Anyone here has skin issues?
Hi everyone.
I would like to add a few more things about laboratory tests.
Some people recognize by their symptoms that what they have is an inflammation.
Also, that, in some cases, it is inflammation, is officially recognized. Just to give an example, they talk about inflammation (paragraph two):
The benefit of nonsteroidal anti-inflammatory drugs, of steroids, to so many people, proves that they are an inflammation, in so many cases.
Another medical article talks about related to inflammation biomarkers, that appear to be altered in some people, post vax:
https://www.ahajournals.org/doi/10.1161/circ.144.suppl_1.10712
But these markers are not common, they are used in universities, in research: IL-16, soluble Fas, hepatocyte growth factor (HGF).
That's why, I really wish to be understood, I am aware that misunderstandings can occur:
I understand that you, Dee, have done a number of investigations and would like to repeat some or make new ones, in particular the inflammatory tests. I'm not saying don't do them.
This is good and useful, anyway, even if it all comes out normal, but my point is that this can be done by those who do the tests through the insurance system.
To do a large number of investigations, on your own, when there is a high chance that it will indicate nothing, this is only for those who have good economic resources.
This aspect, the financial one, is important, especially now.
Everyone must evaluate how much they can dedicate for tests, given that many say that many investigations have shown nothing. And everyone must think that the most important thing is to have the economic resources for treatment. Depending on the severity of the symptoms, as many already say, some people were no longer able to work, to be financially insured.
It is a very tonic idea that the symptoms gradually reduce and disappear, hopefully this is the case for everyone.
But because there are people who say they have not recovered, it is wiser to consider a good organization of financial resources.
It's up to you, Dee, to decide. This, allways. Ans it is true, some inflammatory markers may not be expensive.
The most commonly used in practice are erythrocyte sedimentation rate, C-reactive protein, white blood cell count and differential.
Among rheumatological tests, it makes anway sense to be controlled anti-CCP.
I really hope I can be understood correctly.
Best wishes!
Hi everyone.
I would like to add a few more things about laboratory tests.
Some people recognize by their symptoms that what they have is an inflammation.
Also, that, in some cases, it is inflammation, is officially recognized. Just to give an example, they talk about inflammation (paragraph two):
The benefit of nonsteroidal anti-inflammatory drugs, of steroids, to so many people, proves that they are an inflammation, in so many cases.
Another medical article talks about related to inflammation biomarkers, that appear to be altered in some people, post vax:
https://www.ahajournals.org/doi/10.1161/circ.144.suppl_1.10712
But these markers are not common, they are used in universities, in research: IL-16, soluble Fas, hepatocyte growth factor (HGF).
That's why, I really wish to be understood, I am aware that misunderstandings can occur:
I understand that you, Dee, have done a number of investigations and would like to repeat some or make new ones, in particular the inflammatory tests. I'm not saying don't do them.
This is good and useful, anyway, even if it all comes out normal, but my point is that this can be done by those who do the tests through the insurance system.
To do a large number of investigations, on your own, when there is a high chance that it will indicate nothing, this is only for those who have good economic resources.
This aspect, the financial one, is important, especially now.
Everyone must evaluate how much they can dedicate for tests, given that many say that many investigations have shown nothing. And everyone must think that the most important thing is to have the economic resources for treatment. Depending on the severity of the symptoms, as many already say, some people were no longer able to work, to be financially insured.
It is a very tonic idea that the symptoms gradually reduce and disappear, hopefully this is the case for everyone.
But because there are people who say they have not recovered, it is wiser to consider a good organization of financial resources.
It's up to you, Dee, to decide. This, allways. Ans it is true, some inflammatory markers may not be expensive.
The most commonly used in practice are erythrocyte sedimentation rate, C-reactive protein, white blood cell count and differential.
Among rheumatological tests, it makes anway sense to be controlled anti-CCP.
I really hope I can be understood correctly.
Best wishes!
I get what you're saying but it's just a very frustrating stage where you don't know what to do and how to het back to your previous life.
Also how do you know so much about these? It's very informative! Have you been injured too from the vaccine?
Hi everyone.
I would like to add a few more things about laboratory tests.
Some people recognize by their symptoms that what they have is an inflammation.
Also, that, in some cases, it is inflammation, is officially recognized. Just to give an example, they talk about inflammation (paragraph two):
The benefit of nonsteroidal anti-inflammatory drugs, of steroids, to so many people, proves that they are an inflammation, in so many cases.
Another medical article talks about related to inflammation biomarkers, that appear to be altered in some people, post vax:
https://www.ahajournals.org/doi/10.1161/circ.144.suppl_1.10712
But these markers are not common, they are used in universities, in research: IL-16, soluble Fas, hepatocyte growth factor (HGF).
That's why, I really wish to be understood, I am aware that misunderstandings can occur:
I understand that you, Dee, have done a number of investigations and would like to repeat some or make new ones, in particular the inflammatory tests. I'm not saying don't do them.
This is good and useful, anyway, even if it all comes out normal, but my point is that this can be done by those who do the tests through the insurance system.
To do a large number of investigations, on your own, when there is a high chance that it will indicate nothing, this is only for those who have good economic resources.
This aspect, the financial one, is important, especially now.
Everyone must evaluate how much they can dedicate for tests, given that many say that many investigations have shown nothing. And everyone must think that the most important thing is to have the economic resources for treatment. Depending on the severity of the symptoms, as many already say, some people were no longer able to work, to be financially insured.
It is a very tonic idea that the symptoms gradually reduce and disappear, hopefully this is the case for everyone.
But because there are people who say they have not recovered, it is wiser to consider a good organization of financial resources.
It's up to you, Dee, to decide. This, allways. Ans it is true, some inflammatory markers may not be expensive.
The most commonly used in practice are erythrocyte sedimentation rate, C-reactive protein, white blood cell count and differential.
Among rheumatological tests, it makes anway sense to be controlled anti-CCP.
I really hope I can be understood correctly.
Best wishes!
I get what you're saying but it's just a very frustrating stage where you don't know what to do and how to het back to your previous life.
Also how do you know so much about these? It's very informative! Have you been injured too from the vaccine?
I'm a woman with Lyme disease. I found out this diagnosis after a whole year of medical investigations. A serious form of the disease.
From 2019 to the middle of 2021 it was very hard for me.
When covid disease appeared, at the beginning of 2020, I personally could not think about it. I was extremely ill, anyway.
In fact, I remember saying it jokingly: “I would kiss the Chinese! I would like to find the Chinese!”. I mean, to get the covid disease and thus die. And in this way to get rid of all the torment I suffered, due to Lyme disease.
I was joking, but there was something serious about it. It seems more desirable to die than to experience pain for months and years.
I couldn't work anymore.
I did not take the jab.
I've been following this forum since I discovered it, last summer. I also read from other forums.
Problems with vax are actually a problem for everyone, since anyone in the future may have to take it.
I'm so sorry for all those affected by vax.
It could be anyone's problem, anyway.
And I think everyone is to blame, because there is such a thing: people who are not treated, even though they are sometimes very suffering.
Human it is that everyone come to your aid!
What I would like to say is that in the case of side effects in vax, if doctors do not help, the only solution is the traditional medicine.
Of course, it should be clear that the means of traditional medicine can have intense effects, as well as unwanted effects. So caution is needed.
Another aspect is that the responsibility to follow natural treatments, is of the one who uses it, when the treatment is not followed under the prescription of a naturopatic specialist.
So whoever takes the remedies he reads on the internet, must be aware that the responsibility is his alone.
The reason I wanted to post is to let you know that for Lyme disease there is a long experience, of many people, in using natural remedies and over-the-counter medications.
It is not easy to take long-term treatments, so the experience of some who have already been taking various remedies for a long time, is good to be known.
There is information about the tolerance of different products, about the effectiveness and even the prices.
And what is essential, in what I mean, is that the naturopathic treatment of Lyme disease, including various diets and remedies, and which has already accumulated much knowledge, provides a model for a therapeutic approach to a systemic, chronic, inflammatory disease, which mainly affects the nervous system, heart and joints.
I hope that everyone will take only the good part of all this and be helped!
@black21 hello. Are you still experiencing the irritable bowel issue? Or can you explain what was happening?
Hi everyone.
I would like to add a few more things about laboratory tests.
Some people recognize by their symptoms that what they have is an inflammation.
Also, that, in some cases, it is inflammation, is officially recognized. Just to give an example, they talk about inflammation (paragraph two):
The benefit of nonsteroidal anti-inflammatory drugs, of steroids, to so many people, proves that they are an inflammation, in so many cases.
Another medical article talks about related to inflammation biomarkers, that appear to be altered in some people, post vax:
https://www.ahajournals.org/doi/10.1161/circ.144.suppl_1.10712
But these markers are not common, they are used in universities, in research: IL-16, soluble Fas, hepatocyte growth factor (HGF).
That's why, I really wish to be understood, I am aware that misunderstandings can occur:
I understand that you, Dee, have done a number of investigations and would like to repeat some or make new ones, in particular the inflammatory tests. I'm not saying don't do them.
This is good and useful, anyway, even if it all comes out normal, but my point is that this can be done by those who do the tests through the insurance system.
To do a large number of investigations, on your own, when there is a high chance that it will indicate nothing, this is only for those who have good economic resources.
This aspect, the financial one, is important, especially now.
Everyone must evaluate how much they can dedicate for tests, given that many say that many investigations have shown nothing. And everyone must think that the most important thing is to have the economic resources for treatment. Depending on the severity of the symptoms, as many already say, some people were no longer able to work, to be financially insured.
It is a very tonic idea that the symptoms gradually reduce and disappear, hopefully this is the case for everyone.
But because there are people who say they have not recovered, it is wiser to consider a good organization of financial resources.
It's up to you, Dee, to decide. This, allways. Ans it is true, some inflammatory markers may not be expensive.
The most commonly used in practice are erythrocyte sedimentation rate, C-reactive protein, white blood cell count and differential.
Among rheumatological tests, it makes anway sense to be controlled anti-CCP.
I really hope I can be understood correctly.
Best wishes!
I get what you're saying but it's just a very frustrating stage where you don't know what to do and how to het back to your previous life.
Also how do you know so much about these? It's very informative! Have you been injured too from the vaccine?
I'm a woman with Lyme disease. I found out this diagnosis after a whole year of medical investigations. A serious form of the disease.
From 2019 to the middle of 2021 it was very hard for me.
When covid disease appeared, at the beginning of 2020, I personally could not think about it. I was extremely ill, anyway.In fact, I remember saying it jokingly: “I would kiss the Chinese! I would like to find the Chinese!”. I mean, to get the covid disease and thus die. And in this way to get rid of all the torment I suffered, due to Lyme disease.
I was joking, but there was something serious about it. It seems more desirable to die than to experience pain for months and years.
I couldn't work anymore.
I did not take the jab.
I've been following this forum since I discovered it, last summer. I also read from other forums.
Problems with vax are actually a problem for everyone, since anyone in the future may have to take it.
I'm so sorry for all those affected by vax.
It could be anyone's problem, anyway.
And I think everyone is to blame, because there is such a thing: people who are not treated, even though they are sometimes very suffering.
Human it is that everyone come to your aid!
I'm sorry! I know how it must feel now that even I'm suffering from this nameless shit.
How are you managing with it? I don't know much about Lyme disease but has it gotten better?
At the moment even I'm suicidal so I don't have much to say on it.
@maxx126 Any change? Any help/Our 48 year old son is in his 10th month of suffering, which began 2 wks after 2nd Pfizer shot.NOTHING has helped so far..
Hi folks! Been on this forum for a while, and really appreciate the opportunity to read in so much detail about what everyone's been dealing with (It's a safe haven in a world that truly hasn't acknowledged what we're all going through here). I wish you all well and hope that you find some relief from these awful side effects. Has anyone had the booster shot yet? If so, what has the experience been like? What kind of symptoms have you been having? How long did they last? Did you switch your vaccine type? If so, how? Did this have any change in the side effects following?
For some context: I got 2 shots of the Pfizer in late May and late July last year, had 24/7 dizziness, rocking, swaying for 2-3 months post each of the vaccines. Extremely debilitating and scary, but it did eventually fade away. Still not at 100% though (I'm close to totally normal most days but it'll flare up from time to time).
I had my booster about 36 hours ago. I originally had J&J, and then a moderna some time later (too soon as it turns out). I had really bad vertigo for a few months and ongoing vertigo since then, but not as bad. I would say I was back to maybe 85% before the booster. The reason I got it is my vaccine passport will basically expire if I don’t have my last shot within 9 months, and I don’t want to be stuck at home in the summer. I figured if I was going to have side effects I’d rather deal with them during winter.
They gave me the moderna booster, which is 0.25ml. Other than a sore arm, I so far feel fine. Also strangely today I went for a walk and didn’t have any vertigo. It’s too soon to tell but I was wondering (and I asked this on here previously), if anyone had remission of their symptoms after another shot. Long COVID sufferers sometimes have remission after a vaccine. It’s too soon to tell but I felt pretty good all around today, other than my sore arm.
I’ll post an update in a few more days. It wasn’t until day 6 after my shot in July that I felt pretty bad, so I’ll wait a bit more with this one. But so far it’s been a non event, thankfully.
Hello everyone, I have read the latest publications and I have realized that many people talk about static in their body, it seems curious to me because lately I have felt a current in the left arm of the vaccine and that some people tried the "clinoptilolite zeolite" , Someone has tried? Did it work for them?
Anyone here has skin issues?
I have a rash on my forearms and legs and a couple on my cheeks...It looks like freckles...went to my GP and she said maybe it's eczema and gave me a topical steroid cream...it's not eczema...it's not really itchy...I am now going to be getting an appointment with an allergist...
Hi! I haven’t posted on this forum in about 3 weeks and I wanted to check in and also spread some good news. January is my 5th month dealing with this bullshit but it definitely has been my best month!
The peak of my symptoms started last month but I have been dealing with them since september. Before I felt like a completely different person and now I just feel like a sick version of me. I can think better, can write my poetry again and even some days get back into my sewing. There are still some days where it feels like i’m slipping but it goes away quickly. ALL OF MY SYMPTOMS HAVE SUBSIDED TREMENDOUSLY!!!!! I remember reading posts on this forum of people talking about feeling better and always wondered when was I going to get here! And here i am, I have days where i feel 100% fine and then two days later i’d go back to 60%. But it shows that there is improvement!!!
I haven’t changed anything that i have been doing other than cutting down on fruits & not eating spinach much. I was eating strawberries, blueberries, bananas and black berries before but just stopped randomly. I modulated the spinach because it aids in histamine released but it’s good for the brain cells, b12 and gluthiamone.
But I have been eating and drinking the same things consistently; chicken, black beans, white rice, ginger tea, nettle tea, tumeric, 2 red apples a day, cayenne (every now & then) thyme, parsley, italian seasoning, brococli, red onions, peppers (modulated bc makes me have palpitations).
I also don’t take any vitamins at all. But i have been contemplating on bringing vitamin C and D back into my routine since my body has relaxed some.
I wanted to spread some good news for people who are still at their peak or just now having these symptoms and are confused and scared. It will definitely get better, i promise you! Take the time to search positive terms on here to find success stories and things that work.
Has anyone tried Eastern White Pine Needle Tea? I am told the shikimic acid can help.
Searching for other Cov-vax side effects forums, I came across a page where it's mentioned that Facebook removed the side effects pages with hundreds of thoudands of users. No wonder I couldn't find anything.
Lost for words...!! I'm not into conspiracy theories etc, but I am starting to get the unconfortable feeling that there's something seriously rotten in the state of Denmark!!