Today is World Parkinson’s Day. I have looked on Mastodon for fellow Parkies and found almost none. If you suffer from Parkinson’s or are a caregiver and want to chat, feel free to add me. I am an early-onset and my father-in-law was diagnosed just after me. Awareness is key to working on treatments and someday a cure!

(I just wish “our” color wasn’t orange, lol!)

#WorldParkinsonsDay #ShareYourSpark #Parkies

@AncTreat5358

I haven’t found a good Parkinson’s hashtag but have been looking for a group too. There are message boards at the Michael J. Fox Foundation but wondering where the Mastodon peeps are. Replying to boost visibility.

I wish you all the best with your health journey!

#Parkinson’s #PD #Parkies #MovementDisorders

If anyone reading this has worked for the US National Park Service / BLM / other public land agencies, and has struggled with housing, Molly McCluskey is working on a piece for Sierra magazine and could use your input. It's a big issue for park employees, so I hope as many as possible talk to her.

#parkies #PublicLand #housing

(LinkedIn request) https://www.linkedin.com/posts/mollyemccluskey_attn-current-and-former-parkies-im-writing-activity-7168270943818125313-glex?utm_source=share&utm_medium=member_android

Molly McCluskey on LinkedIn: ATTN current and former parkies - I'm writing an article for Sierra…

ATTN current and former parkies - I'm writing an article for Sierra Magazine about housing challenges for park staff. If you've had any issues…

Women with Parkinson’s or female caregivers, submit your story! The Women’s Parkinson’s Project is looking for glimpses into a day in the life of women with PD. Any language is fine, but English translation must also be submitted. Link to Submit: https://rb.gy/prjfh4.
#Parkinsons #Women #WomenWithPd #YOPD #parkies
grryboy’s house of horror (@[email protected])

Attached: 1 image A bit about my #Parkinsons for #Parkies and others: I was diagnosed with #YOPD in 2011, by 2020 meds were maxed, movement, balance, speech, rigidity and dystonia made it difficult to enjoy life. People think tremor; it’s the least of problems. #DBS was a relief. Brain surgery is scary. I had to be conscious, but it was'nt painful. Moving the probes and adjusting power changed my me from complete constriction to rubber. But we found a happy medium in each limb. Each #Parky is different.

HorrorHub Social

Good Morning, #Mastodon !!!

For #FollowbackFriday I'm looking for people who want to be active members of #horrorcommunity #horrorfam #horrorfamily #mutantfam in discussion of #horror #horrorfilms #fiction #writing #horrorart etc.

Also interestred in #scifi #sciencefiction #Parkinsons #YOPD and my #Parkies #PwP and #UnixPorn

I'm not concerned with quanity of followers but quality. For the like minded #followandboost and I'll do the same.

A bit about my #Parkinsons for #Parkies and others:

I was diagnosed with #YOPD in 2011, by 2020 meds were maxed, movement, balance, speech, rigidity and dystonia made it difficult to enjoy life. People think tremor; it’s the least of problems.

#DBS was a relief. Brain surgery is scary. I had to be conscious, but it was'nt painful. Moving the probes and adjusting power changed my me from complete constriction to rubber. But we found a happy medium in each limb.

Each #PwP is different.

@cceaough I should say for fellow #Parkies this is not necessarily a typical progression, especially for #YOPD. I don’t want to scare anyone.

It’s only my #Parkinsons