Thank you very much for telling Diane's story. There is so much that needs to be said about EHS and electrosmog symptoms. I have written a great many articles and will continue to do so. This is just the latest: https://francesleader.substack.com/p/sudden-deaths-by-parasites
Thank you, Frances. I've seen a bit about this angle and have been meaning to dig deeper. My husband and I are Chinese medicine practitioners, so we've been following the impacts of EMFs for a while now. Ross (my husband) specializes in Chinese pulse diagnosis and has been noting the impact of EMF's via the pulse for many years. But we haven't really explored the link to parasites. It feels important now, given what we're seeing...
I am a retired Barefoot Doctor of TCM. I have been raising the alarm about the impact of electro-magnetic radiation since 2016 when I was asked to investigate the subject by fellow activists.
Since then I have churned out a huge amount of research and articles, been de-platformed from every major social media for my efforts, and find myself side-lined here in the Substack Ghetto aka The Naughty Step.
Frances, your work is so thorough and unique, which is why I subscribe. I have meant to ask you: do you know of a resource for EMF injury? Is there a specific professional association(s), hospital, clinic, group, or private practice that specializes in EMF diagnosis and treatment?
I wish I could help everyone everyone because when I read these stories, I literally stop at the part where the patient is unable to get a diagnosis. If you can't get a diagnosis, you can't get treatment. And that means you can die. That's not right. I know that I can help. I promise you we shall make this condition better.
When I got POTS 18 years ago, not one doctor had heard about it. After being bedridden for 12 years and losing everything the world holds dear, I got my miracle from God and rose out of bed to fight for medical freedom. I learned how to fight.
I wrote The Rebel Patient: Diagnosis and Treatment because I had to fight for my life. For example, people can use medical insurance for what they need and want. They have to learn "How to Be a 'Professional Patient'" I will have to write on this, and more.
In the UK we have only one form of medical insurance for the vast majority of us, the National Health Service. It is abysmally establishment and so slow to learn new diagnosis techniques and therapies that many of us are turning away and resorting to folk medicine and old remedies that our grannies would have used a hundred years ago.
The whole idea that electro-magnetic radiation is a health hazard is completely denied and so more and more 5G towers are blighting our lives without a shred of opposition. Did you know that the only grounds we are permitted to use in objection is aesthetics? If it looks an eyesore, and we complain the companies make the damn things look like trees or sculptures. We are expressly FORBIDDEN to object on the grounds of health!
Because of this, to dare to suggest that people are sickening and dying because of these monstrosities, is laying ourselves open to abuse and even accusations of insanity.
As a result there are no efforts being made to identify which sick people really should be diagnosed as EHS sufferers!
Personally, I would go as far as to say that anyone who has been diagnosed with Covid19 or even a vaccine injury is potentially a victim of electromagnetic radiation overload and until that possibility is eradicated it will remain a suspicion for me.
My research has suggested that people have been getting very sick from wireless telecommunications for at least a decade and each generation of technological advance is compounding the issue further and further.
We have no representation. We have no voices in the media. Those of us who were putting two and two together at the beginning of 2020 have been heavily censored and de-platformed under the label of 'conspiracy theorist' and purveyor of disinformation.
As you can tell - I am beyond angry about this. But I have no choice. I have to keep bashing at this taboo because my own health has been decimated since 2016 and the only relief I have ever discovered has been to dress in EMF Protective clothing 24/7!
We are left to fend for ourselves, and in that effort, we build community. My website has a drop down menu for EMF Protection, and I believe you are right that for those with "Long COVID" or "post-vaccine injury", there is a need to first look not only at electromagnetic hypersensitivity (EHS) but MCS, Multiple Chemical Sensitivities, which may present earlier than EHS. I will be developing more on this subject next week. Thank you. I support you 100%. (https://arandaMDenterprises.com)
A VERY needed article! Starting a few years ago, any time I was startled, I felt a jolt of electricity go through my body. It was quick, but painful, like electrocuting yourself on an outlet. I didn’t know what it was until recently. Everything from earbud usage, to screens, to Bluetooth devices, to a smart meter that was installed has contributed to the issue. Agonizing!
I have asked my endocrinologist (Hashimotos for 15yrs) if this would be a symptom of my autoimmune, but he had no ideas. Recently, I began the Pompa Detox Program. During my first conversation with the Program’s functional nutritionalist, I mentioned this sensation to her. She immediately nodded knowingly and said explained the way the radiation around us effects each of us differently. Since I am still new to this, I don’t have any tried and true strategies to recommend, but I’m starting with things that would be calming to my immune system/adrenal glands - yoga, breathing exercises, LED light therapy for inflammation, nootropics, and 15 min of daylight a day.
What a most wonderful and important article, thank you for all your work. I will help collect information on symptoms, getting a diagnosis, and then getting the needed treatment. It shouldn't be that hard.
So much appreciate all of us getting together to help get this situation under control. For goodness sake, they trained us how to think about a problem, collect information, look for commonalities, try different tests, and finally implement a variety of stepwise therapies - to come up with a plan that works.
For someone to gather this type of effort together, we would need to have everyone involved as a research participant in a trial.
Thank you very much for telling Diane's story. There is so much that needs to be said about EHS and electrosmog symptoms. I have written a great many articles and will continue to do so. This is just the latest: https://francesleader.substack.com/p/sudden-deaths-by-parasites
Thank you, Frances. I've seen a bit about this angle and have been meaning to dig deeper. My husband and I are Chinese medicine practitioners, so we've been following the impacts of EMFs for a while now. Ross (my husband) specializes in Chinese pulse diagnosis and has been noting the impact of EMF's via the pulse for many years. But we haven't really explored the link to parasites. It feels important now, given what we're seeing...
https://rossrosen.substack.com/p/emf-exposure-and-fragility
I am a retired Barefoot Doctor of TCM. I have been raising the alarm about the impact of electro-magnetic radiation since 2016 when I was asked to investigate the subject by fellow activists.
Since then I have churned out a huge amount of research and articles, been de-platformed from every major social media for my efforts, and find myself side-lined here in the Substack Ghetto aka The Naughty Step.
You can find my archive of research here:
https://francesleader.substack.com/p/all-my-substack-articles-on-emfc19
My latest rage is here:
https://francesleader.substack.com/p/a-diagnostic-taboo-which-is-killing
Thank you for your work and your voice, Frances. I look forward to checking it out.
Frances, your work is so thorough and unique, which is why I subscribe. I have meant to ask you: do you know of a resource for EMF injury? Is there a specific professional association(s), hospital, clinic, group, or private practice that specializes in EMF diagnosis and treatment?
I wish I could help everyone everyone because when I read these stories, I literally stop at the part where the patient is unable to get a diagnosis. If you can't get a diagnosis, you can't get treatment. And that means you can die. That's not right. I know that I can help. I promise you we shall make this condition better.
When I got POTS 18 years ago, not one doctor had heard about it. After being bedridden for 12 years and losing everything the world holds dear, I got my miracle from God and rose out of bed to fight for medical freedom. I learned how to fight.
I wrote The Rebel Patient: Diagnosis and Treatment because I had to fight for my life. For example, people can use medical insurance for what they need and want. They have to learn "How to Be a 'Professional Patient'" I will have to write on this, and more.
Regarding POTS, you might want to take a look at this: https://acupunctureandherbalmedicine.com/pots-diagnosing-treating-postural-orthostatic-tachycardia-syndrome-as-a-sequela-to-covid-19/
I've been seeing this in my office for a very long time, and it has been exploding over the past few years.
In the UK we have only one form of medical insurance for the vast majority of us, the National Health Service. It is abysmally establishment and so slow to learn new diagnosis techniques and therapies that many of us are turning away and resorting to folk medicine and old remedies that our grannies would have used a hundred years ago.
The whole idea that electro-magnetic radiation is a health hazard is completely denied and so more and more 5G towers are blighting our lives without a shred of opposition. Did you know that the only grounds we are permitted to use in objection is aesthetics? If it looks an eyesore, and we complain the companies make the damn things look like trees or sculptures. We are expressly FORBIDDEN to object on the grounds of health!
Because of this, to dare to suggest that people are sickening and dying because of these monstrosities, is laying ourselves open to abuse and even accusations of insanity.
As a result there are no efforts being made to identify which sick people really should be diagnosed as EHS sufferers!
Personally, I would go as far as to say that anyone who has been diagnosed with Covid19 or even a vaccine injury is potentially a victim of electromagnetic radiation overload and until that possibility is eradicated it will remain a suspicion for me.
My research has suggested that people have been getting very sick from wireless telecommunications for at least a decade and each generation of technological advance is compounding the issue further and further.
We have no representation. We have no voices in the media. Those of us who were putting two and two together at the beginning of 2020 have been heavily censored and de-platformed under the label of 'conspiracy theorist' and purveyor of disinformation.
As you can tell - I am beyond angry about this. But I have no choice. I have to keep bashing at this taboo because my own health has been decimated since 2016 and the only relief I have ever discovered has been to dress in EMF Protective clothing 24/7!
We are left to fend for ourselves, and in that effort, we build community. My website has a drop down menu for EMF Protection, and I believe you are right that for those with "Long COVID" or "post-vaccine injury", there is a need to first look not only at electromagnetic hypersensitivity (EHS) but MCS, Multiple Chemical Sensitivities, which may present earlier than EHS. I will be developing more on this subject next week. Thank you. I support you 100%. (https://arandaMDenterprises.com)
A VERY needed article! Starting a few years ago, any time I was startled, I felt a jolt of electricity go through my body. It was quick, but painful, like electrocuting yourself on an outlet. I didn’t know what it was until recently. Everything from earbud usage, to screens, to Bluetooth devices, to a smart meter that was installed has contributed to the issue. Agonizing!
Thank you for sharing. It’s amazing how many people are impacted by emr and don’t realize it. Have you found any helpful tools?
I have asked my endocrinologist (Hashimotos for 15yrs) if this would be a symptom of my autoimmune, but he had no ideas. Recently, I began the Pompa Detox Program. During my first conversation with the Program’s functional nutritionalist, I mentioned this sensation to her. She immediately nodded knowingly and said explained the way the radiation around us effects each of us differently. Since I am still new to this, I don’t have any tried and true strategies to recommend, but I’m starting with things that would be calming to my immune system/adrenal glands - yoga, breathing exercises, LED light therapy for inflammation, nootropics, and 15 min of daylight a day.
Thank you. Sounds like you’re working off some good instincts.
What a most wonderful and important article, thank you for all your work. I will help collect information on symptoms, getting a diagnosis, and then getting the needed treatment. It shouldn't be that hard.
So much appreciate all of us getting together to help get this situation under control. For goodness sake, they trained us how to think about a problem, collect information, look for commonalities, try different tests, and finally implement a variety of stepwise therapies - to come up with a plan that works.
For someone to gather this type of effort together, we would need to have everyone involved as a research participant in a trial.
Thank you for your kind words. Yes, we will need to work together to create a better understanding of this problem as well as better solutions.
Meanwhile, the continue to rollout this toxic program. I really feel for these kids.
https://anntomokorosen.substack.com/p/t-mobile-defends-its-right-to-ignore
Very sad, indeed! There needs to be more protection for our children!