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Chronic Fatigue: Bemer vs iMRS vs Rife vs PERL m+

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Chronic Fatigue Syndrome
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Posted 5/27/2018 3:30 AM (GMT 0)
I have had CFS for 13 years, have tried diets, pills, everything I came across, no results.

Recently, I came across this new technology, but they all make claims theirs is the best.

Bemer, iMRS, Rife, PERL m+, and it seems there are countless others.

Any ideas how I can find out which really is the best?
Any proof of which one is best to cure CFS (caused by high stress, resulting probably in adrenal fatigue)


Also interested in helping my daughter's Lymes.

Have been taking ASEA as well. Any comments on this? I have had no results at ALL yet.

Tried iodine for a few months, no results.


Thanks so much!
Posted 7/31/2018 1:36 AM (GMT 0)
Hi Stella Maris and welcome~

If it were me I'd ask my regular doctor about these. I'll admit that I haven't heard of any of them so I went looking.

Bemer & Rife: "pulsed electromagnetic fields (PEMF) interact with the body to trigger beneficial changes." Seems the Bemer device and the Rife machine are tied together.

Perl m+:" We took the Rife machine… and gave it a PEMF twist. The PERL M+ is a non-contact, non-invasive research device that emits a Pulsed ElectroMagnetic Field, commonly referred to as PEMF. It creates an electrostatic charge at the deepest cellular level in the body with the ability to create optimal environment for beneficial change. The particular frequencies carried on the emission from the plasma tube not only target the problem area but help bring the entire body to a level of homeostasis – boosting the immune system, detoxing, repairing tissue, enhancing bone regeneration, strengthening the organs, increasing energy, reducing stress/inflammation and creating an ideal environment inside and outside of the body for optimal wellness."

This one sounds too good to be true IMHO. They say as long as you're within 30' of the machine it will do all of this.

IMRS: It replicates the natural magnetic field of the earth making it one of the most effective and tolerable systems out there.

Hope this may help you with your decision.
Warmly,
Chutz
Posted 7/31/2018 9:54 PM (GMT 0)
Thank you so much, Chutz, for taking the time out to research this for me.

If any one else has information on these topics, I would really appreciate their insights.

I have now come upon another PEMF device, the QRS. www.QCMedicine.com/qrs

They claim they are the first and best, with all the patents.
Each claim they are the best. It is hard to determine the facts from fiction.
Any one with knowledge on these, I would appreciate to hear their thoughts.
I asked my doctor, but they have no experience with these machines.

Thank you again, so much!
Posted 8/2/2018 2:25 AM (GMT 0)
Stella Maris, welcome to the forum. This is a very quiet forum but I have often hoped it would get more active. I am sorry you have CFS/ME it is a debilitating illness with no cure. I am sorry to say that but it is true. A lot of PWME find some relief of symptoms but no cure. Believe me if this technology cured PWME it would have gone through the forums like wildfire & everyone would be using it. I hope it gives you some symptom relief if you try it but please do not expect a cure. Acceptance is a big part of living with any illness & the stress of looking constantly for a way out is hard. I, too, tried everything that came my way but nothing helped, total disappointments. I am waiting for the legitimate research that is happening now, more then ever before. I do think a cure is coming & I just live my life, such as it is, until then. I hope you will find some relief, hugs, Denise
Posted 8/2/2018 5:48 PM (GMT 0)
Thank you , Denise! Unfortunately at this point I am almost bedridden, sleep most of the day, or am on the couch. I can't think or concentrate well. But I have 3 young children, so you see, any improvement is important I find, or I'm not sure what will happen to my children. Thank you for your comments, what you say is very true! I am so sorry you have this also, but it looks like you have learned how to manage it better than I! smile God bless you! Stella Maris
Posted 10/22/2018 4:11 AM (GMT 0)
Hey Stella just wanted to say with respect to ladybugdreams. It is absolutely false that there is no cure for it. Yes I understand the magnitude of that statement and the weight it carries. A bit of a double edged sword here... yes there is no cure for cfs in the cfs/me does not define the problem. You cannot solve an equation of you do not know the problem. The body never just decides to quit functioning properly outside of dna disease. So yes cfs is real but can be caused by ... to start with lymes, Candida, heavy metals, sibo, parasites, latent viruses, latent bacteria ig streph (pandas) root canals done the triational way, Mercury fillings. To just name a few these burden the body and slow down important metabolic and biological processes in the body thus impeding ultimately energy production.

So to say there is no cure is correct in your problem isn’t defined, a medical doctor ran test couldn’t find anything and gave you “chronic fatuigue syndrome” because they are out of answers (none of which the issues listed above can be tested for in a conventional doctors office) To say there is no cure for the way you feel is unbelievably irresponsible and haphazard. I have known and read countless litterly countless success stories and I and one of them (not out of the woods yet but much better) if you have any questions feel free

Stella Maris said...
Thank you , Denise! Unfortunately at this point I am almost bedridden, sleep most of the day, or am on the couch. I can't think or concentrate well. But I have 3 young children, so you see, any improvement is important I find, or I'm not sure what will happen to my children. Thank you for your comments, what you say is very true! I am so sorry you have this also, but it looks like you have learned how to manage it better than I! smile God bless you! Stella Maris

Posted 1/14/2019 11:13 PM (GMT 0)
One device that combines PEMF with rife and other technologies is the AmpCoil. It was developed by folks with Lyme, and treats a variety of chronic conditions including CFS/ME, Lyme and co-infections, and autoimmune conditions. It's very expensive, but after spending $12,000 per year to treat my chronic Lyme and ME for three years, the price seemed worth it, and financing is available. Folks all over the country will come to your home for a free demo if you are curious, and could talk to you on the phone about their experience. Additionally, there's someone who will allow you to rent a device for a monthly fee. According to the company, 90% of users feel a 90% reduction in symptoms in 90 days with standard use. Honestly I can't tell you personally whether it works because I have to go very slowly with treatments, but I can keep you apprised if you are interested, and I find it very promising! I know one practitioner who uses it in a holistic Lyme practice, and she tells me amazing stories of success with her patients. Out of hundreds, everyone has seen improvement with the AmpCoil if they used it for any length of time, many reportedly feeling entirely better.

You might also find the website of Dr. Bill Rawls helpful, rawlsmd.com. He offers free webinars and has lots of articles about CFS/ME, fibromyalgia, chronic Lyme, adrenal fatigue, and all the possible causes and treatments from a very grounded, realistic, holistic perspective.

An app and approach I also find promising is a chronic pain app called Curable. Go to their website for a demo and see if it resonates with you. It basically re-trains your neural pathways to stop your symptoms from continuing, and it's only $15 per month.

Many of us know the agony of being so sick for so long. People get better from this every day, but in all different ways. I hope that you find the thing that works for you!

Sara (Lyme, ME, POTS, HPA axis dysfunction)
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