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    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

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Exclusive care for complex pain and fatigue disorders

SWAlexander

Senior Member
Messages
1,944
Bragée Clinics is proud to introduce our international clinic catering to patients with complex conditions such as Post-Covid, ME/CFS, Dysautonomia, and severe chronic pain.

With a team of over 100 professionals, including top-notch specialist doctors, our state-of-the-art facility is located in the heart of Stockholm. While we currently serve patients from all across Sweden, we are excited to extend our services to patients from the United States and beyond. Our highly skilled specialist doctors provide comprehensive diagnostic evaluations and treatments, both in-person and remotely. For those seeking advanced diagnostic procedures or treatments, we offer nearby accommodation options.

You can access our services either through your insurance provider or as a private-pay patient, with no waiting times.

Equipped with cutting-edge diagnostic equipment, such as radiologist-guided ultrasound examinations, sensitivity labs, and access to university hospital-based laboratories, we offer the latest evaluated techniques and methods for treatments.

We have established strong partnerships with surgical units and nearby rehabilitation facilities to ensure seamless care for our patients.

If you're interested, please fill out the form below to express your interest.
https://www.bragee.se/international-clinic-stockholm
 

SWAlexander

Senior Member
Messages
1,944
This and for many other reasons regarding medical incompetence, I have sent out a Google translation of "Osler's Web" review to my primary, who told me this morning that neither "Parsonage-Turner Syndrome" nor ME/CFS is a real illness.

What has changed for ME/CFS patients since Hillary Johnson´s book “Osler's Web” was published in 1996? NOTHING and NOTHING at all.
 

ruben

Senior Member
Messages
296
Just where does all this fit in with that article in "The Times" recently saying doctors must concede this isn't a mental thing?
 

lenora

Senior Member
Messages
4,926
As I recall 'Osler's Web' was a really good book. A lot of research went into it. I still have it somewhere in what passes for our library.

We have made some progress with pain, but it seems we're heading backwards in doctors actually thinking there is something wrong with us.

I really don't have a clue about what is wrong....in my case, it seems to be one layer on top of another. Mind you, I'm 76 so perhaps that's to be expected. COVID hasn't exactly helped and I still keep thinking that I'm just lazy. I now have something else going on and I can only hope the neurologist I'll be seeing in about 2 wks. will actually take me seriously. Who knows? But I'll keep everyone informed. Yours, Lenora