I HAVE BEEN STRUGGLING (PROBS DELETE THIS LATER)

I am Struggling with my Chronic illness & Pain this Life is so Draining.
Thanks for Watching
I Hope 2023 Brings happiness to your life and you reach Your Goals.
"Always Remember to be Happy, Smile and Enjoy Life because that 3 things main things of life”
And Don't Forget to Subscribe to My Channel.
*Please go Check Out Work on Wattpad (Sharing Awareness and Information on Pots):
www.wattpad.co...
Follow all my social media for Updates:
Social Media:
Instagram- SARAHCVLOGS
Health Journey Instagram- / myhe.althjourne…​
Snapchat- SARAHWEEKLYVIDS
Twitter-Sarahvlogs8
TikTok- MedicallySarah
Also go check out my Sports channel:www.youtube.co...
Business Email
Email- [e-mail]
#youtuber #chronicillness #potssyndrome #iamstruggling #chronicpain

[@seanknox5785]

No idea why this popped up on my home page. I’ll give it a like for you. Hope you feel better lady.

[@gabrielleg.1347]

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.

[@jeannespratt1235]

Hi Sarah, I'm so sorry your feeling down. I hope you start feeling better soon♥️

[@normajeanmcdaniel4491]

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

[@PatriciaBrown1711]

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

[@ginobee]

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.

[@fitwithdiana]

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

[@jenncoker6950]

Sending you prayers from Florida in the states

[@AprilMontgo]

best wishes! hope everything gets better love

[@Ida-Adriana]

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

[@meja2546]

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

[@sunshine9122]

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

[@oshifish2]

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

[@gabbysade6477]

Sending u lots of love💕

[@scotchbonnie4122]

Praying for peace and healing 🙏🏿💗

[@normajeanmcdaniel4491]

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 💪.

[@madisonr7995]

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. :)

[@chummicrisologo2474]

feel better!

[@caliking916]

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

[@thapuiiroyte5035]

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

[@shettikkawoods3248]

❤❤❤🙏🏽 ❤❤❤❤😊

[@caliking916]

I wish you the best new here

[@smootherzzz]

Im so sorry you're going through this :(( lots of hugs!!!

[@anisyadewi2878]

Hi Sarah, I’m sorry that things are not easy for you right now, hopefully you feel better and could find joy and peace again! ❤ sending hugs!

[@su_baby88]

Feel better beautiful girl ❤ we have matching glasses

[@EmmaAnna_]

I hope you feel okay!

[@sh4un333]

Hi Sarah. I don’t know how you appeared on my front KZbin 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. :)

[@janettep]

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

[@Ida-Adriana]

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.