FIBROMYALGIA SYNDROME is Not a Fashionable Label


Stop telling people that you “think” Fibromyalgia is a symptom of something, or a “catch-all” label for something that can’t be otherwise identified.  If you are a public speaker, or have any kind of a public following, you are not helping us by doing that.  If you are not a physician educated on the topic, or a patient living with this SYNDROME, just stop.  It has taken many, many years, and a lot of blood, sweat, and tears, to finally be taken seriously by the medical community and even a portion of the public, and it is a very definite individual diagnosis even qualifying as a stand-alone application for disability!  Quit trying to drag us backwards.

Educating yourself on this topic is not all that difficult these days.  This is not about conjecture and philosophizing about the causes of it.  You can speculate all day long about why you think it happens to *some* people but that does not make it any less legitimate, nor does it invalidate the diagnosis and make something unworthy of proper medical recognition.  It is a neurological condition.  Some choose to use medication to manage it, and some of us choose to stick with natural means, but it does require management and treatment either way.

When someone with a public following makes a proclamation that they think something like FMS is some kind of emotional issue, it only makes life more difficult for those of us trying to manage it in our lives.  You are validating completely uneducated and critical friends and family of ours and creating more problems that we don’t need.  Do us a favor and just don’t try to speak on the topic if you can’t be bothered to catch up with current info.  I am not advocating for anyone to not deal with emotional damage if they have it.  Please just do not label Fibromyalgia as being solely an outcropping from something like that.  The two issues are distinctly individual, and can exist independent of the other.  Even if some traumatic event was the trigger that set it in motion, mending emotional pain is not a guarantee to end the manifestation of the syndrome.  It shows up quite often in autoimmune patients for a reason.  Nobody has figured that out yet but it IS on the suspected list for being autoimmune itself.  Stop making our work harder for us.

T

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About Tala

-Livestream Broadcaster - Active in Periscope & Busker -YouTube, Twitter, Instagram, & Facebook Pages www.talanoexcuses.live Advocacy for better quality of life with catastrophic illness & injury. Conditions I live with myself are my awareness platform: rheumatic autoimmune & neurological, women's heart disease Traditional First Nations (Native American) -Training: Tai Ch'i Chuan, medical terminology, cultural Medicine -Avid about hiking, camping, & outdoor adventure Special Interests: Natural health, everything from East Indian to East Carolina cuisine, 16th Century German fencing Favorite Travel Spots: Yosemite, Catalina Island, E. North Carolina, Northern CA redwoods/coastal rainforest ~I live as naturally as I can, stay on a whole foods diet (as in what I eat, not as in "a diet"), avoid as many synthetic meds as I can, and do not consume artificial sweeteners and most preservatives. If you're curious about why, see my posts.~ Periscope/Twitter ID: Tala_NoExcuses https://badges.wegohealth.com/ha-awards-2016.js?referrer=Owb2x2Nb8L81mhJHyfwGcg

Posted on March 24, 2016, in General Blather, I Am That Wolf, Things That Make You Go... AAAaaaauuuggghhh!!! and tagged , , , , , , , . Bookmark the permalink. 1 Comment.

  1. Barbara Marincel

    AMEN!!

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