Randi Chance
randi615.bsky.social
Randi Chance
@randi615.bsky.social
ME/CFS for over 3 decades. JAFF (Jane Austen Fan Fiction) is my jam. Don't know what I would do without my Christian faith and my husband and daughter.
Reposted by Randi Chance
HOPE

It's 1001 nights since I got COVID-19. 1001 nights of uncertainty, instability and loss. My world turned upside down. But somehow, after 1001 nights, hope is still alive.

#ME/CFS #LongCovid

1/-
March 23, 2025 at 1:21 PM
Having a debilitating chronic illness like #MECFS is hard enough, but when your already-disabled spouse suddenly develops serious physical and cognitive problems, needing your constant care, it's a whole new level of shit-show. 😢😫🫨🤯
March 23, 2025 at 7:37 PM
Reposted by Randi Chance
Just a little reminder for myself not to do that this year!
#mecfs #chronicillness
December 22, 2024 at 8:05 PM
I love this. So many of us with #MEcfs and #LongCovid have wrestled with the same compromises in order to see people. For me, not only am I usually sporting dirty hair, but my bedroom is a mess! I am trying to get more comfortable with people coming in to say hello to me. Very poignant and relatable
(3 minutes)
A man with long Covid shares how he chose "vulnerability over isolation" so we could see his daughter (and her friend)

www.youtube.com/watch?v=WNqs...

#LongCovid #chronicillness #MEcfs #Spoonielife
Vulnerability Over Isolation
YouTube video by Long Covid Musings
www.youtube.com
December 22, 2024 at 10:31 PM
Reposted by Randi Chance
If you’re struggling to learn how to rest and really take care of yourself - you’re not alone.

I wrote an entire article about it - and then immediately went into a flare because I was unable to follow my own advice.

It’s ok - all we can do is get up the next day and try again:
It's Time to Throw Away the 'Coulda, Woulda, Shouldas' and Practice Radical Rest
When you're chronically ill you can't push your body the way non disabled people do. You have to learn to rest. There's few words more damaging to us than the 'coulda, woulda, shouldas'
www.disabledginger.com
December 9, 2024 at 3:48 AM
Reposted by Randi Chance
Welcome Collective: 'Living with ME'

'Jeremy Jeffs is a filmmaker and photographer whose experience of living with ME/CFS inspired him to talk to and photograph others with the same illness.'

wellcomecollection.org/stories/livi...
Living with ME
Nine people with ME reveal their unremitting struggles as they negotiate life with their illness, including their battles to be believed, diagnosed and supported.
wellcomecollection.org
December 3, 2024 at 7:38 PM
📢📢📢 PUBLIC SERVICE ANNOUNCEMENT:

One month from today, we will be entering the calendar year in which the oldest 👩‍🦳👨‍🦳 members of Generation X will turn 60! 😳

and yes, I 🙋 am one of this group 😳😳😳 Trying to wrap my head around it but not entirely sure of how I feel. How about the rest of you?????
December 1, 2024 at 10:34 PM
Reposted by Randi Chance
. @meresearchuk.bsky.social :
Today (20th November) is World Children’s Day - UNICEF’s global day of action for children. A key aim of the day is to highlight critical issues affecting children’s lives – regrettably, this includes ME/CFS.

Read more: bit.ly/4hY2xXw

#MEcfs #PwME

#WorldChildrensDay
November 26, 2024 at 6:00 PM