chronicallyparkyr

31yo person with multiple chronic illnesses. Hypothyroid, EDS, intestinal dismotility, POTS, intestinal malrotation, MCAS, and migraines diagnosed so far.

[Hamkae Center 🥁 #KnowYourRoots @hamkaecenter]

why Youngkin's SOLs- that got 4 hrs of verbal criticism + thousands of written comments in opposition, had no public involvement in its making + no transparency, and is literally white nationalist revisionism of U.S. history- are even being CONSIDERED is beyond me #TeachTheTruth

[chronicallyparkyr @chronicallypar1]

Checking In with Your Caretaker https://t.co/QlGmofqEVh

[chronicallyparkyr @chronicallypar1]

Strep, Pneumonia, and Sepsis Oh My! https://t.co/3Hd4nJxkH5

[chronicallyparkyr @chronicallypar1]

Depression surrounding my Chronic Illness https://t.co/Q4Z3N9cLLq

[chronicallyparkyr @chronicallypar1]

How to Get Your Doctors to Work Together https://t.co/a9Ufy7xvGd

[chronicallyparkyr @chronicallypar1]

COVID-19 Vaccine and Chronic Illness https://t.co/JybWtPz3h5

[chronicallyparkyr @chronicallypar1]

Therapy Is Okay https://t.co/uxQQaNKTcs

[chronicallyparkyr @chronicallypar1]

Medical Burnout https://t.co/U0XMZhAglq

[chronicallyparkyr @chronicallypar1]

MCAS Attacks https://t.co/3SKKiB5FIX

[chronicallyparkyr @chronicallypar1]

I’m really feeling this lately. #POTS #posturalorthostatictachycardiasyndrome #chronicillness #ChronicPain

[chronicallyparkyr @chronicallypar1]

This Weekend https://t.co/evDO9II2UX

[chronicallyparkyr @chronicallypar1]

Giving a presentation today for a class and my tongue is numb because I have a rare side effect from my medication 😜

[chronicallyparkyr @chronicallypar1]

About Me https://t.co/h5z6CuOMFS

[chronicallyparkyr @chronicallypar1]

How do you explain Ehlers-Danlos Syndrome to people?

#EhlersDanlosSyndrome #EhlersDanlos #ChronicPain #chronicillness #connectivetissuedisease #connectivetissueissue

[chronicallyparkyr @chronicallypar1]

The days when the pain makes me shaky and upset are the worst. #chronicillness #chronicpain #ehlersdanlossyndrome #hEDS #Dysautonomia #MCAS

[chronicallyparkyr @chronicallypar1]

How I felt yesterday. #chronicillness #ChronicPain #EhlersDanlosSyndrome #hypothyroid #MCAS #POTS #hEDS

[chronicallyparkyr @chronicallypar1]

If you ever feel medical burnout, you are always welcome to come talk to me. #medicalburnout is something a lot of chronically ill people feel, and it’s time that we talk about it. #chronicillness #ChronicPain #EhlersDanlosSyndrome #hypothyroid #mastcellactivationsyndrome

[chronicallyparkyr @chronicallypar1]

Sometimes I catch myself sitting in some not-normal positions. Thanks, EDS! #chronicillness #chronicpain #EhlersDanlosSyndrome

[chronicallyparkyr @chronicallypar1]

When does it ever end? I’m forever exhausted and nauseous #chronicillness #chronicpain #chronicnausea

[Princess, The Tower @APainPrincess]

“People with #chronicillness and #chronicpain are very keenly aware of how everything affects their bodies. Usually, more than you’ll ever hear us talk about.” Sometimes I Choose The Cost https://t.co/nmiysfTTR7 @KimberlyJPenix #invisibleillness #disabilities #spoonies