As I become more involved with #DisabilityTwitter I wanted to pin this to my profile in case anyone was curious about my experience with chronic illness, misdiagnosis, etc. #NEISvoid#disabilityinclusion https://t.co/usCDHwwYeW
Tagging you so you don’t miss the $AEGIS led by @Vet_X0..
I putted 2,500 XRP in on https://t.co/Fs0UMvaf4N.
Could retire me if this moons 😂 You putting any bags on this?
Hey , was you able to get Loyaly Badge at https://t.co/RP2A5F68gE?
I tried but got unlucky , was not eligible😕 , you are really lucky if you get one..
Oh , site will look better and smoother in pc btw, GL!
Hey , was you able to get Loyaly Badge at https://t.co/RP2A5F68gE?
I tried but got unlucky , was not eligible😕 , you are really lucky if you get one..
Oh , site will look better and smoother in pc btw, GL!
Hey , was you able to get Loyaly Badge at https://t.co/RP2A5F68gE?
I tried but got unlucky , was not eligible😕 , you are really lucky if you get one..
Oh , site will look better and smoother in pc btw, GL!
I’m glad to see POTS is getting more awareness now that it’s a #LongCovid consequence but we should be talking about it anyway. It put me in a wheelchair for months. My doctor told me it was hormones. #DysautonomiaAwarenessMonth#DisabilityTwitter
#POTS is MUCH more than lightheadedness and a racing heart, but we're glad to see @HarvardHealth talking about this common autonomic nervous system disorder during #DysautonomiaAwarenessMonth.
October is #RaynaudsAwarenessMonth Raynaud’s affects 5-10% of Americans and causes constriction of the blood vessels in your hands and feet, usually in response to cold. My Raynaud’s is severe enough that I can’t walk on tile without socks. #DisabilityTwitter
Niagara Falls is lighting up turquoise tonight to help us kick off our 10th Annual Dysautonomia Awareness Month campaign! You can view the lighting on our social media channels at 10:00PM ET. Learn how to get involved with Dysautonomia Awareness Month at https://t.co/dzYfauuxZr!
POTS Walk volunteers have raised over $91,000 for POTS research! We only have one more day to reach our goal and we are so close! Can you help raise $100K to fund an AMAZING new #POTS research study by donating at https://t.co/55fazrtcH2?
We are recruiting two editors to join the @Nature team! One with expertise in biochemistry/molecular biology and the other one in immunology. Please spread the word! Details for application 👇🏼
https://t.co/IpNH2HTjYI
https://t.co/iJP7RHbQ33
Here's our first story from a staff member.
Faculty, staff, and students we want to hear your stories anonymously. We want to hear from you!
Click "share your story" in our LinkTree. https://t.co/UtfTjYg2xz
#OkState#ProtectOkState
@kaylejh My personal favorite is when they try to blame your symptoms on something you’re doing. I had severe chest pain from arrhythmias and a doctor I saw (did not return) told me it was because of the medication I had to take for my chronic fatigue. I’d be non-functional without it.
@fatalmoth It took 8 years for me to get diagnosed. Mostly because I had other chronic conditions and weird symptoms so it was hard to figure out what was causing all the fatigue. I’ve finally gotten to where good days outnumber the bad days.
@SophieMattholie There has been research linking trauma (psychological, physical, etc.) to an increased risk of chronic pain disorders, particularly fibromyalgia.
Mayor Will Joyce just declared a State of Emergency for Stillwater, saying it’s based on “medical health of the community.” State Health Dept. will be assisting with deployment of Medical Reserve Corps.