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  1. 5 giorni fa · Chi c'è in linea. I nostri utenti hanno inviato un totale di 748264 messaggi. Abbiamo 886 utenti registrati. L'ultimo utente registrato è Simo57. In totale ci sono 71 utenti in linea :: 1 Registrato, 1 Nascosto e 69 Ospiti [ Amministratore ] [ Moderatore ] Il massimo numero di utenti in linea è stato 399 il Ven Apr 26, 2024 12:02 am.

  2. 16 giu 2024 · Discuss the various forms of orthostatic intolerance (OI) found in ME/CFS, including orthostatic hypotension (OH) and postural orthostatic tachycardia syndrome (POTS). (Other symptoms of dysautonomia are discussed in the "Dysautonomia: Cardiovascular, Respiratory, etc." forum.)

  3. www.fibromyalgiaforums.org › communityFibromyalgia Forum

    1 giorno fa · Fibromyalgia forum is a support group community that provides help to people affected by fibromyalgia, chronic fatigue syndrome, and chronic pain.

  4. 5 giu 2024 · A place to discuss treatments for ME/CFS and related conditions, excluding psychosomatic treatments.

  5. As someone who identifies with an ME/CFS type long covid, I have been letting this get to me. It's a terrifying thought to be doomed to this condition forever. My heart is broken every time I read some of your stories, especially those dealing with some serious mental health issues.

  6. 19 giu 2024 · Dysautonomia in its classical sense is not just a clinical syndrome. POTS is meant to be diagnosed based on subjective and objective features but there remain questions as to the relevance of the objective measures being used. And the "30-100%" estimate just tells you that we have no reliable prevalence data.

  7. 23 giu 2024 · This forum is for your chronic pain related questions and symptoms for CFS and fibromyalgia.