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@adamslilith-msart
🧡😍 😍🧡
Me and my MS art project A Thousand Faces was featured in my local newspaper and I'm still speechless
check out my latest YT video for more infos on this :)
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. 🧡
Pretty much 6 months ago I had my first clinic flare up and got diagnosed with MS.
And here I am now.. again with a flare up. Again my immune system is destroying my central nervous system. This is way too early. This is not good at all.
So once again I can post "Gloria" who is my visualisation of Multiple Sclerosis.. from my art project A Thousand Faces created to raise awareness of this invisible illness by visualising every aspect of it.
I talk about this on YT... go check it out
u all ever lose the ability to socialize in the middle of a convo like.... ok i’m done now there’s no more words in here brain shutting off
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.
Happy MS Awareness Month! 🧡
New MS symptom painted to raise awareness of the complexity of this autoimmune disease!
Go check it out 🧡
When a doctor seems really promising and gets your hopes up but then disappoints you at the next appointment:
let's end misconceptions about MS 🧡🎨
Longer version with more infos ⬇️
Find out more in the video below 🧡
I'm an artist and in summer of 2022 I was unexpectedly diagnosed with Multiple Sclerosis. Now I create art to visualise my invisible illness to raise awareness of it! Check out my video to find out how and WHY I do this!!
(And don't forget to subscribe; like; comment to support my mission, thx💕)
I'm not "letting my disability win".
Bitch has already won long ago. There was never even a contest.
Let's talk about paresthesia...
that's the medical term for abnormal sensations of the skin, that is pretty common when you got MS for example..
Now, what I've experienced is ... kind of specific and maybe a little weird, watch the video to find out more and please let me know if you've ever experienced something similar 🤔
For someone who is tired 100% of the time, I sure am bad at sleeping.
sorry for documenting my suffering and delusions online do you still think im hot
Pretty much 6 months ago I had my first clinic flare up and got diagnosed with MS.
And here I am now.. again with a flare up. Again my immune system is destroying my central nervous system. This is way too early. This is not good at all.
So once again I can post "Gloria" who is my visualisation of Multiple Sclerosis.. from my art project A Thousand Faces created to raise awareness of this invisible illness by visualising every aspect of it.
I talk about this on YT... go check it out