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My Autonomic Dysfunction/POTS story

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  • Опубліковано 25 вер 2018
  • First video in what I hope to be a series of videos of coping with being diagnosed with Autonomic Dysfunction/POTS. This first video covers my story of how it all started and how I plan to treat it.

КОМЕНТАРІ • 25

  • @germanotamendi7878
    @germanotamendi7878 5 років тому +2

    How positive you remain is incredible

  • @144EARTH
    @144EARTH 5 років тому +5

    I'm a guy and I was recently diagnosed with POTS also

  • @vaudgumm
    @vaudgumm 2 роки тому

    I was just diagnosed with POTS post covid. Thank you for this video. It was so helpful!

  • @TheCriscantu
    @TheCriscantu 4 роки тому +1

    I have to say that this was one of the most informative videos I’ve seen of POTS. When people ask me what symptoms I have a exclude anxiety, because peoples first thought is you must have anxiety or depression. But that’s not the case the autonomic dysfunction is causing me anxiety. I feel like I can share your video to explain to others what it is that I feel. Continue making these videos, they truly are very helpful

    • @tyleroconnor6683
      @tyleroconnor6683 4 роки тому

      Thank you!! I made a few other videos under this account

  • @davebeck3157
    @davebeck3157 5 років тому +1

    I've had the pots curse for 20 years. Been to Mayo, Vanderbilt, Cleveland clinic and dozens of cardiologists and neurologists. Had every drug and test known to man. Been bedridden for the last 10 years. I recently figured out on my own that it was caused by small fiber neuropathy.
    Get tested for it. You're still young, there is still hope. I'm 70 and screwed. Don't give up.

  • @chronically__emily6531
    @chronically__emily6531 5 років тому +1

    Thank you for sharing . It is so frustrating when you keep getting normal test and everyone looks at you like it is in your head and you know something is not right. I am on the journey through this too and it is nice to hear others stories .

    • @1jazzyphae
      @1jazzyphae 5 років тому +1

      I thought I am going crazy too. But now that the doctors are seeing my symptoms they're realizing they are wrong. You really have to fight for yourself.

  • @8XxFlameThrowerxX8
    @8XxFlameThrowerxX8 5 років тому +2

    Stay strong brother it gets better with time. BTW research mast call Activation Syndrome it's a secondary syndrome associated with pots.

  • @rufioshaw5441
    @rufioshaw5441 5 років тому +1

    Im a guy, Iv got pots. Keep going with the uploads man. Not going to lie, it sucks having pots.
    One day your living a normal life then its hard to stand up. It does get easier with time. You basically have to learn how to relive your life, understand you have new limitations etc.
    Working outs also hard man, id suggest swimming as its not to hard on the body. If your going the wieghts route then it depends on what you can do. I do a 5x5 workout which is simple enough, or try 5/3/1 Its so much less than i used to do but its something.
    Should join the Reddit community brother, its good. r/pots. Best of luck.

  • @heatherchristenson187
    @heatherchristenson187 2 роки тому

    Thank you for this... :(

  • @MultiDom20
    @MultiDom20 3 роки тому

    I’ve been worried that I’m going through this as well

  • @MATT-ij6wo
    @MATT-ij6wo 5 років тому +1

    Hopefully the Cleveland Clinic helped you. Hope you've been able to kick the tobacco chew addiction as well..

  • @ari9313
    @ari9313 2 роки тому

    I'm here for you. How are you now?

  • @blainecatron7328
    @blainecatron7328 5 років тому

    Good luck bub! Hope you can find some help up there!

  • @hunterj.hughes7252
    @hunterj.hughes7252 5 років тому

    I don't have POTS but I do have a autonomic dysfuction. I unknowingly had mono for a year and then got sibo for a year after that from a weakend immune system. I got rid of the sibo that took 10 fukin months for the egghead doctors to dignose. And finally I see a autonomic doctor in a week. Lucky the doctor is one of the best in the country and wrote "thee book" on autonomic dysfunction.. they use it to teach in colleges. 2 fukin years of hell, put my whole life plans, education, work, relationships, everything you name it on hold. I've been to all the doctors.. I've been to a lightworker who I meet with every 1 to 2 months. I should make a video when its over, but God I don't want to waste one more second talking about the dumb shit that took 2 years from me. I will make a video tho because people don't know what this is.. many.. almost all doctors don't either.. and alot of people have it and suffer for a long ass time.

  • @lesquis
    @lesquis 5 років тому +1

    How you doing?

  • @losserrano9367
    @losserrano9367 4 роки тому

    Look into vitamin b1 deficiency also focus on electrolytes potassium,magnesium,vitamins D3,sodium good sodium not table and processed food type of sodium

  • @barlowpenny
    @barlowpenny 5 років тому

    I just got told a week ago that my my autonomic system malfunctions and that’s why I passed out. Along with all the other symptoms. Is pots the same thing??
    So confused! Iv suffered from migraines. Low blood pressures 80/40, nerve damage, bladder problems, high heart rate 118 to low rate. Face rifles or burns or

    • @barlowpenny
      @barlowpenny 5 років тому

      On and on. Used to walk 2 miles a day and unload pallets at work. To exsuasted!

    • @tyleroconnor6683
      @tyleroconnor6683 5 років тому

      Sounds like possibly syncope? Which is the most common type of autonomic dysfunction!

  • @kyrickpannell4032
    @kyrickpannell4032 3 роки тому

    Sounds like Lyme Disease

  • @tyleroconnor6683
    @tyleroconnor6683 5 років тому +2

    Updated video under this account..... check it