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HaylenView Thread
Thank you for the reply and the further clarification. I truly appreciate your efforts to help me out. From looking for definitions of Bradykinesia and Adiadochokinesia on the web, both seem to be treated as separate symptoms and not as a subset of one another.
Bradykinesia seems to refer to slowness of movement and is seen a neurological issue whereas
Adiodochokinesia seems to be more cerebral and refers to the "Lack of ability to stop movement in one direction and follow it immediately with movement in the opposite direction."
Thanks once againView Thread
I hope these arrticles give hope.
Just think maybe this is part of the solution for all neurological disorders
This article gives me hope that they will be able to stop the domino(SP) destruction of our brain cells.combine this with astrocytes taking over dopamine production we would not have to worry about further loss of movement and memory. Eventually No one would have to experience Parkinsons, Alszheimers, MS etc.
w
IView Thread
View Thread
I know that my own nursing training was over 30 years ago, but I don't remember learning too much about PD. All we really knew was that patients with it had tremors.
Okay, that's about all my caffiene buzz can handle this morning, Thanks for all of the advice! And, thanks to the strangers on this site who are becoming friends!View Thread
I think thousands, maybe tens of thousands, of people are looking for a cure for PD. Take heart - I am hopeful and optimisticView Thread
Sorry for my long and continued rambling. but these were the questions bothering me the most
1. what could be the reason for the chronic fatigue on waking up in the morning and why would it decrease during the day along with other symptoms?
2. could the carotid artery stenosis of 25 % be symptomatic for my dad to cause all this (like the cardiologist alluded?)
3. if not then is there any benefit to doubling aspirin dosage to 150 mg every day ?
4. his mri was done without contrast (no dye injected). i understand that to be ur recommendation
5. the cardiologist put him on gabapentin when he first complained of numbness in his toes. dad thinks it neither had any positive nor negative effect. could it be the cause for parkinsonism symptoms?
6. what could be our next course of action/ questions. we do believe getting a blood test done to determine any deficiencies is very important. i guess thats the MCV test is that you also mentioned.
any other recommendation for tests or diagnosis would be very helpful
Thanks
ShyView Thread
Unfortunately, restless legs syndrome and painful leg and moving toe syndrome are not the same, and it is unfortunate that we have blended this nomenclature. Sadly, RLS medications and everything else usually do not help PLMTS.View Thread
the viartis website is at http://www.viartis.net .
-- susie margaretView Thread
i googled ("deep brain stimulation" parkinson's pros cons); take a look at http://www.google.com/webhp?sourceid=toolbar-instant&hl=en&ion=1&qscrl=1&nord=1&rlz=1T4DMUS_enUS305US305#hl=en&gs_nf=1&cp=48&gs_id=1c&xhr=t&q=(%22deep brain stimulation%22 parkinson's pros cons)&pf=p&sclient=psy-ab&qscrl=1&nord=1&rlz=1T4DMUS_enUS305US305&site=webhp&oq=(%22deep brain stimulation%22 parkinson's pros cons)&aq=f&aqi=&aql=&gs_l=&pbx=1&bav=on.2,or.r_gc.r_pw.,cf.osb&fp=ba8047ecf031fabe&ion=1&biw=1280&bih=715 .
-- susie margaretView Thread
I do think yo need to see your family physician. While PD can present with these symptoms, it may be more likely be a result of severe depression. Please remember, both of these conditions can be treated, and it is very likely you will feel better just knowing whether it is one or the other.View Thread
It is very frustrating. You try so hard to keep a positive outlook, but sometimes it is just too hard. I hope the next dilation works for you. I am going to see a GI doc that specializes in treating people with PD.
Keep in touch, and best wishes to you.View Thread
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As far as my carpal tunnel, I haven't had an "explosion" of electrical type pain in almost two weeks, which is the length of time I've been wearing the braces. Not to say that the pain is gone, just the BAD, explosive pain.View Thread
Another aspect of his future treatment will be to reduce the dopaminergic or dopamine agonist replacement drugs that he has gotten used to over the sixteen years he has been treated for PD. It is an extremely painful process and mwy take a year or two.View Thread
webMD info on atropine drops is at http://www.webmd.com/drugs/drug-6687-atropine Oral.aspx?drugid=6687&drugname=atropine Oral&source=2 . you may also want to take a look at http://www.mdvu.org/emove/article.asp?ID=364 .
-- susie margaretView Thread
it is time to see a neurologist or a rheumatologist. i suggest starting with a neurologist.
obviously, no one can diagnose you over the internet (see PS1), but i have found several articles suggesting that a rash, followed by weakness in the arm or leg, could be caused by the virus that is responsible for shingles (PS2) or could signal an autoimmune problem. whatever it is, a dr needs to figure it out and start treating it.
i send you caring thoughts and hope you will keep us posted.
-- susie margaret
PS1 -- i am not a medical person; i welcome, solicit, and indeed beg for correction, amendment, or replacement of inaccuracies in this post.
PS2 -- shingles is a viral infection of the nerve roots.View Thread
I am fairly certain that the PD is/has played some part in this development, along with my neuropathy. Has Dr. Stacy ever had patients with this combination before?View Thread
HaylenView Thread
HaylenView Thread
Thanks so much for all you do!
HaylenView Thread
When you are first diagnosed with Parkinsons you want to sit down and cry and at the same time you are relieved that you finally know what is wrong with you. You are scared that you are going to be dependent on others. You do not want to go to a nursing home but that is what you keep thinking about. Until your father starts his own research into this disease he is going to be scared. He will not show it. If he researchs this disease he will see how far research has come in treatment. The medication available will help immensly with the symptons. He is going to have a rollcoster at first. Some days he will be the energizer bunny and some days it will take everything he has to move. It is important to keep a journal to keep track of everything that is happening. An adjustment or addition of drugs may help. I have yet to meet a parkinson person who is not a lousy speller with a bad memory. Also he may loose part of his vocabulary. Tell him not to worry about the loss of vocabullary, my sister says she now understands what I am talking about.
He must exercise. the old saying use it or loose it applies with parkinsons. The more exercise you do the better you feel. Look at it as fighting back. If you cannot move parkinsons wins. Parkinsons affects everyone differently. I think attitude along with exercise plays a big part along with support from familly, friends and co workers. Keep away from negtaive people. They suck the life out of you and turns your positive attitude into bad attitude whick helps parkinsons . I do not hide the fact that I have parkinsons. People ask question which I answer. With an open discussion it helps take away the uncomfortable feeling that some people get when they do not understand. Even though I do have parkinsons I do not let it slow me down and I keep a postive attitude. I always go fot the brass ring. Admittedly it has caused some problems. I have no sense of balance and when I tried to lift and move the glass top off of a 5 ft round coffee table I ended up falling face down on the glass top with my hands pinned under the edge. I had to laugh as the only thought that came to mind is I've Fallen and can't get up.YOU must keep a positive attitude and help with the research. Talk about other things besides parkinson If he brings up the subject talk and listen.. If he dosn't have a hobby get one. Exerscise body and brain. Take up golf--great exercise, social life. Remember dogs or cats are good therapists. Make friends with the neighbors dog or get one. Dogs are people magnets and if your dad is single a chick magnet.---life goes on-- please do not take offense but making and keeping friends is vital to his emotional well being. Also walking the dog is great exercise. Goldens, Labs or any mutt that is friendly will work. I have 2. Besides great exercise I have met more of my neighbors in 1 week than I had in years.
Back to one of your questions. Parkinsons disease progresses at different speeds in every one. I have had parkinsons since the 90's. My medicatioins of stalevo, mirapex,azlect and the exelon patch for parkinsons has not changed since i started taking them. I was so far along she started me on the big guns except for the exelon patch which was added last year for memory. It has helped. With the medication you cannot tell I have parkinson.
So stop worrying about what can happen and enjoy life.
If you have specific questions ask.Someone can answer your question. It may not be what you want to hear but you will be given an answer.
Don.t let parkinson stop you from enjoying life.
wView Thread
I know that you and your husband are dealing with a lot. Because his memory is worse when he is on medications, I think this can get better. However, you will need to be prepared the next time you go to his Neurologist - and remember that we neurologists have very short attention spans...
Of the medications he is on, amantadine can cause problems with memory. Ask if this can be stopped.
The other PD meds can cause confusion and sometimes anxiety. He is on the "psych meds" for one of these symptoms. Ask which one.
Finally ask if the doctor thinks he is overmedicated, and if so, is he a candidate for Deep Brain Stimulation surgery. This is a surgical procedure, that in the right patients will allow for more mobility and less dyskinesias, with less medications. That would be a good outcome.View Thread
We cut back on that and he sticks to "natural" sugars (still in small doses) and it seems to have helped.View Thread
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