Anonymous wrote:How do you explain my cardiac issues that are very clearly seen via MRI and echocardiogram? And no, they weren’t there previously. I am in my 30s, incredibly fit, was running 35-40 miles per week before I got sick (this was pre-vaccine; first wave). Literally couldn’t breathe even though my lung capacity is usually off the charts. I needed inhalers for the first time in my life and even those didn’t work super well. Ekg and blood work showed many abnormalities. I was declared disabled for 1.5 years because I had medical evidence of my persistent illness. These are all very objective measures. Nothing psychosomatic about it.
Anonymous wrote:Anonymous wrote:This is an important study and jumping off point for long-haul Covid issues. If you've taken a research methods class, you know that one can only fail to support or support a hypothesis. This study did not test whether anxiety or mental health concerns were the cause of long-haul Covid symptoms, so we can't draw any scientifically supported conclusions about the syndrome being all "in your head." This study did not evlauate the "realness" of post-Covid symptoms, only some possible causal factors.
Some medical professionals believe that mast cell activation syndrome (MCAS) and/or postural orthostatic tachycardia syndrome (POTS), a dysautonomia, may be the cause of long-haul Covid symptoms. As far as I can tell from a keyword search of the article, none of the diagnostic blood or urine markers for MCAS were tested in this study. Nor were study participants subjected to a tilt table test, the diagnostic standard for POTS. As well, the possible causes of dysautonomia, like an imbalance the renin-angiostensin-aldosterone system were not tested in this study. It is a great start, and I it is good that we have this research, but it still leaves more questions than answers when it comes to post-Covid symptoms.
Agree, though I would amend your statement to "some medical professionals hypothesize that mast cell activation syndrome (MCAS) and/or postural orthostatic tachycardia syndrome (POTS), a dysautonomia, may be the cause of long-haul Covid symptoms." Not belief. A lot of what gets discussed as fact or belief around long Covid is really just scientific speculation. Similar to speculation early int he pandemic as to why Covid was so mild in young children -- there were medical professionals who hypothesized that hit had to do with frequent recent exposure to other coronaviruses, and other people speculated that certain childhood vaccines could be offering a stronger immune response. Neither of those are medical facts, it's just people thinking critically about something and speculating on possible causes.
I think it will be difficult to design a study into MCAS/POTS as possible causes of long Covid until the medical community can narrow the meaning of "long Covid". One thing making it hard to do research in this area right now is that the current trend is to constantly expand the definition of long Covid, to include literally any symptom that occurs in a person who at some point tested positive for Covid. You can't run studies into that. Most likely future studies will be limited to people with the most severe or debilitating long Covid symptoms, which is probably as it should be. I think with time many people who are currently considered to have long Covid will no longer be treated as such. A lingering cough after a respiratory virus is not uncommon. Mental health issues like anxiety or depression can have many causes and will be very hard to link to Covid itself.
I think in a few years, the idea that "most" people who get Covid have long Covid will be considered silly.
Anonymous wrote:This is an important study and jumping off point for long-haul Covid issues. If you've taken a research methods class, you know that one can only fail to support or support a hypothesis. This study did not test whether anxiety or mental health concerns were the cause of long-haul Covid symptoms, so we can't draw any scientifically supported conclusions about the syndrome being all "in your head." This study did not evlauate the "realness" of post-Covid symptoms, only some possible causal factors.
Some medical professionals believe that mast cell activation syndrome (MCAS) and/or postural orthostatic tachycardia syndrome (POTS), a dysautonomia, may be the cause of long-haul Covid symptoms. As far as I can tell from a keyword search of the article, none of the diagnostic blood or urine markers for MCAS were tested in this study. Nor were study participants subjected to a tilt table test, the diagnostic standard for POTS. As well, the possible causes of dysautonomia, like an imbalance the renin-angiostensin-aldosterone system were not tested in this study. It is a great start, and I it is good that we have this research, but it still leaves more questions than answers when it comes to post-Covid symptoms.
Anonymous wrote:This is an important study and jumping off point for long-haul Covid issues. If you've taken a research methods class, you know that one can only fail to support or support a hypothesis. This study did not test whether anxiety or mental health concerns were the cause of long-haul Covid symptoms, so we can't draw any scientifically supported conclusions about the syndrome being all "in your head." This study did not evlauate the "realness" of post-Covid symptoms, only some possible causal factors.
Some medical professionals believe that mast cell activation syndrome (MCAS) and/or postural orthostatic tachycardia syndrome (POTS), a dysautonomia, may be the cause of long-haul Covid symptoms. As far as I can tell from a keyword search of the article, none of the diagnostic blood or urine markers for MCAS were tested in this study. Nor were study participants subjected to a tilt table test, the diagnostic standard for POTS. As well, the possible causes of dysautonomia, like an imbalance the renin-angiostensin-aldosterone system were not tested in this study. It is a great start, and I it is good that we have this research, but it still leaves more questions than answers when it comes to post-Covid symptoms.
Anonymous wrote:Anonymous wrote:Anonymous wrote:yup its the new fibromialga
Ugh. My dh has new anxiety/panic after covid. He literally never had any anxiety history until he was sick with covid. I lost my taste and smell for 3 weeks. They came back, but I experience a phantom smell of sewage and burning rubber, intermittently. It has been 2 months since we were sick. I'm not thinking of it as "long covid", but, it's not nothing, ya know?
The onset of his anxiety post Covid may just be a coincidence. There is no proof that the virus caused the anxiety.
Anonymous wrote:Anonymous wrote:Anonymous wrote:How do you explain my cardiac issues that are very clearly seen via MRI and echocardiogram? And no, they weren’t there previously. I am in my 30s, incredibly fit, was running 35-40 miles per week before I got sick (this was pre-vaccine; first wave). Literally couldn’t breathe even though my lung capacity is usually off the charts. I needed inhalers for the first time in my life and even those didn’t work super well. Ekg and blood work showed many abnormalities. I was declared disabled for 1.5 years because I had medical evidence of my persistent illness. These are all very objective measures. Nothing psychosomatic about it.
I think what you are describing is quite different from “brain fog”, “fatigue”, “lingering cough” and supposed “shortness of breath”.
I think it is important to sort out the above symptoms from physical conditions that occur as sequelae to Covid. These can include heart, lung or kidney impairments that are measurable through standard tests. I believe the latter do not belong in the category of long covid.
Anonymous wrote:Anonymous wrote:yup its the new fibromialga
Ugh. My dh has new anxiety/panic after covid. He literally never had any anxiety history until he was sick with covid. I lost my taste and smell for 3 weeks. They came back, but I experience a phantom smell of sewage and burning rubber, intermittently. It has been 2 months since we were sick. I'm not thinking of it as "long covid", but, it's not nothing, ya know?
Anonymous wrote:Anonymous wrote:yup its the new fibromialga
Ugh. My dh has new anxiety/panic after covid. He literally never had any anxiety history until he was sick with covid. I lost my taste and smell for 3 weeks. They came back, but I experience a phantom smell of sewage and burning rubber, intermittently. It has been 2 months since we were sick. I'm not thinking of it as "long covid", but, it's not nothing, ya know?
Anonymous wrote:Anonymous wrote:Anonymous wrote:How do you explain my cardiac issues that are very clearly seen via MRI and echocardiogram? And no, they weren’t there previously. I am in my 30s, incredibly fit, was running 35-40 miles per week before I got sick (this was pre-vaccine; first wave). Literally couldn’t breathe even though my lung capacity is usually off the charts. I needed inhalers for the first time in my life and even those didn’t work super well. Ekg and blood work showed many abnormalities. I was declared disabled for 1.5 years because I had medical evidence of my persistent illness. These are all very objective measures. Nothing psychosomatic about it.
I think what you are describing is quite different from “brain fog”, “fatigue”, “lingering cough” and supposed “shortness of breath”.
I think it is important to sort out the above symptoms from physical conditions that occur as sequelae to Covid. These can include heart, lung or kidney impairments that are measurable through standard tests. I believe the latter do not belong in the category of long covid.
Anonymous wrote:Anonymous wrote:How do you explain my cardiac issues that are very clearly seen via MRI and echocardiogram? And no, they weren’t there previously. I am in my 30s, incredibly fit, was running 35-40 miles per week before I got sick (this was pre-vaccine; first wave). Literally couldn’t breathe even though my lung capacity is usually off the charts. I needed inhalers for the first time in my life and even those didn’t work super well. Ekg and blood work showed many abnormalities. I was declared disabled for 1.5 years because I had medical evidence of my persistent illness. These are all very objective measures. Nothing psychosomatic about it.
I think what you are describing is quite different from “brain fog”, “fatigue”, “lingering cough” and supposed “shortness of breath”.
Anonymous wrote:How do you explain my cardiac issues that are very clearly seen via MRI and echocardiogram? And no, they weren’t there previously. I am in my 30s, incredibly fit, was running 35-40 miles per week before I got sick (this was pre-vaccine; first wave). Literally couldn’t breathe even though my lung capacity is usually off the charts. I needed inhalers for the first time in my life and even those didn’t work super well. Ekg and blood work showed many abnormalities. I was declared disabled for 1.5 years because I had medical evidence of my persistent illness. These are all very objective measures. Nothing psychosomatic about it.
Anonymous wrote:How do you explain my cardiac issues that are very clearly seen via MRI and echocardiogram? And no, they weren’t there previously. I am in my 30s, incredibly fit, was running 35-40 miles per week before I got sick (this was pre-vaccine; first wave). Literally couldn’t breathe even though my lung capacity is usually off the charts. I needed inhalers for the first time in my life and even those didn’t work super well. Ekg and blood work showed many abnormalities. I was declared disabled for 1.5 years because I had medical evidence of my persistent illness. These are all very objective measures. Nothing psychosomatic about it.