How I got diagnosed with young onset Parkinson’s Disease

[@PatFerry]

I was also diagnosed with MS 14 yrs ago. Then PD 8 yrs after that. Thankfully my MS has been quiet, b/c just having PD symptoms has been challenging. Keep the faith, good luck, and exercise!

[@shakinginmyboots1]

Oh wow! That’s great to hear. I mean the doctors don’t seem to have much to say. And yes PD is more than enough

[@GaryPack-l4u]

Thank you for this. I have LBD-basically the same thing. It’s hard to accept, but it’s not the end. Stay positive, stay strong.

[@shrinjoymukerji6833]

You are a warrior ❤️

[@paultoensing3126]

Hang in there dear. We have a large support group. Not just for commiserating, but for finding effective approaches. I’ve done stem cell treatment for mine and it really helped.

[@adawehi55]

Thank you for sharing. I should have been diagnosed years ago. Actually, a nurse practitioner thought I had PD 7 years ago. Low B12 and a clear MRI changed her mind. Diagnosed with DATScan in 2022. I was actually relieved. The medication has helped with the stiffness and pain they said was caused by fibromyalgia.

[@shakinginmyboots1]

I was relieved too! I think the stress of not knowing was worse than the diagnosis.

[@Mortenlu.kungfu]

Almost exactly my story 5 years ago. I'm 54 now. Positive thoughts from here ❤

[@MikeMercury]

sympatise with you
also have parkinson

[@kendc4725]

I’m not too far behind-hitter a year on April 3. Had a similar path of random symptoms until an MDS put it together.

[@shakinginmyboots1]

Hope your first year was smooth sailing

[@jodydaguimol]

im hoping to see if im a candidate for focused ultrasound

[@MikeMercury]

you take medication ?