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danelle

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Thanks to your replies and finding a Dr who knows about POTS(finally!), I have decided to start my meds. I will start the MIdodrine in about 30 minutes when my husband gets home from work. I am determined to try whatever I can to get better before going the disability route. Maybe they will work, maybe not. We shall see shortly!!! I'm scared but now I'm determined! :)

Thanks for all your support and wish me luck!!

danelle

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Danelle,

I'm on midrodine as well. I started slow having 3 tablets a day of 2,5 milligramme. The first time I felt tingling all over my head and body where I touched myself. It was a bit scary but it doesn't hurt or doesn't make me feel sick or something. Since I'm building the medicine up (is this good english?) I still feel this tingles but it becomes mild. I also feel what I call "cold sensations" but it's not too bad. I'm on 3 tablets of 5 milligramme right now and my body still handles this. It's just a pity that it doesn't work yet but who knows, I keep on trying. My neuro said this midodrine can be build up till 30 milligramme a day. I hope it will work for you and that you don't feel too bad!

Best wishes,

Corina

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Hi Danelle,

Good luck with the midodrine! I've taken it in the past. The tingly feeling didn't bother me at all. It's just like being cold and getting the goose bumps...not a big deal. I'm proud of you for getting up the nerve...I know it's not always easy.

Michelle

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