 20 years ago. Recently diagnosed with MG, he now has firmer and less frequent stools. I’m curious if anyone else has experienced anything similar? TIA!
My husband was diagnosed with myasthenia gravis in 2016. He is extremely weak now. Takes 60 mg. Pyro 3 times a day. Trying to get in to see Dr., but can’t get in until middle of August. He was diagnosed also with dementia just after that at Center for Senior health in Akron. After much urging by family Dr. We went to a psychologist and after much testing he said he does not have dementia,...