#youdontlooksick
#ProudBlue

Infusion day. Time to shut down my immune system again.

Will treatments like this soon be banned here under RFK Jr? Definitely concerning to me.

#mecfswarrior #interstitiallundisease #spoonie #youdontlooksick #Dysautonomia #mecfs #chronicillness #invisibleillness #sjogrens
March 2, 2025 at 6:31 PM
#ProudBlue

This is HUGE News for the ME/CFA community.

They have found some links to a person’s genes & this illness. This could lead to better testing & possible treatments soon.

#mecfswarrior #spoonie #youdontlooksick #myalgicencephalomyelitis #mecfs #chronicillness #invisibleIllness
August 7, 2025 at 2:06 AM
#ProudBlue #MomSky

I so appreciate those protesting for those of us too sick to attend.

Medicaid cuts will be devastating to the ME/CFS & Long Covid communities.

Tell Congress NO to Medicaid cuts

#mecfswarrior #youdontlooksick #myalgicencephalomyelitis #mecfs #chronicillness #invisibleillness
Myalgic encephalomyelitis (ME), Long COVID, and other chronic disease advocates demonstrated outside the Capitol Building in Washington, D.C. yesterday. #MillionsMissing.

Read more from @mileswgriffis.bsky.social at The Sick Times: thesicktimes.org/2025/05/12/m...
May 13, 2025 at 7:01 PM
September 1, 2025 at 2:29 AM
#ProudBlue #MomSky

I am one of the millions missing.

Help me & others fight for our lives! ME/CFS steals the lives of millions across the world. Let’s raise awareness.

#mecfswarrior #spoonie #youdontlooksick #myalgicencephalomyelitis #mecfs #chronicillness #invisibleillness
Protest in DC happening now!
Here are action items for today and the rest of the month. Links can be found here: Action items for the coming week and beyond:
🔗 linktr.ee/maggieboxey
#MEAwareness #momsky #mecfs
May 12, 2025 at 9:09 PM
The #youdontlooksick issue leads to extensive time (often years of gaslighting) before diagnosis, and when that eventually comes, treatments are often barely effective, leading to isolation, forcing sufferers to mask symptoms which feeds the whole cycle. The system fails people with chronic illness.
SBS: 'Chloe's been called 'hysterical' and has lost friends — because of something we can't see'

'Brett has been living with Long COVID since 2022 and believes his symptoms are getting worse.'

'..he finds it challenging to gain empathy for his Long COVID..'

www.sbs.com.au/news/insight...
Chloe's been called 'hysterical' and has lost friends — because of something we can't see
Chloe has an invisible illness. She says the world makes her feel like she's going crazy — and she's far from alone.
www.sbs.com.au
April 21, 2025 at 8:01 PM
Did you know❓

Not all disabilities can be seen.

Did you know❓

Millions of people live with disabilities that you can't see like #fibromyalgia❓

Our fibromyalgia may be invisible, but we are not!

#InvisibleDisabilitiesWeek #YouDontLookSick #EndTheStigma #SeeTheInvisible
October 19, 2025 at 1:08 PM
So I am on the sofa, ankles, knees and hips burning, but the view (and the challenge) was worth it. I went into it with planned recovery time, so it is okay. But sometimes I feel that the #youdontlooksick thing is insurmountable. More than a climb of 225 steps, anyway. #cfs #sarcoidosis #spoonie
September 13, 2025 at 2:57 PM
Some days are harder than others. Most “get unblocked” programs don’t consider that.

The Two Rule Recovery does. Having a rough day? Creative, you are in the right place.

#2rulerecovery #chronicillness #artists #writers #youdontlooksick
——
My weird books: ruthannereid.com

youtu.be/Ac9TsijKWOw
Having a bad brain day? So am I.
YouTube video by Ruthanne Reid
youtu.be
September 16, 2026 at 7:18 PM
May 29, 2025 at 8:22 PM
Another Tradition has come to visit:
Holiday Cheer Aftermath
Flaring the Day Away

#chronicillness #selfcare #youdontlooksick #fibroflare #spoonie #autoimmune
a man laying on a couch covered in christmas lights and tinsel
ALT: a man laying on a couch covered in christmas lights and tinsel
media.tenor.com
December 26, 2024 at 3:22 PM
I would really love to be able to work consistently, or at least predict when I'm going to feel like crap. Today should have been very busy but instead I'm stuck in a dark, quiet room with a migraine while me teeth feel like they're trying to escape my head. #invisibledisability #youdontlooksick
August 12, 2025 at 9:32 PM
June 12, 2025 at 4:36 PM
May 25, 2025 at 5:19 PM
#InvisibleDisabilitiesWeek – Day 2

#Fibromyalgia is an invisible illness. You can’t see the pain, fatigue, or brain fog, but it’s real

People often have to explain or hide what others can’t see. What they need most is understanding, compassion & belief

#YouDontLookSick #FAC #EndtheStigma
October 20, 2025 at 7:13 PM
Depression is a bitch. Job searching isn't helping. I just keep being told "we have a lot of applications" they won't even let me say my name. But at least it's on my resume 🤷‍♀️
#mentalhealth #depression #youdontlooksick
February 17, 2025 at 9:43 PM
Today's spotlight author is Clarence Carter. His story is titled "Unraveled" and features themes of anxiety and depression.

#fridaynightwrites #seemeasiam #fnwanthology #books #invisibleillness #youdontlooksick #weeseeyou #charityantho #disabilities #invisibledisabilities #mentalhealthawareness
June 7, 2025 at 12:26 AM
See Me As I Am, a charity anthology that seeks to bring light to illnesses that hide in the shadows, unseen. #fridaynightwrites #seemeasiam #invisibleillness #youdontlooksick #weeseeyou #charityantho #disabilities #invisibledisabilities #mentalhealthawareness
May 20, 2025 at 10:51 PM