Parkinson’s Disease Misdiagnosis
I am 74 years old and I was diagnosed with Parkinson’s disease in 2019 at the age of 69 years old and I still do not have any symptoms of the disease, no constipation, tremors, pain, I do feel dizzy often and fatigued and blurred vision at times but I am sure that the blurred vision is not due to a disease like Parkinson’s disease. I have no tremors at all, I do not have any problems with my bowel movements.
My neurologist said it could be a disease that is similar to Parkinson’s disease. What could that disease possibly be to mimic the symptoms of Parkinson’s disease? I think he was lying to me about the diagnosis and the disease. Or else he made a mistake in his diagnosis and he sounded like he was trying to come up with something that sounded logical, which it didn’t make sense to me.
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It sounds like you need a second opinion. Maybe you might get some information that helps you. I hope you find some answers.
My good friend was diagnosed with PD but had no tremors, still driving, participating in social activities. Sinemet didn’t seem to make a difference with occasional focus issues. He’s 80. Finally got in with Mayo Dr. who said if anything he has a nickel’s worth of Parkinson’s. They are doing other Neuro tests. Do get a second opinion from very experienced neurologist with movement disorder testing and scans.
Hello @mamasmeeve,
That is an interesting term, "nickel’s worth of Parkinson’s." Do you know if this was this meant to describe a mild case of PD?
My husband was diagnosed with PD about 6 years ago. To look at him, you would never know it. He’s doesn’t have the typical tremors associated with PD. His pain is mostly muscular. PD is very difficult to diagnose. We were told, it takes a good 7 or so years to really diagnose. He is diligent with PD exercises. He has joined a Boxing group just for PD and exercise program. The program is strictly for PD. It seems exercise is one of the most important thing that you can do to keep your PD under control. Also there are other Movement Disorders out there. They are realizing that everything that may look like PD may not be PD. I would suggest finding a really good Neurologist or movement disorder doctor. I would seek out a teaching hospital with a good reputation versus a local hospital/dr. Good luck.
If you have access to a university or tertiary care clinic with a neurology
Department there is a new PD skin biopsy with genetic test sent out to a referral lab.
It is more accurate than a clinical
diagnosis and the new technology
may be helpful.
Agree.
Several symptoms are related to Parkinson's.Yes it varies for each person. My experience with my husband was first.Loss of smell, constipation, vivid nightmares and not getting REM sleep, sleep apnea, falling and difficulty with his posture. He was not able to write his name. He did not have the classic symptom of jerking of his left arm and hand . My brother has Parkinson's as well as my father. My father is deceased and my brother is in hospice. He is 67 yo. This terrible disease has been heartbreaking and sometimes bitter sweet. Movement Disorder's are hard to manage. Continue to take care of yourself as best you can .