#multiple sclerosis awareness

[thebeesbox]

Day 42 of Pride Flags Drawn as Foxes: Multiple Sclerosis (yes it is technically a symbol not a flag but I couldn't find a flag)

#digital art #art #artist #digital arwork #digital painting #artists on tumblr #painting #fox art #multiple sclerosis #multiple sclerosis awareness #disability pride #disability #disabilties #disabled artist #disabled #disability pride month #actually disabled

[kindajd]

#multiple sclerosis #ms #esclerose múltipla #em #multiple sclerosis warrior #autoimmune disease #chronic disease #chronic illness #ms flare up #ms relapse #multiplse sclerosis flare #multiplesclerosis #chronically ill #chronic fatigue #chronic pain #multiplesclerosisawareness #multiple sclerosis awareness #TN #trigeminal neuralgia #pins and needles #trigeminalneuralgiaawareness #trigeminalneuralgia #pain #invisible illness #chronic ill #illness and disability #illness #invisible disability #disabled #fatigue

[unave]

March is Multiple Sclerosis Awareness month, you all have to be nice to me

#jk tho I’m not demanding that lmao don’t worry I’m just trying to be funny #multiple sclerosis #Multiple Sclerosis awareness #ms awareness #multiple sclerosis awareness month #ms awareness month #autoimmune disease

[adamslilith]

In July of 2022 I was diagnosed with Multiple Sclerosis and on New Year's eve the same year I ALREADY had my second flare up. On YT I talk about this, the symptoms, the denial.. the treatment, and what this might mean for my future.. here's a sneak peek..

And here's the full video ⬇️

#multiple sclerosis #chronic illness #invisible illness #chronically ill #spoonie #disabled artist #spoon theory #multiple sclerosis awareness #multiple sclerosis flare up #multiple sclerosis relapse #rrms #ppms #Youtube

[terrisha-of-the-abyss]

I’m taking part in The May 50K challenge this May to raise funds for life-changing research into multiple sclerosis!

MS strikes young people in the prime of their lives. The average age of diagnosis is around 30 years old, although myself and many others I know have been much younger. There is no known cure, yet.

With how amazing and fast the medical field and the knowlage we gain evolves I hope in my lifetime to see MS be a thing of the past. As an example of how much this research is truly impacting on our live in th MS community let me share a part of my story:

Five years.

If I had been diagnosed five years earlier(and I could've been since I had been exhibiting symtoms for well over a decade) I would be dead right now.

The kind of MS I have was a death sentence only /Five Years/ prior to my diagnosis but thanks to how fast medical science progressed and the timing of when my symptoms were noticed(thanks to some "awesome" seizures)I am here now, alive and breathing.

At the time of my diagnosis there was no treatment I could take to manage the symptoms, all the doctors could do was prescribe strong anti-epileptic medication to prevent seizures but that medication didn't prevent the damage, the demyelination and subsequent haemorrhaging, that caused the seizures in the first place.

But! Two years after my diagnosis there had come a new medicine that I was abe to take and that managed my symptoms for nearly a decade, now when that one stopped working(as is sadly the usual with autoimmune disorders) I have almost six different medicines to chose from to treat my rare form of MS.

In such a short time so much has changed and it gives me so much hope that we can oneday be free of this illness.

So please donate, participate yourself, spread the word and please support my challenge to leave MS where it belongs, in the past far behind us.

Your donation will support research into the prevention, treatment and finding a cure for multiple sclerosis to change lives.

Thank you!

#TheMay50K #ms #multiple sclerosis #ms awareness #multiple Sclerosis awareness #ms Australia #balos ms #balo ms #rare ms #put ms behind us #chomp chomp brain

[adamslilith-msart]

ARTIST with and despite Multiple Sclerosis.

Watch my latest YT video to find out how I manage to keep pursuing my dreams even though I've wanted to quit many times.

#multiple sclerosis #multiple sclerosis awareness #ms artist #chronic disability #chronic pain #chronic illness #invisible illness #invisible illness club #MS #auto immune #spoonie #spoon theory #spooniestrong #motivation #keep going #don't give up #love life #chronically awesome #Youtube

[sashathethundercuhntofficial]

#auto immune disease #multiple sclerosis #ms #ms warrior #ms awareness #chronic illness #chronically ill #chronically chill #Multiple Sclerosis Awareness #Chronic Fatigue #So tired #sleepy #always sleepy #nap #nap time #napping #sleep #sleeping #comfy cozy #exhaustion #exhausting #exhausted #too tired #way too tired #rest #need rest #immuno compromised #immuno suppressive therapy #physically weak

[invisiblepiecesofme]

Have you heard of me?

Have you heard of me? 

My invisible foot steps 

The unscented toxicity of my breath 

My razor-sharp depth in my lashings 

My negative influence. 

I am: 

Toxic 

Narcissistic 

Stress inducing 

Debilitating 

Behavior changing 

Life - bending. 

Have you heard of me?

My residency is permanent 

The feelings I bring are torturous 

I steal all of your senses 

Shatter all of your dreams 

Re – arrange your ways of thinking 

Your, seeing your feeling, 

Your life. 

I am: 

A thief 

A bully 

A terrorist 

Emptiness 

Seclusion 

Sadness 

And loss. 

Have you heard of me? 

I am: 

Multiple sclerosis. 

#gbuda #mental health #awareness #mental illness #emotions #understanding #multiple sclerosis #poets on tumblr #poetry #poem #original poem #writers and poets

[sshonuu]

why does nobody represent physical illnesses?? I mean... Most people don't know what cerebral paralysis, epilepsy, etc are, and in the end laughing at it, or saying stupid and disrespectful things about it. I think we should spread awareness about physical illnesses, because they're hard to deal with alone, and also could lead to a mental illness. Please, someone, spread awareness about physical health...

#physically ill #physically disabled #physically and mentally #illness tw #chronic illness #chronically ill #chronic pain #chronic fatigue #epilepsy #actually epileptic #non epileptic seizures #epileptic problems #seizures #cerebral palsy #disease #pansy parkinson #parkinson's disease #norman parkinson #huntingtonsdisease #high blood pressure #tachycardiac #nervous system #awareness #self aware au #hard to deal #multiple sclerosis #shout out #sad thoughts #sorry for being depressing #tw depressing stuff

[pleasetakethis]

Rick and Morty got me in my feels tonight...

#multiple sclerosis #fuck yeah morty #ms fucking sucks #rick and morty #rick and morty s7 #rick and morty s7 spoilers #rick sanchez #morty smith #fuck ms #ms awareness

[intentkitten]

The fridge M (she/them/their/theirs) stores bulk frozen foods and prepped meals for their kids went out, ruining $750 worth of food. So their monthly medical budget went to replacing food for their children.

Please donate.

Intentkitten.gay is a quick link to the gofundme account. Or send funds directly to

Venmo SojournerT91

Cashapp $Mo2391

Paypal.me/niconiche and I will send the funds directly to M from my account. She doesn't have PayPal

$40 today would help them get food ordered so she can eat

#queer pride #queer artwork #chronically ill #creative #cancer awareness #fuck cancer #multiple sclerosis #cerebral palsy #epilepsy #sjogrens #lupus #lgbt pride #pride month #pride 2023 #trans pride #happy pride 🌈

[gbuda73]

20 things only people with MS or other chronic illness would understand

1. My hair hurts

2. My brain feels numb

3. The air blowing on my hurts

4. Hugs hurt

5. I can't remember how to get home

6. I can't remember what I was doing

7. Just the smallest fever makes me feel like I got hit by a truck

8. I'm to tired to eat

9. Baths/showers exhaust me

10. It hurts to move

11. I need to sit down and cook dinner

12. I feel like I'm thinking in slow motion

13. My teeth break of no reason

14. I feel so guilty about stuff I can't do

15. I fear my daughter will be sick too

16. Most doctors don't really get it

17. Sweeping the floor makes me feel sick and dizzy

18. I tripped over nothing

19. I hope this place doesn't have stairs

20. I hope I don't pee in my pants

I'm sure there's so many others.. you are not alone we understand

#invisibledisabilities #invisibledisease #budas warriors #mental health #awareness #multiple sclerosis #advocacy #chronic pain #advocate #spoonie

[kindajd]

HELP ME! I can't deal with this pain anymore.

#multiple sclerosis #ms #em #esclerose múltipla #multiple sclerosis warrior #autoimmune disease #chronic disease #chronic illness #ms flare up #multiplesclerosis #multiplesclerosisawareness #multiple sclerosis awareness #TN #trigeminalneuralgiaawareness #trigeminal neuralgia #chronically ill #chronic fatigue #chronic pain #chronic disability #disability awareness #disabled #invisible disability #disability #pain #help me #pins and needles #pain flare

[adamslilith]

MS: when your brain hates you so much it literally kills itself.

#ms #multiple sclerosis awareness #ms relapse #mainz #multiple sclerosis #autoimmine disease #artists on tumblr #disabled artist #spoon theory #spoonie #invisible illness #chronic illness

[revenantcarnival]

Our cane sits in the break room of a full time job we don’t get breaks in because the tile floor is too slippery and the job requires both hands.

All we want is a home we don’t feel like an intruder in, to be able to afford to eat without working ourselves sick for it, to receive help without feeling indebted, and to rest when we are hurting.

#disability awareness #invisible disability #multiple sclerosis #osdd 1b #chronic pain #critical role #talesin jaffe #ashton

[adamslilith-msart]

ARTIST with and despite Multiple Sclerosis.

Watch my latest YT video to find out how I stay motivated to pursue my dream of becoming a full time artist even tho I've wanted to quit many times. 🧡

#multiple sklerose #multiple sclerosis #multiple sclerosis awareness #ms symptoms #ms awareness month #motivation #love life #love yourself #don't give up #take care #artist #disabled #actuallydisabled #disabled community #chronic disability #chronic illness #invisible illness club #Youtube