Speech problems symptoms and conditions

Dizziness, back ache, severe hip and shoulder pain, transient global amnesia, after discontinued taking of Lipitor, speech problems, loss of words.

I took Lexapro for several years without many side effects. Yawing and sleep problems. Then I had an aortic anysrem and kept taking the Lexapro. Then for money savings I switched to Celexa. I started losing weight, great. Then I start talking like a drunken sailor. I couldn't find any symptoms of speech problems so I figure it was a stoke. MRI says no stoke. I am getting off Celexa and SSRI's all together. I think the panic attacks i was having was my body telling me something was wrong and the doctor and I didn't listen. I just about cost me my life. NO TO CELEXA.

I just found this post by accident. I also am on Topamax 200mg daily. I have tingling in my feet especially in my heels. I find myself being very forgetful. I will be doing something and completely forget what I was doing. I am also having speech problems. This is very frustrating to me. I don't know that I could ever go off the medication. When I first went on the medication I lost a total of 80lbs. This was very scary. It seems now that I can eat whatever I want and not gain a pound. This is weird. I heard that the FDA is trying to approve the RX for weight loss. Just wanted to post my problems too.

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 have taken Lamictal for 2 years now, I increased my dose a few months ago. It curbed my rage issues, and continued to stabilize my mood swings.I have had the side effects of some memory loss, problems recalling things in the past, minor things, like what happened in movies I may have seen in earlier months. I have hair loss, more than usual when not on the drug. I have definite speech issues, I can never relay what I am trying to say. I feel stupid. I am consulting another psychiatrist to discuss the side effects. I really don't like not being able to remember things as much as I did before I took this drug. I really, really don't like the lack of the ability to speak fluently or even to get the words out. It is embarrassing, it makes me look almost like I have a mental retardation. It sucks. I also am disappointed that my spouse seems to think all "our" issues are because of my mood disorder and if I somehow when I disagree with him and want to address these issues, then my medication is not working. I know if I am raging more or if I have an increase in anger, then I need to go on higher meds or change meds. But, as my psychiatrist said to me, not all my issues in life are all my fault.
Generally, lamictal is working, but I would like to have a greater memory recall and I would definitely like my speech problems to be resolved and it sure would be nice if my hair would become thick again.Also, I have some twitching problems occasionally, it is annoying too. I still have racing thoughts and panic attacks too, it has not changed those issues. Oh, and another side effect is headaches in the back of my neck at the top where my head meets the spine, they are annoying and if I take ibuprofen, I get even more stupid and spacey, almost like I am checked out. My older kids notice more than my spouse does. My older kids also let me know when I am raging more, in a better way than my spouse does. My advice, let those whom you can trust be the one's who give you feedback on how you are doing, rather than someone who doesn't want to take ownership for their own issues, that way you can truly trust if the med's are working or if they are at the right dose. This along with your psychiatrist's help and help from family and your own assessment will keep you on the right track.

Hello-
I am here to share my story about topamax in hopes that others may read this and not have to go through what I did. I went on topamax for the prevention of migraine headaches. It worked great to prevent my headaches but gradually I could not talk, I stuttered severely, and I have memory and other cognition problems. At my doctors recommendation I stayed on the medicine for about 6 months because he assured me that the stuttering would go away. I was in such awful pain that I agreed with him. Needless to say that 6 months was not me. I couldn't talk and I couldn't think. Now when I think back on it, I wish I had just endured the pain. When I went off of the medication I still stuttered. It was not quite as severe but it was bad. It effected my work, my personal life, and daily menial tasks. I could no longer communicate. I was devastated. My doctor was puzzled and said that he had never heard of this before. So to make a long story short I went to a speech clinic, bought casa futura techs small talk device, and tried some anti-stutter meds. My speech now, 2 years later, is much improved thanks to the smalltalk but guess what,? I still stutter. Manageable and not very noticeable to others at times but my speech has not returned to pre-topamax status. I looked into sueing the drug company to bring awareness about this issue but did not get much positive feedback from attorneys. IF YOU ARE ON TOPAMAX AND ARE STUTTERING, STOP TAKING IT. IT MAY NOT GO AWAY WHEN YOU DISCONTINUE THE MEDICINE. It is not worth it. You cannot put a price on speech. I don't care what the physicians desk reference says, what your doctor says, what the corrupt drug companies say. I know my experience and it has been a catastropohic effect from topamax. Find a different med if you have speech problems! Please, for your own sake. Thanks for letting me share my story.

I am relaying the story of the granddaughter of my boss. She was 15 when she got the first shot of Gardisil in May of 2007. Within hours of the shot, she collapsed and an ambulance was called because she had distressed breathing. She was taken to a hospital and was in intensive care for 2 weeks in and out of consciousness. In the meantime, her mother tried to get the shot records from the doctor's office that gave the shot. They did everything in their power to:
A.Dismiss the correlation between the shot and the girl's collapse, despite the girl being in good health before the shot.
and
B.Keep the parents from getting hold of the vaccination records.
It was like pulling teeth to even get the vaccination batch numbers, and finally the office told the parents that somehow, the girl's health records went "missing". Luckily, the parents still had copies of most of the doctor visits, plus the "aftercare" paper following the shot with vital information on it.

When the girl finally began to be able to sit up again and eat on her own, she experienced mental fuzziness, memory problems, and speech problems. She had perpetual tingling and jolts of pain on the arm that had gotten the shot, in her side and abdomen and down both legs. Three weeks after the shot, she tried to get up out of bed and found she could not walk. She was diagnosed tentatively with Guillain-Barre Syndrome, also with nerve damage. It took her three full months to walk again without help, and even now, a year and a half later when she comes into the office she still has a bit of a limp. She lost over 25 pounds, which is pretty sad as she was not overweight or anything. She now looks very skinny and sickly. She had to quit school and started being home schooled because of the physical and memory problems and depression. I feel so sorry for her and her parents, who thought they were doing the right thing.

I just went to the Dr. for my second Lupron injection and to get some help with the side effects. Menopausal/emotional me, started crying!!! Gawd! I went in with my list of side effects from the last 3 months (and it was long!) and wondered what was worse, the pain of endometriosis or the life changing side effects of Lupron. My Dr. is wonderful and spent an hour with me; he decided to put me on Provera (progesterone or add-back therapy) for a week to see if the side effects improve. If they do, I get my second dose of Lupron in a week. If not, we stop it all and let my body slowly try to get back to normal (although I have never known what "normal" is since endometriosis) and see how the "therapy" worked. He is strongly encouraging me to follow through with the 6 month course as that is the recommended length of time for the best results. I'm 5'8" and have lost 10 lbs. in the last three months, I'm down to 107 lbs. He told me to try and eat more if I could (although my nausea is constant 24hrs. a day) and make sure to take a daily vitamin and calcium for bone loss. He said that he has never heard of blurred vision to be a side effect of Lupron, "But every woman is effected differently." I'm really hoping the Provera works - any kind of relief is better than this! I'm still having 3-4 hotflashes every hour with extreme exhaustion/fatigue, night sweats, daily migraine headaches, nausea 24hrs. a day, life changing mood swings, and shaky hands. He kept reminding me that this only 6 months out of my life - it's not forever ... forever feels like an awful long time when you can barely get out of bed!

Hi I've been on topamax for 4 years . Had all the side effects...weight loss,tingling in hands and feet,no memory and speech problems! I was taking 600mgs a day! I take it for epilepsy! I was on the highest dose. my doc then weened me from top. to zonegran 600mgs. It's very similar to topamax. For me it is not helping me as much as the topamax. I think it's a great drug!!!! I did not loose hair, no constipation, no rapid heartbeat for me! I am going back on it . Yes sometimes I would get in a hostel mood and can't spell shit , but for me it's all GOOD !

I gotta tell ya this is scary. I am a 30 yr old guy my wife is 27 we have four children.Our last one was born Mar. 2007 She has been on Yasmin 6months or so.She has never been regular on periods. Well a few weeks ago she started having massive headaches.As of June 31st her doctor said she has migraines. Well by July first her left eye went blurry by the 2nd she has lost vision in both eyes.She only sees light and is very cloudy and can see shadows. We made 3 trips to ER. They did Cat scan and it was neg. the doctor said she might have even had a mild stroke because her left cheek went numb. By the 2nd we were in ER again because of total vision loss. They did a lumbar punture and no Meningitus. cat scan again neg. blood work neg. except UTI sound familiar ladies??? By the 3rd we visited her doctor and she passed out and was rushed by EMT to Hosp. They did and MRI,MRA,had a eye Doctor called an ophthalmologist clear her of vision problems.She has talked to a neurologist. So here is a 27 yr old female with all the test's coming back normal but she can't see.They even had a psychiatrist talk to her because she is on Prozac because she has PCOS and had half her ovaries removed and almost died.They even suggested that she had conversion disorder(google it).Finally I decided to check side effects for all her meds. When I checked this one I almost jumped outta the chair.She has about 10 symptoms. But before I get too excited has anyone had vision loss for a period of time and did it come back once off of it?? I'm throwing these away

I'm glad to have found this website posting as tonight I decided it's time to do further research on Singulair and check the issues I'm experiencing. I've decided tonight that I'm going off so I can do some testing and rule out whether they are causing the following side effects for me:

I've been on Singulair for almost 6 months. When I first started, I had a heck of a time getting through the drowsiness but it got easier each day and gradually after a month, I stopped being so "spacey". I started Singulair primarily to address my asthma issues and the tightness in my chest and as an added bonus, it helps my allergies so I went off the Claritin as well. Singulair has done wonders for my asthma and I have rarely had to use my inhaler or have asthma attacks. (I should note, I wanted to eliminate steroids in my life since it causes acne etc. etc.)

Meanwhile, I've noticed changes in myself. I'm more lazy, take naps on the weekends, less hyper (which is a good thing on my stressful job) but I've lost my "edge" where I should be quick on my feet and responses. Recently, I've noticed that I'm slurring my words and having speech problems. I have got lost a couple times in my train of thoughs. I also seem to experience being dyslexia - I frequently type letters and numbers jumbo'd around. Very unlike me!

I also have severe dry mouth almost like an infection. I tend to get itchy around my neck and arms for no reason - almost like a mild form of nerves twitching simulation. I've got more sinus infections but that could also be due to not using Claritin and perhaps, I need to be on it at the same time.

I've cut back to 5mg (I cut my pills in half) for a few months and felt less tired but my speech and other side effects are still present. Heck, it could be a sign of aging or other things occuring but I need to start somewhere. I am sad that it could be Singulair because it's the best drug for my asthma but I have concerns about the other impacts it might have on my health and well being. I'll post updates in a few weeks.

Feel free to email me to talk about anything offline - I'm eager to hear from others!

-S

I've been on topamax for 3 1/2 months & was on 25 mg & then was pushed up to 100 mg when I started to have more severe migraines & "seizing" in my arms & legs. Here are a list of my symptoms: increased sleepiness, gait problems, word recall, more difficulty w/dysgraphia, increased ADD problems, increased lability, increased hypersensitivity to stimuli (seizing in limbs increased), pins & needles, metallic taste in mouth, asthma worsened, sleep became more disrupted, lost weight (already skinny), increased facial hair, strange menstrual symptoms, basilar migraines worsened, hemiplegic migraines started occuring at increased rate, suspicious that it may cause or excacerbate pre-existing sleep apnea (haven't been evaluated yet), feel like a stroke patient, weakness on right side of body, can't drink soda, increased impulsiveness, confusion, increased speech problems, increased GERD...this has really messed me up.

you really should be careful giving this to patients who may have a sleep disorder, previous head injury or breathing issues...Is this safe for people w/ asthma, sleep apnea, cerebral palsy, sleep disorders, etc.? Will these side affects wear off or is permanent?

I have nothing to thank Topamax for.

my side effects : - Tingling hands and feet which are going away now, memory problems, word finding difficulties, speech problems, visual hallucinations. Mine ball of light flashing, red/orange colour lasting seconds, then also a white out line of doors or bjects or my body. ( even neurologist's are not aware of these visual problems and because they don't fit into the normal visual aura pattern they may think you are made. The drug company need to put out a visual hallucinatinatinations as a noted side effect. I'm taking Topamax 50mg twice a day for migraine for the last for months. It is only just now controling the migraine. I have lost 12lbs in weight.

Has anyone encountered any speech issues while on yasmin? I mysteriously have developed sort of a stuttering/speech problem over the last few years, and (coincidentally or not) around the same time I started yasmin. Of course, the yasmin could be creating the anxiety which is causing the speech problems.

Any feedback?

I thought this stuff was going to kill me! Sure I could live with the bad taste and the feeling like I was going to hurl, I could even handle the thrush. But then it started to effect my mind. It made me feel so ill. I had confusion, I would get disoriented. Then it got to the point my arms head and neck would have uncontrollable jerky movements. Then it messed with my speech. It was hard to get the words out. While trying to talk I would just start to cry, all the while my arms are flaring. Some thought I must have had a stroke. I looked like I had Parkinson Disease. I took this for about a total of 5 days. The first 2 days were okay, just felt pressure in my head behind my eyes and in my ears. By day three I felt like someone slipped me something bad. That was when the jerks and speech problems started. Once the medication was stopped, it was 72 hours later that the jerking movements stopped and I could speak normally. I was prescribed this for c-diff. The c-diff was a walk in the park compared to what this drug did to me. The doctor says those side effects can happen but it was VERY rare. I guess I was the rare one. So I say it is a VERY bad drug. But it is hard to say if I may have an underline condition that is not known and this drug just brought it to the surface. Either way I would avoid this like drug, that is just my opinion. I now know what hell must be like.

Incredible weakness, back pain, tinnitus.
During surgery for sinus disease, had levaquin administered through iv with general anesthesia. I was supposed to go home in the afternoon, but couldn't walk or even talk coherently. Intense back pain followed along with difficulty hearing and pains in shoulders as well. My tongue was thickened and I had trouble talking for three days. Today I saw the doctor and he feels that leviquin caused the problems. The back pain and speech problems are slowly disappearing. This drug is dangerous to anyone who is sensitive or allergic to medications. I once went into shock from three compazine tablets, and had to have adrenalin administered, so I know how very powerful medications can be.

my husband is dignosied with als and lyme. our dumbss* Dr. had him on lipitor 20mg for a month. my husband has taken a serious dive in condition. how could i be so stupid as to trust a Dr. and this medicine. jon is now having speech problems and extreme lung problems. he was all ready unable to walk and has extreme muscle wasting. help please !!!!!!!!!!!!!!!!!!!!!!

Pfizer doesn't admit that Lipitor has this side effect, but it does. I have swallowing and speech problems plus memory loss. I am under care of a neurologist who who originally diagnosed me as having Bulbar ALS. After an EMG test he realized that my nerves were regenerating AFTER I had stopped taking Lipitor for a few months. He now things that my problems were caused by Lipitor and that I do NOT have ALS. My speech and swallowing have not deteriorated further since stopped Lipitor one year ago; however, they have not improved very much either.

Positives: I lost the ninety pounds I put on with Depakote in just over a year. Full seizure control.

Negatives: Occasional tingling in extemities. Hands and fingers feel cold frequently. Speech problems--can't recall the words I'm looking for.