Can we stop overworking healthcare professionals, so they can actually do their job? 😩 the current healthcare system isn’t benefiting anyone.

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I’m happy to message my doc in the meantime… but, I know his nurse will reply and just tell me to go to urgent care/ER. I asked my home health nurse about it, and she just said I needed to talk to my pcp, of course. I was supposed to have an appointment with my pcp on the 19th of October, b

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Look out for my next video on the diagnoses that can cause joint hypermobility. (Because hypermobility on its own is not a diagnosis) ❤️‍🩹

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I don’t even know if anyone can see the vibrating, but I have a feeling other hypermobiles know what I’m talking about. 😭

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The joy of having POTS with sluggish digestion. 🤪 based on true events from last night. I feel like I’m always regurgitating something. 😭

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My test results are normal? Omg! Thank you, doc! I’ve been cured! All my symptoms magically disappeared when you told me that. 😭❤️‍🩹

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I’m so sorry. I just have POTS. 🤪

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I’m a totally different person when I’m all alone and free to let it all out. I would rather fake being well, then be a burden on anyone. 🤪

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Who else does this to avoid flaring up their POTS? I’m so grateful for my monkey feet. 😅❤️‍🩹

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The undiagnosed are still chronically ill and/or disabled! ❤️‍🩹

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Which type of hypermobile are you? 🤪 …as someone who needs to pee or get sick to their stomach straight away in the morning, I don’t have time to get my joints back in place before I get going. 😅

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Anyone else unaffected by the ‘October Slide’? 🤪

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Is this just my cats? Or can anyone relate? (With their cats needing to be held when you’re going to the bathroom - not the overactive bladder, chronic constipation and diarrhea, and homebound part) ❤️‍🩹

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Super original… haven’t heard that one before. /s 🤪

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Where are all my hypermobile babes at? 🙋‍♀️❤️‍🩹

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What else do you wish everyone knew about POTS? ❤️‍🩹

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It’s really ok to use mobility aids. ❤️‍🩹

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In honor of Dysautonomia awareness month, if these 5 signs reasonate with you, I recommend networking with people who live near you to find a Dysautonomia specialist to evaluate you for POTS. ❤️‍🩹

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I share about my chronic conditions, because I don’t think anyone should have to wait decades for answers. ❤️‍🩹

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I haven’t had any side effects from the Hydromorphone (and I’ve been getting it continuously with the addition of my 10 boluses for over 24 hours now). ❤️‍🩹

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Allison Tennyson