What's the Truth About Long Haul, POTS, and Dysautonomia? An Exclusive Interview and Case Study
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- Опубліковано 3 жов 2024
- 🚨 LIVE EVENT: What's the Truth About Long Haul, POTS, and Dysautonomia? An Exclusive Interview and Case Study 🚨
Hello health take chargers & wellness enthusiasts! 🌟
Are you ready to uncover the real story behind long haul COVID, POTS, and dysautonomia? Join us for an exclusive UA-cam live interview and case study that you won't want to miss!
💥 What You'll Learn:
• The REAL truth about long haul COVID, POTS, and dysautonomia
• Insights from the top health expert solving these problems every day
• A detailed case study that sheds light on these often misunderstood conditions
• What can be done instead
✨ How You Can Join:
📅 Date: Thursday May 30th
🕒 Time: 2:30pm PDT/4:30pm CDT/5:30pm EDT
📍 Where: ua-cam.com/users/li...
Don't miss this chance to get the facts straight from the experts and learn how to take control of your health. Click the link to set a reminder and join us live! 🌟
Get your FREE tickets to Dr. Maggie’s upcoming workshop Uncovering Long Haul, POTS, Dysautonomia. www.eventbrite...
Get started with our comprehensive multi-part training series on POTS. Start feeling better today! drmaggieyu.res...
#LongHaulCOVID #POTS #Dysautonomia #maggieyumd
I have longhaul from Epstein-Barr, mono. It took many years to distinguish between my genetic connective tissue disorder and Dysautonomia from long mono or long-haul. Looking back I always had issues that are explained from EDS and/or RA. With a high rheumatoid factor it’s hard to know. I’m 46 and fully disabled. I am in chronic pain 24 hours a day. I’m diagnosed with everything in the book from Reynards to IBD, POTS, ME, I have over 20 diagnoses. I take eight medications a day. And I’m going on my seventh year. my body inflammation flares regularly, causing major spinal and neck pain. Early onset, osteoporosis causes bulging discs and pinched nerves, chronic calcific tendinitis on my joints. I’m very blessed to have an amazing life and amazing people in it. I am very happy and don’t have much stress in my life yet my body does not want to kickstart back to work again. I feel like I’ve tried everything. Including homeopathic. I take lots of supplements. I have to lay down 80% of the day. So far docs have been minimally helpful. I feel like they are taking a stab in the dark hoping we hit the right thing. I do not eat sugar, flour or red meat. I drink liquid IV, and lots of water. Still I get monthly UTIs, and yeast infections. I also got sick overnight just like your guest when I turned 40. 2 years after mono. I had always been extremely healthy and athletic. I rarely got sick.
I will be asking my doctor to test for adrenal hormone. I take estrogen now. Had a partial hysterectomy 20 years ago.
I’m glad to hear doctors are finally starting to understand what’s going on with me. It’s like living with cancer and never dying.
I'm so sorry you have to go through all of this Sarah, I appreciate you taking the time to share. It's ridiculous-- having to live with this for years and years, becoming essentially bed ridden, and still not receiving the help and understanding you absolutely deserve. I would love to see how we can further help you, you can text our team directly at 503-647-4568 :) I would also recommend checking out my pain protocol drmaggieyu.com/PainProtocol! Who else is dealing with debilitating symptoms?
This long haul is a very insidious monster. MCAS, POTS, disautonomia, neurological etc.. involuntary, adrenaline rushes that make you feel doom, tremors. It seems impossible to figure out how to get back to baseline
What would be your best medical approach/advice to someone who lost a job they loved and experienced workplace PTSD symptoms after losing the job due to disclosing medical conditions as outlined below & requested for accommodation at work . Medical conditions & symptoms included general anxiety disorder, major depression, brain fog, dizziness, headaches, vertigo, chronic fatigue and body muscle pains, chest pains and difficulty in focus and concentration. Then after that there is constant tingling and burning sensations of the left feet and it’s worst at night while in bed. Thank you for taking the time to read my question/comments. ❤️🙏❤️
Wow, that's ridiculous! I'm so sorry you had to deal with that from your old workplace. This is why it is so key to have positive support systems around you and people who recognize and understand what you're going through. I would love to have you in our facebook community at facebook.com/groups/transformautoimmune/, absolutely no gas-lighting here!
With all that you are dealing with when is it time to say enough is enough? If you are ready to take the next steps in getting better you can speak to my team directly by texting 503-647-4568!
Multi part training
Here you go drmaggieyu.respond.ontraport.net/training-pots!
How do you get over brain fog 2 years now Psycology says ptsd from long covid could be causing brain fog plus now cataracts
Multipart training
Here is a link to the POTS and Dysautonomia training series drmaggieyu.respond.ontraport.net/training-potsdrmaggieyu.respond.ontraport.net/training-pots! You can also reach my team directly at 503-647-4568
Long haul caused a aneurysm on my pancreas
how do you help your spouse understand what you are going through when as you said it is all a silent illness going on?
Hey Cherie! Communicating about a silent illness can be difficult, I would encourage you to share this video with your spouse. A huge part of dealing with autoimmunity is going to be involving your partner in your journey as much as possible. Would love to have you in our facebook group: facebook.com/groups/transformautoimmune/ ! Here is a link as well to the multi-part training for POTS and Dysautonomia: drmaggieyu.respond.ontraport.net/training-pots !
My feet are aging, getting wrinkles and thin skin 😢 my feet do burn and have blood pooling.
I'm so sorry to hear :( Would love to connect with you further on this!! You can join our facebook group for more information at facebook.com/groups/transformautoimmune/, or you can speak to our team directly by texting 503-647-4568!
Linda from Maine. I was left with being wobbly.
Hey Linda, are there any other symptoms you're dealing with? I would love to hear more about it. It would also be great to have you in our Facebook community ttps://facebook.com/groups/transformautoimmune/!
@@DrMaggieYu I was diagnosed with COPD back in the 90's. I went to a naturopathic doctor in 2020 and discovered that I have an abundance of food allergies. When I stopped eating those foods I was able to breathe much better. I started on oxygen in 2010. I also have lots and lots of environmental allergies as well. I have had covid 3 times. I recently had an appendicitis attack.
I am 77 years old. Thank you for getting back to me, I wasn't expecting a response.
Mine is chronic Lyme. Babesia I believe is my Pots and treatment I think has almost non existent. I'm struggling to see the symptoms. My HR is now not going high on standing.
Hey! Here's a video I've done on Lyme that you might find helpful: ua-cam.com/video/TuWrCR_nrZs/v-deo.html! You can also access the pots training series here: drmaggieyu.respond.ontraport.net/training-pots!
Light and sound sensitivity, full body crash , PEM , debilitating fatigue , chest / heart pain , derealization, palpitations, concussed feeling ,and many more in a wheelchair if i leave the house . My baseline is about 1500 steps a day on a good day . 31 months after reinfection. 2x long hauler
I would love to connect with you further on this, reach out to my team directly by sending a text to 503-647-4568
Forever grateful for your advice long hall for sure power on warriors Az
I would love to have you in our facebook community Always more to share, always more to learn 😊 facebook.com/groups/transformautoimmune/
When will there be treatment for LC
Important to note that treatment isn't going to be a CURE, it's going to look a lot more like management of symptoms, pain reduction, etc. Here's a link to a video of our alumni Cara who dealt with LC and how she's managed to transform her symptoms ua-cam.com/users/liveNXTeVPf4IZU!
@@DrMaggieYuthats odd because dr maggie says lc can go away with time ?
Multipart training please
Sure thing! You can get ahold of that here drmaggieyu.respond.ontraport.net/training-pots What are the worst POTS symptoms you're dealing with right now?
Excellent information yay Joel ❤
multipart training