@gabrielleistired: Yes I have always “seemed” okay. I am a natural performer at heart. I have always gone far out of my way to make people comfortable and not worried about me. I don’t like adding stress to peoples lives. Although I did notice that anytime I let my guard down and told someone how I really felt physically & mentally people didn’t believe me anyway. I had undiagnosed Multiple Sclerosis & Hypermobile Ehlers Danlos. Friends and family were accepting of my mental illness — my diagnosed OCD, depression and CPTSD. Debilitating anxiety. Even then no one knew how bad it was. The suicidal ideation. Living in constant physical pain and no one there to help. Doctors didn’t know what to do with me. I’m so thankful for finally getting some answers, but the struggle forever changed me. I have been at this since I was 11 years old. The aloneness in my health battle has really hurt. If this is a familiar story to you, I stand with you. ❤️‍🩹⚔️ #multiplesclerosis #multiplesclerosisawareness #medicaltrauma #medicaltiktok #CPTSD #trauma #chronicpain #chronicillness #invisibleillness #medicalmystery #invisibledisability #hypermobileehlersdanlossyndrome #hypermobilejoints #ehlersdanlos #POTS #spoonielife #spooniesoftiktok #suicideprevention #mslife #painmanagement #multiplesclerosiswarrior #chronicillnesswarrior #healthjourney #disability #invisibledisabilityawareness #msstrong #zebracrossing

Gabrielle | life with MS & EDS
Gabrielle | life with MS & EDS
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Region: US
Saturday 03 December 2022 21:07:29 GMT
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miatraplin
Mia :
for 6 years i had doctors tell me my back pain was in my head. i had a tumour, two herniated disks, and my nerves were literally being crushed
2022-12-04 06:23:33
9
pantsingtonlarooson
Pickles Momma :
Did you have a brain MRI that was normal early on or was your first one the one that showed it? I have all these symptoms but my brain MRI was clear
2024-01-13 15:20:10
2
nicolefrances1011
Nicole Frances 1011 🇨🇦😍❤️ :
I felt like I was dying. took years to figure out I had chronic hylori infection with very low vitamin d, B12 and ferritin. plus I have a tumor on my
2022-12-08 14:49:33
2
dkwhat.to.put.here
⠀ ⠀ ⠀ ⠀ ⠀ ⠀ :
I kind of think i have ibs, I’m gluten and dairy intolerant and i have most of the symptoms but I know my mom will probably just brush it off and say-
2022-12-05 19:16:59
1
sheenalee204
Sheena Lee :
My mom has MS and I have many symptoms and struggle everyday but everything is testing normal. How were you diagnosed?
2022-12-12 05:42:04
2
ellieblanton
Ellie :
Took 4 years of “everything came back normal” to figure out I have rheumatoid arthritis
2022-12-04 08:06:52
1618
meghansandra_
meghan :
told i was 14 and just had anxiety, im now gonna be 18 with 5+ chronic illnesses getting worse, fainting daily:/
2022-12-08 16:09:50
2
idk_what_username_2use
(∩`-´)⊃━☆゚.*・。゚ :
I have all the symptoms of fibromyalgia and the doctor wont diagnose me neither refer me to a specialist. 🤬
2022-12-04 06:02:31
36
psythecompany
PSYcompany :
my grandma had eds and multiple sclerosis. I'm sending you so much love and support, no one truly knows the struggle
2022-12-26 15:58:25
2
sarahfetherman
Sarah Fetherman :
I either have ms or a brain tumor. I couldn’t walk for months and my old neurologist lied to me and said everything was okay. I have lesions or tumors
2022-12-04 18:56:59
2
brainfrog10
The Berrywoman :
Oh hun, hugs. That's a tough diagnosis for one so young. A friend of mine got diagnosed at 19. Anyone feeling apologetic to you?
2022-12-11 22:13:08
1
mossfairy3468
Jenn :
My doctors are telling me I have something neurological that we’re trying to diagnose and my mom keeps saying she thinks it’s MS… she’s always been
2022-12-04 00:24:44
2
iachzne98
High Lady of Tiktok 🎀🦈 :
you got this! my MS turned aggressive recently and I'm starting mavenclad in 9 days. I'm only 24. 😔
2022-12-03 21:50:34
16
beccamartin28
Becca Martin6259 :
8yrs of trying to figure out my daughters health..they now think MS. She’s 16. Hoping the specialist is quick to work it out.
2022-12-05 03:13:57
1
enfysciel
ana/enfys 🧚🏻‍♂️ :
my breathing is getting worse but they say im fine, my symptoms match POTS and/or heart failure 🥰🤪
2022-12-04 23:49:13
1
graceisgayashell
Grace🏳️‍🌈 :
I feel like I've been gaslit so much that I truely think all this pain is normal for everyone🤡
2022-12-13 00:02:53
1
zainy.rainy
Zainy Rainy :
They just checked me for MS bc I have a lot of symptoms but say the MRI is normal and now I'm still fighting for help. I'm glad you found an answer
2022-12-04 01:21:39
21
ativanluvergrl22
Julia Ford :
How did you get them to listen to you? Already ruled out thyroid. My neurology apt is until March
2022-12-03 23:00:32
3
catnaps18
Patricia :
Please get tested for Lyme disease ! Lots of time ms is just undiagnosed Lyme. Happened to me and. Is that I am in treatment getting better
2022-12-20 22:23:26
0
divarayne
divarayne :
i've been dealing with chronic health issues for years now and nobody listens. i get so scared thinking i have something that's just getting worse :(
2022-12-08 07:52:46
3
spongebobsq89
?????? :
hey, i have chronic migraine disorder and i relate. health trauma is something so lonely. i’ve yet to meet someone who understands the battle of being
2022-12-04 23:05:07
2
azakiah
Azakiah :
🥺well it’s been almost 3 years for me… I’ve been gaslight for that time frame…. Now I’m scared for my heart I’m always out of breath
2022-12-05 04:52:12
1
smokescreen11111111
Smokescreenxx :
Big hugs to you x I know this too well. the hardest transition is to let myself be ill. my mum thought I was being a hyperchondriac &my doctors didn't
2022-12-03 22:26:34
1
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