@racheledek: Myasthenia Gravis is an autoimmune disease where the immune system attacks communication between nerves and muscles. Your brain tells your muscles to move, but the signal doesn't get through and everyday movements are exhausting or impossible. People have even been mistakenly kicked out of bars or arrested for DUls because our speech can be slow and slurred, coordination is poor, and it affects our vision and eye movements. It can also be deadly if without warning the muscles that control breathing are affected. But one thing about me is even in a flare my skincare routine is getting done one way or another. #myastheniagravis #invisibleillness #invisibledisabilities #chronicillness #skincareroutine
So sorry. My MIL had my myasthenia gravis. She was my hero♥️
2026-03-17 13:12:45
2
Chaney :
Put all that stuff by your bed and do it laying down. I do all my skincare in bed. 😭😂
2026-08-25 20:04:00
3
Gillian :
I was diagnosed three months ago. It has been such an adjustment mentally and physically. I am finally on medication for 2 1/2 months. It’s been working. I was seriously asking and praying to be not around anymore, but I am adjusting now and hoping for the best, I am wishing you the best with hugs and love and support.
2026-08-02 01:18:36
3
Porscha :
Our routine is exactly the same.
2026-08-28 05:11:10
2
💕 LISA G. | D(M)V | 40+ Crew :
I have MG as well, have they tried IVIg?
2026-03-24 16:38:42
1
Jackie & the Ghost 🤍 :
Oh queen, i hate this for you so much 😭 is there medicine to help manage this?
2026-03-15 02:20:54
3
🖤🖤🖤 :
Oh girl, I’m so sorry. One MG queen to another • you’re killing it! We find all the ways to compensate for our challenged bodies 😂 When I’m flaring and have to wash my hair, I have to rest my arms up against the wall in the shower, and put my forehead on the wall and try to wash as quick as possible. Feel free to DM if you ever want to chat 🖤
2026-03-14 12:59:57
12
roses :
this is me some days girl I get it
2026-07-02 03:31:55
1
Ashley Cowan :
I was diagnosed when I was 21. Still trying to figure out how to live with it. But seeing other people with the same struggles is so refreshing knowing I’m not alone 🥺
2026-03-18 03:03:31
3
🪽 :
I have MG, T1D, PCOS and Celiac and I genuinely don't know what to do...
2026-03-23 00:22:21
1
velvetsprouts4 :
I have the same illness. And I completely understand. Even with my expensive treatments, it still takes me hours to get ready to go to work.
2026-05-13 23:34:20
1
RACHEL CHAVA RAIZEL :
I have it too
I feel for you
stay strong
xox
2026-04-20 14:24:35
1
Aminaaa :
Having MG too, and I trumy feel you ❤️
2026-03-17 02:04:18
1
LIA 💕 || TTS • UGC :
proud of your strength !
2026-03-13 20:13:15
1
Lord Almighty :
It happens to me most of the time and if i can’t get it done, I will get mental breakdown and cry, which makes my MG even worse 😭
2026-06-02 14:23:02
2
Rossibel :
You are amazing!!
2026-03-13 16:50:53
1
Allie / Working Mom 💖💖💖 :
You are so strong! Some people would just lay down and give up. You got this!! 🥰🥰
2026-03-14 13:51:32
1
Kaitlin | NJ :
❤️❤️❤️❤️❤️you are amazing
2026-03-13 19:10:47
1
Em💘 :
I love that we all have our ways to get things done 🥹💗💗 I’m with you boo x
2026-03-15 00:01:47
2
lexiegee_sahsm_ :
you are so amazing and so strong ❣️
2026-03-13 17:02:13
1
A🫧👩🏼🍳 :
This is how I am when I’m flaring up really bad 😭
2026-03-20 02:13:49
1
chronicallyillandfab :
Love a chronically ill queen figuring it out 💪🏼💪🏼💪🏼💪🏼😘😘
2026-03-14 05:33:42
2
kareng :
okay I have no excuse for not doing my skin care. you're doing amazing girl!
2026-03-14 01:29:59
1
The Dailey Advocate :
Definitely can relate this is how I was in the beginning before diagnosis in 2015
2026-03-14 11:31:15
1
Chaney :
My right side is weaker. When I change the radio in my car I use my left arm to prop my right arm up to touch the buttons. 😂😂
2026-09-07 10:24:28
0
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