@ashleylou.09: My Autoimmune Disease (Lupus) Symptoms. We know our bodies better than anyone else. If something feels off, advocate for yourself and for answers. #greenscreen #chronicillness #autoimmunedisease #autoimmunediagnosis #autoimmune #diagnosis #lupus #lupuswarrior #lupusawareness #medicalgaslighting #lifewithlupus #advocateforyourself #advocate

Ashley Lou 🦋
Ashley Lou 🦋
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Region: US
Saturday 30 November 2024 23:34:26 GMT
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itsjustkait_
itsjustkait_ :
It’s so interesting how so many autoimmune disorders have overlapping symptoms. I have a different one and almost all of these
2024-12-01 03:01:18
1145
c.chesterrr
Carrie :
Yep. Literally had all of this and more. It’s exhausting. I hope you’re feeling better and are on meds now??? Plaquenil changed my life.
2025-02-11 20:27:52
1
elisabethwhiteside
Elisabeth Whiteside :
I have most of those but they said “you have Hashimotos” 🙃 I have brain fog, eye issues, extreme fatigue, pain and positive Ana also
2025-02-24 05:39:31
1
ms_leigh
Morgan :
What helps you more with the breathing???
2025-08-29 00:00:40
0
yrolfy
yana :
I have most of these and I haven’t been diagnosed with anything. Everything “comes back normal” no matter how hard I try to get answers. I’m lost
2024-12-01 05:16:01
202
kellyalwayskravin
alwayscravin :
How long did it take you to get diagnosed?
2024-12-02 20:47:50
2
lola8242020
Irma Otero :
I was told my symptoms indicated lupus, but my bloodwork doesn’t. I’m sure they’ll just blame it on the fibro like they always do! 🤦‍♀️😭
2025-01-21 03:19:18
1
shyanneordonez
Shyanne Ordoñez :
Do you by chance have issues with gluten as well? I feel like I have all of these symptoms and no one will take me seriously but one trigger I’ve noticed is gluten and rashes and weight gain etc
2024-12-17 17:31:40
2
bmwgirlm240i
M240BMW :
What about dry eyes blurred vision
2024-12-01 03:35:41
20
kyleejordan1012
Kylee :
I just got diagnosed with membranous neuropathy (an autoimmune disease)not to long ago and I thought all my symptoms leading up to it were normal come to find out if it would have gotten worse I would
2024-12-03 03:08:48
2
tinacolada85
TinaColada :
do you itch often?? I just got diagnosed and freaking out
2024-12-04 21:18:25
2
maritzaavi1
Maritza Aviles :
I’ve just been diagnosed with CLE and going to be running more tests to check for SLE. I have all the symptoms you have as well but did you have nonstop migraines?
2025-02-28 00:18:18
2
invisibledisability
💜🐧P E N G U I N🐧💜 :
Have you had an echo done?
2024-12-03 01:50:20
2
valeriee_1111
Valerie❤️‍🩹 :
Question i have an autoimmune disease got the stomach flu and i was dying normal people got it and they were fine but i feel like i got it 10x worse
2024-12-01 03:45:54
2
deanaace
💋Deana Acevedo ❌ :
same same
2024-12-03 02:19:05
1
kelleyi0828
Kelley0828 :
I’ve had that butterfly rash every time I get remotely warm for 15 plus years. It’s very defined. They say mine is just fibro and hashimotos but I have every symptom in this video and more
2024-12-01 15:04:24
37
00sandie
Sandie Kirkpatrick :
I’m having some health issues right now and I have most of these things going on.
2025-01-20 19:06:39
1
kazberry26
kazberry26 :
My rheum said my butterfly rash is just ✨rosacea✨ and that there’s no way I have lupus despite having positive sx and high ANA. No smiths AB so no dx. 😭
2024-12-01 04:12:04
39
mrspeacock12
Jessica P :
I’m in the process of being assessed for viral-induced lupus (caught Parvo/Lyme/Covid within 3 weeks of each other) Positive ANA until prednisone. Then negative work up. Symptoms still after 6 months
2024-12-21 18:14:47
2
aryel_like_the_mermaid
Aryel :
I have POTS and have similar symptoms
2024-12-01 23:54:47
87
quinnrclark1
quinnrclark1 :
If you don't mind sharing, what's your course of treatment?
2024-12-01 06:05:44
71
libbymurphy18
Libbymurphy :
Any dizziness or vertigo?
2024-12-04 02:38:42
2
xsnowyyx
xsnowyyx :
Which lupus do you have? As I have sle systemic lupus erythmatosis and it’s been at bay for a few years now
2024-12-01 20:09:27
2
rebeccatruitt
Rebecca Truitt :
I have most of these plus a lot of joint pain and they say I don’t have it.😳
2024-12-01 04:23:57
8
mom_wife96
Photographer & •SAHM• 🫶💕📸💍 :
WAIT BUTTERFLY RASH AFTER SHOWERING? My face does that too! I have EDS & they talked about Lupas but it’s SO hard to diagnose. I’ve heard you had to get tested during a flare up????
2024-12-03 18:28:04
2
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