As someone who has pots and has passed out before it’s very discouraging. Just last night I was at work and suddenly just had to stop and sit down and had to go home early. It certainly does suck. I am fearful of passing out everywhere I go and I find this very encouraging. Thank you for this I truly needed it.
"Those things are happening to me but they are not who I am.. " thank you so much... I really needed to hear this today 💜 wishing the best to you and your husband. Thanks for your great and inspiring content
I‘m new to the channel and I‘m already so thankful for your videos. I‘m still a teen fainting pretty often and it absolutly sucks. I mostly faint in the tram on my way to school and most people I see everyday saw me fainting at least ones. It‘s honestly so anoying to expirience such things especially at a young age(I started fainting at the age of ten)but thank you for your videos and helping people who are struggeling and also making me feel a bit more normal❤
Happy I found you! I am 28 years old and was also diagnost with POTS when I was 16. My symptoms are very similar to yours. Watching your fainting videos and just knowing we are going through the same experience, was very comforting. Thank you for sharing. Just subscribed :)
What she is saying takes years to accept. And once you do, you can explain to others how to push through it. I have epilepsy since age 10. And my mother saved my life as I had drowned in the tub. Great way to find out I had a medical problem. At this time there's no internet. So there was no way to tell and explain to others what was going on. So I got picked on. Until I was willing to explain that it was not catching and not to take lightly. I gained great friendships with the people who picked on me. And haveing the highschool football team on my side. Helped also. It was not easy. Am 48 now and have done more than most people at my age. Knowing that at anytime something could happen. Medication helps some what. But my body fights to keep the drugs from working. The positive of all of this is am a speaker on Epilepsy. And have done TED TALKS. The one question that I have to answer to doctors. Are you depressed or feel like hurting yourself? My answer is always no. I accept my way of life. It's not easy,, but everyday is not a guarantee. So I make the best of each one. Staying positive and accepting is the key. But it takes time. It doesn't happen overnight.
i dont get why you keep posting you fainting..To make people feel sorry for you really? your syndrome is treatable with blood pressure meds and you know what you can do , and not do to ease the symptoms ..but yet you aggravate your symptoms to video you fainting??? wow anything for likes huh? stop making people feel sorry for you when you know you are doing it on purpose
As someone who has pots and has passed out before it’s very discouraging. Just last night I was at work and suddenly just had to stop and sit down and had to go home early. It certainly does suck. I am fearful of passing out everywhere I go and I find this very encouraging. Thank you for this I truly needed it.
sending you love!!! you got this!
I really loved this a a younger person with multiple chronic illnesses.
Thank you so much! ❤
thank you so much!
"Those things are happening to me but they are not who I am.. " thank you so much... I really needed to hear this today 💜 wishing the best to you and your husband. Thanks for your great and inspiring content
I‘m new to the channel and I‘m already so thankful for your videos. I‘m still a teen fainting pretty often and it absolutly sucks. I mostly faint in the tram on my way to school and most people I see everyday saw me fainting at least ones. It‘s honestly so anoying to expirience such things especially at a young age(I started fainting at the age of ten)but thank you for your videos and helping people who are struggeling and also making me feel a bit more normal❤
sending you all the love, i’m so happy you found my channel!
thank you so much for this i also have POTS and have really been struggling lately and seeing i’m not the only one really helps
Happy I found you! I am 28 years old and was also diagnost with POTS when I was 16. My symptoms are very similar to yours. Watching your fainting videos and just knowing we are going through the same experience, was very comforting.
Thank you for sharing.
Just subscribed :)
It's so great to see you back on TH-cam, I can't wait to see what you create on here!
Thanks for sharing! I honestly didn’t even know what POTS was until now. I love how positive you are and how you manage it ❤
THANK YOU. YOU ARE SO BEAUTIFUL.
My partner has POTS as well. Thanks for sharing your positivity living through it
God bless you always be safe I just find your channel ….❤🙏🙏🙏🙏🙏🙏🙏🙏
Thank you I really needed this
Sending you so so much love and so many hugs i am so so sorry for everything that you are going through xxxxxx
love it!!
What she is saying takes years to accept. And once you do, you can explain to others how to push through it. I have epilepsy since age 10. And my mother saved my life as I had drowned in the tub. Great way to find out I had a medical problem. At this time there's no internet. So there was no way to tell and explain to others what was going on. So I got picked on. Until I was willing to explain that it was not catching and not to take lightly. I gained great friendships with the people who picked on me. And haveing the highschool football team on my side. Helped also. It was not easy. Am 48 now and have done more than most people at my age. Knowing that at anytime something could happen. Medication helps some what. But my body fights to keep the drugs from working. The positive of all of this is am a speaker on Epilepsy. And have done TED TALKS. The one question that I have to answer to doctors. Are you depressed or feel like hurting yourself? My answer is always no. I accept my way of life. It's not easy,, but everyday is not a guarantee. So I make the best of each one. Staying positive and accepting is the key. But it takes time. It doesn't happen overnight.
I used to have POTS. I quite birth control pills, and it went away.
i dont get why you keep posting you fainting..To make people feel sorry for you really? your syndrome is treatable with blood pressure meds and you know what you can do , and not do to ease the symptoms ..but yet you aggravate your symptoms to video you fainting??? wow anything for likes huh? stop making people feel sorry for you when you know you are doing it on purpose