#InvisibleDisabilitiesWeek
It's #InvisibleDisabilitiesWeek 🌻

Repost this and read the thread below to help bring awareness to and support #InvisibleIllnesses & #InvisibleDisability!
October 23, 2024 at 3:23 PM
This week is #InvisibleDisabilitiesWeek. My chronic illnesses are an invisible disability, especially #MECFS. ME/CFS is a neuroimmune disease that has a worse quality of life measurement than any other. This #Sciart #symptomatology #embroidery, body map, maps out my symptoms as they were in 2016.
October 20, 2025 at 5:25 PM
Just because someone looks “fine” and “okay” doesn’t mean they can’t be fighting a constant battle. Be kind!

❤️

#InvisibleDisabilities #ChronicIllness #DisabilityAwareness #Autism #hearthealth #invisibledisabilitiesweek
October 22, 2025 at 3:19 PM
it's #invisibledisabilitiesweek ! invisible disabilities are valid & can be just as debilitating, chronic migraine, cervical spondylosis & occipital neuralgia have unfortunately defined my life the last 4 years & it's taken a LOT to get to where I am now mentally & physically
i have zines where i talk about both my chronic migraine & occipital neuralgia, a real pain in the ass headache condition, that is now (???) kinda under control since last year

ko-fi.com/s/bdeeb336ee

ko-fi.com/s/d380d80496
October 20, 2024 at 4:28 PM
When I asked my Dr. to fill out my disability tax form, she did it reluctantly, saying, this is for people who are REALLY disabled.

#LongCovid #ME/CFS #invisibledisabilitiesweek
"Most disabled people don't claim #DisabilityBenefits.
Many would be eligible, but they choose not to, or are alienated from the process by how horrific it is. People overestimate how many claim, how we are deemed eligible, and how much we get."
@adamfare1996.bsky.social
#InvisibleDisabilitiesWeek
October 23, 2025 at 5:14 PM
Beautiful expression of one person's somatic experience of ME/CFS

Happy to have found this artist here, thanks to #InvisibleDisabilitiesWeek
This week is #InvisibleDisabilitiesWeek. My chronic illnesses are an invisible disability, especially #MECFS. ME/CFS is a neuroimmune disease that has a worse quality of life measurement than any other. This #Sciart #symptomatology #embroidery, body map, maps out my symptoms as they were in 2016.
October 24, 2025 at 8:57 PM
For #InvisibleDisabilitiesWeek: One of my main #MECFS symptoms is multiple paresthesias (tingling). This #SciArt #symptomatology #embroidery maps the paresthesias in my face. 🐡🧪🩺🧶
October 22, 2024 at 5:00 PM
This week is #InvisibleDisabilitiesWeek. My chronic illnesses are an invisible disability, especially #MECFS. ME/CFS is a neuroimmune disease that has a worse quality of life measurement than any other. This #Sciart #symptomatology #embroidery, body map, maps out my symptoms as they were in 2016.
October 19, 2025 at 4:03 PM
This year #InvisibleDisabilities Week is October 15-21. Invisible symptoms are real. Patients with complex illnesses deserve recognition. This is my tribute to everyone living with an invisible disability. #POTS #MEcfs #longLyme #longCOVID #dysautonomia #brainfog www.lymedisease.org/invisible-di...
October 14, 2023 at 11:58 PM
Compassion, awareness, and respect help make the “invisible” visible.

#InvisibleDisabilitiesWeek #DisabilityAwareness #AccessibilityMatters #InclusionForAll #NotAllDisabilitiesAreVisible
October 21, 2025 at 4:15 PM
It’s #InvisibleDisabilitiesWeek.

I dream of an education system that proactively meets the needs of ALL students.

I dream of a world that doesn’t make people beg for the accommodations they need to be safe and successful.

I dream of acceptance, inclusion, and celebration.
October 20, 2024 at 12:46 PM
For #InvisibleDisabilitiesWeek: One of my main #MECFS symptoms is multiple paresthesias (tingling). This #symptomatology #embroidery maps the paresthesias in my face: paresthesia (face) 2016
October 21, 2025 at 4:06 PM
"Most disabled people don't claim #DisabilityBenefits.
Many would be eligible, but they choose not to, or are alienated from the process by how horrific it is. People overestimate how many claim, how we are deemed eligible, and how much we get."
@adamfare1996.bsky.social
#InvisibleDisabilitiesWeek
October 23, 2025 at 3:41 AM
"When a disabled person asks for help, we've likely exhausted all options before asking. We've tried everything before coming to you. Believe us & offer the help requested (if you can)...
Follow Kelly @broadwaybabe for more!

#SeeTheInvisible #InvisibleDisabilitiesWeek
October 21, 2025 at 4:17 AM
⇢ use your voice to advocate for them (and ALL disabled people)
⇢ use your platform and RT this post to bring awareness

If you yourself have an invisible disability - comment down below so we can connect 🤎

#InvisibleDisabilitiesWeek #MakingtheInvisibleVisible
October 23, 2024 at 3:25 PM
For #InvisibleDisabilitiesWeek & #WIPwednesday: May Thurner Syndrome (#IliacVein compression syndrome) seems to be a common comorbidity with #MECFS. This #symptomatology #embroidery in progress is based off a venogram of my stent. 🧶🩺🧪🐡
October 23, 2024 at 4:54 PM
Another for #InvisibleDisabilitiesWeek

On #cognitivedecline / #dementia
And the idea of still providing “light” and joy to your children who are trapped growing up in your diagnosis.

#tradart #acrylic #chronicillness
October 23, 2025 at 7:01 PM
ADHD can present differently from student to student, and there are strategies that support not only their individual learning needs, but also benefit the entire classroom community. #InvisibleDisabilitiesWeek
How to Support Students with ADHD | NEA
From strategic seating to brain breaks, educator-recommended classroom strategies that help students who have ADHD.
www.nea.org
October 23, 2025 at 7:19 PM
Thanks to the Neurological Alliance of Ireland for raising awareness of those living with invisible, unseen or hidden neurological symptoms.

Many people living with #FND have such symptoms and awareness and education is critical to feel more visible and understood. 💚🧡
#InvisibleDisabilitiesWeek
October 23, 2025 at 3:20 PM
This week is #InvisibleDisabilitiesWeek. My chronic illnesses are an invisible disability, especially #MECFS: a neuroimmune disease that has a worse quality of life measurement than any other. This #SciArt #symptomatology #embroidery maps out my symptoms as they were in 2016. 🐡🧪🩺🧶
October 20, 2024 at 5:00 PM
💜 Invisible Disabilities Week – Final Day 💜

As the week ends, let’s keep the conversation going.
Invisible doesn’t mean forgotten or judged. 💜

#InvisibleDisabilitiesWeek #Fibromyalgia #EndTheStigma #Listen #Believe #YouAreNotAlone
October 25, 2025 at 2:44 PM
I heard it’s invisible disability week! I had an undiagnosed lifelong calcified herniated disk slowly severing my root nerves and I had to get an emergency decompression laminectomy on my L5-S1 on November 19, 2024. It was traumatic and I almost died.

#SeeTheInvisible #InvisibleDisabilitiesweek
October 21, 2025 at 10:07 PM
For #InvisibleDisabilitiesWeek: This #SciArt #symptomatology #embroidery explores the sensation of post-exertional malaise (PEM), the hallmark symptom of #MECFS. When I overextend myself physically, cognitively, or emotionally, I am too fatigued to even wash myself. 🧶🩺🧪🐡
October 21, 2024 at 5:00 PM
#InvisibleDisabilitiesWeek ❤️
#SemaineDesHandicapsInvisibles ❤️

Be kind always. 💛
Soyez toujours gentil. 💛
October 23, 2025 at 11:22 PM