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If becoming chronically ill has taught me one thing - it’s shown me who and what really matters 💘 #chronicillnessawareness #medicallycomplex #posturalorthostatictachycardiasyndrome #mcas #sibo
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It’s NOT “cool” to have a chronic illness. It’s “cool” to accept the way your body is functioning and live life despite all of it. It’s “cool” to be empowered to seek the answers you deserve and not stop fighting for the care you need. It’s “cool” to have limitations and choose to see the abundance in them, using creativity to expand your life. We create content and be loud because community is incredibly valuable. It’s the reason some people have the strength to keep fighting, find the answers
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links in bio check me out 😳 | AITAH cause I told a chronically late person an earlier time than everyone else? #sarby
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Chronic illness larping has flooded the Internet in the last few years #ehlersdanlos #chronicillness #heds #hypermobileehlersdanlossyndrome
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I’m here to advocate for the people living with “hidden” chronic illnesses—the ones you can’t always see just by looking at someone. I went from being the healthiest I could be, living my life at 21, to having my entire world change in a split second. A “normal” life has suddenly became something I have to fight to have. • MANY hospital visits • Being admitted • Being put on 3 different diets • Tons of medications • Weekly/monthly infusions • Fluid retention and swelling that people assume is si
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Someone needed to say it and I’ll definitely get some unfollows for this but it’s so true when
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