Wow. This is a very accurate anecdotal account of my lived experience for the past 19 months with LH covid and resulting POTS/dysautonomia. My dysautonomia has caused paralysis and oxygen saturation issues which has stumped all of my doctors thus far. Thank you for highlighting the tremendous amount of medical gaslighting that has been occurring. It is VERY REAL and can be a barrier to seek care. It’s nice to know that I’m not alone on this journey. Thank you for helping to spread awareness about the long term effects of this awful virus. Every patient needs advocates like you to help spread the word so we can start to receive the care we deserve. Sending you love and light. ❤
Thank you for this. I’ve had pot since 2011 I am a health expert and have an extensive biological science background. I’ve had full fledged arguments with cardiologists both in New York and Florida for three years before I got diagnosed. I am a sports biomechanics, athletic injury correction and conditioning expert in nyc. And I know that I was only diagnosed because of my background and being able to speak the language. I was able to get myself back to full capacity for working, although I was not able to run anymore, I was able to work on all of my athletes and that was my work out. I’ve been a dancer since I’m three years old and that was ripped from me as well, I was able to dance again but nothing like I used to. Dancing would not make me feel very sick at the drop of a hat. I have extremely low blood pressure and very high heart rate but now I can’t get my heart rate very high and it feels like 120 is 200 in my chest. I also do athletic heart conditioning so I’m also well-versed in The cardiovascular system. I got Covid in May 2022 and it sent me back about eight years with my pots. Covid felt like the worst parts flair I had ever had and I am still managing it to this day as Pots is progressive and we really don’t know what the next day is going to be like. I originally got pots from a really bad flu in Feb 2011 But my diagnosis didn’t come until Sept 2013 by an electrophysiologist. I was maxed out on the only medication that raises your blood pressure, beta blocks, steroids and sodium medication all of which was actually making me 10 times worse than I was ordered to stop them all immediately. I’ve not had any medication since December 25, 2013. I’ve worked with many athletes that have had pots but can still actually do cardiovascular work where I cannot. However my programming works very well on people with pots because of how it’s delivered and received to and from the body. Yet and still I cannot run and I do struggle to dance again now since I’ve had Covid it’s made me much much worse my G.I. issues are much worse my body aches are much worse my migraines are much worse my vision is much more blurry my chest pains are pretty consistent and the palpitations gel kind a-fib now. there’s really nothing anybody can do. If I have one piece of advice for anybody reading this is don’t you ever tell somebody with pots they have anxiety because none of us have anxiety we have a heart working its ass off to help us because nothing inside of our processing systems is actually processing properly and the entire system is tripped up and the whole body is over working to complete exhaustion to do basic tasks like talking, breathing, heart control, digestion, thinking…even urinating. It’s debilitating and steals your life from You. People are getting this from Covid the same way I got it from the flu it’s a bad virus that completely rattles your autonomic nervous system. I have actually personally worked with a lot of long haulers and they’ve all recovered and are running marathons with no problem, the difference I see in pots from people who got Covid versus people who had pots pre-Covid is that the people who have gotten pots post Covid are recovering, whereas people like me our pots is just worse.
I just made a video on a similar experience regarding post covid pots..I also had pots as a preexisting condition that got worse from covid and I was a competitive runner before. I'm a Healthcare worker.
@@Truerealism747 pots. I don’t have anything else. Ive had it 12 years now, but when i was diagnosed everyone had the same as me. Now, however, it’s said that inputs is the more severe. Covid inflated pots and since no drs know to treat it OR mistreat as ok seeing more and more overstepping in the medical fields, it makes people sicker. Muscle aches with pots is from not getting suffice oxygen to them, blood pump deficiency and muscle loss. I’m much better now thankfully. But it’s daily work to do so.
I’ve had long Covid since my last flu/Covid jab in October 22…the fatigue, low blood pressure, low oxygen, rapid heartbeat is a nightmare. I’m thinking of going to alternative therapies as the medical system won’t acknowledge it and all my tests come back fine. Can you explain to me what exactly pots is??? Thx
I never had COVID but suffer from all these symptoms and more since Feb 2019. I really don't think life will ever improve. Want to get approved for dignity to die but since it is not " terminal" it's impossible. So where does that leave patients with no treatment or hope and that's finding their own way out which is unfair.
Absolutely agree. I have lived with long Covid now for over 3 F’N YEARS!!!! I want to end it all some days. I used to be active and hike with my husband. Now I can barely get up a flight of stairs. Severe congestion and respiratory issues, cognitive decline and I’m only 43! Used to be happy and vibrant. “Pharmaceutical agents” is what I call them, and they’re USELESS! Just passed from one “specialist” to the next… It’s infuriating!!! 🤬 I have become my own Dr and advocate. They could care less!
I have long COVID and it’s been 17 months I think. I get sick every single month for 3 weeks. Bad headaches, dizzy spells upon standing, racing heart. Out of breath , coughing and runny nose constantly. I can no longer breathe out all my air. My breathing function is not functioning very well. Scars on my lungs. Do I have Pots? Great question.
Did we know at what tissue temperature did SARS COV2 better replicate ? Why ? Because at TWiV 659 at min29 Christian Drosten suggest that SARS COV2 better replicate at very low tissue temperature.
What does it matter? Most people that have " Long Covid " have been jabbed, but this is happening to a ton of people that haven't as well. The jabbed aren't your enemies either. Many are victims that were coerced into taking it without informed consent, as you know. Not everyone that took it was vaccine Nazi or a Covidian.@@SurvivorDiariesOfficial
Just want to say, this condition is not only in vaccinated people. I have not been vaccinated for anything, since 1997 and that was tetanus. I am a long hauler, since Jan 2020. I have not taken any pharma drugs, only vitamins, herbs and various supplements this whole time. Just now, beginning taking Colostrum, which seems to be helping to correct this horrific poisoning of my body.
Mes commentaires sont effacés, d'après les commentaires je trouve qu'il y a un maximum de personnes qui sont accrocs aux médicaments et la vaccination 😂😂 Prenez vous en charge sinon bigpharma se fera un plaisir de s'occuper de vous
Google image vitamin compatibility chart (it is a picture of Red Yellow and Green squares)// these combinations are for the nervous system (also mental health) B1 (Thiamine) + B5 (Pantothenic acid/avocados) // The reason there is 4 or 5 different clusters is because if you look at this chart some vitamins cancel the other ones out// B6(Pyridoxine/ causes lucid dreams), B2 (Riboflavin/ dairy products), B3 (Niacin), Zinc /// B12, B9, B5, Calcium, Magnesium/// Vitamin D + potassium ( this is a good combination after work really easy 10,000 IU vitamin D and a banana/// Vitamin E, beta carotene (carrots/synthetic vit A is toxic) , Alpha Lipoic Acid, Vitamin C// To make red blood cells you need Iron + Vitamin C and then two hours later B9 and B12// Vitamin C destroys Vitamin b12 and vitamin C makes Iron absorbable// Good luck with the leap of faith trusting this information!! More red blood cells = Faster healing
![Long Covid: The Shadow Pandemic | Covid-19 Survivor Diaries Episode 2 [ NO MUSIC ]](/img/n.gif)
Wow. This is a very accurate anecdotal account of my lived experience for the past 19 months with LH covid and resulting POTS/dysautonomia. My dysautonomia has caused paralysis and oxygen saturation issues which has stumped all of my doctors thus far. Thank you for highlighting the tremendous amount of medical gaslighting that has been occurring. It is VERY REAL and can be a barrier to seek care. It’s nice to know that I’m not alone on this journey. Thank you for helping to spread awareness about the long term effects of this awful virus. Every patient needs advocates like you to help spread the word so we can start to receive the care we deserve. Sending you love and light. ❤
I just made a video on my post covid Pots story as a NYC healthcare worker...its a tough condition to have.
Thank you for this. I’ve had pot since 2011 I am a health expert and have an extensive biological science background. I’ve had full fledged arguments with cardiologists both in New York and Florida for three years before I got diagnosed. I am a sports biomechanics, athletic injury correction and conditioning expert in nyc. And I know that I was only diagnosed because of my background and being able to speak the language. I was able to get myself back to full capacity for working, although I was not able to run anymore, I was able to work on all of my athletes and that was my work out. I’ve been a dancer since I’m three years old and that was ripped from me as well, I was able to dance again but nothing like I used to. Dancing would not make me feel very sick at the drop of a hat. I have extremely low blood pressure and very high heart rate but now I can’t get my heart rate very high and it feels like 120 is 200 in my chest. I also do athletic heart conditioning so I’m also well-versed in The cardiovascular system. I got Covid in May 2022 and it sent me back about eight years with my pots. Covid felt like the worst parts flair I had ever had and I am still managing it to this day as Pots is progressive and we really don’t know what the next day is going to be like. I originally got pots from a really bad flu in Feb 2011 But my diagnosis didn’t come until Sept 2013 by an electrophysiologist. I was maxed out on the only medication that raises your blood pressure, beta blocks, steroids and sodium medication all of which was actually making me 10 times worse than I was ordered to stop them all immediately. I’ve not had any medication since December 25, 2013. I’ve worked with many athletes that have had pots but can still actually do cardiovascular work where I cannot. However my programming works very well on people with pots because of how it’s delivered and received to and from the body. Yet and still I cannot run and I do struggle to dance again now since I’ve had Covid it’s made me much much worse my G.I. issues are much worse my body aches are much worse my migraines are much worse my vision is much more blurry my chest pains are pretty consistent and the palpitations gel kind a-fib now. there’s really nothing anybody can do. If I have one piece of advice for anybody reading this is don’t you ever tell somebody with pots they have anxiety because none of us have anxiety we have a heart working its ass off to help us because nothing inside of our processing systems is actually processing properly and the entire system is tripped up and the whole body is over working to complete exhaustion to do basic tasks like talking, breathing, heart control, digestion, thinking…even urinating. It’s debilitating and steals your life from
You. People are getting this from Covid the same way I got it from the flu it’s a bad virus that completely rattles your autonomic nervous system. I have actually personally worked with a lot of long haulers and they’ve all recovered and are running marathons with no problem, the difference I see in pots from people who got Covid versus people who had pots pre-Covid is that the people who have gotten pots post Covid are recovering, whereas people like me our pots is just worse.
I just made a video on a similar experience regarding post covid pots..I also had pots as a preexisting condition that got worse from covid and I was a competitive runner before. I'm a Healthcare worker.
Is your muscle pain.from.pots or cfs
@@Truerealism747 pots. I don’t have anything else. Ive had it 12 years now, but when i was diagnosed everyone had the same as me. Now, however, it’s said that inputs is the more severe. Covid inflated pots and since no drs know to treat it OR mistreat as ok seeing more and more overstepping in the medical fields, it makes people sicker. Muscle aches with pots is from not getting suffice oxygen to them, blood pump deficiency and muscle loss. I’m much better now thankfully. But it’s daily work to do so.
@@Ririsimi hope you’re feeling better! Thank you for commenting!
I’ve had long Covid since my last flu/Covid jab in October 22…the fatigue, low blood pressure, low oxygen, rapid heartbeat is a nightmare. I’m thinking of going to alternative therapies as the medical system won’t acknowledge it and all my tests come back fine. Can you explain to me what exactly pots is??? Thx
I never had COVID but suffer from all these symptoms and more since Feb 2019. I really don't think life will ever improve. Want to get approved for dignity to die but since it is not " terminal" it's impossible. So where does that leave patients with no treatment or hope and that's finding their own way out which is unfair.
Lmao, if you have all the symptoms without having Covid the. That means long Covid dosent exist
Absolutely agree. I have lived with long Covid now for over 3 F’N YEARS!!!! I want to end it all some days. I used to be active and hike with my husband. Now I can barely get up a flight of stairs. Severe congestion and respiratory issues, cognitive decline and I’m only 43! Used to be happy and vibrant.
“Pharmaceutical agents” is what I call them, and they’re USELESS! Just passed from one “specialist” to the next… It’s infuriating!!! 🤬
I have become my own Dr and advocate. They could care less!
THIS IS IT!!! Thank you so so very much ♥️
Thank you for the encouragement!!
I just made a video about my personal post covid POTS story . Its a tough condition to deal with!
Very tough! Thanks for sharing your story.
Interesting. Can't wait.
Thank you so much for this.
You are so welcome! Have you had a similar experience?
My goodness hearing from another long hauler who also went through Rheumatic Fever that resulted in a heart murmur, just dropped my jaw.
I have long COVID and it’s been 17 months I think. I get sick every single month for 3 weeks. Bad headaches, dizzy spells upon standing, racing heart. Out of breath , coughing and runny nose constantly. I can no longer breathe out all my air. My breathing function is not functioning very well. Scars on my lungs. Do I have Pots? Great question.
Tough having POTS then given covid. Blows up Dysautonomia into overdrive
Sounds like you’ve had experience?
Thanks for watching!!
Best hypothesis ever from the JHH profressor. But what is the cure?
NAC
POTS spelt backwards = STOP
Sorry if you are experiencing similar symptoms… you are not alone!
What other content would you be interested in seeing on this channel? More info about POTS or survivor stories on other topics?
BRAVO. You said it.
Did we know at what tissue temperature did SARS COV2 better replicate ?
Why ?
Because at TWiV 659 at min29 Christian Drosten suggest that SARS COV2 better replicate at very low tissue temperature.
Thanks for watching!!
Did any of them get the COVID jabs?
Thanks for watching!
What does it matter? Most people that have " Long Covid " have been jabbed, but this is happening to a ton of people that haven't as well. The jabbed aren't your enemies either. Many are victims that were coerced into taking it without informed consent, as you know. Not everyone that took it was vaccine Nazi or a Covidian.@@SurvivorDiariesOfficial
Just want to say, this condition is not only in vaccinated people.
I have not been vaccinated for anything, since 1997 and that was tetanus.
I am a long hauler, since Jan 2020.
I have not taken any pharma drugs, only vitamins, herbs and various supplements this whole time.
Just now, beginning taking Colostrum, which seems to be helping to correct this horrific poisoning of my body.
@@dianarhyne Look into Low Dose Naltrexone. Alot of long haulers are having success on it.
Of course. That's why they did this "documentary"; to deal with the fallout.
wow
Thanks for watching! I hope it was helpful for you.
How many boosters have you had?
Thanks for watching!!
Could it be the jabberwocky?
Mes commentaires sont effacés, d'après les commentaires je trouve qu'il y a un maximum de personnes qui sont accrocs aux médicaments et la vaccination 😂😂
Prenez vous en charge sinon bigpharma se fera un plaisir de s'occuper de vous
Google image vitamin compatibility chart (it is a picture of Red Yellow and Green squares)// these combinations are for the nervous system (also mental health)
B1 (Thiamine) + B5 (Pantothenic acid/avocados) //
The reason there is 4 or 5 different clusters is because if you look at this chart some vitamins cancel the other ones out//
B6(Pyridoxine/ causes lucid dreams), B2 (Riboflavin/ dairy products), B3 (Niacin), Zinc ///
B12, B9, B5, Calcium, Magnesium///
Vitamin D + potassium ( this is a good combination after work really easy 10,000 IU vitamin D and a banana///
Vitamin E, beta carotene (carrots/synthetic vit A is toxic) , Alpha Lipoic Acid, Vitamin C//
To make red blood cells you need Iron + Vitamin C and then two hours later B9 and B12// Vitamin C destroys Vitamin b12 and vitamin C makes Iron absorbable// Good luck with the leap of faith trusting this information!!
More red blood cells = Faster healing
Always cool and happy to wants to blood donation daily 1 time is a oxygen is in mumbai maharashtra india 400095 is called information platform .