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My dear followers who wear compression socks: Not Your Grandma's hands down got the best selection, if you happen to be looking to add more pairs to your collection!
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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me rn 😍🙏
Fellow POTSies: I’ve seen people downing straight salt, but have we considered doing shots of soy sauce?
Cons: less portable than packets of salt
Pros: so tasty!
Thoughts and prayers to potsies during the warm months
So far my new meds are working!! I’m so excited I may be able to function probably without worry of fainting!
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
Last year right around this time. I had a scary experience in the back country. I have have several chronic illnesses including Ehler’s Danlos Syndrome and Postural Orthostatic Tachycardia Syndrome. I felt fine until I didn’t and then I really didn’t feel fine. I fainted several times and was four miles into the backcountry. I don’t remember a lot of water happened. But thanks to a friend and fellow hikers who helped get me out, I was able to get out safely and narrowly avoid the ER. I have been thinking about this a lot recently especially is we go into the summer hiking season. I have always been a ‘what if’, dead in a ditch, worse case scenario type of person. I always take precautions especially now. But I still have this nagging thought in the back of my mind. What if it happens again? The list of ‘what ifs’ goes on and on. I have always been active and outdoorsy. As I head into this season, I am nervous but these places fill my soul. They quiet my racing mind and give me so much. I don’t really have any answers yet as to figuring out when and where to push through, and when to take a step back. Chronic illness can be all encompassing but even with all the ‘what ifs’, all you can do is keep moving forwards.
I got a meaningful tattoo today. It’s hard to come to terms with chronic illness. I have had chronic fatigue and POTS for years now.
I sleep... A lot. And I mean a lot. I feel like a lump blocking people’s paths and generally like a nuisance if I’m honest.. But I choose to believe that’s what makes me lovable.. and perfect for all the same reasons I fucking love snorlax. And sometimes I need patience from others and myself and sometimes I need to take it Slow.
I didn’t angle my snorlax for everyone else’s eyes. I faced it towards me as a reminder. As one thing I love (Snorlax) and another I choose to love, (being chronically exhaustedly me)
Also, it’s a great conversation starter and a segway into spreading POTS awareness.
If It means something to you, then get it. Your significant marker doesn’t have to be a ribbon or a color or a day. Make it bold, as bold as you. Even a slumbering Snorlax is bold. 💪🏻💪🏻
