Oh yeah, I know exactly what you're talking about. Life on earth is a constant journey of ups and downs, but long haul and any post viral malaise is like existing underground. On good days I feel like I have managed to pop my head up and can once again see the sunshine. Then, for some unknown reason, the ground beneath my feet gives way and I slip back into dark murky heaviness. Like you, I use whatever methods I possibly can: mental; emotional and spiritual as well as physical to keep going and think positively. To continue on with whatever may be my purpose in this world. Then there are the times that I feel like I'm buried just too far down to stand a chance. It all feels so hopeless and I find myself giving up. At these times, the only force I can find within myself is simply the desperation to escape from that deep dark miserable life. What choice do we have? Somehow we keep on trying. Wishing that you, and all who are in need will keep on healing to full health, strength and happiness x
Thank you for sharing your experience, I can completely resonate. It is such a struggle at times for the brain to adjust to the constant ups and downs of this healing journey and also release our expectations of what healing should look like. On the days when it all feels to much I am trying my best to allow these feelings to be felt and experienced, to give the body and mind the space and respect for whatever it is going through. It is not easy as my mind associates ease and increased energy with healing and it is far easier to feel good mentally and trust the process on these days. When symptoms resurface or relapses occur my mind beings to grapple and struggle and try to understand and put labels of bad or failure and blame on everything. I notice I feel much better once I take a step back and allow the fatigue or discomfort to be felt, when I release the expectation of how I believe my body should be feeling and also release the expectation of doing anything that day. Instead of saying and thinking “I feel awful” I have started saying and thinking “today my body is asking for deep rest.” Wishing you so much healing and full vibrant health and happiness.
I had long covid from covid in March 2020. I was super fit before that. Recovered tried to go back work on day 8, wham never felt so ill in my life. Long covid start. Lots of relaspes over the next 18mths. My world shrunk. I slowly built up my excercise starting with tiny walks around the house, then the garden. I always felt better outside in the fresh air. I made sure that i nevet pushed myself even if i felt well always rested afterwards any excercise. I take Vit D which helped. Ibuferon later on when i felt exhausted but not everyday so i didnt upset my tum. The big game changer was to accept my limitations, looked for something nice everyday, listen to bird song, a coffee sat in the sun, little treats. Was kind to myself. I watched nice utubes, chateau diaries seeing happy people having a good time was stangely helpful, i couldnt take part but i think hearing laughter helped. I am well now working as a gardener, riding a pony, walking the dogs havin fun. You will get there, be brave. Hugs from the UK.
Thank you for sharing your LC healing experience. I am so happy to hear you are doing so well. I have also found that respecting limitations and the bodies need to rest rest rest has been an important key to feeling better. Sending hugs 🤗
I can totally relate to these relapses, they are SO brutal! I almost feel that the longer time goes on the harder it is mentally to deal with. Things that help me are meditation, deep breathing, my acupressure matt, lavender oil, crying. I recently recorded a video for myself when I was feeling good, giving myself a pep talking that 'you will get through this, just like you did the last time'. The relapses during menstrual cycles are SO crazy too. I wish there was more knowledge in the medical world about it. Wishing you all the best x
Thank you for sharing the practices that help you to deal with relapses, these are some really great and inspiring suggestions. I really love the idea of recording an encouraging video for yourself. I wish you all the best with your continued healing.
I’ve never had Covid. But I do have Chronic Lyme disease, and research is beginning to show that we share many of the symptoms. I started my Lyme relapse in November 2020. Thank you for sharing your experience. I’m strengthened by it!
Thank you for sharing. Yes I have heard this as well and have just have started seeing someone who specialises in Lyme disease to try and help with LC.
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.
Yes!! You are the same as me!! March 2020 is when this all started. I have the flares and worsening flares with cycle. I was very healthy prior. None of the physicians understand or even acknowledge Long Covid. They look at you like it's a stress response.
Hi Olivia, Thanks for sharing that you are in the same boat. Yes, I completely relate. It has been so hard finding physicians that understand or even really listen. I used to get so disheartened and frustrated each time I spoke to my doctor or the long covid clinic.
@@njoyliving my last bad relapse was in February and around my cycle. However, once I'm in a flare, it takes weeks to come out of. I didn't have a muscle and joint flare this month ( happy). However, I caught a non-covid virus that caused laryngitis and chest congestion/post nasal drip. ( currently have). However, when I'm sick with a cold, my long haul muscle, neck pain, and joint pain disappeared 🙃. Not sure if I should be happy and sad, at the same time. On inhalers now since 2 years ago. My theory is that our overactive immune systems focus on the new virus and almost stop the long-haul haul symptoms( besides mt chest).
I'll let you know. Having a post covid asthma flare with lungs, however. :( Been in contact with doctor today) The albuterol makes me anxious and shaky). I'll come back and update to see of symptoms are back or stay away.
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. ❤️
Thank you for sharing, I know so many of us who are experiencing LC can relate to this. One of the hardest things is constantly having to asking for help. I have struggled so much with feeling like a burden on my loved ones. At times I often felt like I had used up all the support allocated to me in this lifetime. What really helped me was putting myself in their shoes, I knew that if our roles were reversed I would do all I could for my family if any of them needed me. My husband often reminds me when I feel guilty about yet again having to ask for help that he is not exhausted like I am and what feels so huge for me is usually easy for him. I always look to blame myself after a relapse. I got myself into a pretty big mess earlier this week simply by eating a little too much. It really is impossible to do everything perfectly all the time. I think part of recovery is testing our perimeters and it is inevitable that sometimes we push too far. At the moment I am focusing on being grateful that when I do trip up I am able to recover so much faster. I really hope that this relapse passes quickly and that you feel increased ease each and every day. Stay strong and rest lots!
Totally relate to all of this and great to find someone I can relate to as I don’t know anyone else with this… I have loads of releases and fear of them along with fear of getting covid again incase I go right back to the worst of my symptoms.. I find any form of stress makes it all worse but yoga meditation and lots of fresh air helps all things Ive never done before all of this. Certain foods flare things up especially palpitations/ arrhythmia’s
I'm seeing electronic vagus nerve stimulation being mentioned more and moRe .There isn't much We can do for ourselves but I think working on the vagus nerve is one of the best things we can do
For me, the third moderna shot got rid of the sinusitus and tinnitus. Magnesium taureate and beetroot for the high blood pressure, thiamine and potassium iodide for the arrthymia. Zinc, multi vitamins lots of rest helped me the most. Taking aspirin for the micro clotting was a quantum leap in the right direction too. Learn to breath with the diaphragm again. Listen to your body, rest accordingly. Good luck.
In regards to the impact on the 28 day cycle, it might be helpful to explore putting those cycles on hold so that you can help your body heal. I do feel mor unwell / triggered in a relapse… talk with doctor as there are ways to put the cycle on hold.
Thank you for sharing Leslie. Although this may be very useful for some I have thought about this for awhile but at the moment feel that my system is too sensitive. I am cautious to experimenting with different contraceptive methods that may aggravate my symptoms in the process of finding the right product for my body.
@@njoyliving it sounds like hormone fluctuation could be at play in your long covid experience! *IF* you feel up to it, I do suggest talking in-depth with a women's health doctor about a hormone therapy that could be right for you. I have had many chronic illnesses in my life and also dealt with endometriosis via a low-dose birth control. I know this is all hard and there are so many unknowns. Possibly explore the option of hormone/birth control therapy right now if you sense a cycle? That said, please do whatever you can to feel well.
Long Covid stopped my cycles for more than 1 year. Now they are back, but last for weeks, and that’s exhausting too. I wish it had stopped permanently.
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
I’m having long covid symptoms. Dry cough, sore chest and my glands were up at for months. I had covid pneumonia and I was in hospital for 9 days on oxygen and ill for a week before that and yes it’s up and down.
Hi Paula, Thank you for your message and sharing your experience. I am so sorry you are experiencing long covid too and have had such a rough time. The up’s and down’s are a roller coaster. I really hope you make a full recovery and begin to feel some relief and stability.
Hi Teddy, I am based in the UK and it was and still is a challenge to get ones hands on Ivrmct. I was able to try a couple of courses but only 1 year after covid infection. Although I experienced no adverse reaction it is impossible to say if it was beneficial. I believe it works best when taken immediately during active covid infection and as a prophylactic.
Im one year in and its still hard to get out of bed for more than an hour. I get really delirious and light headed. Feels like my brain is not getting enough oxygen, my doctors are useless.
Hi Chael I am so sorry to hear your having such a rough time of it at the moment. I can completely relate to what you have shared. I think 1 year in I was also at my worst. In my case my body was so depleted from being ill for so long that I felt weaker over time. I have not received any guidance from Doc’s this seems to be a common issue. I really hope that you feel some improvement and stability soon and are able to find treatments that help you in recovery. Rest and sleep are some of the most wonderful healers and honouring your bodies needs can’t be a bad thing.
@@maxim__prokhorov Im at about 65% of what I was precovid. I got covid a third time and that seemed to knock away some of my long covid symptoms. Time is the only cure everything else is snake oil.
Hi Michelle, Thanks for sharing your experience and I am sorry to hear it is currently so challenging. I can completely resonate with what you have said, it can sometimes feel like balance is a very narrow tightrope and even the smallest exertion can push you over the edge. I really hope you are able to find some more stability.
Thank you for sharing your experience. I am so sorry you are experiencing long covid too and have had such a rough time with heart palpitations. I really hope you make a full recovery and begin to feel some relief and stability.
I am sorry to hear you feel so isolated, I have learned the importance of a support system during recovery. If you haven’t already I recommend joining a couple of LC groups on Facebook. Sometimes it can simply help to know you are not alone in this experience.
Hi Njoyliving, I’m day 50 post infection. My symptoms crushing head throbbing, sinus throbbing, head fullness, head fog, fatigue, upper back pain, nausea, dizziness, eye pain, heat sensitivity water and air, night sweats, neuropathy, weight loss, anxiety and insomnia. How long have you been recovering? Have symptoms dropped off? Have symptoms died down? Do you feel you are getting better as time passes?
Hi Luke, I am sorry to hear you are experiencing these challenging symptoms. I went through many of the same symptoms you have listed especially during the 1st year of LC. It has been almost 2 years for me and there is definitely less severity in many symptoms especially within the last 2 months. Symptoms can still be triggered by stress as well as over exertion, but within 2 years I have learned so much about managing my energy and caring for my body which I believe is vital for healing. I wish you a full and speedy recovery and hope that you begin to feel some improvements soon.
Hey Luke, thanks for sharing your experiences and hoping you have a speedy recovery. I don't know if I have or have had Covid since I never tested for it but I have also been experiencing a fullness feeling around my face and head along with clicking sounds when trying to swallow and body aches since October 2020. My symptoms come and go but they always seem to come back around noon everyday until sometime during the night. Are you taking anything to help deal with that fullness feeling in your head? Is anyone else experiencing these symptoms as well?
@@chrisjoe145 yeah my symptoms are one and off all day long never a break. Many people are suffering the same thing. Try getting a naturopath and starting there. Regular family doctors will dismiss you and say your healthy.
@@lukesmith3283 Hi Luke 2+ years shortness of breath and lung burn, muscle and bone pain. Especially brain fog. I got infected again and all my symptoms are back to square one!! I'm disgusted.. How are you now? Any better
@@chrisjoe145 How are you now Chris! My symptoms after 2 years were getting better then I got reinfected and back to breathing issues. Lung burn you name it I got it all back. Exactly 2 years later this May.
Oh yeah, I know exactly what you're talking about. Life on earth is a constant journey of ups and downs, but long haul and any post viral malaise is like existing underground. On good days I feel like I have managed to pop my head up and can once again see the sunshine. Then, for some unknown reason, the ground beneath my feet gives way and I slip back into dark murky heaviness. Like you, I use whatever methods I possibly can: mental; emotional and spiritual as well as physical to keep going and think positively. To continue on with whatever may be my purpose in this world. Then there are the times that I feel like I'm buried just too far down to stand a chance. It all feels so hopeless and I find myself giving up. At these times, the only force I can find within myself is simply the desperation to escape from that deep dark miserable life. What choice do we have? Somehow we keep on trying.
Wishing that you, and all who are in need will keep on healing to full health, strength and happiness x
Thank you for sharing your experience, I can completely resonate.
It is such a struggle at times for the brain to adjust to the constant ups and downs of this healing journey and also release our expectations of what healing should look like.
On the days when it all feels to much I am trying my best to allow these feelings to be felt and experienced, to give the body and mind the space and respect for whatever it is going through.
It is not easy as my mind associates ease and increased energy with healing and it is far easier to feel good mentally and trust the process on these days. When symptoms resurface or relapses occur my mind beings to grapple and struggle and try to understand and put labels of bad or failure and blame on everything.
I notice I feel much better once I take a step back and allow the fatigue or discomfort to be felt, when I release the expectation of how I believe my body should be feeling and also release the expectation of doing anything that day. Instead of saying and thinking “I feel awful” I have started saying and thinking “today my body is asking for deep rest.”
Wishing you so much healing and full vibrant health and happiness.
How you feeling right now?
I had long covid from covid in March 2020. I was super fit before that. Recovered tried to go back work on day 8, wham never felt so ill in my life. Long covid start. Lots of relaspes over the next 18mths. My world shrunk. I slowly built up my excercise starting with tiny walks around the house, then the garden. I always felt better outside in the fresh air. I made sure that i nevet pushed myself even if i felt well always rested afterwards any excercise. I take Vit D which helped. Ibuferon later on when i felt exhausted but not everyday so i didnt upset my tum. The big game changer was to accept my limitations, looked for something nice everyday, listen to bird song, a coffee sat in the sun, little treats. Was kind to myself. I watched nice utubes, chateau diaries seeing happy people having a good time was stangely helpful, i couldnt take part but i think hearing laughter helped. I am well now working as a gardener, riding a pony, walking the dogs havin fun. You will get there, be brave. Hugs from the UK.
What a fabulous comfort you are Sharon. I know many will feel great encouragement from your experiences. So happy you are feeling well now.
Thank you for sharing your LC healing experience. I am so happy to hear you are doing so well. I have also found that respecting limitations and the bodies need to rest rest rest has been an important key to feeling better. Sending hugs 🤗
@@njoyliving thank you. Hope you make a full recovery soon.
@@kara2310 thank you. Hope you recover soon. It was very lonely experience going through it, i really feel for anyone who has it. You take care.
How you feeling right now?
I can totally relate to these relapses, they are SO brutal! I almost feel that the longer time goes on the harder it is mentally to deal with. Things that help me are meditation, deep breathing, my acupressure matt, lavender oil, crying. I recently recorded a video for myself when I was feeling good, giving myself a pep talking that 'you will get through this, just like you did the last time'. The relapses during menstrual cycles are SO crazy too. I wish there was more knowledge in the medical world about it. Wishing you all the best x
Thank you for sharing the practices that help you to deal with relapses, these are some really great and inspiring suggestions. I really love the idea of recording an encouraging video for yourself. I wish you all the best with your continued healing.
How you feeling right now?
I’ve never had Covid. But I do have Chronic Lyme disease, and research is beginning to show that we share many of the symptoms. I started my Lyme relapse in November 2020. Thank you for sharing your experience. I’m strengthened by it!
Thank you for sharing. Yes I have heard this as well and have just have started seeing someone who specialises in Lyme disease to try and help with LC.
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 totally understand why is this long Covid not more on the media I’m struggling every day we left behind
Yes!! You are the same as me!! March 2020 is when this all started. I have the flares and worsening flares with cycle. I was very healthy prior. None of the physicians understand or even acknowledge Long Covid. They look at you like it's a stress response.
Hi Olivia,
Thanks for sharing that you are in the same boat.
Yes, I completely relate. It has been so hard finding physicians that understand or even really listen. I used to get so disheartened and frustrated each time I spoke to my doctor or the long covid clinic.
@@njoyliving my last bad relapse was in February and around my cycle. However, once I'm in a flare, it takes weeks to come out of. I didn't have a muscle and joint flare this month ( happy). However, I caught a non-covid virus that caused laryngitis and chest congestion/post nasal drip. ( currently have). However, when I'm sick with a cold, my long haul muscle, neck pain, and joint pain disappeared 🙃. Not sure if I should be happy and sad, at the same time. On inhalers now since 2 years ago. My theory is that our overactive immune systems focus on the new virus and almost stop the long-haul haul symptoms( besides mt chest).
@@oliviaelliott4623 That is interesting! I wonder what will happen once you get over the virus. Really hope that you feel better🙏
I'll let you know. Having a post covid asthma flare with lungs, however. :( Been in contact with doctor today) The albuterol makes me anxious and shaky). I'll come back and update to see of symptoms are back or stay away.
@@oliviaelliott4623 I am sorry to hear you are experiencing an asthma flare, I hope you find something that helps. Yes do let me know🙏
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. ❤️
Thank you for sharing, I know so many of us who are experiencing LC can relate to this.
One of the hardest things is constantly having to asking for help. I have struggled so much with feeling like a burden on my loved ones. At times I often felt like I had used up all the support allocated to me in this lifetime.
What really helped me was putting myself in their shoes, I knew that if our roles were reversed I would do all I could for my family if any of them needed me. My husband often reminds me when I feel guilty about yet again having to ask for help that he is not exhausted like I am and what feels so huge for me is usually easy for him.
I always look to blame myself after a relapse. I got myself into a pretty big mess earlier this week simply by eating a little too much. It really is impossible to do everything perfectly all the time. I think part of recovery is testing our perimeters and it is inevitable that sometimes we push too far. At the moment I am focusing on being grateful that when I do trip up I am able to recover so much faster.
I really hope that this relapse passes quickly and that you feel increased ease each and every day. Stay strong and rest lots!
How you feeling right now?
Totally relate to all of this and great to find someone I can relate to as I don’t know anyone else with this… I have loads of releases and fear of them along with fear of getting covid again incase I go right back to the worst of my symptoms.. I find any form of stress makes it all worse but yoga meditation and lots of fresh air helps all things Ive never done before all of this. Certain foods flare things up especially palpitations/ arrhythmia’s
Thank you for sharing! Meditation and fresh air help me too 🙂
I'm seeing electronic vagus nerve stimulation being mentioned more and moRe .There isn't much We can do for ourselves but I think working on the vagus nerve is one of the best things we can do
For me, the third moderna shot got rid of the sinusitus and tinnitus. Magnesium taureate and beetroot for the high blood pressure, thiamine and potassium iodide for the arrthymia. Zinc, multi vitamins lots of rest helped me the most. Taking aspirin for the micro clotting was a quantum leap in the right direction too. Learn to breath with the diaphragm again. Listen to your body, rest accordingly. Good luck.
How you feeling right now? Better?
@@maxim__prokhorov Yes. Off the beta blockers now, reduced the iodine intake and have lost weight.
@@TrustMeiamaD.R. glad to hear that!
In regards to the impact on the 28 day cycle, it might be helpful to explore putting those cycles on hold so that you can help your body heal. I do feel mor unwell / triggered in a relapse… talk with doctor as there are ways to put the cycle on hold.
Thank you for sharing Leslie. Although this may be very useful for some I have thought about this for awhile but at the moment feel that my system is too sensitive. I am cautious to experimenting with different contraceptive methods that may aggravate my symptoms in the process of finding the right product for my body.
@@njoyliving it sounds like hormone fluctuation could be at play in your long covid experience! *IF* you feel up to it, I do suggest talking in-depth with a women's health doctor about a hormone therapy that could be right for you. I have had many chronic illnesses in my life and also dealt with endometriosis via a low-dose birth control. I know this is all hard and there are so many unknowns. Possibly explore the option of hormone/birth control therapy right now if you sense a cycle? That said, please do whatever you can to feel well.
Long Covid stopped my cycles for more than 1 year. Now they are back, but last for weeks, and that’s exhausting too. I wish it had stopped permanently.
@@CourtneySchwartz That sounds absolutely exhausting to go through each cycle. I really hope that this improves quickly for you.
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
How you feeling right now?
I’m having long covid symptoms. Dry cough, sore chest and my glands were up at for months. I had covid pneumonia and I was in hospital for 9 days on oxygen and ill for a week before that and yes it’s up and down.
Hi Paula, Thank you for your message and sharing your experience. I am so sorry you are experiencing long covid too and have had such a rough time. The up’s and down’s are a roller coaster.
I really hope you make a full recovery and begin to feel some relief and stability.
@@njoyliving thank you. You too x
How you feeling right now? Better?
I'm on birth control that blocks periods, I couldn't imagine dealing with that plus long COVID
Me too. It keeps dysautonomia symptoms under control. It's been a life saver. Its just continuous use, under the doctor's recommendation.
Have you tried the medicine that starts with an I and a V and an E and and R? Curious what your experiences with it are if you have.
Hi Teddy, I am based in the UK and it was and still is a challenge to get ones hands on Ivrmct. I was able to try a couple of courses but only 1 year after covid infection. Although I experienced no adverse reaction it is impossible to say if it was beneficial. I believe it works best when taken immediately during active covid infection and as a prophylactic.
Yeah period relapses. Grr
Im one year in and its still hard to get out of bed for more than an hour. I get really delirious and light headed. Feels like my brain is not getting enough oxygen, my doctors are useless.
Hi Chael
I am so sorry to hear your having such a rough time of it at the moment. I can completely relate to what you have shared. I think 1 year in I was also at my worst. In my case my body was so depleted from being ill for so long that I felt weaker over time. I have not received any guidance from Doc’s this seems to be a common issue.
I really hope that you feel some improvement and stability soon and are able to find treatments that help you in recovery. Rest and sleep are some of the most wonderful healers and honouring your bodies needs can’t be a bad thing.
It's a little unfair to have a crack at Doctors when there is no known cure that they can prescribe. Anyway good luck to us all, fingers crossed.
How you feeling right now?
@@maxim__prokhorov Im at about 65% of what I was precovid. I got covid a third time and that seemed to knock away some of my long covid symptoms. Time is the only cure everything else is snake oil.
@@chuteboxegod try take vitamins C D B Zinc and for brain. Glad you improving
I have a lot of bad symptoms
I'll feel like I'm getting better start walking on my treadmill then I'll feel like crap where everything hurts
Hi Michelle, Thanks for sharing your experience and I am sorry to hear it is currently so challenging. I can completely resonate with what you have said, it can sometimes feel like balance is a very narrow tightrope and even the smallest exertion can push you over the edge. I really hope you are able to find some more stability.
How you feeling right now?
@@maxim__prokhorov mostly better. The bad days happen a lot less often
@@mtrocine glad to hear that you improving!
Please pray the healing prayer to our Heavenly Father by Padre PIO, the divine power of God, our Creator, God bless you
Wouldn't it be great if that actually worked....
long covid for 2 months...The hardest symptom is my heart palpitations ..for the past month i get it when i relax and my heart rate go down to 69 ...
Thank you for sharing your experience. I am so sorry you are experiencing long covid too and have had such a rough time with heart palpitations.
I really hope you make a full recovery and begin to feel some relief and stability.
@@njoyliving also anxiety... panic attakcs...chest pain...ibs
How you feeling right now?
Wish I have someone to talk to
I am sorry to hear you feel so isolated, I have learned the importance of a support system during recovery. If you haven’t already I recommend joining a couple of LC groups on Facebook. Sometimes it can simply help to know you are not alone in this experience.
Hugs😢
How you feeling right now? Better than it started?
Hi Njoyliving, I’m day 50 post infection. My symptoms crushing head throbbing, sinus throbbing, head fullness, head fog, fatigue, upper back pain, nausea, dizziness, eye pain, heat sensitivity water and air, night sweats, neuropathy, weight loss, anxiety and insomnia.
How long have you been recovering? Have symptoms dropped off? Have symptoms died down? Do you feel you are getting better as time passes?
Hi Luke,
I am sorry to hear you are experiencing these challenging symptoms. I went through many of the same symptoms you have listed especially during the 1st year of LC. It has been almost 2 years for me and there is definitely less severity in many symptoms especially within the last 2 months. Symptoms can still be triggered by stress as well as over exertion, but within 2 years I have learned so much about managing my energy and caring for my body which I believe is vital for healing.
I wish you a full and speedy recovery and hope that you begin to feel some improvements soon.
Hey Luke, thanks for sharing your experiences and hoping you have a speedy recovery. I don't know if I have or have had Covid since I never tested for it but I have also been experiencing a fullness feeling around my face and head along with clicking sounds when trying to swallow and body aches since October 2020. My symptoms come and go but they always seem to come back around noon everyday until sometime during the night. Are you taking anything to help deal with that fullness feeling in your head? Is anyone else experiencing these symptoms as well?
@@chrisjoe145 yeah my symptoms are one and off all day long never a break. Many people are suffering the same thing. Try getting a naturopath and starting there. Regular family doctors will dismiss you and say your healthy.
@@lukesmith3283 Hi Luke 2+ years shortness of breath and lung burn, muscle and bone pain. Especially brain fog. I got infected again and all my symptoms are back to square one!! I'm disgusted.. How are you now? Any better
@@chrisjoe145 How are you now Chris! My symptoms after 2 years were getting better then I got reinfected and back to breathing issues. Lung burn you name it I got it all back. Exactly 2 years later this May.
With your giggles,, I don't believe you..