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He thought it maybe Manieres and had me tested for it as well as checking for a stroke or any leasions by means of M.R.I's and CT scans.All showed neg.As time went on My balance and coridination have gotten worse and started haveing problems swollowing food or liquids with out sometimes chokeing, and my vision has gotten blurred and even at times seeing double. And hard to look down or up with out the feeling of being dizzy,and the balance is way worse in doing that as well.
My neck is so sore and stiff that I find myself tilting my head against my shoulder most of the time just to get relief from the pain because my head feels like a gaint weight and trying to find balance all the time my head bobbels alot. My thinking process is so messed up I find it very hard to stay focused and planning, problem solving is very difficult,and short term memory is very bad. Slurred speach and finding the right words that I want to say is very difficult.
I have a constant feeling of cotten mouth and no matter how much I drink water I can never keep it from drying out. I have a lot of other things going wrong but they seem to be related more with the Parkinsons Symptoms like ED and lots of numbness in one leg and mucle and joiunt pain and stiffness. I feel like my movements are in slow motion and even sometimes freezing up. I thought I needed new glasses and saw my optomitrist and he found that one of my pupils is bigger than the other and asked if I could feel it being bigger than the other,I didn't, Hummm something new there.and he believes it to be corrilated to what is going on with me and said my perscription hasen't changed and the blurred vision is also related to what is going on.
All I know is that feeling this way is not normal and something is very wrong and this is progressing very fast. Unlike what I have found out about Parkinsons its self this is not really going in stages but seems to be developing symptoms faster and more agressively than in stages. I know that I maybe jumping the gun and self diagnossing maybe more harm than good but the Doc seems stumped about how this is progressing so fast and the tests are just showing normal for my age he tells me.I know I'm only fifty but I don't think either condition is very discrimitive with how old you are.
I'm just trying to get a grip on what this could be and with doing alot of research on my own It just keeps comming up in my mind Parkinsons or P.S.P. but I'm no Doc. So all I can do is educate myself and try to better prepare myself .....
Am I over stepping my bounds here or am I justified in doing this.....View Thread
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The E.N.T. Doc's also have told me that I do have a 98% loss of function for balance in my right ear and was starting to progress to my left ear, and that it has been progressivly getting worse sense my first test and something is causing it to happen. They have also told me that once it is gone you can never get it back and that if I totaly loose that function in both ears I will not have any balance at all..That was over a year ago.
I feel dizzy and off balance 24/7 365 and never goes away, Have lots of joint pain and muscle pain, hard to swallow food at times and choke sometimes even on my own saliva .I have a hard time finding my words and have major problem solving issues as well short term memory issues, as well as speech problems.I have blurrred vision and double vision at times, especially when I follow movement. Trying to focus on the object when motion stops is the hard part.I have numbness burnning and tingleing sensations in my left leg and my right arm has the shakes and tremmors. sometimes when at rest and sometimes while I'm using it.
My reactions and actions feel as if were being slowed by something even boardline being stopped by something. I guess I should explaine the dizzieness better, It's not a spinning sensation but like being Very Very drunk and haveing no control of your movements or ability to walk straight and your sense of balace is way off kilter. It never stops until I fall asleep. and every morning I wake the same way. I found out that I have E.D. never even thought that would happen.
My Neuro want's to dissmiss this as Vestibular issue and keep testing for a vestibular issue. I feel that this is a wrong direction and have no way to get a new Neurologist who will listen or treatment. I guess I'm looking for some guidance and or some help in getting Help....Any thing at all would be very appreacted thanks for listening......
I get sick alot ( throw up) I think it's because of the dizzieness and trying to do things and I over do it, because movement and motion dose make it feel worse. My neck and shoulders are so sore and stiff all the time because I have a hard time keeping my head balanced all the time and I believe it's because of the need to keep my sense of balance. If I'm makeing sense there I hope you under stand.View Thread
wView Thread
what supplements can anyone suggest that you have found to help with parkinsons symptoms?View Thread
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My mom have Parkinson Disease and she's being treated with Sinemet.
Before PD appeared she was suffering from depression and she was taking Deanxit for a couple of years.
Her PD doctor stopped Deanxit saying this medication should not be given with PD, he prefers Cipralex ! But Cipralex seems to have
more side effects on her (dizziness, fatigue).
I'm confused. Is Deanxit really bad with PD & why ?
What can be done against dizziness?
Thank you
RashadView Thread
PROBLEM: He's experiencing severe anxiety attacks when his levodopa medicine starts to wear off. How can we prevent these? Will taking more levodopa or the dissolve-on-your-tongue version instead help?
Many thanks for any advice.View Thread
i just wanted to tell you again that you're the greatest!
-- susie margaretView Thread
wView Thread
So right now my uncle faces 2 problems : he cannot take any regular Parkinson's medications due to dysphagia and is there any treatment for the Parkinson's dysphagia itself ? Thanks for your time.View Thread
I don't have tremors persay but have noticed over past 2 years that i would be sitting resting and all of a sudden my legs or hands will jump for no reason. I have been diagnosed with restless leg syndrome and have fallen a lot over the past 2 years but one of my Doctors blames it on hip and lower back problems. I am now concerned with Parkinsons.
Tell me how to discuss this with my Doctors.View Thread
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