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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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#11 | |||
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I am. Especially for headaches. It's tedious because they want me to write it down in a journal aswell. But a few times i've just pushed it and not recorded it. It's all going to the cardios anyway
![]() Thx. Night. I hope they can find what is wrong so I don't look like a fluke. |
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"Thanks for this!" says: | Nicknerd (03-09-2010) |
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#12 | |||
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No problem, Tyson...I'm like you in that I didn't think that BP would be a problem for me for one thing, because I'm pretty young too, and for another, because I had always had low/normal BP prior to starting prednisone (110/70)...I also had never thought sugar would be a problem either because of my age.
I wasn't really informed of the side-effects of prednisone prior to starting. In fact, one day the nurse came to me in the morning, when I was at the comp. in the entertainment room, and there were some new pills in her hand. I was like, "What are those?" She's like, "oh this is your prednisone." I was really upset, and protested. I hate taking pills (as everyone does) and I especially feared prednisone (but knew I'd have to take it eventually 'cause of the way things were going). Mental illness runs in my family (many have bipolar disorder, OCD and one has Schizophrenia), and I was terrified of losing my marbles from the 'roids. Moonface, blood sugar, salt, and all those other things, were the least of my worries at that time...My dad has been taking prednisone for over 12-years, and went psychotic when he first started taking them...He'd still have psychotic episodes every now and then...Don't ask me why they didn't try a different immunosuppressant for him... So anyway, I was sitting in the hospital eating the delicious food *barfs* ![]() I think I was under the impression that the sides from prednisone only affect a small percentage of people, like other medications...Was I wrong when you pretty much get every side effect listed...Taking it is essentially having Cushing's, so it's not really surprising... Anyway, I'm glad that you're getting some help, and I hope things with your heart get sorted out...I want you to get the answers, and on that road to recovery, without all the potholes! ![]() Nicky |
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#13 | |||
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Tyson, I'm so relieved that you're getting the work ups from your doctor. The event monitor is a pain, but it is a necessary tool. Writing a Journal while you're not feeling well,is also a real pain, but it does help them. When you're feeling better hope you'll be able to look up those fun MG links.
The famous ones are interesting. Feel better soon. Love ![]() Lizzie |
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#14 | ||
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Tyson,
I wasn't going to post about this but I will say something now. Remember I only take Mestinon for my MG but I also get a weekly I.V. infusion for my Alpha-1. The last couple of weeks I have been getting chest pains and have ignored them {yes, I know, dumb} on Thursady my throat swelled up so bad my husband freaked out {never happened like that before} again, I ignored it, thinking well I can still breath so I am OK and besides I knew I had a Dr. appt on Monday. Monday, went to Dr. EKG came out bad, but I was feeling good, the pain {actually in my upper back} had subsided, so Dr. is setting me up with cardio Dr. and I am under STRICT orders to go to E.R. should anymore pain start. The problem with us is that the pain comes and than goes so we never know what is "real" and what isn't. I am soooo glad you went to the E.R. {I know I may be doing it myself} Any pang you feel, you let them know and write down everything, I went to the Dr. and forgot my "list" and couldn't remember anything while I was at the office..LOL If your lips tingle, write it down, if your shoulder hurts, write it, if you feel sick to your stomach, write it, even if these things last only a few seconds. Keep us updated kiddo and know you are in so many peoples thoughts and many of us here really care about you! ![]() |
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