Parkinson’s or Parkinsonism?
I was dx on Wednesday with Parkinsonism..I think it is Parkinson’s tho…should I see a specialist? I have loss of balance, which means frequent falls, can’t drive, slow speech and thought along with extreme fatigue. I’m being treated for depression which hasn’t gotten better after 8 weeks. Does anyone know what the stages are?
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@mondo3019 That’s a good sign. Keep thinking positive thoughts. 😊
I got rear-ended in 2019. The pain went from 0 to a 8 instantly. I was taken to the hospital where they did a ct scan, probably looking for blood on the brain, I guess. The guy had a jeep and I was my Honda accord, which they totaled, I think he actually picked up the car and placed it in the other lane, I don’t think there were any brake marks at the scene..I asked whether or not that could be contributing to the falling and the dr. from the movement center said no….
Thx.. it is hard to do, considering..
I had a brain mri and it came back unremarkable. Is that the same kind of thing?
I am sorry, but not a good person to ask. I know there is a scan called a DAT scan which is a brain scan specifically for PD. I would think a regular MRI would not be the same. Do you live near a major medical center or university? You definitely should see a specialist if there is a possibility of PD or other serious condition. I hope you can get good care in help.
There are other tests a specialist could do to identify possibility of PD.
I answered this last night and my answer is not here! Basically you should have a DAT scan which looks at dopamine in brain. That pretty much confirms PD. There are other tests too. Find a specialist. I have limited knowledge only. I hope you get good care.
Hi @tsch, your response to @mondo3019 is here https://connect.mayoclinic.org/comment/1340657/
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For some reason it was in the forum and then it was after I wrote that it wasn't. Thanks tho.
I was dx with psp, so my head is spinning.
No test to diagnose PD 100% . my brother had DATScan, professionals said PD, now they say maybe not. I'm taking my brother to a PD movement specialist in Sept. Hope to learn a little more at that appt. Leva/Dopa DID NOT Help my brother. He was also born with a somewhat rare disease called Sturge Weber Syndrome(SWS), his Parkinson like symptoms started when he started taking Lamictril for seizures that are a part of the SWS. His neurologist INSISTS, the lamictril is not the cause of symptoms. I will ask the PD specialist. The human body is a mystery for sure....