Parkinsons symptoms and conditions

I'm 54, started taking lisinopril in jan 09. I took for about 3 months and noticed a decrease in libido. My pressure was pretty much in control, so I stopped taking it. I started again around 1st of Aug 09. Approx 3-4 weeks later, I began to experience severe pain in my left shoulder and arm. It began to move into my neck and back. I went in for an EKG to ensure I wasn't having a stroke. It was normal. I experience dizziness and headaches. I wake in the night and my 2 left fingers on the left hand are completely numb. The pain in my neck is now moving to the right side and some shoulder pain seems to be apparent. I noticed pain in other joints as well. I'm unable to work out at the gym as I usually do due to the pain my my left arm. I highly suspect these symptoms to be caused by lisinopril. I've been taking 20mg and was just switched to 20 mgm Hct. a week ago. X-Rays were taken of my neck and shoulder last week. Haven't' heard from the doctor as of yet. I was on Diovan before I lost my job and health benefits. As a vet, the VA put me on the Lisinopril. The Diovan worked fine for me, too expensive for us vets I guess. I am discontinuing the Lisinopril as of today 10/24/09. I feel like I imagine a ninety year old would feel with these aches and all. I havent' admitted it, but I believe I'm feeling mildly depressed as well. Let's see what a week of purging this from my system does. f. D.

My 62 year old husband has had Parkinson's for about 10 years now. The other day he was prescribed Prednisone (20 mg tablets, twice a day) for 5 days. After the first day his pinched nerve problem was greatly improved, and as a side effect, his Parkinson's symptoms disappeared completely and he was like normal again! This is a miracle to us and we are looking for medical research to help prescribe Prednisone for Parkinson's', or some agent similar. Did the Prednisone make the other Parkinson's drugs more effective; or did the Prednisone fix the Parkinson's on its own. We don't know. For 5 days, it was bliss; I hope we can get someone to weigh the side effects against the miracle of being normal without any Parkinson's symptoms!

I had muscle aces and pains most of that time but near the end of the 3 weeks I would loose the use of my left arm for periods. I would feel faint and very weak. I have had restless leg since I was a child but my legs got much worse during the 3 weeks. Finally I remembered that if you had muscle weakness you were to stop Zocor so I did. The daily muscle weakness gradually went away but I developed severe restless leg and had to go on Requip. I also started having face spasms and “turrett” type spasms in my legs that would travel up into my arms and hands. My hands would clench and I couldn't talk plain. My head would jerk and my body would shake inwardly as if I were freezing. These symptoms were worse when I was stressed or got too hot. Eventually I had to quit my job, it was very high stress. Five years have past. I now stay home and garden and paint. I very seldom leave my home and my stress level is low but when I do get into a stressful situation I still have to deal with the “loss of control” over my body. My sleep is a nightmare every night. My restless leg syndrome is getting worse and I've had to increase my Requip and will probably have to do so again soon.

My cholesterol is very high and my doctor keeps trying to get me to go on some meds for that but I would rather die than add to the painful, exhausting struggle I go through now because of what Zocor did to me.

memory loss, headaches, tias/mimi strokes, kidney stones, blood clot,vertigo, disorientation, muscle spasms, shaking, trembling could not control , dry eyes, stiffness in neck, back pain, twitching of all muscles , blackout when really sick, cant hold arms up, thought I had Parkinson, ms or Muscular dystrophy, motor skills are no longer great, arms and leg muscles bad, cannot write much at all, no strength in fingers or toes.
chronic fatigue and fibromyalga diagnosed not so sure after reading all these side effects.

Here's a way out theory about my unique and to me mystifying medical situation....

I recently read where Singulair, an asthma medicine, is suspected of causing suicides, obviously an effect on the brain function. The FDA notes that over the past year, Merck has updated Singulair's prescribing information and patient information to include the following post marketing adverse events: TREMOR (March 2007), (April 2007), suicidally (October 2007), and anxiousness (February 2008). (the tremor highlight is mine since this is a major symptom of Parkinson's )

Well, I took Singulair from 1998 to 2004 and I wonder if maybe, just maybe Singulair could be a contributing factor to my strange Parkinson's but not Parkinson's problems that is
gait,
balance,
freezing of gait problems

Any thoughts or ideas on how I might follow up on my hypothesis?

Within 5 days of beginning course of Geodon, 40mg daily, doc doubled my dosage to 80mg, began to have problems. Intensely manic, easily frightened, insomnia, terrifying dreams. I decided to get out of hospital ASAP and decide if to quit taking Geodon.
On day six already my face was twitching, was irritable and manic, pacing, increasingly manic throughout day, decided to skip evening dose, keep total dosage same as before, 40mg. Began tripping around midnight and it was all downhill from there. Sleepless all night, by morning I had convulsions, increased heart rate, fear and anxiety, psychosis, uncontrollable crying. Had another seizure 12 hours later. Slept a little with help of Valium. Next day developed Parkinson's like symptoms, had my father not been there to help me, Lord knows what would have happened to me. Still awake in day 3 of withdrawal. Hoping the worst is over.

My husband is taking Lipitor for high chol. just like all of you. In June 2007 he began to complain of mild pain in his body...including joints and muscles. He also had a very painful stomach ache with a feeling of tightness. He takes many meds. due to Parkinsonism and depression. As time has passed the pain has become so increasingly bad that I took him to a neutologist to determine if the pain could be a Park. symptom. His doctor is no dummy. He first determined that it was not parkinsons, but did order some tests to analyze a number of other possibilities....one being a form of rheumatiod arthritis that suddenly attacks the entire body without warning. ..it is very rare. In addition he ordered an immediate rheumatology appointment to have another doctor give him an opinion from that specific area of expertise. When we get there the rheumatologist will determine if it is a rheumatoid syndrom or not and then put him on a regimen to help that.if necessary...BUT, HERE IS THE THING THAT THIS FANTASTIC NEUROLOGIST ALSO DID....HE ORDERED HIM TO STOP TAKING ....LIPITOR.....FOR A MONTH AND SEE HIM AGAIN AFTERWARD FOR A FOLLOW-UP FOR THAT POSSIBILITY...LOVE HIM...DON'T YOU!!!!!!
For all those doctors out there who don't want to test the possibility that LIPITOR could be the cause for these life dibilitating symptoms....may ALL THE ATTORNEYS BONE UP ON THIS PROBLEM...AND PREPARE TO GO TO COURT. WE WILL BE FIRST IN LINE.....I am almost positive it is the Lipitor...and I will try to get back to this site and let you know what happens.
God Bless you all.....and God help all of the care givers who also feel pain from their loved ones' physical dilemas.

my husband took permax for parkinsons and complained of severe exhaustion and dizziness.

This is for a friend of mine diagnosed with Parkinson's and dystonia. All her big problems began shortly after hypothyroid diagnosis and her starting on Synthroid. Is it coincidence? Or has anyone heard of synthroid or thyroid meds promoting or mimicing Parkinson symptoms,or involuntary muscle spasms? Am I just imagining a connection?

Can you please tell me some common side affects for the drug which my mother is taking to treat Parkinsons. Carb/Levo 25-100 mg, substitute for Sinemet. Thank you

tremors, imbalance, dizzy, sore neck, shoulders, weak right arm, unresponsive right foot, night twitching right leg. About the time I got off lipitor diagnosed w/ early onset parkinsons. Add me to the hundreds...or more.

I went into the hopital for a bowel resection. They gave me Reglan after the surgery. Within in a day. I had strange feelings, restlessness, edgy and could not stop moving. I walked the hopital for hrs and hrs. One nurse said I was having anxiety attacks and gave me ativan. They released me after 9 days. I was back in another hospital that same night with a bowel obstruction. They pumped me with more reglan. I became very shakey and felt like I was going to fall apart. I stayed in that hospital for 19 days. When they released me I had to go back and see my original surgeon. I told her I thought the reglan was doing strange things to me. She just increased my ativan and told me I had to take it for at least 3 more mos or I could end up back in the hospital with another bowel obstruction. I started to have head shaking episodes about once a week but I still thought it was anxiety. Then after being off reglan for 1yr, I was still having attacks only every night. I saw a neurologist and she said I had permanent damage to my brain from taking Reglan and now I"m on Parkinsons medicine and ativan to try and control the symptons. I will never be the same and would not recommend this drug to anyone.

poor small motor control, difficulty swallowing,tremors,not swinging arm when walking, weakness,confusion,anxiety/panic attacks,constipation,stacked writing, getting tested for Parkinsons and am thinking it may be my 3-4 year use of Lipitor.