Відео

Hey, just checking in. You okay?

Loved it. Thank you ❤

You described long covid perfectly!!!! It's crazy to feel normal, then relapse, and feel terrible, for no reason, it makes you scared of life, scared to push yourself in anyway, as a relapse feels awful and you don't know how long the relapse will last, my mental and sleeping problems can be terrible!!!! my anxious and weird mental thoughts can keep me awake for weeks, and there are times I feel completely normal, like a lot of people mine started in March 2020 when I first got covid, it's a very weird how covid causes so many different problems to the body, Time does help I know this for a fact!!!!!! Maybe there is a little bit of covid in our body's that sleeps, then it wakes up every now and then, which gives us a relapse every now and then, maybe it's damaged a part of our central nervous system that regulates our bodys functions!!!! And are bodies is slowly repairing this damage (but it takes years)!!!!! 3 years now of covid problems, I must admit there not as bad as they first was, (as I would be dead now I would not be able to handle the inner torture) so why does my relapses hurt me still so bad..... So it's a waiting game till they find out why this is happening!!!!!! I wish you long covid sufferers, strength to get though these strange and debilitating symptoms , your not alone and it's very real.

I hear you. It's been a long 2 year journey. I pray to get better and keep trying supplements and thinking of hyperbaric oxygen therapy.

Hey how many sessions have you done so far?

What is the optimal pressure in the chamber? Is mildHBOT also beneficial? 1.4 ATA?

How much does it cost where you went ? In the US its $300-400 per session 🙄

treatment for the rich

I’m still getting flare ups and it’s been 3 years for me as well. It’s frustrating. I feel absolutely normal one day, but for 2 to 5 days after my “normal day” I get so exhausted again, my cheeks turn red. I get aches and chills. I can’t get a doctor to take me seriously. So, I’m in this alone.

I'm literally doing the very same thing. Early bedtime also

This is a helpful video that does show how much better you are doing. Even when you are having a flare up, you are making sure to eat a well balanced diet. Some good ideas here for meal choices too. My favourite, of course are the cookies. Always have room for cookies! It's impressive that you manage to make these videos when you feel so unwell. I find them very comforting and encouraging. So, thank you very much. You have my prayers and best wishes for your continued healing and full recovery. x🤩

Glad to see where you're at on your journey. Your video were so valuable to me during the darkest phase of this journey.

What a wonderful and inspirational video. So, so happy that you are feeling better and you do seem to be well on your road to recovery. Can't wait to hear more about how you revised your healing protocol. All your meals look so yummy. Especially the cookies! If you did not manage to finish the tray I can volunteer to share . Wishing you continued success and joy and lots of fruit and pancakes and cookies 😋 in all your days 😍

Thanks for posting this, so good to see your journey is progressing. Wishing you all the love and healing xxx

the banana oatmeal pancakes without any additional ingredients are a revelation, I will be trying it!

How are you now?

It did not work for me. What pressure are you using?

If you're still doing HBOT, you may look into lower pressure. There are studies that show it to be more effective for some ailments. I do HBOT in soft chamber at 1.3 ATA and it seems to help but I haven't tried a hard chamber at 2+ ATA. Hope you turn a corner. I'm on second long haul after a full recovery from the first. This time I have dyautonomia, shortness of breath, GI and thyroid issues. It's no fun.

I tried it and didn't feel like it helped much. After 3rd treatment had pretty bad chest pain so i stopped. I was in a tube. Different than what you did. I also ended up with collapse lung which I think caused it. But not sure just got covid 2nd time but don't think its from covid.

audio is so low... cannot hear anything

Hey i know this is a strange question but i wanted to ask how it feels wearing big mask in the chamber? Does it force you to breathe ? Your breathing sounds are intense when you are breathing through mask.

How are you currently doing?

Where are you getting the HBOT therapy?

This is such an interesting video of your recent experiences and very well presented. I agree that you do look a lot better after starting the HBOT. I have had several sessions myself recently. Not for long covid but symptoms similar to many long covid issues. I hoped it would help me with autonomic dysfunction, neuropathy, IBS/C, gastroparesis and digestive issues, chronic fatigue, weakness etc. I absolutely loved my sessions feeling better immediately after each one. After my 5th treatment I managed to start wiggling my toes which I had not been able to do for at least 5 years. My pain also has reduced considerably. Unfortunately, like you, I recently contracted covid. For me it was the first time, but also, like you, the virus went directly to my most sensitive area, my gut and played havoc there. Months later I am still suffering from the effects. Barely able to eat or sleep and much weakened by it. And most unfortunately, I too can no longer tolerate the pressure of the HBOT treatment. I am eagerly waiting to heal enough to be able to return to HBOT. Wishing you and all us chronically ill people a full and speedy recovery

Im just about to try this and iv vitamins ..thankyou for using your spoons on helping inform us ..praying for you ❤️

thank you for the expressing the frustration and despair of "when am I going to feel better?!" so many valuable snapshots of what it can be like in this video!

Sending you so much love from the Netherlands! I wish I could do magic and make you better. You are so strong! Please never give up hold on! I have long covid too, it is so frustrating at times, sometimes i feel hopeless and depressed. I also spent a lot of money on a functional doctor, supplements. I have low cortisol, high adrenaline, hpa-axis out of balance, fatigue, sleep issues, brainfog, pain in my body, tingling in my feets, histamine intolerance, gut issues and now i have Sibo(small intestinal bacterial overgrowth). Some weeks i feel a lot better and then it is there again. Things that helped me. ATP FUEL it is a supplement for your mitochondria, people use it also for Chronic fatigue syndrome really felt so much more energy after taking this. And Cytozyme AD is a supplement for your adrenal glands maby you will benefit also from this. I am sending you so much strenght to hold on 🫂♥️🙏🏼! I wish i could take all of your sufferering. Sending you lots of love ♥️

Proud of you for continuing even when it’s hard! Take big care xo.

You look fantastic! You gave me hope when the times were so dark!

I typed in, stomach problems, I have reflux, this class was so interesting. Make more stomach, acid reflux videos! 🎉

I really felt alone today in my relapse. After a string of a few good weeks, I had just written in my journal the day before yesterday that the worst feels behind me. The irony. This isn't my first relapse, and they are so demoralizing. Thanks for being that friend that understands today. Spot on about the menstrual cycles too, the relapses my cycle triggers seem to be getting better as the months wear on, but it's still a thing. Are you always able to pinpoint triggers for your relapses? I find myself always looking for a way to blame myself for my relapse, probably not healthy, but I always feel guilty for being a burden to my family yet again when I get flattened. Take care, and thank you for making videos and sharing. ❤️

I have a lot of bad symptoms

With your giggles,, I don't believe you..

I totally understand why is this long Covid not more on the media I’m struggling every day we left behind

You seem to be doing well. Most of us can’t get out of bed.

It’s a long process

Iv been struggling close 2 years at times I felt like giving up

I can so feel your pain Having the same symptoms as yours from past 6 months plus I am in my postpartum phase too.. I can provide one person, she is from India only and I hope she can help you as she is surely helping me Take care 🧿

Thank you for your video. I’m struggling bad, 5 months 🥲

You should never reduce exercise . Exercise is important for inflammation can’t believe theses doctors keep saying no exercise .

Have you found vagus nerve exercises help?

I an a long hauler. You might call them flares. Research on night histamine, night gut health, b vitamins for neuropathy, c foods for skervy. Also research on cold ease. Sunlight and exercise

Tremendously relaxing Qi Gong exercises

Got severly ill in April 2020, so 27+ months here. NO day since the infection that I havn´t had a hard time breathing, horrible vibrations and clinical proven arrhytmias. These are the two worst symptoms, the other 25 I just try to suppress. Still cant walk more than 2-400 meters. I am certain that the brain (medula oblongata) is damaged and/or the connections to the vagus nerve, hence there is no sign of any organ damages. Life is..... shattered... and a living nighmare. I am almost certain now that this state could be permaent hence the long time that has passed since i got infected. I would like for all of you to get well again! Keep strong

This is very encouraging and reassuring. Thanks for posting xx

Check ur vitamin d...?

Thank you so much for making these videos, it really does help underscore that many of us are going through the same problems and we really have no time table for when we will be able to stop thinking about our health all the time.

Do you have any prior health conditions before covid? I hope you get better.

SOrry to hear this, r u vaxxed? i'm not and i'm 6 1/2 months in.