December 20th
2006
1:03 PM
Kim,
I totally agree with Sarah! And another thing: You should really try to stop caring that much about what others say or think about you!! One very important thing, Kim!! Only you can feel, what you need right now and if it's the Lexapro, than you should try.
And as I know, what we all are or were going through I'm sure, that you're not weak, if you don't get through this nightmare without help!! Looking back I really don't know, how I stood all this without medication (ok, besides my Valerian, which I had always with me for about 6 months, just to know, that I had them with me, most of the time already helped....). And believe me: Some days I thought "Please give me ANYTHING, I WILL TAKE IT, I can't stand this any longer!" And I think the only reason, why I nevertheless took nothing was, that I knew, that my body didn't tolerate this kind of medication.
Everything went even worse only after taking one of that pills (they tried to put me on an antidepressant in hospital because of my very bad constitution!!)... But this also happened WHILST TAKING YASMIN! So it might be, that my body would react different about that stuff today...
Kim, I wish you best of luck, that the Lexapro will help you somehow through those hard times. But nevertheless I'm also sure, that you won't have to take it over a very long time!!
Sounds very interesting, what your pharmacist told you! One thing I found out first about Yasmin and bcp in general: They deplete you nutritionally, which makes things as anxiety, weakness, dizzyness and everything else definitely much worse!! And I think the fact, that makes Yasmin even worse than other bcp is that diuretic in it!! The more water we loose, the more electolytes and vitamines we loose!! And I wondered for so long why I had to get up sometimes 2 times at night with an urge to urinate.......
Best wishes to you Kim and all the others and keep it up!! We're all on the right way, I'm sure!!
Silke
-- By voicesi | Reply | Private Message me
October 17th
2008
2:25 PM
I've been on Topamax for almost a year. I've had auras for years which were misdiagnosed as hypoglycemia episodes, then started having grand mals after detoxing from alcohol (I'm sober now), continued to have them in sobriety (I guess I messed up my brain from alcohol). I tried Tegretol but it made me groggy. Anyway, a few months into using Topamax I stopped sweating completely and got the numbness and tingling in my extremities, which drives me crazy. I also have trouble with urination, I've been put on water pills. I live in a desert climate and during the summer had bad problems with overheating, had to drink so much water that I had trouble with water retention and my electrolytes got messed up. I had no idea that it was the Topamax--the doctors put me through multiple blood tests, I discovered it might be the medicine by doing my own research online. I'm tapering off Topamax and trying the Low Glycemic Index Treatment to see if I can be off meds and not have auras because I don't want to be on seizure meds if I can help it. The withdrawal is pretty bad--anyone else have the problems with no sweating and wicked withdrawal?
-- By melaguas | Reply | Private Message me