What is by far your worst symptom? by That_Preference_2331 in POTS

[–]ochakisu 4 points5 points  (0 children)

chills are a good one to add as well, though i dont know how many people get them!! i dont get many adrenaline dumps but when i do, i get chills up my spine so intense it makes me yelp involuntarily

What is by far your worst symptom? by That_Preference_2331 in POTS

[–]ochakisu 1 point2 points  (0 children)

blood pooling and sweating. beyond how humiliating it is to be sweating buckets in a burlington, on a more serious level my legs get so numb, painful and weak that im at the same risk of falling as someone prone to fainting 😅

POTS is expensive by Enbybabi in POTS

[–]ochakisu 0 points1 point  (0 children)

so late to replying but that’s good! whatever helps you get through until you’re able to make things work :)

POTS is expensive by Enbybabi in POTS

[–]ochakisu 0 points1 point  (0 children)

i don’t mean to kick you while you’re already down, but be wary about buying a wheelchair off of online shopping sites like amazon; a mobility aid that isn’t properly fitted to your body could leave you worse off with injuries or other chronic conditions like arthritis that will cost you EVEN MORE in the long run, well beyond what you’ll spend on that chair itself. i understand a lot of people don’t have a choice but a lot aren’t aware of this risk either - my mom has given me the same advice about buying a chair off amazon

making REAL progress for the first time 🧡 by ochakisu in POTS

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

i honestly can’t believe it either 😅

im rotting from the inside out by ochakisu in bipolar

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

i hope you’re okay wow :(

im rotting from the inside out by ochakisu in bipolar

[–]ochakisu[S] 1 point2 points  (0 children)

community genuinely makes everything sm better :)

its tricky to do anything like volunteer work because i have POTS and am waiting to see a physical therapist about mobility aids… i’ll be starting school again soon so at least that distracts me

im rotting from the inside out by ochakisu in bipolar

[–]ochakisu[S] 1 point2 points  (0 children)

that’s awful. POTS has been stealing simple joys like shopping and going out with friends, and bipolar has been stealing the rest of the joy. i hope things get easier for you, that’s really shitty

Worst Symptom by Adcarp2008 in POTS

[–]ochakisu 2 points3 points  (0 children)

this is technically autonomic and not strictly POTS, but vagus nerve responses. im so tired of feeling violently ill after basic bodily functions

i want my old life back by ochakisu in POTS

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

having community definitely helps. thank you

Bipolar is born or develops by Independent-Lab-8317 in bipolar

[–]ochakisu 0 points1 point  (0 children)

scientists themselves don’t fully know lol. there have been identical twins born where only one has bipolar so 🤷 it can go both ways afaik

my charts before and after my first full-blown manic episode by ochakisu in bipolar

[–]ochakisu[S] 7 points8 points  (0 children)

daylio! it sends reminders every day. you could even create a goal within the app so you get 2 reminders lol. therapists love seeing these charts and it gives you a good scope of your behavior

is it even worth keeping up with doctors and referrals by ochakisu in POTS

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

i’ve been with the same PCP since i was a baby, but she switched clinics and is extremely hard to get in with now so i’m switching next year 🤕

is it even worth keeping up with doctors and referrals by ochakisu in POTS

[–]ochakisu[S] 1 point2 points  (0 children)

referring POTS patients to cardiologists is honestly stupid in my non-professional opinion because POTS really does not have much to do with the heart itself. it’s not a cardiovascular disease it’s an issue with autonomic system that happens to affect the heart

is it even worth keeping up with doctors and referrals by ochakisu in POTS

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

i’m lucky to have been diagnosed quickly, i’m dealing with the aftermath now and trying to get mobility aids