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Sometimes EDS makes you Exhausted...

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Uploaded by on May 15, 2009

Hey everyone... I'm really exhausted, so this video and description will be short. I started a new medicine for my POTS, as I was just diagnosed on May 8, 2009. Another fun thing associated with Ehlers-Danlos Syndrome.

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Uploader Comments (jkweirich)

  • Thank you for your support! It means a lot!

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  • I know exactly how you feel. I'm 18 with EDS (Classical Type)

    We just get so tired.

    I have super low blood pressure too..

    Stay strong girly!

  • I can feel your pain, my wife gets upset with me for not wanting to go shower on my days off.

    Yet I am 52 with EDS and the breadwinner for our family, most days I would prefer to die than to keep plugging away with the pain and all the meds they are having me take.

    I am glad your husband has some understanding for you.

    I know it is hard to accept having something like this, I always had held out hope that one day they would be able to fix my pain, and then to find out there is no cure.. sigh.

  • You're so strong!

  • I'll pray for you. You are so courageous for your videos and I know what you mean about "caring less about getting dressed" because of the pain. I feel you----and am in the same boat. Chronic pain in many areas of the body. Good luck!

  • Hey there, May be we can find out where the next EDS support group meeting is and we can go together. I wrote u a few notes through the e-mail thing on here. We should get together, and share stories, I have the eds Type 4 and yea, it sucks. I left u my phone numbers on the e-mails, Hope to talk with you very soon, Hang in there!!! -----Nick-----

  • I know that sucks...I have EDS and POTS as well...just keep breathing in and out!

  • that sounds rough. Sorry to hear about the effects of the medicines.

    Sending you my best wishes. Don't know if youre religious, but I'm going to say a prayer for you now.

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