"Post-acute COVID-19 Syndrome": COVID "long-haulers" suffering symptoms months after initial diag…
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- čas přidán 1. 06. 2024
- Doctors are still searching for answers to why a portion of people who were diagnosed with COVID-19 are still suffering symptoms months later. Anderson Cooper reports. cbsn.ws/2Vi2oFy
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Most doctors, when they don't understand something, say "it's just in your head". Instead of admitting that they don't know, they inflict additional pain on sick people.
Yes, and waaaayy too often!
I know how meaningful it is to be told that they don't know, but willing to listen and listen and listen and document and document and research and research and research and listen. Too infrequent. There is so very much to our bodies and medical staff can't know it all, but to acknowledge someone can be comforting. What was described here is just some of the things that Fibromyalgia throws at you. You can look fine when you're not fine. My heart goes out to everyone everywhere.
@Macca McDonald Doctors have had about a year to learn about CoViD-19, but most haven't even started doing research, and simply talk trash to their patents.
It's hard for ignorant people to do a diagnosis.
Always take responsibility for your own care and keep pushing for answers move on to another doctor if you get BS answers from the first second or third doctor these guys are not infallible and often overworked and just in it for the money and really have no interest in patient care this is the reality of the American Health system.
@@rainmon
Not just in the USA. Over a period of 4 years I consulted 17 doctors in 3 European countries before an illness was correctly diagnosed. 12 doctors told me to "think positive", 4 said they didn't know. The last doctor I saw had had the illness himself and could diagnose it. I was unable to work for almost two years, got bankrupted and was left with permanent physiologial damage.
It makes me so angry that the doctors in the emergency room told that woman her symptoms were caused by anxiety. So typical, and so infuriating.
I'm currently realizing this is happening to me. My doctor has been telling me everything is from my anxiety
That happened to me too unfortunately and I suffered for 3 months
I was told the same. They still have no answers for me
I got told anxiety too, it sucks
@Anonymous ty, I'll look into it
I totally relate to this story. I’ve been dealing with “Long COVID” for about 9 months now. It caused Fibromyalgia and I hurt all day every day. Life is totally different now. I can’t do the things I used to enjoy and it’s very very upsetting and frustrating. I’m 40 and most days I feel like I’m 80. On top of it all I think the worst is the short term memory loss issue. It’s been getting worse. I sometimes forget what I’m saying as I’m talking. And yes the only ones that seem to understand are those of us dealing with it ourselves
Wow, I glad I stumbled onto this 60 minutes video and all these responses. I had covid a year ago now. I was in the hospital for almost 5 weeks. I was intubated for 7 days of that 5 weeks in the hospital. The nurses were telling me I was going to die. I didn't thanks to many, many prayers. Jesus heard those prayers and brought me through. But....I'm having long term affects, aside from the "normal" things like memory loss, and forgetting words, I have developed high cholesterol and I'm pre diabetic. I'm now on thyroid meds for hypothyroidism. I had none of these problems before I got sick. Prayers to all of you that are suffering post covid. Hang in there!
I have all kinds of new problems. Sjogren's, hair thinning, tired,fibromyalgia. All kinds of health issues!!!
Did you get covid after being vaccinated?
Did you get covid after being vaccinated?
Did you get covid after being vaccinated?
This is heartbreaking...I hope for healing for everyone effected by this illness. Thank you to our doctors and nurses for their care. I believe everyone is just trying their best.
"COVID" is communism hiding behind a fake medical issue. All this for a virus with a 99.5% or greater survival rate. A virus so bad that most people have to be tested to find out if they have it! You’re right it’s about control, and also a big distraction over all of the other BS going on.
Annoys me when medical professionals claim that something is psychological when they can't explain the problem yet.
That’s because they’re lazy
They just need something to write down in your medical file so they go with that
So true
They did that to me before my diagnosis of Fibromyalgia. That only causes more depression and anxiety.
@@ceedee410godschild2 my mom has fibromyalgia and I’ve watched her suffer for years. I cried to her last night because I finally felt how it feels to have an invisible chronic condition. It feels like the doctors don’t take you seriously and it’s so frustrating!
Welcome to the journey of a chronic illness sufferer trying to get help from a medical community who thinks it is all in your head.
And people be like “but 99% of people survive!!!” Would you want to survive with this? Death isn’t the only bad outcome of this virus
It's not. Suggestion: Read The Deepest Well - by Dr Nadine Burke Harris - about the impact of childhood trauma on later life health/well-being.
The doctors are no longer debunking this
@@ew2755 if we did that we would all be 6 feet under
@@ew2755 you just made your beloved religion a cult
This has been my experience with Chronic Fatigue Syndrome. My long haul was triggered by a mono virus 25 years ago. I have coped with these symptoms and the feeling that society has ignored patients with mystery illness. Very depressing experience on earth.
Same here. My fatigue supposedly adrenal related. Even all replacement hormones I don’t have a normal day. I should be in the military. I went from being able to hike 12 miles with 80 pounds on my back to basically not being able to walk to the front of my lane then the Covid came over along. I got over it, but it left me with information of my lungs, and either a bronchitis or a COPD type condition oh Lord every day, I pray that this will leave my body and I will at least be able to live a normal life. I’m in my sixes now time is getting short.
I feel as if I’m dying a slow death. There is something very very wrong with me. I’m fairly certain I had Covid at the beginning of the pandemic when testing wasn’t available. I was evaluated at urgent care and told that I “have a virus”. Since that visit, I’ve developed an autoimmune disease, elevated platelets, vertigo, hypertension, extreme fatigue, severe depression and more. Before this, I was an active, happy person. I’m currently able to work one to two days a week but can’t function for days afterwards. My quality of life is poor. I’m in the absolute worst physical and mental shape of my life. I’m not a complainer so I try my best to function without complaining. I just desperately want to feel better
The same. Wish you all the best. Greetings. 🙋♀️ 🌍
Same. I’m so sorry
The first two women described my daily symptoms, but l’m a 73 year old stroke victim with a heart condition. The virus aged them.
That’s exactly it. I’ve never seen it stated so well.
Well said Vivian.
This sounds exactly right
Thank you, Vivian for sharing your story. It really makes sense
I'm 55 years old, and I know I look older than my age. I have days where I feel good and days where I have no energy at at. So far I have survived 5 strokes this year and they weren't little mild strokes. My doctor said that I am extremely lucky to be alive.🙏.
This is what living with chronic pain and an autoimmune disease is like...24/7.
Yes! I have autoimmune issues that have similar symptoms. I've been able to be of support to a friend that has survived Covid-19, because I can relate to her symptoms.
They keep talking about how they have never seen this before but these seem like symptoms of a chronic illness.
@@abbyehrenstein2550 yes but as a long hauler myself, nothing shows up on the test.
@ 👍
I already had auto immune disease before I got covid this is worse I'm devastated
OMG....I AM GOING THROUGH ALL THIS THESE DAYS....😭😭😭😭I AM NOT ALONE ..
I've had M.E. for over 35 years. Welcome to my world, longhaulers. And good luck getting medical care.
Hey, Attention;
60 minute, Deaf community and Hard of people need closed caption/ subtitles please.
My parents are deaf, if you are on mobile, press the 3 dots on the corner of the screen, click CC, english. You can do this on PC too.
@@xmidgewon736 I just tested this and the captions option within the three dot menu is not clickable.
edit: im on mobile
@@xmidgewon736 There are no captions available for this video.
@@xmidgewon736 6tyu
M 23 will cool I'm joining him I'm thinking io pop
In the bio, third line down gives link to transcript cbsn.ws/2Vi2oFy
Folks with chronic illness live this way. Life can turn on a dime, I know from personal experience.
@Lexi Cat
These ladies are living the typical Multiple Sclerosis "lifestyle". I'm dealing with same symptoms for three years now.
You're so right. I experienced the same thing. From pro sports coach to bedridden in the blink of an eye.
Best wishes to you ❤
I was left like this with Bacterial Pneumonia, you just don't seem to get past it.
I have psoriasis, psoriatic arthritis, and asthma. I was diagnosed with covid19 last July. I have some of the same symptoms they have like memory loss and light-headedness but I also haven't gotten back my full sense of smell and taste.
@@rumblefish9 Hope you get through it.
My brother has a lot of these symptoms and never had Covid, but has had 3 shots. The symptoms began immediately after the second shot!
i think the vaccinations might be to blame in much of this.
I was curious how many of the long haulers have had the jab?
I never had covid, but my 1st vaccine did a number on both my kidneys. Extreme tenderness for months. It's been 18 months now and my left kidney still is sore.
My immune response to the shot was just too much.
Ah, there it is.
Sorry, there is absolutely NO evidence TV at these vaccination
I just got over Covid and pneumonia and I am exhausted. I force myself to get out of bed, but I can only stay up for a short time. I went to the grocery store and couldn't even go through the whole store. I got so tired that I had to set down several times. Then I didn't want to carry the 4 bags in. I am sad and glad that I watched this. It's just comforting to know that I am not alone.
R.I.P Doctor
Condolences to the family and friends of Dr. Mary Fowkes. What a loss, especially of one doing critical work during this pandemic. Rest in peace, Dr. Fowkes.
@TIME TRAVELLER < Joined November 24th, 2020
@TIME TRAVELLER Hey loser, I see ya ‘joined’ 17 hours ago, what’s the chances you’re one of them tRumpet desperate losers, pathetic..
😒🍊☠️
Hmm, only thing ‘fake’ here is YOU..
It's so shocking.. it feels like she must have died from Covid after effects.
@TIME TRAVELLER STFU you goon.
@TIME TRAVELLER You're a coward.
This is what those of us who have chronic illnesses feel like. I wouldn't wish this on anyone. I hope these people can recover, without any real meaningful diagnosis I doubt I ever will.
Used to have a throat condition which would make swallowing and breathing painful.
Every second of my day was horrible and I'm 25.
I somehow no longer suffer from that condition but I am now extremely grateful for my health.
God bless you.
Everything in this video seems almost word for word like just daily life for me/us. (chronic illness largely effecting lungs).
I feel really sorry for anyone who needs to live like this, especially after being used to an active lifestyle.
I don't understand why it's so hard for people to care about others health.
Agree. The symptoms they describe sound like what people who suffer with chronic autoimmune disorders also feel.
Absolutely agree. Chronic illnesses, a disability now... &.... impact/trauma coming out of a super confusing, scary, toxic, abusive relationship. Phew, add in what's going on now.... never knew this burden & alone, could be SO heavy. Things I shouldn't & cannot do.... what choice do I have? Livng every day, atm..... just trying to get through, find a way to make sure my son eats, renting a room in hiding that he has to share w/ his mom (poor kid, he's been through enough) for now, trying to save what I can on disability alone. W/ a toxic ex who pays nothing, after SO many yrs of me doing evvvvverything... Realizing taking care of myself has to happen, yet.... neat trick, ya know? All, while .... for so much of it, family, friends.. those who are left anyway, simply don't get it OR, shockingly... even have compassion empathy for anyone BUT themselves. I'll never understand what's happened to people. Not what I imagined life... or this age... or my son's.... phew, anyway. (HUGS) of strength & wellness, at least some good days & smiles... hopefully, coming your direction! :) Stay safe & be well.
Exactly!
Having chronic fatigue and fibromyalgia suffering chronic pain for 30 years was challenging enough until I got Covid, and I hit a new low. It’s no joke, it messes with your entire system. I feel bad for people who were healthy, at least I was used to feeling crappy all the time. At least now, doctors are going to take these conditions seriously, chronic pain patients have been ignored for years.
Hello mate, I feel you and wish you keep strong and clear mind while you fight all those problems. I went throu life or death covid where I was put in artificial sleep.It has been tough one year and I have survived, but It took a lot of discipline to get back on track.I stil lhave mild neuropatia in my thighs but the rest is fine.I wish all the best to you everyone.God bless you all.
Agat
the one place that listened to me was Mayo clinic with chronic pain. They have a 4 week long program where you go through it with other people in chronic pain conditions. You get validated, taken care of, and taught how to deal with the pain symptoms in ways that arent "take a pill". They have the most research done on pain in the world and address it in some really diverse ways. See if you can get yourself into the program, it seriously changed my outlook on life. I am not "cured" but damn I am a lot better than rock bottom now.
Yeah I have fibrmyalgia and small fiber Neuropacy. Every since I had covid it's all I can do to get up everyday. And I Developed Sweating nonstop between that and being cold. It's really exhausting. Idk if they will ever figure it out.
D3/k2
Zinc
Magnesium
Vit b complex
My condolences to the family of Dr Fowkes. Omg how shocking and what a seemingly sweet woman on a mission to research and help ppl find relief. Prayers for all suffering and that you make full recoveries
This is just one of many reasons why mortality rate alone is not sufficient to describe COVID's risk.
This is one of the most frustrating things for me when dealing/arguing with the morons that downplay the seriousness of the virus. Even if you are completely incapable of showing compassion for those who are suffering just think of the long-term economic impact this could have on society.
@ltlblugrl I agree, but what will the protracted economic cost be over the next 30-40 years if 1 out of 20 working-age tax payers are A. not capable of holding down employment due to debilitating chronic issues and/or B. a burden on the health sector financially?
Or an excuse to keep the lockdowns going. Because in the beginning it was deaths, now it is cases.
@@RMokros Yep right. Governments across the world are involved in a big conspiracy to decimate their economies for.... what exactly?
@@timothyjennings9520 The politicians still have jobs. The WHO said end lockdowns and Gavin Newsome and Cuomo continue the lockdown.
This brings me comfort knowing that I’m not the only one.
I hope this is only temporary and wish everyone a complete recovery🙏🏼
I was diagnosed with Chronic Fatigue Syndrome in 1987 when I was 26 years old. So many doctors put me in the too hard basket. I am now 60 and it still affects me in so many ways. It is also a post viral syndrome. I would suggest the medical profession expand their views on how to understand, diagnose and treat post viral syndromes.
Still waiting for treatment that works after 34 years.
I haven't been the same after covid19.. I can't even climb the stairs without feeling extremely tired.. I have extreme fatigue which makes it hard to work.. I work outside the heat and is killing me😥
@@Tonatiuh27 do you have chest tightness when climbing stairs?
@@ThePrashanth66 yes. I have chest tightness when i climb stairs.. It feels like I'm going to die.. Shortness of breath and head ache..
Try Naturopath remedies. NAC/N-Acetyl L-Cystein is great for detoxing the lungs, liver and kidneys. Drink lots of ginger tea, honey and lemon. Get to a Naturopath doctor for real medicine.
Lord have mercy. ❤️ 🙏🏻 It's been almost 2 weeks since I first got this illness. It's worse than anything I've had in my life. I'm comforted knowing I'm not alone in this fight to get better. I'm praying for all those who have Covid and the long haulers. Wish you a speedy recovery and great health! ❤️
Most serious cases of flu will last for weeks.
Did you have the vaccine prior?
How are you doing, now?
@@johnpglackin345 I am on my fourth month
@@orange222... and it looks like the flu last more than week. Almost every year my cough would last for months but I did not feel sick.
I had Covid almost a year ago. I’m still dealing with the after effects. It gave me high blood pressure , rapid heart rate , exhaustion, and the worst headaches that anyone can imagine.my prayers are with each and everyone of you who are dealing with the after effects .❤
We’re u vaccinated?
My sister who has long covid found taking glutathione helped reduce her symptoms.
Hang in there, your not alone
@@sylviaking8866 what dose?
@@angelasmith257 Start with 250 mg am then go up slowly to 500 mg am and 500 mg pm.
My son is 20 and is describing the same symptoms. And everyone thinks he’s making it up
I know the feeling.
I’m 20 and experiencing a lot lol this is scary
Yeah,,uh...it's flu season..get over it, happens every year!!!
Look up Postural Orthostatic Tachycardia syndrome.
I fear I'm going through the same thing! I realize one thing though I feel better when I don't think about it
The Black woman in the blue seems so sweet it broke my heart to hear the doctors weren’t taking her seriously when she’s not making it up she’s having real health issues she deserves better care
Her and the MD saying that when she goes home she will curl up with a splitting headache...so sad. People are at their breaking points.
black women are not taken seriously VERY often in the healthcare system.
@@katelynknopp8397 Actually it’s just women in general...
@@shelly7269 black women are MUCH more likely to die during childbirth and major surgery, so not really.
@@shelly7269 Black women especially. Don't minimise the effect of racism. Black people are underprescribed pain medication compared to white people for the same conditions. Thats statiscally proven.
RIP Dr. Mary, thank you for your work.
Sounds just like an autoimmune disease! I've been living with chronic illnesses for almost 25yrs. So after having Covid twice, the after effects are just like what I have already been accustomed to. I feel so much empathy because I know how they feel!
I was one of the early infected ones when it comes to COVID-19. I had it in December 2019 (NYC). I was sick for the entire month of DECEMBER and a couple of weeks in January 2020. It’s now January 2021... and I’m having chest pain, insomnia, heart palpitations, weakness, heavy limbs, heartburn.... difficulty breathing. My doctor also said that I was depressed and anxious. 🙄. NO...I AM NOT DEPRESSED....IM SICK OF FEELING SICK.
Bibi I'm going through that now post covid-19. It sucks it seems like the medical field doesn't have enough data and don't have the answer we need.
I had it in January 2020 and I’m only starting to come back to myself mentally now
@@jajajajajaja867 base on my research the past year is that people are starting to feel like themselves at the 15-18 month range. i just hit my anniversary with long covid. i'm about 80%. The fatigue is debilitating. I havent worked in 10 months
I have this and nobody believes me
Yes this sounds like my problem
This is actually what needs to be covered
True. There are more long haulers than deaths.
Stop ignoring ME/CFS! For over 30 years same symptoms after EBV infection, yet no help or understanding or acknowledgment.
I’m a 62 years old woman, got COVID in July, I’m still struggling with fatigue, balance, dizziness, brain fog, double vision loss of smell, and appetite, and more anxiety all that stays with you. I went back to work and while there I tried not to dwell into my symptoms and get going with my life, good luck to all of you and a little advice is drink plenty of water 💦 but lots of it and with the balance walk around home without 👠
You have "vaccine" damage
Yeah or water is probably tainted also.i had omicron 18 months ago it messed me up good,especially my vision
@@johnnyv673 Let me ask you one thing. Are you stupid, delusional, or just dumb?
It’s vaxx damage.
I have the same thing than you. I really have problems with my balance and it’s really difficult for me to walk a straight line. I tend to lean on one side. How do you deal with the balance and the dizziness?
This long hauler thing exactly describes what autoimmune disease feels like for me everyday for last 15 yrs. I'm so sorry to hear about Dr Folks.
It's worse
Yep
Watch "Dr. Chris Knobbe - 'Diseases of Civilization: Are Seed Oil Excesses the Unifying Mechanism?'" on CZcams
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Yes exactly I have ankylosing spondylitis
@@kimberlyk2530 I have R.A Sjogren's and Fibro. As I listened to their stories on how they were feeling it was exactly how I felt in the beginning and everyday since
These ladies are telling my story 😢 Us long haulers!! God help us all 🙏🏾
It is same with me
Me too
I am going through it now. Have you recovered from it?
how are you now?
2 years in. It still feels like a 40% energy level. I haven't checked myocarditis since diagnosis. Rash still hits every few days.
People don't understand if they have never had it. I don't want sympathy, I just want understanding that I'm not what I once was. I want patience from those who are use to getting more from me. I WANT TO FEEL BETTER. I WANT MY LIFE BACK!
👍
You’re not alone!
@@HaveaVH5150 I'm sorry to hear your going through it as well, how long has it been for you? Did you get covid shot? My Dr. diagnosed me 6 months ago and said to expect it to last 8-9 months but how would he know? I hope he's right though!
@@tina5670 I understand because it changes your whole surroundings. My personality/life has taken a 180. Friends are giving me a hard time but family is great. I just found out 3 weeks ago about this. Segment on CBS Sunday Morning 7/17/22. To be short,got Covid last year and a lot of symptoms lasted but gradually wasn’t as strong . 8 months straight this year with a permanent headache among all the other symptoms that are crushing me.It started when I got the booster,hyperdrive Covid. Didn’t know there were others out there. Wishing you and all the others a light at the end of the tunnel. 🙏 🤘🏻
@@HaveaVH5150
That's sad. What a big lost for her family and so many people she was helping in her work. RIP
OMG! I feel like crying right now. My breathing hasn’t been the same since COVID. I’m constantly winded, even from simple task. I’m tired every second of the day. I thought I was going insane. I’m praying for everyone suffering from Covid and the aftermath of it
Yes, very scary when you can't take a deep breath...Hugs😢
I’m the same , can’t breathe,I don’t think I be normal again
You are now alone..... There are thousands of us and I am making it my business to speak out because where I live in Daytona Beach the medical professionals don't know anything about it which is sad because I see it all over the news how can they not know?
But I have found help with the long haulers support groups on Facebook so if you have that join one of the groups please and if you have a way to message me back I can try to give you any information that I have acquired over the past few months because I felt the same way I was in bed and I was thinking my God what is going on I have no energy I can't even roll over without feeling like I'm running 10 mi LOL it's insane and other people don't understand and we are not being heard and I am not sure why but we need a lot of assistance now many of us like myself are in a pickle because I am used to working several jobs and being self-supporting and I'm not able to now and I'm terrified about losing everything off work so hard for so please hang in there there are others just like you and hopefully you can get some support and get the medical care you need
Amen. You are not alone.
I feel the same way
Im 24 years old, i got covid 3 months ago . Its hard to not be emotional but im literally crying typing this. Ive always been active, healthy . Now, not only is it emotionally draining , but i throw up every day since , i haven’t been able to smell or taste the same , I recently rushed the emergency, my mri my blood work , everything came back fine . They asked if i was stressed. I was convinced i was until i watched this🥺 i feel so sick, now I know everything I’ve been saying has been right! Im not crazy🥺 i am sick 😔
I am 28 in the same boat it a struggle but for your smell try smelling essential oils but dont over do it I hope it helps❤
@@mrmojorisin6951 hang in there, praying for you!
@@marinaperez2714 Thank you. Praise God for other believers. Prayer works. His blessings to you also. Peace 🙏
My family had Covid about a month ago. Husband and I had severe cases with him spending 8 days in hospital. For those with long term struggles, try treating for parasites. There may be some natural parasite cleanses on the market? Also take vitamins NAC, D, C, zinc, perhaps a probiotic. Spend time sitting in the sun. Do deep breathing exercises to strengthen your lungs. Physical therapy may help with proper diaphragm exercises. Jesus Christ is the ultimate healer. Come to Him in prayer and repentance.
I hope your fully recovered now !!!
I am 75 and have been having all of these symptoms for the past 6 months after a mild bout of covid. It is the worst thing I have been through, and I have been through a lot in my 75 years. Very hard to deal with. Horrible experience.
I'm an American living in Malaysia. I just recently (2 months ago) had Covid and the symptoms described in this video are what I am experiencing now. I was feeling numb hands, dizziness so I feel faint, swollen sore knees (so I can't squat to use our squat toilet or kneel for praying). I also felt tired and weak. So, I started intermittent fasting, taking B vitamins, cut down on sugar, and started eating salads for supper with live active-cultured yogurt to improve gut health. This caused me to drop some weight and I started doing 15 min calisthenic workouts. I take it easy and do what I can on workouts and walk 20-30 min every day. I've gotten stronger and the hand numbness is gone. Still, I do feel like my heart rate is abnormally high and my head sometimes feels as if I have mini strokes or imbalance. . Hard to explain...it's like something is crawling inside my skull. It's why I do low impact workouts. I'm 60 and my parents & grandparents lived long lives 90s or above 100. As a stock broker I anticipated living into my 90s so I focused on saving money to last. Now I think I won't live so long with this feeling of mini strokes so I think I should spend my retirement savings. I know we never know when we will die but these long haul symptoms make the possibility of death, sooner than later, feel real. So sad that the doctor passed away. 🙏
It's just amazes me how people take care to read the food labels to find out what in the food they put in their mouth but never bother to find out what in d jab they let people out inside their body. Pfizer is a company that been slapped with the highest criminal fine around the world... and people happily line up for their products ... loving it
Much the same here . I caught it about 8 months ago . I took a lot of elderberry zinc vitamin c combo , Some Silver bathed in Pink salt for fever . After about 6 days I started feeling better . No jab here. Never will
My husband bikes up to 20 miles 3-4 times a day.. He just contracted the virus and he didn’t show any symptoms but today he mentioned congestion.. Please keep us in your prayers.
Tanisha Brown: How is your husband doing? I caught this virus back in February of 2020…..and believe me…it is no joke. Heart palpitations, fatigue, heavy breathing, loss of smell and taste, joint pain and inflammation. The virus is no joke…..
@@dman221 How are you doing these days?
@@robg8033 : I am doing okay….I have my moments of flare ups.
@@dman221 Oh really , wow even after all this time.
Did any of you get Vaccinated afterwards? I heard some of the long hauler symptoms possibly go away after Vaccination.
I had it in March, haven’t been the same since, I honestly thought I was crazy until I saw this video
We’re in the same boat. I had it in March as well. I have these headaches that are debilitating. I go next week for MRI and MRA finally. I’ve never had headache issues before the virus.
Me too!!! I don’t feel as weird/crazy/alone
Ian, I've been there and I know exactly how you feel. For some reason It was worse during night time, after I had dinner. It took me about 4-5 months to fully recover. My advice to anyone going through this is to rest as much as you can. Take small steps, literally, don't work yourself out too much. Combine that with a good diet, meaning no salt or sugar, consume food that's good for your heart and lungs. Avoid eating seafood and pork. Also I found it supper helpful taking supplements and vitamins such as Omega 3, probiotics, vitamins C and D. Don't underestimate the power of your mind, stay positive and trust you'll get better. If you can, take short walks under the sun, doing breathing exercises, I did this every day from 10-15 minutes and I'm happy to report I'm back to 100%. Good luck and take care of yourself.
OMG! I'm having the same issues! I thought I was the only one!
@@leodelrio3458 thanks man, actually a lot of help, and my symptoms also come around nighttime
I got covid nov 2020, I have cognitive issues, I have fatigue high anxiety, headaches daily, I sleep all day sometimes or take naps, I look at instructions and can't figure them out. I have memory issues. Muscle aches heavy limbs this list goes on. This has ruined my life. The care providers look at me like I am crazy and say get counseling. One of my last dr visist she looked at me and said" you're still having these issues?" Omg! Really! They don't want to believe me.
I am 62yrs old with All the symptoms you described. I had covid19 in July 2019 and still haven't recovered. Brain fog, memory loss, edema, no smell or taste, diabetes, cataracts, no concept of performing tasks. I am an engineer with a masters degree in commerce and can't perform basic duties
I’ve survived COVID 19. But I still have shortness of breathe and my stamina isn’t the same. It’s not a joke. Stay safe y’all.
Fingers crossed for you pal
I have shortness of breath too. It's been just over 3 weeks since my diagnosis. I had every symptom and just existed the 2 weeks I had off. Im still not 100% but had to go back to work. I come back to work to find my so called friend/co-worker absolutely hates me now. She texted me everyday with 20 questions about covid /gathering info and wanting to know my symptoms so she knows what to expect IF she gets it. On the 4th day I collapsed on the ground. I got instantly hot/dizzy and a sharp pain traveled up my thigh that was so painful - I passed out on the living room floor. I gently asked her to give me sometime to get better and stop texting me. I didn't feel well enough to have to answer her daily questions. I can't believe her she hates my guts now. No compassion. I'm still dealing with stuff and hope to God it's not a long hauler situation.
@@blacksunshine5758 I've been there and I know exactly how you feel. For some reason It was worse during night time, after I had dinner. It took me about 4-5 months to fully recover. My advice to anyone going through this is to rest as much as you can. Take small steps, literally, don't work yourself out too much. Combine that with a good diet, meaning no salt or sugar, consume food that's good for your heart and lungs. Avoid eating seafood and pork. Also I found it supper helpful taking supplements and vitamins such as Omega 3, probiotics, vitamins C and D. Don't underestimate the power of your mind, stay positive and trust you'll get better. If you can, take short walks under the sun, doing breathing exercises, I did this every day from 10-15 minutes and I'm happy to report I'm back to 100%. Good luck and take care of yourself.
@@blacksunshine5758 she was not your friend, or she would’ve honored your wishes. Hope you feel better! 🥰
Yes I am also a survivor... And still have shortness of breath... Fatigue ...it's awful....
That blood clot observation seems REALLY important.
I am on a Blood Thinner, after having 5 strokes this year 2020. I had no underlining health conditions. After a zillion different tests, they said No Damage to my Brain, Heart, No Clogged Arteries, No Eye Damage. Nothing. It was never verified that I had Covid 19, but my doctor went into quarantine, I didn't see my regular nurses anymore and when I went to the ER, someone did check positive for Covid 19. 🤔🤔🤔🤔.
The Chinese doctors in Italy were calling this a Blood Virus in March
Radiation does that.
# Ride the wind. Yes I think you're right. Radiation from technology! Cell phones!
That has been known about since 2019. Most Doctors in the USA are clueless, and lost. The virus targets the Endothelium leading to apoptosis of the cells. This raises Angiotensin II levels and reduces Angiotensin-(1-7). That leads to more damage to the Endothelium. The destroyed Endothelium allows von Willebrand factor to spill into the blood causing clotting. The virus also targets red blood cells using CD147 as opposed to ACE2. The virus should bind to the 1-beta chain of hemoglobin dislodging the iron used to carry O2. This causes hypoxia(lack of oxygen in the blood) in addition to the blood clots that lodge in the capillaries in the alveoli of the lung. If the red blood cells begin to rupture(lysis of erythrocytes), the free heme then binds to von Willebrand factor, preventing it's breakdown. The iron is also a factor. The resulting clotting cascade can be so severe that anti-clotting drugs don't work and the heart explodes due to the blood turning hard. It is doing the opposite of Ebola that prevents clotting.
Also viral bound Porphyrin could be infecting cells without ACE2 or CDE147 receptors. The virus is also targeting T-cells like HIV. They need to look at CoViD-19 AIDS, as half of those without symptoms have a suppressed immune system and are being eaten alive by the virus. The immune system causes people to feel sick, so not having symptoms can be due to having AIDS. This virus has inserts from Measles, Mumps, HIV-1, SARS, MERS, and rabbis. It does seem to usually need a high initial exposure dose in most people to get a fatal case, but many will never fully recover.
I’ve had Covid twice: once at the end of 2020 and once at the beginning of 2021. Here it is 1-2 years later and I still have long symptoms from Covid, terrible headaches, muscle pain and heavy limbs, and breathing has never been right since, balance issues are terrible, also my heart rate has been high since and weird irregular beats. Was told at the ER it’s anxiety and was asked about mental disorders, they say nothing is wrong. It’s a shame they don’t listen to people, we may all learn something and stop this from destroying lives.
I recently had COVID in October 2022 and I’ve been suffering with a high heart rate that comes out of the blue I have to sit still most of the time and I suffer with ptsd/anxiety what helps me is taking a spoonful of sea moss in a warm glass of filtered water squeezed lime, lemons, oranges and ginger
I also was given paxlovid that cause me to have problems with breathing and what I found out about this medication is one of the 3 pills is used for HIV symptoms that I do not have
@@gaildickerson8499 how do you feel right now? any improvements?
As a Covid ventilator survivor, this is 100% accurate. If someone told me what to expect 1 year after this ordeal, I would’ve laughed in their face. Life is not the same and it’s been 1 year since I’ve been able to go to work due to the aftermath of the virus. No income, no Medicaid, no unemployment, no disability. Furious is an understatement
How do you survive?
@@juliagarbmy life savings. It’s been 2 years now and not one single penny from our lovely govt. it took 14 months for them to deny me for disability. However, I am getting a little stronger but still nowhere near as strong as I was. Mentally, physically, emotionally, financially… and so on.
I just got over covid and now my legs randomly give out on me at night so i’m really glad this came out and i’m not alone
Give out means feel weak and wobbly ?
Give out is unable to control and move them at will.
Eat as healthy as you can, rest extra, and exercise when you can. I pray for your recovery. 🙂
Gabriela I'm so sorry. This was very hard to watch. I hope you recover fully and don't be discouraged.
This happened to my dad he’s pushing 60 he felt weak and wobbly for a month or two after. Now luckily has been perfectly healthy for months I am hoping you have the same outcome!
Stay strong.
thank you for reporting on this. it's truly scary.
stay safe people
Those at greatest risk from Convid-19 & Long Haul Covid are people whose ancestors didn't live with their farm animals for millennia, basically people of color. Being of European & First Nations Ancestry, I was warned early in the Pandemic by a retired physician at church while we were waiting to talk to our pastor to explain to him why the service had to go virtual...
Especially over Thanksgiving!
@@davidhollenshead4892 that makes no sense
David Hollenshead , Do you have a reference for that?
It’s all for show
I got covid in Jan of 2022. Cold symptoms is all I exhibited (I'm 65, fully vaxxed at the time) 2 weeks after symptoms stopped, I had difficulty breathing, fatigue and headaches. I've had my lungs and heart checked out, everything is good. I get out of breath just putting on my seat belt. I was walking 4+ miles a day prior to Covid-19. I'm lucky if I can walk to the mailbox without getting out of breath. Drs ruled everything else out and believe it is long haulers. I feel for these people, I am lucky I have milder symptoms than they do.
Heard this from another fully vaxed person, they ended up not being able to breath and emergency went into ER , had water in lungs. Seems common after vax
how do you feel right now? any improvements?
Feeling great. Several days after posting this I was back to normal. I'm obese and out of shape, for sure. This experience shouldn't have surprised me.
So glad I watched this. I feel crazy when I tell people I have most of these same symptoms, I didn't know there were others having the same.
I had Covid in the wind of February and I cannot walk up my steps without coughing. I am 37 and I deliver mail. I use to run every day I no longer can. Covid is very serious.
😳😳😳😳😳
@@Kathrynlove good luck hope you regain your energy and you life back. i have chronic fatigue syndrome mamy years i lnow how frustrating it is.
Get either Clear Lungs or NAC at the health store. These really work to clear the lungs naturally.
A friend of mine still can't go back to jogging like he used to -- it's been more than a year now
I’m so sorry .. I hope you get well soon 🙏🏽
I thought I was crazy, but this has opened my eyes.. Honestly thought I was the only one going thru this😭
I still suffer, to this day, after battling COVID 3 times! Violent asthma attacks, body aches, headaches, unexplained increase in fluids in my brain, issues with vision, memory loss, etc. This stuff is real. I'm praying for relief!🙏🏽🙏🏽
It’s been almost four months since I had Covid. I had mostly bad GI symptoms during this time. I developed numbness in my legs, fast hard heart beat, ringing in my ears, and brain fog. The fatigue can be very bad at times. If I have errands to take care of one day, the next day I’m wiped out. Aches and pains In muscles come and go as well as chronic constipation. It’s a very depressing thing.
I’m going through this right now😢
@@deandre22 Sending prayers to you 🙏🏻
The gaslighting by employers and many physicians is horrific.
yep
I'm currently dealing with COVID syndrome. 6 weeks off work with no sign of when I'll be able to return. Started off with upset stomach, cough, aches and pains then tiredness and fever, diminished appetite, and hardly any voice. Then a rash on my hands and knees every two days for a fortnight. My voice has practically gone, I'm walking very slowly and can't go far without being exhausted. Things I love doing takes me longer. When I asked my GP what can he recommend apart from electrolytes and rest ...nothing as they don't know enough about it. Had bloods done ...perfect, lungs, blood pressure and pulse ...perfect. Time seems to stand still and becomes like groundhog day, utterly fed up. Hoping all those going through this recover, no one deserves this.
Please continue to keep this topic in the news. So many are still suffering terribly.
I had to pause this video at 2:20. I broke down in tears because I feel like I’m not alone. I have the same thing.
Your not I feel the same way
I have had Long- COVID symptoms since 11/2030 and the Health Clinic I go to since then dies not take my concerns and problems seriously. I have had Strep Throat 2 times within 2 months lately. I was so use to Walking & running 1- 3 miles at a time many times per week, yet now I become " winded" and so fatigued doing minor tasks which take small effort. Doing my full- time job is so difficult for me.
You're not ! Stay mentally strong that's very important if you don't you will fall into depression.
You are not alone ..it is wonderful putting it into words ...I have been wondering why I have these symptoms since covid ,lost my balance quite a few times..headache , my brain sometimes feel like in a fog ...
I'm in the same boat. Lost almost all my hair. It was down to my waist now so thin you can see my scalp. I Forget how to talk constantly. My vision is off. Can't remember things. Too much to list. This is awful I pray for all of us going through this.
Sounds like chronic fatigue syndrome- awful wouldn’t wish it on anyone.
Yes I have lupus and CFS. It sucks I am just here.
I think they are onto something with the autoimmune response. As a result of getting the Epstein Barre virus, my thyroid went into overdrive with Graves Disease and microscopic colitis. Autoimmune diseases suck the life out of someone. Very sad.
@@caseybc6342 Sorry for you.. I will 🙏for your good days❤
Yup exactly! I have CFS, developed it after an acute “mystery virus” in 2014. Hoping this is going to lead towards CFS treatment or cure
@@HannahLucia Only lots of small cures. Take zinc and minerals, sage tincture, meditate, stop eating animals.
Extreme anxiety and vertigo now when driving a vehicle me and three others have they exact same thing . We all three have had this happen to us after getting over covid . After seeing this I feel blessed. I pray we will all be healed.
The jab is a BIO WEAPON !!!!!! The govt and their globalist billionaire masters DO NOT LOVE YOU. THEY WANT YOU DEAD. "The welfare of humanity is always the alibi of tyrants." Albert Camus
I am one of the long haulers as well and it's crazy! I'm so glad to know I'm not alone, because you feel like you're going crazy! I hope we all heal soon.
You dont have to live with symptoms forever.
ArtemiC Rescue is used for Covid Short, and ArtemiC Support is used for Covid Long. Ordered online on the shop and shipped worldwide.
For prevention, on flights or vacations, take one drop of ArtemiC Support daily to help in not getting corona.
keep it ready in the fridge.
Do you feel you are recovering?
@@enlightenfitness in some aspects yes, but then having issues in others. When j think I'm getting better, something else pops up.
@ Samantha Sunshine
You are definitely not alone! I am 11 weeks post Covid. Been dealing with debilitating fatigue and muscle weakness. Mostly in my arms. I’m so discouraged. Right when I felt like I was getting better. I got hit with food poisoning that pushed me back 10 steps. How are you feeling today? Wishing you good health always!🤍
@@MK-gy1ug I'm so sorry to hear that! One day at a time is all you can do. It's ongoing but I can only take one situation at a time. I'm wishing you help throughout all of this.
There are millions of us that have had these symptoms for years that never had covid19. They don't know what to do with us. "Adrenal fatigue", "fibromyalgia". Drs throw their hands up and tell us to do yoga. I hate this is happening to a new wave of people but maybe this attention will shine a light on the millions that have been here for decades already.
Yes, I've been living with Fibromyalgia and Polymyalgia Rheumatica for many, may years. Every day is a trial. It's a shame SO MANY have these diseases but can get no help and are made to feel like they are stupid and don't know what pain is! The pain CAUSES the anxiety!
@@michelesettle its a vicious cycle
I have ME/CFS and it sounds like that too. I'm also hoping treatments come out of this tragedy, but I'm not holding my breath.
This is textbook CFS, many organizations are finally starting to look at the connection, disappointed that they didn’t even mention it. Check out the open medicine foundation for more information.
I agree!!!! I have fibromyalgia, EDS and Autonomic dysfunction
You are describing every single person who has an autoimmune disease. Millions of people have been living with these symptoms for years and fighting a healthcare system that doesn't believe them. Perhaps now things will change.
Doubtful but I'm still hopeful
Yeah, when they said doctors hadn't seen anything like this before I literally yelled out loud at my phone, "THE F**K THEY HAVEN'T!"
I had mono when I was younger. I have had all kinds of symptoms, but to simplify greatly, the main one has been full body pain. For the first two years I had mixed good and bad days, probably half of them bad. The next 12 years have been nothing but constant pain, and doctors don't believe me.
@@winterinbloom Understand totally -have had many many skeptical persons who then sent me to Doctor after Dr. Was diagnosed with autoimmune disorder and finally when my Doctor (Rheumatologist) referred me to a neurologist and then they finally began working and understanding on me. I hope that the Medical Community gets the message. I had very good care and I worked in a lab which helped me. WAKE UP PHYSICIANS-YOU HAVE NOTHING TO LOSE BUT YOUR COLLEAGUES.
It is frustrating to those who have been suffering from autoimmune issues for decades.
Exactly
You guys are not alone. Unfortunately many people (me) are going through the same ordeal. ❤ 🙏
Rest in peace Dr. Fowkes. Thank you so much for your diligent work.
嗯嗯
I'd rather wear a mask and stay a good distance from others, than go through something like this - possibly for life.
First thing turn off the satanic lying MSM! Then seek God and truth. Bless You!
You need to seek help, learn to think for yourself lady
You guys are disgusting. If yall get covid you dont deserve a ventilator
Tell folks that that don't believe Covid is real.
Best response from this thread, wise words.
This is the same effects many people are getting after the vaccine, including myself, after my second Pfizer vaccine. That was back in November 21, and it’s now Near the end of July 22 and while I am a lot better, I have the same symptoms. I cannot run, my heart races and pounds when I lift heavy things or go from crouching to standing. I still get chest pain,chest pressure, severe numbness in my limbs, random angry red rashes on my hands, searing sharp pain that spreads in my thighs and the back of my head, and the brain fog. There is no support for people like me. I wish we could go to a clinic like this one and have some help to get better. I’ve lost my main job because of this and there’s zero support in NZ. It’s so hard being alone in this.
Definitely not alone. Changed me and the way I do everything now,not in a good way.
I'm suffering from the pfizer shot and wondering where do i get help 😪 😢😢😢
Never got the shot and never got covid. Whats your take on that? Glad you believe the same "science" destroying women.
Sorry! Please look into Dr. Mark Ghalili in Los Angeles, CA - able to do miracles helping people who were harmed by these shots 🙏🏽
czcams.com/video/dIVZ5ssWB-o/video.html
Thank you for the report Anderson
Huuggss and prayers to everyone who has been experiencing this. You are not alone! 🫂
Hugs and prayers to you, also. Thank you for your kindness.
Have 6 months of long hauler it suxs
@@phoebedirks8186 ARTEMIC can be a potential lifesaver in the fight against covid 19.
ArtemiC has been used by many people to help the immune system to prevent covid or alleviate covid, Long or other infectious diseases.
Type it in on CZcams and you will find more info. It can be ordered online but theres a possibility of a backlog so its best kept in the fridge until symptoms occur. 🤧🤧 We have personally tested it on two occasions of covid and had great results with it. ArtemiC Support is used as a preventative measure on vacations or other travel when you dont want to catch covid.
Everybody should watch this video.
@Buddy Dawson stfu
Why
@Buddy Dawson I just don't get people like you...I do However feel sorry for you..
@@suehowie152 That is because you may lack intelligence. That is why you lack understanding. Why did they only have two patients? In NYC they should have had rooms full of patients like this.
@@RMokros I don't lack intelligence and Neither do I fight reality..
What's crazy I got their symptoms with the legs feeling like weights like you're going to fall over after going up a pair of stairs and feels like somebody's sitting on your chest along with memory fog big time fumbling for words no fun going through this stuff
I'm so glad I came across this program, I'm experiencing the same symptoms and experiences, it's dilibetating.
My husband went back in December and they kept telling us he had anxiety. COVID has been here longer than they said.
My 1 year old was very sick and hospitalized in December. The doctor's said RSV... But I bet it was covid
the US was several months behind in testing compared to the rest of the world, so there are probably many more people who never got tested that were infected and died.....scientists say that at least 104 mil Americans are probably infected....almost one third of the population
@@Lo0622 I’m sorry to hear that. It’s very stressful not knowing how to help. My husband still has health issues since last December.
@@cherieestbien1902 definitely agree! Even now I still believe testing is behind.
@@g.g2248 thank you. She recovered quickly... But I'm sorry that your husband still has issues! Praying for you!
Rest in Peace Dr. Fowkes. You are a hero.
I am glad someone is listening.
Knowing you are unwell but not knowing why will cause high anxiety but that is secondary to the true ailment and patients are entitled to proper answers, not sarcastically brushed off by doctors to egotistical to say, "I don't yet know but let's work together to find out".
Dr. Fowkes, I'm so sorry we lost a vitally needed doctor and to a heart attack at such a young age. 💐😔🌾
I'm a long hauler, the most frustrating part is the doctors who can't fix anything. The migraines are AWFUL, I get exhausted going grocery shopping, vertigo, IST, nausea. Its... awful. :(
Hugs. I can relate.😢
how long your symptoms persist?
How long did it take to see symptoms after you got the virus ?
I know how you feel X
What's your diet like? I can tell you I got Covid, but I also got Jesus and when this virus hit in Dec. I told myself if 99% are going to get it I"m cleaning up my diet! I believe these two things saved my body from experiencing symptoms. Also what about vitamins, do you take any?
are doctors still telling patients with legit physical symptoms they're having anxiety attacks? so disappointing and disheartening.
To be fair, those with panic attacks can experience physical symptoms. With nothing else to point to, it’s the default explanation.
@@Jack-gl2xw it is one of the worst things that can happen when you are experiencing these kind of symptoms, people do not have continuous panic attacks, by definition panic attacks are temporary. Medicine and science should not be dismissing people with such symptoms and conditions, it should be listening to them and working with them. Patients are not there to get diagnoses that shore up their medical professionals insecurities, they go to their doctor for help and to find out why the physical issues they are experiencing are affecting their lives so badly.
I’m so tired of hearing ER doctors and EMTs say sounds like you’re having an anxiety attack. Well why is that doctor?! WTH
@@lindyashford7744 That's not entirely accurate. Not all anxiety sufferers have these dramatic "panic attack" events. I myself have had GAD for years and have only had 2, one of which was a reaction to medication. Anxiety can also cause some persistent physical symptoms--headache, fatigue, general pain, dizziness, rapid heartrate, etc. And they don't just hit and go, they'll stick around for a while. Might leave you desperately trying to find ways to relax just to feel normal-ish again. Sometimes events that feel like emergencies or symptoms that seem like chronic illness really can be anxiety.
@@TsukiNaito1, I agree with you in one respect, but the point is that patients are getting told they are having panic attacks, not that they are anxious. Anxiety conditions are ongoing but what is being described by people is not the same. They HAVE a condition they know is physical, they go to find out why they are unwell and their condition is dismissed on the basis of being a panic attack. Even when they are not anxious but are feeling unwell. It is tantamount to saying you are a hypochondriac, and is a kind of put down. I was told this on presenting with breathing difficulties after what could have been a brain event. I was told it was a panic attack, then later when symptoms continued I was given a fibro diagnosis, even without the signs that normally fall into the fibro category. Nearly a decade later I was diagnosed with Atypical Parkinsons and actually I DO have an old infarct that could have been a brain bleed or similar. The default position is to shove you into a box that says MH issues. I had a friend with MS who often got treated like this too, she regularly had to undergo resuscitation due to eosaphageal spasm, and emergency room doctors don’t do resus for nothing. Yet doctors would happily discuss her MS as a ‘functional disorder’ which is medical code for ‘all in the mind’. I feel for you in your suffering from GAD, I know others with it and worked for a while with people who had acute anxiety, but what I and others are describing is different. It is beyond bad to be treated as if you have a behavioural disorder when you are finding that you cannot put one foot in front of another and your quality of life is plummeting. Hopefully now they will start to recognise that they do not have explanations for everything yet, and far from being at the peak of medical understanding there is still a long way to go.
This is chronic fatigue syndrome. I got it after shingles 9 years ago. I thought it would go over time but no looks like it's here to stay. It scared me so much at the time and for many years. I couldn't make sense of it. Now I'm just resigned to it. My energy is 30% and this hasn't changed for almost a decade. It's depressing and so many people don't believe me. I've lost family and friends. I lost my job,family,house and now I'm off sick. It's driven me crazy at times. I hate it. I was 37 when my life ended.. not even middle aged. It's the only illness / condition / disease where doctors just give up on you. I think it's actually brain damage from a major cytokine storm..from virus and multiple stressers. Very scary.
Edit: oh! They do say this by the end! 👏
Edit: oh 😥..she died.. .....🤔
Oh my word...my sincere condolences to her family and friends 😢 🙏
How unreal that the doctor passed when she was trying so hard to help with long covid. What a loss. Bless her and her family.
RIP Dr Fowkes
ONLY THE GOOD DIE YOUNG ..... SHE LOOKED VERY HEALTHY TO ME. THAT WAS LIKELY,, A INDIRECT MESSAGE 🤪 TO THE MEDICAL COMMUNITY TO BACK OFF. IF THEY GET IN FRONT OF WALLSTREET ::: @ ALL THE GREED MONSTER'S. 😎🖕
Not surprising, but so very sad.
If you read the Bible you will understand what is happening.
I’m struggling with the same symptoms, but didn’t take the shot cuz I don’t trust anything rushed, not tested or being Forced on us.
I have always took all my shots, but too many red flags. Ironically the guy mentioned 911 terror attack.
That makes me think that this probably use the same
Wow this is familiar to anyone who asks questions or studies anything this man made virus has caused.
Could have been the stress of it all or complications from Covid or the vaccine. This is so baffling and depressing. Furthermore, worry and misinformation are making me ill, physically and mentally. GOD Comfort!🙏.
WTF, she "died suddenly of a heart attack"????? That's a strange way to end this!
You have to wonder if they did a Covid autopsy on her to see if she got infected at work and it caused the heart attack. I bet they did not do it because their lawyers told them not to for liability reasons. Damn that is sad to lose a researcher just when we need them most.
@@markpashia7067 I was thinking the exact same thing.
The long term effects of Covid. I have constant burning lungs and heartburn. My God.
I feel like I just met her like I met her in person. It's a weird feeling like just watching a video and seeing someone then being told they're dead. I guess I feel sadder since they are working so hard to help people and then die mostly likely from a COVID infection that wasn't reported or even tested for. There has been plenty of corruption in hospitals so I hope this isn't the case.
Covid is causing long term myocarditis (inflammation of heart tissue) even in patients who had a mild case or had no symptoms while they were infected. There are likely a lot more long haulers than anticipated
Same here. Thank u for sharing
So very sorry to learn of the passing of Dr Mary Fowkes 💔. Thank you for all you’ve done to research this condition. I have been recently diagnosed with what is suspected to be a post-COVID condition affecting my balance. The audiologist says she’s been seeing an uptick in this condition since COVID.
Just the fact doctors are starting to believe us brings me to tears. I said 'yup, same girl' too many times, as I watched this.
I’m 4 months in post COVID, my body still feels heavy but it’s got significantly better over time, my breathing has improved and my sleep has gotten better, still have anxiety/depression and brain fog issues but it’s gotten better. My memory has gotten better but my difficulty finding words is still affecting me tremendously. I hope that everyone that has this illness recovers fast. Trust me, you’re not alone❤️
I was there too. Bedridden for 4 months, read about megadosing vitamin B1. 30 minutes after the first dose my symptoms were 50% reduced, by the end of the week I was completely cured. I took 500mg (5 capsules) with each meal for ten days. Look into it! It's a miracle.
Try drinking lemon balm tea. It will help a lot of the symptoms. I had COVID in November 21. I do breathing exercises. Breathe in through nose to count of five. Hold to count of five, breathe out through mouth count of five. Regular breath and repeat.
Did you take a vaccine shot?
Please eat plant based
Plzz stop blaming covid blame covid vaccine instead
I can relate to the symptoms … unless u have it . u won’t understand this … best thing I did was consult a homeopath, take good supplements, eat good wholesome food and rest when I knew I had too.
The fact that they keep telling you that you can’t feel a way irritates me
Since I've had it in March i have felt:
-constant back pain
-vertigo
-more frequent migraines
-exhaustion
Truly, my heart goes out to you.
i wanted to respond to your comment by saying I have close to similar symptoms post covid;
- neck, jaw, back pain
- tension headaches
- fatigue
I’ve improved over time as I try and manage each symptom I experience, I truly wish you a healthful future
Thanks for the support. I was hoping to put this up to see if maybe it would be helpful.
@joe, can you describe your back pain? I have experienced constant back pain as well.
I'm in day 13 of my quarantine, and I just got my taste, and smell back. I felt back pain, but it's going away. I don't wish this virus on anyone.
how sad that there are still people who thinks COVID is just like a flu
That’s because it is. How sad the gullible believe anything they see on tv
@@jamiec4478 And you believe what you hear where?
@mr burg Really?
@Lance Mullholland sure they are. But every other funeral home on the planet have record lows....
@Lance Mullholland nice try. Is that your comeback when proven wrong ?
Poor loves. What a cruel twist. 😢
This is not new with viruses. Years ago I caught Tasmanian flu in the UK from a work colleague. 1 by 1 we all caught it from him in our small, poorly ventilated, team office.
Most had coughs & shortness of breath for some weeks & months after, including me. Mine continued for 18 months+. I ended up having tests on my heart rate. 1st test normal, 2nd test picked up a missed heartbeat. Years later & I still couldn't do the workouts at all that I once did 3-4 times a week. I still live in hope that I will be able to do them again albeit gentler & no strain on my heart. I'm not old.
One of my work colleagues had sleep apnea. So getting that strain of flu none of us had any resistance to was a double blow for him.
Long respiratory virus issues needs exploring I think.
Yes, brain fog just like taking Benadryl. I can relate to that. Stiff and heavy legs, numbness and tingling on my face, feeling dizzy, vertigo, get out of breath from vacuuming and I use to walk 3-4 miles a day
This is really terrifying, people who are healthy experience these symptoms
This is serious. Very serious😵
@@tanyawilliams823 After watching this video im scared 😅😂
I had it until a week ago.I didn't have any lung issues while I was infected.But now days later I feel like coughing each time I take a deeper breath.I have to keep chugging mentols
@@ivonastrukar4715 wish everyone could have gotten what trump got. That antibody cocktail and all
It happened to me. My lungs still hurt and its been months. The worst part is the headaches and mind fog. I was a runner in my early 20s. Mine isn't as bad as most these people's conditions though.
So shocked and sad for this dedicated doctor and her family. In Gods hands now.
When a Dr. Doesn't believe you, where do you go for help? I feel so bad for them. .
The doctor who had long haul covid herself is a hero
No she not. She's a liar spreading fear.
@@mattjacobs414 she's not the liar, the people you listen too and idolize are
@@77maggiemae this has been planned for a long time. Research event 201 then get back to me. Read this if you have the guts.
@Lance Mullholland you tell me zombie.
Adding L-Lysine, Vitamin C, Zinc and B vitamins to my diet has helped. Also as long as I’m taking a digestive enzyme and probiotic and drink lots of water the I usually feeling better energetically. It’s so odd though cause that fatigue will hit me hard and I’ll be out for the day. And all I can do is sleep. Then I’ll be fine for a few days. Also when I drink water all the sudden I have to blow my nose like crazy and a lot of stuff comes out. Invest in a good massager like a massage gun and use it on your feet and back and wherever there is pain. My massage gun has helped me break up knots in my muscle and heal quicker. I try to run my massage gun over the pressure points in my body. Prayers for healing for all of us.
🎄🎅🎄🎅🙏🙏🙏🙏🙏🙏🙏🎄🎅🎅🎄
The digestive after effects can be so challenging. I've literally had debilitating stomach pain. I realized recently that I may need a probiotic daily for relief. Appears if I'm anxious, the pain will creep. Year later, still having a plethora of issues. Best Blessings to all.
I didn't realize digestive issues were connected to covid. Ive been having the same issues including the energy or lack there of. There are days where all i do is sleep.
I take the 90 essential nutrients in optimal doses, and I cant function still. Losing my oxygen is the biggest frustration.
Very true I’ve been doing the same thing...it’s very important this Information gets spread
I just acquired Covid-19 two days ago. Day two was horrible. Today, is better but now I feel my left arm very hot. I’m doubled vaxxed and boosted. I hope everyone recovers quickly! ❤