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7:28 Sarah, don't you think your speaker is too hidden behind the monitor?

Wonderful❤🎉❤🎉vlog❤🎉❤🎉

Happy weekend

So happy to see an update. Can’t wait to see more videos from you. Continued prayers to you sweet girl

Good ❤❤❤

Looks like you are coming strong girl! Sarah you are brave. This is inspiring to all who are suffering the same. I wish you well girl! Stay strong!

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Been praying for you Sarah

😮never heard of this before I hope they find something that helps. 🙏🏼

Arnt u ever afraid to faint while driving? I customized my cane. Trying to figure out what to do with my walker lol

I have 2 different accounts don’t mind me lol anyways how did u know the brain fog was from pots and not epilepsy? I have an Apple Watch too and right now it’s 110 and all I’m doing is laying down 🤦🏻‍♀️ glad I haven’t fainted yet but I have had the feeling of faint. Going thru the process but my dr has already been treating it like pots so I’m learning to eat more salt lol that table tilt test scares the crap out of me

I’d love a bed like that but I just have a queens bed cuz my bf sleeps in it too lol took me a while to know that my breathless thing is called air hunger lol cute pup

Missed when my only problem was just my epilepsy 🤦🏻‍♀️

I’m going thru the process of finding out if I have pots. Thank u for sharing!

NATAIYA

I’m glad you are getting answers. My son was told he has asthma as a kid. Turned out he had SVT and needed a heart procedure.

Stay strong!!!

Prayers!

Hang in there. ❤❤❤

I had all that and much much more went even blind from the seizures, kidney, liver, heart insomnia, panic attacks, anxiety, wheelchair, hospice they even gave me time at one point until one day me and one of my friends who had MS he’s been in a wheelchair chair since he was I believe 10-11 years old he’s now 42 yrs old and we were talking about our health how our diagnoses are all incurable and than he asked me if I prayed to be healed and I told him yes almost everyday but never got healed because I believed a false doctrine when “Paul” in The Bible asked God to remove the thorn from his side many pastors and teachers say it was a sickness but it actually never days exactly what Paul’s thorn in his side was and God said no to taking it away because it kept Paul humble but it could of been anything? A person, there was also a witch that use to harass him as so on… so my friend told me “don’t you know it’s always in Gods Will to heal us and that’s when I found out it’s one of God’s promises to ask anything in His Name “Jesus Christ” and it will be given on to you PRAISE YOU JESUS 🙌🏼🙌🏼 pray for your healing in Jesus Name I pray a complete healing upon you the same way God had healed me completely THANK YOU JESUS 🙌🏼

Wish you the best

Thank you for this. I deal with daily, chronic pain and have been dealing with it for almost 6 years. I assume ill probably be dealing with the pain for the rest of my life, but it gets easier with acceptance. I wish you all the best, and thank you for letting me feel less alone ♥

Waxed!!?

Praying for you. Do they have any explanation on why this has developed so suddenly?

Like my great great grandfather once said #It gets greater later with time he was born in 1898

I wish you the best new here

❤❤❤🙏🏽 ❤❤❤❤😊

Lots of love and hugs to you, Sarah. Would you please let us know how you're doing?❤

Sending you lots of love and prayers. Glad you are staying connected to family and going out. Stay focused on the “can” and “can do’s”. Thank you for sharing.

I got ideas for fidgets for my family 😀

Did this all happen to you out of the blue about 18 months ago? This does coincide with a major global mandate. You are not alone, there are many support groups on the internet with plenty of valuable information to help clean out the poison from your system. Do not give up. Believe in yourself and your own healing. Those conditions you wrote out are only labels...they are NOT YOU. Blessings xx

Please look into an iteracare device, it uses terahertz frequencies to help you heal ♥️

❤

Stay strong

Have you spoken to your doctor or specialist about Low Dose Naltrexone .

I'm not sure why your video showed in my feed, I am sending SO much love your way ❤💕 I don't believe I have seen your channel before, I feel your message is strong for many to hear so maybe keep it posted. ~ Big hugs from Arizona

I am sending you love and lhealing for your condition. Pleaae do not delete this because it somehow found its way to me. My dear niece struggles with POTS and she lives in Florida. She is 23. I can share your video to show she is not alone. Sometimes she feels that way. Your video came up for me twice so it seemed like a sigh for me to watch and I am glad I did. Sending you prayers from Scotland.xx

Sorry to hear about your struggles. Take care and stay strong.

FWIW, pls don't erase this video. It helps others to see the good and bad times. 💯✌️🌴

Been there. It's an awful feeling and I hv no magic words -- except my Old Gen-X butt is still here, and I was supposed be gone by 22. Fibro sucks bc it's invisible. My other autoimmune disease is the life-threatening one. I just subbed. Sometimes, it helps to know some stranger out here cares. Be nice to you. - just me in Palm Springs 🌴 (bad day here, too; Temps near 120 + beta blockers... ) Stay 💪.

Praying for peace and healing 🙏🏿💗

Feel better beautiful girl ❤ we have matching glasses

What are you eating? I heard that some people had success with a basic elimination diet eating meat/organs/bone broth/animal fats.... have you checked your prolactin levels? I bet they are high.

Hey Sarah, I hope you’re feeling ok, rest and take it easy and don’t try to force your body

Hi Sarah. I don’t know how you appeared on my front CZcams page. I’m not subscribed or seen any of your videos before and there isn’t any related videos but I take it as a sign for you that your gonna be okay. The world meant your video to be seen by people and that everything is gonna be okay. :)

wow I literally didn't even click on this video and it still popped up! Like the Universe wanted me to see it. I'm so sorry about your new diagnosis and having to leave the job you love! That is so so hard and sad. I totally get where you are coming from because I have several chronic illnesses myself (very similar to what you have), and have had to stop working for 3 years now. I have found some things that have helped me improve this year though and I am hoping that by next year, I will be able to work again. Things can turn around! My biggest advice is to not rely on standard doctors to help you much. Become a medical researcher yourself, find the right health mentors, and don't be afraid to trial new or unconvential treatments. And make sure you find the root cause of the POTS and Fibro because neither of those are "root cause" illnesses. For instance, I was diagnosed with ME/CFS (which 50% of people with that also have POTS), told there was no cure and limited treatments and I would probably be bedbound for the rest of my life. But I started digging and figured out that I actually have Lyme Disease and mold illness and those are the actual root causes of my ME/CFS, which similar to Fibro, is kind of a catch all diagnosis they give you when nothing else really fits. So I started working with a health coach who specializes in lyme and mold, and I started to get better. Both Fibro and ME/CFS are often undiagnosed lyme disease. You can't trust the standard lyme tests either, they give false negatives 60% of the time. I can recommend a good lab test that will scan you for over 400 stealth infections and root causes that you can do at home and mail out. It saved my life to know what was really going on. You should find me on instagram yeshe_khandro11 and I can send you more info on it if you want. I hope your week gets a little easier.

Sending you prayers from Florida in the states

Am praying for you Sister, am hoping you feel better , God bless you ❤

I'm really sorry to hear that you're struggling right now. I also have pots and you remind me of myself from a couple years ago. I was at a very low point and it was simultaneously debilitating as well as frustrating because it felt like no one understood me. I think a huge helpful aspect is having a mindset change and trying to see things positively. And I think as more time goes on, it's also something you will get more used to, though I'm not sure when you were diagnosed. I think it's amazing you're trying and doing the best you can because that's all you can do, and you should feel very proud. :) It's important to not let an illness define you, though easier said than done. What's helped me is trying to have a healthy balance and not putting as much focus on pots as I once did. And I think just choosing to focus on all of your other amazing attributes as well as putting more focus into your hobbies and taking baby steps is so huge. Sorry, I know you weren't asking for advice but just figured I'd leave this comment. I know things will get better for you. :)

i wanna give u a hug right now .. i hope u feel better 🫶🏻