rach73 Posted November 26, 2011 Report Share Posted November 26, 2011 Hi,Something strange has happened - a good strange lol. Since starting midodrine my ptosis that I've had for nearly 4 years has resolved.My eye closes completely when I am having a bad spell and most days I look like I have a lazy eye. The only thing that ever resolved it before was mestinon, which is why I had years of tests for myasthenia gravis.The first day I took midodrine I had really bad ptosis and one hour after taking the tablet it resolved. 2 weeks on I woke up with bad ptosis and one hour after taking midodrine it was gone. In 4 years the only thing that ever resolved my ptosis without taking drugs was bed rest, it never resolved without medication (mestinon) or bed rest.I have measured by BP when I have ptosis and it can be low or it can be normal so I am struggling to comprehend why the midodrine works. Obviously both mestinon and midodrine up my blood pressure and resolve my stroke like symptoms ( I not only get ptosis but my whole face drops also so I look like I've had a stroke).I just wondered as I know there are a few on you on here with ptosis found the same thing when taking midodrine or am I still a medical mystery lol!ThanksRach Quote Link to comment Share on other sites More sharing options...
ramakentesh Posted November 30, 2011 Report Share Posted November 30, 2011 I get this as well. One doctor said it was because I was depleting my norepinephrine or showing signs of too little norepinephrine with paradoxical hyper symptoms. Another doc suggested its because POTS and MG are related in that they may be related to similar autoantibodies. The autoantibodies in MG are more related to all acetylcholine receptors whereas in POTS they seem specific or may be specific.Interestingly, MG patients also exhibit autoantibodies to A1 and beta 2 receptors both implicated in POTS. Quote Link to comment Share on other sites More sharing options...
rach73 Posted December 2, 2011 Author Report Share Posted December 2, 2011 Thanks for the reply, its very interesting.Ive had to stop taking the midodrine at the moment due to a uti. Midorine makes it difficult for me urinate so my GP has said better to stay off it whilst the infection clears.Rach Quote Link to comment Share on other sites More sharing options...
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