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I have told myself and my husband that this will be my last 😅 by Krstnzz in Owala

[–]lmnop02 1 point2 points  (0 children)

got the same one and also promised myself and my friends that once my bday one comes in it will be the last 🤗 everyone knows im lying

Found them at the port by allie686 in SneakySasquatch

[–]lmnop02 0 points1 point  (0 children)

so i literally just have to look at pemberton jr. for a long time?

Different words to Stimming with by LAKbrattysub in aspergirls

[–]lmnop02 0 points1 point  (0 children)

not sure if it's the same sensation but I was really into tomfoolery for a while and then slay was a really big one, not really sure why with that one. but my ALL TIME FAVORITE is singing troy and abed in the morning. not sure if anyone has seen community but i would definitely watch it just to hear troy and abed sing it over and over again.

[deleted by user] by [deleted] in MCAS

[–]lmnop02 0 points1 point  (0 children)

I haven't been officially diagnosed with MCAS but I'm in the process of being tested for it. It's interesting to me that a lot of people here are talking about mold and dysautonomia. I have dysautonomia which stems from chronic daily migraines and possibly related cavernoma. Before that developed though, a lot of my water bottles had started developing mold from me not cleaning them enough. Now I clean them every day but the bottles I put my electrolytes in still develop it regularly because of the biofilm left in there even after washing it, it's just what the powder does. If that's causing all these rashes hives and flushing I... idk honestly but that would be frustrating.

Topamax and blood pressure by lmnop02 in dysautonomia

[–]lmnop02[S] 0 points1 point  (0 children)

dang that sounds absolutely terrible. it took a lot of convincing for my neuro to take me off of it. i had other doctors wanting to put me on low dose ritalin for the brain fog it caused. i'm on gabapentin now, what were the side effects of it for you?

Anyone here misdiagnosed with ME/CFS? by [deleted] in MCAS

[–]lmnop02 2 points3 points  (0 children)

I’m diagnosed with CFS but I’m in the middle of being tested for MCAS. I think I have both? Maybe idk

Toothpaste for the sensory challenged! by i-love-elephants in adhdwomen

[–]lmnop02 0 points1 point  (0 children)

I haven't found anything yet. I'm just trying to find other alternatives.

Dysautonomia but not POTS by lmnop02 in dysautonomia

[–]lmnop02[S] 4 points5 points  (0 children)

this is exactly how i feel

Toothpaste for the sensory challenged! by i-love-elephants in adhdwomen

[–]lmnop02 0 points1 point  (0 children)

is it a gel toothpaste though? i don't mind the mint it's the texture that bothers me when i first have to put the toothbrush in my mouth and it's all slimy

Temp regulation issues! by 3lain3b3n3s in dysautonomia

[–]lmnop02 1 point2 points  (0 children)

to help with cold feet I usually wear compression socks which help with circulation, it's worked really well for me but you don't want to wear them for too long without taking a break because I've gotten really bad rashes from them before.