POTS (postural Orthostatic tachycardia Syndrome)
Uploader Comments (chocolatemusica)
Top Comments
-
I have POTS too. I know how hard it can be sometimes... hang in there!!!
-
Look into Lyme disease. I didn't know I had it, but got a clinical diagnosis and getting better with treatment. Many on lymenet report getting POTS during their Lyme and I can vouch, because I just had a pos. Tilt Table test, but I'm killing it with my Lyme treatment. Many case of Chronic Lyme. Big debate about it, but it is real and it does exist. I have a support site at lymechatnework with a period and a come minus the e. You should check it out and see what I'm talking about.
All Comments (15)
-
Such a true song. Great job capturing the true feelings behind the POTSIE, I am sure these are all things you can all relate too. My 15year old daughter has POTS and has just had to leave school for home learning. Stay strong and promise yourself to never give up the hope of all these dreams coming true.
-
I have POTS too:(. We'll hang in there:) God bless you!!
-
I have POTS too:(. We'll hang in there:)
-
Anyways, you're not alone. stay positive, and keep fighting to get better. Good luck!
-
You are not alone, I am the same way. I struggle with nausea, dizzyness, anxiety/panic attacks, muscle pain, etc. etc. the list goes on. The last year and a half, doctors just thought I had an extra sensitive stomach and an anxiety issue. After switching doctors and insisting they find what's wrong, I met with a nurse practitioner, and she diagnosed me with POTS.Some of my friends are so rude to me, thinking I'm faking or making excuses.
-
I have Pots I just recently got diagnosed with it. I think ive had it for about 3 years tho, but knowbody knew what was wrong with me at first, and knowbody believed I was sick my mom was the only one who did. Not even the doctors. I got diagnosed with conversion disorder 3 years ago before they found out I had Pots. Turns out that I never had conversion disorder it was the POTS. Many people think I'm faking. If theres anybody who has the same story to tell please talk to me.
-
I have had pots syndrom for 3 years its difficult to live with but all that can be done is to have the hope and the strangth and hope to hold on every day.



By the way what the name of this song?
XoxUhlyssaXox 1 year ago
@XoxUhlyssaXox Billy Gilman "i could if they would"
chocolatemusica 1 year ago
i have been tested for that but thanx
chocolatemusica 2 years ago