Citizen Scientists Take on the Challenge of Long-Haul COVID-19
Posted on by Dr. Francis Collins
Coronaviruses are a frequent cause of the common cold. Most of us bounce back from colds without any lasting health effects. So, you might think that individuals who survive other infectious diseases caused by coronaviruses—including COVID-19—would also return to normal relatively quickly. While that can be the case for some people, others who’ve survived even relatively mild COVID-19 are experiencing health challenges that may last for weeks or even months. In fact, the situation is so common, that some of these folks have banded together and given their condition a name: the COVID “long-haulers.”
Among the many longer-term health problems that have been associated with COVID-19 are shortness of breath, fatigue, cognitive issues, erratic heartbeat, gastrointestinal issues, low-grade fever, intolerance to physical or mental activity, and muscle and joint pains. COVID-19 survivors report that these symptoms flair up unpredictably, often in different combinations, and can be debilitating for days and weeks at a time. Because COVID-19 is such a new disease, little is known about what causes the persistence of symptoms, what is impeding full recovery, or how to help the long-haulers.
More information is now emerging from the first detailed patient survey of post-COVID syndrome, also known as Long COVID . What’s unique about the survey is that it has been issued by a group of individuals who are struggling with the syndrome themselves. These citizen scientists, who belong to the online Body Politic COVID-19 Support Group, decided to take matters into their own hands. They already had a pretty good grip on what sort of questions to ask, as well as online access to hundreds of long-haulers to whom they could pose the questions.
The citizen scientists’ group, known as the Patient-led Research for COVID-19, brought a lot of talent and creativity to the table. Members reside in the United States, Canada, and England, and none have ever met face to face. But, between their day jobs, managing time differences, and health challenges, each team member spends about 20 hours per week working on their patient-led research, and are now putting the final touches on a follow-up survey that will get underway in the next few weeks.
For their first survey, the group members faced the difficult decision of whom to contact. First, they needed to define long hauler. For that, they decided to target people whose symptoms persisted for more than 2 weeks after their initial recovery from COVID-19. The 640 individuals who responded to the survey were predominately white females between the ages of 30 to 49 who lived in the United States. The members said that the gender bias may stem from women being more likely to join support groups and complete surveys, though there may be a gender component to Long COVID as well. About 10 percent of respondents reported that they had ultimately recovered from this post-COVID syndrome.
Another important issue revolved around COVID-19 testing. Most long-haulers in the online group had gotten sick in March and April, but weren’t so sick that they needed to be hospitalized. Because COVID-19 testing during those months was often limited to people hospitalized with severe respiratory problems, many long-haulers with mild or moderate COVID-like symptoms weren’t tested. Others were tested relatively late in the course of their illness, which can increase the likelihood of false negatives.
The team opted to cast a wide investigative net, concluding that limiting its data to only people who tested positive for COVID-19 might lead to the loss of essential information on long-haulers. It turns out that half of the respondents hadn’t been tested for SARS-CoV-2, the virus that causes COVID-19. The other half was divided almost equally between those who tested positive and those who tested negative. Here are some highlights of the survey’s findings:
Top 10 Symptoms: Respondents were asked to rank their most common symptoms and their relative severity. From highest to lowest, they were: mild shortness of breath, mild tightness of chest, moderate fatigue, mild fatigue, chills or sweats, mild body aches, dry cough, elevated temperature (98.8-100), mild headache, and brain fog/concentration challenges. Highlighting the value of patient-led research, the team was able to assemble an initial list of 62 symptoms that long-haulers often discuss in support groups. The survey revealed common symptoms that have been greatly underreported in the media, such as neurological symptoms. These include brain fog, concentration challenges, and dizziness.
Making a Recovery: Of the 60 respondents who had recovered, the average time to recovery was 27 days. The respondents who had not recovered had managed their symptoms for 40 days on average, with most dealing with health problems for 5 to 7 weeks. The report shows that the chance of full recovery by day 50 is less than 20 percent.
Exercise Capacity: About 65 percent of respondents now consider themselves mostly sedentary. Most had been highly physically active before developing COVID-19. Many long-haulers expressed concern that overexertion causes relapses
Testing. Respondents who reported testing positive for SARS-CoV-2 were tested on average earlier in their illness (by day 10) than those who reported testing negative (by day 16). The team noted that their findings parallel those in a recent published scientific study, which found false-negative rates for current PCR-based assays rose as the time between SARS-CoV-2 infection and testing increased . In that published study, by day 21, the false-negative rate reached 66 percent. Only two symptoms (loss of smell and loss of taste) occurred more frequently in respondents who tested positive; the other 60 symptoms were statistically the same between groups. The citizen scientists speculate that testing is not capturing a subset of COVID patients, and more investigation is required.
Since issuing their survey results on May 11, the team has met with staff from the Centers for Disease Control and Prevention and the World Health Organization. Their work also been mentioned in magazine articles and even cited in some papers published in scientific journals.
In their next survey, these citizen scientists hope to fill in gaps in their first report, including examining antibody testing results, neurological symptoms, and the role of mental health. To increase geographic and demographic diversity, they will also translate the survey into 10 languages. If you’re a COVID-19 long-hauler and would like to find out how to get involved, there’s still time to take part in the next survey.
 “What Does COVID-19 Recovery Actually Look Like?” Patient-led Research for COVID-19. May 11, 2020.
 Variation in False-Negative Rate of Reverse Transcriptase Polymerase Chain Reaction-Based SARS-CoV-2 Tests by Time Since Exposure. Kucirka LM, Lauer SA, Laeyendecker O, Boon D, Lessler J. Ann Intern Med. 2020 Aug 18;173(4):262-267.
Coronavirus (COVID-19) (NIH)
Patient-led Research for COVID-19
COVID-19 is a curse. Nobody knows when it’s completely going to end.
Just want to express my admiration for this group of long haulers, spending their (now much more) valuable time on this project. Good luck and do report back.
Does COVID 19 cause Stevens Johnson Syndrome? From the beginning the symptoms are similar. My Stevens Johnson Syndrome symptoms were aggravated by a trip to the VAMC Black Hills, SD in Hot Springs, SD in late February. I visited with the motel owner for a couple of hours twice in the 2 day stay in Hot Springs. He had just returned from India by air.
On August 21, I did an ER visit because the cyanosis of my hands had worsened and I was nauseous. Both a quick test and a Health Department Test for COVID 19 were negative as well as a antibody test. My oxygen level was 94 -97. I was treated with a normal saline IV which improved me greatly for a couple of days. So I have no idea what has worsened my symptoms which is continuing at a much worse level than before February 27.
But it raises the question of does Stevens Johnson Syndrome affect the electrolyte balance? Is that the cause of long term residuals of Stevens Johnson and COVID 19?
As a psychiatrist and psychotraumatologist working in Madrid, Spain, with 35 years of clinical practice, I very much think that the “psychosomatization” of initial COVID symptoms and – at the same time- a negativisation of tests makes clear that the mental helth variable is of great importance here.
Trauma / severe stress reactions / anxiety disorders include often a clinical picture that is to some degreee quite similar as the one described for so called long haulers in the article: “…shortness of breath, fatigue, cognitive issues, erratic heartbeat, gastrointestinal issues, low-grade fever, intolerance to physical or mental activity, and muscle and joint pains”. Is it pure “anxiety plus”, I would ask myself and others?
Often we forget that our alarm systems enhance all somatic reactions and symptoms that were present for another etiology and chronically well tolerated. In stress and insecurity times they come again to clearer expression because we hear our bodies “more and better”.
Despite of all these old knowledge in Medicine, we should not forget the psychosocial stress related to loss of work, death of relatives and a political and social situation in the whole world that is more that worrysome.
All in all, remain calm and try not to medicalize too much, please.
So you are saying they are all psychosomatic, Paco? You are saying my relief from a normal saline IV was psychosomatic? Perhaps you also believe my temporal lobe epilepsy is psychosomatic?
I’d rather believe the objective tests and treatment results. Treat for electrolyte imbalance and get results, then even if it is the psychosomatic start you have an electrolyte imbalance. No amount of talking is going to make that go away. Too many behaviorist think everything is psychosomatic.
It is always both Lemuel: “Psycho” AND “Somatic”. For me and you and for everybody. I care always for both parts. Very much hope you stay well!
I am not well. Whether COVID-19 tested too late (over 6 months) to be antibody positive or a Stevens Johnson relapse. I experience the problem of, “Many long-haulers expressed concern that overexertion causes relapses”. From my exercise days, I know the point to push to improve the following time. But that point makes me worse the following time and is keeping me sedentary. Short winded crossing the room but O2 level of 94-97 which doesn’t make sense. Therefore, there must be a vagus nerve or nerve center involvement to have difficulty breathing without an accompanied diminished oxygen level.
Or maybe those of us who were regular at exercising build up a need for a higher level of blood oxygen?
Check out the exercise studies on the long, long haulers – people with chronic fatigue syndrome – and then let’s talk about anxiety. That discussion has gone for decades in ME/CFS and the psychosomatizing has finally just about run its course. Unfortunately it took several decades of ME/CFS patients with it. Sad but not surprising to see it show up here.
I am telling you, it is not hypochondriasis. Psychosomatic illness is a real illness regardless of the effects of emotional stress on the pathophysiology. Long haul is a prolonged inflammatory reaction which focuses on the nervous system and causes exacerbation of damage in other organs in the inflammatory phase. It is disabling. You are wrong dear colleague. Don’t gaslight thee patients. Please be careful about assuming psychosomatic illnesses can be addressed as a mental health issue, we used to have the same misapprehension about peptic ulcers until H Pylori was discovered …
Nobody is speaking about “hypochondriasis” Denise S. Just you. I never used that word.
I repeat: I just want to remark that the so called mental or psychosocial or just human aspects of any illness, incluiding COVID 19, must be taken into consideration.
Paco unfortunately you did come across like that whether intended or not – it’s not particularly useful or helpful to feel that you are not believed when you are unwell. Of course mental health is important but let’s not forget that ME was only until recently thought to be of a psychosomatic origin and people had to fight hard for biomarkers to be found.
Kelly, read about stress induced hyperalgesia, please. It is not about malgingering or faking symptoms.
Covid 19, as any other stress and virus related illneses are frequently related with later fibromialgia.
Rheumatologists know very well about this.
Paco Orengo Garcia, u have the nerve to suggest all these people have some sort of Hysteria illness from Corona. It’s greedy people like you telling the public that this isn’t a biological after affect from Covid 19 but a somatic affect. It’s people like you that keep the REAL Doctors from studying Viral Syndromes so millions of people can’t get well. These sufferers don’t need YOU the (psychiatrists) they need scientific study in a lab to get to the biologistics of this. You’re doing your covid long hauler patients more harm than good telling them it’s all in their heads, when we’ve known since the Spanish Flu of 1918 that Viruses cause Viral Syndromes in some people…
Experiencing it, I think it is COPD or Stevens Johnson related. COPD should show lower O2 level. Stevens Johnson does not show the lower O2 level by reacts the same way. The brain thinks the O2 level is too low.
I wonder if those patients may benefit from Adipose-derived mesenchymal stromal cells.
It would be interesting to know if this group of individuals may have reactivated a latent Epstein–Barr virus infection.
I had mono 60 years ago. Could be a common cold reactivated it or my Stevens Johnson. I had a low grade fever for 1 day. Or the cold aggravated my diagnosed Stevens Johnson from taking Lamotrigine for temporal lobe epilepsy reactivated it. But I don’t remember getting an IV for mono. Just rest. The body is complex. Paco could be right most of the time, but if he is wrong once his patient could die from the error.
I am a physician and a COVID long hauler. I tested positive for COVID-19 by nasal swab DNA test and had classic acute COVID symptoms for 2-3 weeks and was hospitalized 4 days. I am now 8 weeks from my initial symptoms/diagnosis and still suffer from fatigue, headaches, brain fog and dizziness. I have not been to work in 8 weeks.
About a week ago my Internal Medicine doctor ordered a large number of lab tests hoping to see why I wasn’t getting better. All were normal except Epstein Barr Virus (EBV):
VIRAL CAPSID AG (VCA) AB (IGM) – 750. Off the chart
EBV NUCLEAR AG (EBNA) AB (IGG) = 361 (High)
Notice all my Ebstein Barr titers are very high, except the IgM. My doctor feels this is a reactivation of EBV caused by COVID. He says he has seen EBV reactivation from other viral illnesses. I have no memory of having Mono, but EBV is ubiquitous.
I believe that long haul COVID may, in many cases such as myself, be a reactivation of EBV. This is an hypothesis that should be tested.
I can also attest that the long haul COVID-19 recovery is a very real clinical syndrome.
Thanks for sharing your experience, William B. I have been thinking that we’ve gotten to talking a lot about microbiome over the past decade, but we rarely talk about how viruses too might be part of that in our bodies. Are you taking part in the Citizen Scientist (Patient-led) research? I wish you a complete recovery!
I am based in New York and got sick in early March, my symptoms were very much gastrointestinal breathlessness and horrendous headache, it took weeks for me to recover. I’m still not fully recovered having a variety of the usual symptoms coming and going. Anyway, I finally got to the doctors 5 months after infection to find out why I was still feeling so crappy and all my blood work revealed was very high EBV antibodies. It was not an active infection but incredibly high titer, they also felt I had, had a reactivation of EBV very recently. TMI but in addition (and this is true of 3 of my girlfriends who also tested positive) at the end of menstruation we have 3 to 4 days where we are barely able to function, absolute fatigue, unbearable cramps, dizziness where you have to lie very still and emotional upset. Its unbelievable to me that ALL 3 of us now experience this symptom. We are all in our early 40s and had none of this before the illness. Its a very strange illness to be sure and I do agree with your hypothesis regarding EBV.
@Kelly. I commented on William’s post as I too had the high titer for EBV. Not much has been researched on this, but there has to be something there. Curious did you also have elevated liver enzymes and/or mitochondria? I saw that you also had gastrointestinal issues at the start of the illness. Another finding during my blood work up in April (one months after falling ill) was that I tested positive for h-pylori and had it eradicated in May.
I didn’t have my liver tested but my doctor did say he felt it might be slightly enlarged. I am to return for further testing so I will request this – I have been taking a probiotic which is helping somewhat I have not been tested for hpilori recently but did have a negative test 5 or so years ago. I am interested to know if any long haulers have made any progress in their recovery – I feel like mine is a roller coaster some days I’m 95 percent others I’m 50 it’s very unpredictable and unnerving. I don’t believe there is a current treatment for EBV other than hit or miss antivirals. I wonder if any medical professionals on this thread could advise. I do feel my illness now has a CFS “flavor” to it.
@William B. Thank you for sharing this finding. I too tested with high IGM IGG. Never knew I had EBV and physician said these results mean it was in the past, but if your hypothesis is correct, perhaps we should be treated for EBV? Are there any risks to doing that? I’m currently taking ursodiol as my mitochondria and liver enzymes were also elevated so was given a diagnosis of PBC not Covid since my tests were all negative. My symptoms are many many since March 20th all along the lines of Covid longhauler including glucose intolerance without a high A1C (5.4) No fibrosis either to cause glucose intolerance. It’s has all been unexplainable since March to now. Currently I have heart palpitations when I do not eat in 2-3 hour windows and hair is falling out dramatically, anemia and low iron along with muscle twitching and static energy pulses. Taking B12 and it’s helping, but not with everything.
William, if you see this please reply. I got COVID April 2020 and was a long-hauler. I was treated . . . and have been on meds for 7 weeks. After the first week my long-haul symptoms went away, but my doctor suggested I get a blood test. It showed IgM at 3954 mg/dl and now he thinks I have Multiple Myeloma or Waldenstrom’s Macroglobulinemia. I need to know if there could be a connection between long-haul and very high IgM. This doctor also thinks there is.
I think it’s extremely interesting that only 0.6% of long haulers are obese. (See link to the original research).
In the US, this must be highly statistically significant. They also exercise regularly but if they do so after long haul COVID their symptoms worsen.
I’m a long hauler and all these are true for me.
is there any research to see if the “long haulers” have anything in common prior to infection?
There is no doubt a relationship between Covid 19 and ACE 2 expressions. My thinking is that post Covid 19, the residual complaints might be the result of activations or a post mutation that accounts for some such as the above Epstein Barr?
The challenges that the scientists and the citizens have taken on might be practical because there are no signs of the pandemic ending or settling down. The information was very helpful. Thank you for sharing the information with us through this article.
I am Julie O. I have Had covid for, as far as I know, over two months now. Prior to this I have been treated for Thyroid tumors, fibromyalgia and sleep apnea. I waited too long to take the test and therefore got a negative but… diagnoses. My daughter tested positive after the second test. I have tried to deal with this myself,so as not to infect others. It has been really hard to reach my Drs. Their message boxes are full or they don’t get back to me. I have been on this roller coaster with this. I will start to feel better, get up and try to do stuff and I’m down for days again. The most significant symptoms for me have been intense muscle pain, chills, random and extreme, and violent coughing fits. I am taking a medication for the sleep apnea, which tends to lessen the coughing. When it wears off it is really bad … The fatigue issue I had before covid. I have no idea how much longer this will last. I feel like I can’t get treated for my other issues until this is clear. I have no idea when that will be. I’ll go to the Hospital if I feel the symptoms are life threatening, but don’t want to expose myself to other things. When I first got sick with this people kept asking me “are you sure it’s covid?” It was not until my daughter tested positive, that people believed that I had it as well. The people who live with me Knew. I feel like there needs to be guide lines for when to test for this and people you talk to when you have it
My daughter is a long hauler. Late 30s, very fit, eats healthy, exercised often. Has had a number of neurological issues, about 60% are gone but still experiencing: fatigue, flutter feeling in her head, floaters in her eyes and does not to feel “right” enough to go back to her exercise program. Has seen a neurologist and opthamologist, has modified her diet and added supplements, and had vestibular therapy all of which probably helped some issues go away. She initially experienced a physician who implied it was all in her head and offered a prescription for anxiety. These long haulers need the support of the scientific community to research this aspect of COVID-19. Thank you for this valuable article.
… This started for me back in early July. My girlfriend and I believed to both had have Covid so we quarantined and waited until July 16 to go get re-tested. My first test had come back negative in late June. But I was experiencing the loss of smell and taste, low grade fever. My test from July 16 came back positive for Covid, my gf was negative. I’ve since tested negative August 5th. Here are my symptoms that I’ve been dealing with since July 16, appetite pretty much non-existent. Fatigue easily, Nauseous and here is the one symptom that no one can understand, Im cold all the time, whenever I sit for long time or lay down to go to bed, my body gets cold. At first I was like okay, this is part of it, but we are now Sept. 22 and still ongoing. I’ve down blood work twice, Once in mid July and another just last week. Blood work came back good. Dr. wants me to lower cholest (220). and watch get my glucose under 100, (it was at 108). I have also since had a colonoscopy and endoscopy and all came back good. The one symptom that has been consistent since July 16th, is the coldness. My body just getting cold. Starts at my knees, down to my foot up through my arms. During the time I was sick i felt as if someone was poking me inside my body with a needle of some sort, wasnt painful but felt almost like poking me with a cold stick of some sort. Dr. put me on an anti-depressant really hasn’t helped much. Dr.’s look at me like I’m making this up, this is VERY real symptom. If anyone has heard anything like this please reach out to me, I would really appreciate it. God Bless
Similar negative tests and long haul symptoms. But I have other conditions that could be the cause. And CORVID-19 is not the only virus floating around.
But so many symptomatic with negative test results makes me question the accuracy of the tests and if Labs are charging for tests not done and simply reporting them as negative. Are there any audit controls in the test equipment to prevent this?
I was in the hospital with diagnosed Covid in March, severe double pneumonia and very high fevers. I was released after nine days and have since been suffering with intermittent severe fatigue and extreme body aches several days a week which are completely disabling. All of my blood work has been fine for the last three months and I’m wondering about the extreme fatigue and the muscle aches, has anyone suffered this long with those symptoms.
I’m experiencing the same kind of fatigue as well. Been cleared from COVID since August 5. I did blood work in July when I was sick. And blood work again two weeks ago. All came back good. I went to another physician and he ordered some other blood tests that they don’t do on regular blood work. I’m waiting for those results.
Does anyone have problems with blood oxygen levels?
Thank you for this informative article. What is the risk of future coronavirus vaccine will trigger some of the ” Long-Haulers ” symptoms as chronic side effects?
Byron M, a pretty significant (almost “runaway”) attack on the lungs and body would have to happen for that. That is not how vaccines act. Vaccines stimulate the immune response, but even a live virus vaccine would not launch an attack on the body at the scale that the coronavirus does.
My 21 yo daughter had 1st dose Moderna vaccine last week. About 6 hours later she was excessively tired (sleeping on the floor tired), this lasted ~24 hours then she was fine. On the 5th day after the vaccine she developed a terrible sore throat, swollen white tonsils, swollen lymph nodes and is unable to swallow. She had mono / EBV years ago but appears to have a reactivation caused by the vaccine. The vaccine must cause immunosuppression severe enough to allow reactivation. She is reporting as an adverse event.
I’m one of the March suspected COVID cases. Could not get tested because I was considered not high risk or over 65years. Was in quarantine from my job until all my symptoms resolved, around 28 days. It’s now October. I have a lingering cough that won’t go away. I wheeze and cough on and off at night. I now get random 3 to 4 day Headaches every couple months. I am constantly clearing my throat of phlegm that sometimes impairs my voice when trying to speak when at work.
Virginia, I wish you a better recovery. Have your doctors/providers discussed lung rehabilitation exercises?
I was sick Sept 14th and tested positive for the antibody on October 9th. I had been sick in the Spring as well but unable to get tested – the same as many mention here. I have Epilepsy, Sleep Apnea (recently discovered) and am 52 years old. Hot flashes started in the Spring after I had been sick for the first time. They were AWFUL. The brain fog too…. When I was sick the second time, the fatigue and brain fog seemed to drag on. I started investigating everything I could think of…… My OB/GYN put me on hormones – estrogen patch and progesterone. The brain fog began to clear almost immediately. Could it be that this virus messes with the hormones? I did also hear of a couple patients that were on vents at the University Hospital. They tried a med that does something with the thyroid – it was something they learned about after people died from the Swine Flu here. They did the research and saw what failed so I think I’m not crazy that it may affect hormone levels for some people. Interesting about EBV. I did have mono in High School so maybe that’s why it affected me more severely as well….
I am a Registered Nurse from the Midwest U.S. I have participated in the Nurses Health Study for 40 plus years and take very good care of myself in regards to nutrition, exercise, and mental health. I believe I had COVID -19 in early March 2020 following a flight to Arizona and travel to California for the Tennis Open in Indian Wells, CA. It was the first athletic event to be cancelled. My travel partner and I took precautions as this was very early on. We wiped down table trays on the airplane, wore masks and spent time with one couple for a period of 5 days (they never had symptoms). Upon returning home on March 12 we experienced frontal headaches with discomfort particularly near the bridge of the nose and forehead, minor sore throat, and body aches for several days. We were to get tested through a clinic on March 17 and waited for 2 hours to be tested only to be told that testing was now for emergency cases only. I participated in a CDC webinar in March as a representative of the Future of Nursing: Campaign for Action and stated that perhaps the CDC was misguiding citizens by mentioning only 4 symptoms: fever, cough, shortness of breath, and fatigue. It wasn’t until May 2020 that additional symptoms of COVID-19 were being shared. During the spring and summer I experienced significant anxiety, insomnia, photosensitivity (wore sunglasses to watch TV) and an increase in auditory sensitivity. I believe my brain became even more inflamed following an iatrogenic induced Serotonin Syndrome which I experienced in early October.
In November I again contracted COVID, my partner had it first and I showed symptoms within 3 days – we were both following mask and social distancing guidelines. An annual physical on Oct. 31 showed a Hgb A1C of 5.8 and abnormal pap and positive HPV (never had an abnormal pap or positive HPV in my life). I believe my body was in a state of stress from lack of sleep and the Serotonin Syndrome. I tested positive for COVID on Nov. 10 following a negative test on Nov. 7th. As a public health nurse I was certain I was infected. The virus targeted my weakest organ system – my brain. I experienced the same kind of headache I had in March along with mental confusion, fatigue, weakness, lack of energy, and continued insomnia (treated). I’m wondering what strain I may have had during round two. I suggested treatment of my anxiety and high pulse rate 115 (my normal is around 66 – 70) with propranolol. I am disappointed with treatment by the medical community – not showing much creativity in the treatment of long-hauler symptoms and try to label with other psychiatric diagnoses. My yawn reflex returned in mid January and my anxiety has started to be less problematic. I am now 3 mos. post infection and still have to tell this long story when seeking medical attention. I continue to have slight pressure in the bridge are of my nose (sometimes feels like Rice Krispies popping), occassional bloody nose (once a week), continued intolerance to light and sound, and very mild upper teeth ache throb which may suggest sinus inflammation. Through my own sleuthing, I have had my optic nerve examined by an optometrist – it showed no inflammation. I have taken Ibuprofen 200mg twice a day since the November infection and have taken fish oil for years.
To Victoria V. (Registered Nurse from the Midwest U.S). Sorry about your experience, I hope your recovery gets better.
If you are having nosebleeds weekly, why would you want to be on ibuprofen? If pain is the issue, is acetaminophen not working? Blood pressure normal? ENT exam normal?
The nosebleeds are very minor (little blood mixed with mucus). I notice it because it is outside my normal. Dry air could be a contributing factor. My physician is aware that I am taking a low dose NSAID. The pressure felt at the bridge of nose is not usually pain and so I don’t take Tylenol very often unless the pressure/crackles persist after a dose of Ibuprofen. My blood pressure is normal below 120/80. I have not had an ENT exam. I don’t seek extra medical care with a high-deductible healthcare.gov insurance plan. No benefits when working for non-profits. Thank you for replying to my post! I feel heard!
To Victoria V. (Registered Nurse from the Midwest U.S). Since the discomfort in the nasal sinus/frontal sinus area has lasted since March 2020, i.e. chronic, and you’ve excluded hypertension, maybe an ENT opinion will help. Depending on how much of a DIYer you are, or if symptoms tend to temporarily resolve after a warm shower, you can look into a neti pot. The pot is fairly low-priced at $8-15ish with saline sachets included, but most people hate how the saline solution runs in and out of the nose (and they have to also learn to do it right). Disclaimer – this is not to be considered medical advice. If not alleviated… ENT and they’ll likely ask for a radiology scan. Good luck!
Thanks. CT done 12/30 negative. Wondering if anyone else has prolonged HA and sinus symptoms post COVID?
I have had chronic fatigue and brain fog since last March (2020). I felt run down and had some headaches, but other than that, my biggest complaint is debilitating fatigue and brain fog. I can’t remember things. I was always very active and very sharp. I have been diagnosed with Epstein Barr – but other than that the doctors cannot find anything wrong with me. My liver levels are a little high, but I have been told that is from the Epstein Barr. I have had two antibody tests the past year with zero antibodies. But everything I read about, it sounds like I have long-haul covid symptoms. I just think its strange it all started right when Covid hit.