She is seeing people that are not there at night. Shadows, Hallucinations. At first there was no sleep at night, her Dr gave her a sleep aid witch helped. We both have just this week started Mental health care. What is hard for me is I have no help, she fell and broke her wrist in December, had a plate and screws installed to put it back together in January. It never stops.
AARP article- some of this is redundant but maybe just a slightly different take on things that might be helpful and it does make a person wonder if light therapy during the day might help to some… read more
Newbie here. At a loss of how I can help my family. My father has been on Sinemet for months-- taking the pills makes life "kind of" worth living again, but the negative side effects are beginning to take a toll. He is very paranoid and jealous, accusing his spouse of cheating. It's becoming so difficult for her, who does nothing but love him and take care of him at the expense of her own mental health. She tries to explain to him that this is a side effect of the medication, but he does not… read more
I have not encountered any problem. I take 2ea four times daily and four hours apart..
I'm newly diagnosed and don't know what kind of medical expenses to expect with Parkinson's.
I agree, I wouldn't change. Many doctors don't participate in those plans. At least that's the case in Panama City, FL. However, we lost many doctors after the 2019 (or 2018) hurricane, so that could… read more
https://tafcares.org/upload
This organization helps offset medical costs.
Maria
The last time I looked, I believe there was a year-and-a-half waiting list for patients with Parkinson's Disease.
Thanks for asking about this drug. I have not heard of it. Do you know if it affects blood pressure
For me, reducing my anxiety with medication and controlled breathing, my tremors are almost… read more
I'm shocked and thrilled to learn that this can happen and did happen just yesterday and I really have no idea what to do now after spending most of the past 9 yrs accepting and adapting to PD.
Maria
Hi Maria! There appear to be thousands of research studies on this disorder although the bulk of them are not in this country, mostly in Europe. Many of them are not recruiting. When I applied the… read more
Thanks for the ideas...the reason for my rqueerie was due to a documentary I recently saw, called "Root Cause" which clearly ties in the concept that root canal is one of the worst things people do -… read more
I have to continue working part-time because Disability does not cover the costs of living. I know many jobs and he uses me everywhere. If someone misses work I do my job and theirs. Many times it's 2 other jobs. Today he wanted me to pop his back, both myself and coworker said no. When I reminded him he said I just use PD and Fibromyalgia as an excuse. I know it's because I push myself til I collapse, in a corner where Noone sees
He doesn't pay me a lot because there's just so much I can make.… read more
Hi. First of all, you are not a useless woman! It's normal to feel bad in terms of the weight on your care partner, but you are NOT useless! Everyone ages and changes. People get sick. People get… read more
The APDA recommends the following resources to information about improving the quality of life by reducing OFF episodes
Communicating About OFF Episodes: This helpful booklet explains why OFF episodes occur, the motor and non-motor symptoms that you may experience while OFF, tips for smoothing out medication to reduce OFF times, and so much more.
Motor Fluctuations Fact Sheet: A quick overview of what motor fluctuations are, what causes them, how to treat them, and more. Also available in… read more
No links? Sorry for brevity…I’m in “off” mode myself right now…
Have been diagnosed with Parkinson’s 4 years ago. Doing great on low doses of Sinemet and Mirapex. About a year ago developed muscle pain which is worse in the morning (mostly on the left side buttocks and low back). Increasing med’s did not help. I keep exercising but some days the muscle pain is so bad I do not want to exercise. I have tried everything from exercise, stretching, Tylenol, topical analgesics, trigger point therapy, massage, tens unit etc. Nothing seems to help. I believe it is… read more
Where can I meet this Parkinson’s Ned?