Trish symptoms and conditions

My doctor put me on Topamax for ADD.... I am a 37 year old woman and I'm taking 100mg's of it. 50mg at night and 50 in the AM and have very quickly found that I have had memory LOSS very quickly. I have been on the med for 1 1/2 months. My vision is also getting worse and this medication is not helping me with the ADD. I am a Lab Rat to them... I am going OFF this medication. If anyone out there reads this... please do all the research you can. The side effects are not worth it! Today is Mother's Day and after 37 years.... I called her and could not remember her little sweet nic-name she has been calling me since I was born. My heart sank. IMHO.... This medication is very bad.

I am a little past my 2 weeks with my 1st luprone shot- 1 month. At first my pain symptoms didn't go away at all until one day(after a week and a half after the shot) I got my period and a serious hot flash. From then on I only get sweats and hot flashes at night. I am extremely fatigued. I am used to working long hour days, i.e. +12 hours, but I can't even hack making it through 3 hours these days. Other symptoms include: terrible migraines(all day), nausea, depression, terrible back and joint pain, my arms fall asleep all the time, pain a injection site, loss of appetite-slight weight loss, hair loss, and slight mood swings. This is the second time I have ovarian cysts, but now the doc's think I have endo too.

I had my second Lupron shot this last mid October that lasts, supposedly, 3 months. So I will be 5 months in this mid December and I have to say I was one of the people who was fine with Lupron...up until now. I had and have all of the typical side effects of hot flashes, headaches, memory loss, mental fog, etc. Then I had my first ever migraine a week ago that knocked me on my butt for 2 days. My memory loss and depression are by far, by far, the worst side effect I have experienced. At this point I am concerned my memory problems and mind fog will not go back to normal, which has already adversely affected by daily life. I was one of the people who spoke positive of this injection even after reading all the horror stories but now I am beginning to wonder if they were right on some levels. When reading all the different experiences I would get confused and wouldn't know what to believe. I am not saying I would change things, the jury is still out as to whether the benefits will outweigh the difficulties, but my personal experience and symptoms have been getting worse just in the last few weeks, so that would be between month 4 and 5 on it. I could lead a pretty normal life up until recently and I'm a pretty tough person, I clean houses for a living and work hard with a packed schedule so I am not just stating little symptoms I experience but ones that actually have affected my daily life. Just being honest so you know what to possibly expect, depending on your body's reaction. That is a point to keep in mind, everyone's body reacts differently but if the majority of people are saying the SAME side effects, makes you wonder if there is a consistent pattern.

One thing I will tell you that has helped me is B vitamins regularly in your system and staying as active as possible. Write things down to remind you for the memory issues, don't over-commit to things because of the mental affects-it hits you hard when you can't follow through, and try to watch your sugar intake, which messes with your emotions. Hope this is helpful.
I would love to know from someone who has the same symptoms (which looks like almost everyone who is on it) and who is now off of Lupron for at least a few months, if the symptoms of memory loss and mind fog go away. Is my memory permanently damaged?

Hallelujah, its OUT!

I got mine out today!!! I made sure to take ibuprofen before I went in and thank heavens the removal was NOTHING like the insertion! Quick, easy and pretty painless!
I sure wish I could go "au naturel' at this point but my husband and I just can not risk pregnancy right now. I am grudgingly going to start on a low hormone pill on Sunday...

I will post in the future to share what changes happen now that the thing is gone!

Good luck to all you ladies!

Need some advice for my husband. He has been given Levaquin and he is in alot of pain. Headache, stomach, dizzy, lower back pain..and what ever else you can think of. So my question is, what did you do to get relief from taken the medicine and how long untill you felt better. I have told him not to take anymore, but what else if anything can he do to feel better? Please e-mail me at thetuggles@yahoo.com...thanks, trish

Been on 200mg. tpamax about 6 weeks. Problem swelling of the legs and tingling in toes they sometimes turn blue. Is this a side affect of topamax or something else. Doctors have no clue what the problem is any suggestions on what to do.

I've been on 90mg of prednisone for about a month and a half for nephrotic syndrome and have had some of the more common side effects like the round face, some weight gain, dizzy spells, and some others.

I started to feel better after about 3 weeks on the drug then I started to get a weakness in my legs almost to the point that I can't support my own body. I know that prednisone causes muscle weakness but this seems excessive. I have to keep myself from falling nearly every time I try to walk, even short distances. My doctors are looking into it just to make sure it's not something else but I think it's the drug.
Has anyone else had this problem and does it get any better? As far as my blood work goes, I'm not dehydrated and my potassium levels are fine so we know that is not the problem.

Also, I'm starting to have some heart problems. Before the prednisone my resting heart rate was in the 60's now it's in the upper 90's and even goes up into the 100-120's. And if I even walk to the bathroom it goes into the 150's. And my blood pressure is extremely high. Anyone else dealt with this. It's worrying me and my primary doc seems really worried about it but my kidney specialist just wants me to wait it out and stay on the high dose as long as I can.

I'm at the point where my kindey specialist says if I go off the prednisone it could lead to kidney failure but my primary doc says that if I stay on such a high dose I'm at risk for a heart attack.

extreme muscle pain,especially in the legs.could this be
lotrel?