Showing posts with label stigma. Show all posts
Showing posts with label stigma. Show all posts

Wednesday, February 11, 2015

What is in a Name?

Well the latest in the ME/CFS world is what to call it again?

But how important is a name?  My name is Jane, does that tell you what I am like, how I behave, what I look like?  My name means gracious, gift from god, I guess that would depend who you ask as to whether they think that is true.

Does the name of an illness have to describe what it is?  Cancer doesn't tell you what it is, or Diabetes.  Many illnesses are named after people Parkinson's or Huntington's.  Has anyone ever heard of Guillain Barre Syndrome or Diabetes Insipidus?  Not many, but they don't think less of it because they don't understand the name.

When people hear the word cancer their immediate reaction is that it is fatal, actually y not many people die from it these days, but I am sure that changing the name won't make any difference and the emphasis is on getting quick and effective treatments.

ME/CFS was first called Myalgic Encephalomyelitis, but got changed to Chronic Fatigue as no one knew what Myalgic Encephalomyelitis meant.  Some believe that ME and CFS are different illnesses as there is much more to ME that chronic fatigue.

Literally Myalgic Encephalomyelitis means

Myalgia - Muscle pain
Encephalomyelitis - Inflammation of the brain and or spinal cord.

But does that matter?  What is important is that it is a serious and debilitating condition that is not taken seriously.  The time that is wasted thinking of a suitable name takes away from developing diagnosis techniques and research into causes and treatments.  Whatever it is called it will never lose the stigma attached to being Chronic Fatigue or Yuppie Flu, it might get more respect if it was called We Don't Have A Clue Syndrome!

The proposed new name is SEID, Systemic Exertion Intolerance Disease, hmmmm what does that say, sounds like idleitis to me.  Someone did an internet search for SEID and the first thing that came up was 

Really helpful!  If he wants to come and do my chores though I will happily call it SEID!

Whatever the name is will never describe how the illness affects us and the symptoms we suffer.

How do you condense this into a name?
Headache
Dizziness
Poor co-ordination
Poor concentration
Confusion
Unable to walk far
Unable to stand very long
Tinnitus
Muscle pain
Joint pain
Stomach ache
Irritable bowel
Tender spots in back and shoulders
Weakness in arms and legs
Fatigue
Feeling cold
Sweating
Irritable bladder
Palpitations
Tingling in hands, feet, head and face
Sleep disturbance, Insomnia
Nausea
Bruise easily
Sore throat
Swollen lymph nodes
Food intolerances, gluten, fish, alcohol, sugar, dairy, yeast
Itchy skin
Itchy eyes
Mood swings
Nasal irritation
Restless
Earache
Intolerance to bright light
Intolerance to loud noise
Weight loss
Panic/ anxiety attacks
Visual disturbance
Painful tongue
Shaking
Stiffness in arms and legs
Mouth Ulcers
Adrenaline issues.

They are my symptoms, they vary day to day and some are more of an issue than others.  Not everyone has the same symptoms or the same severity.  It is unlikely that everyone classed as having ME, CFS, SEID all have the same thing.  How can someone who can go to work, walk and run a home have the same as me or someone who is totally confined to bed and needs all care?  It's so confusing, but changing the name won't help.

What is in a name? ME, CFS, SEID? I don't really care what it is called, it already has a stigma and will never lose that, more needs to be put into proper diagnostics and treatment instead of what to call it, why does the name need to say what it is, other illnesses don't and they are taken seriously.







Monday, May 12, 2014

ME awareness Day, week or whatever it is.

There have been a few articles and points of interest on facebook today.  I will share a few of them with you.  In the mind or in the brain? Scientific evidence for central sensitisation in chronic fatigue syndrome a study being carried out in Belgium. Chronic fatigue sufferers push for awareness a campaign in Australia.  Action for ME spread the word and awareness. ME matters a community page on facebook. The big sleep for ME a fundraising initiative.  An article from the Daily telegraph about a 16 year old who has written to her ME. A New Zealand article about stigma and ME. An article from Malta about lack of support in Britain.  There is also an article in the Nursing Times on this subject, but you have to register to read it. It is only a short article, but links to Action for ME campaign Time to Deliver.  Articles were published in Sheffield Star and Sheffield Telegraph about a local lady with ME and her experiences.

Final piece from facebook a photo campaign to fundraise called my two sides set up by Clare Stephanie Cartlidge

Here is a poem by Rosalynde Lemarchand 

Another poem from Sally@blogspot

I don't like to go on about ME I would rather focus on something else in my daily life, but felt today it needs to be highlighted.