International M.E. Awareness Day 2021

Today, 12th May (US May 12th) is International M.E. Awareness Day. In some countries Myalgic Encephalomyelitis (M.E.) is misnamed Chronic Fatigue Syndrome (C.F.S.).

There are three categories of suffering per N.I.C.E.: mild - a loss of 50% of function (what other condition is described as “mild” with a loss of half one’s previous abilities!), but many can still work (G-d knows how!); moderate - mostly house-bound and unable to work; severe - mostly bed-bound. However, the M.E. community is well aware of a fourth category, “very severe”, in which sufferers are mostly blindfolded, earplugged & drip-fed, unable to do anything, not even move (often paralysed), but exist and suffer. Individuals quite literally die from M.E. [The image below is an M.E. taxonomy based on several international criteria - apologies to the sight-impaired, there is far too much text for me to type up.]

I was diagnosed with M.E in 1998. Prior to that I had been diagnosed as having Post-Viral Fatigue Syndrome. Both conditions are classified by the W.H.O. in ICD-10 at G93.3, as neurological conditions (and have been since 1969). Even so, in the U.K., Denmark & the Netherlands especially, where a psychiatric cabal control much of the medical establishment, and in the U.S. until relatively recently, the disease has been treated as a mental-health condition, in contradiction to all the scientific evidence which demonstrates inter alia differences in sufferers’ brains, spinal-columns, hearts, blood-flow, blood-work, biomes, etc.

Recently I have begun to suspect my condition probably commenced at puberty, if not beforehand. Under the current N.I.C.E. guidelines (which are about to be updated) I have been and am classified by my G.P. (family-doctor) and by my N.H.S. hospital-consultant as suffering the severe form. Mostly I am bed-bound, nigh on all the time house-bound. However, with one or two assistants, I am able to travel with lots of planning. This would put me in the moderate grouping. Similarly, there are times when I suffer temporary paralysis, which places me within the very severe grouping. M.E. Is an unpredictable disease that constantly fluctuates. Prior to Severe M.E. Day in August I hope to have conducted some research into my medical history, to attempt to determine the approximate start of my condition, assuming it is not congenital. As long as all goes well, I hope to publish a blog-post on 8th August (August 8th).

[Image Description: the writer in sunglasses and wheelchair enjoying a day out.]

However, for the purposes of my argument today, I am looking at the time-frame 1998-2021. Whilst the numbers of suffers of M.E. is in the tens of millions worldwide, and currently estimated - excluding the new-comers via Covid-19 so-called Long-Covid - to be circa 250,000 - 500,000 in the U.K. That is roughly 1:200 folk having some form of the disease. Every G.P.’s list is estimated to have around forty sufferers. And yet the vast majority of family-doctors know little or nothing about the disease apart from the myths and prejudices, which they (mostly) also perpetuate.

There is NO TREATMENT for M.E.  More than half-a-century has passed since the W.H.O. classified this disease. Until the 21st century very little medical-research was carried out. Even now, most research is funded by sufferers as governments have all but turned a blind-eye to both the disease and especially those who suffer from it. The Pharmaceutical industries have also done very little research (as far as is known), reluctant to invest monies when so little is known about the disease. However, in the past few years the Norwegian Prime Minister apologised to her citizens for their mistreatment by Norway’s health-services. Researchers, especially in the U.S., Australia, the Scandic countries and even the U.K. have been gradually uncovering the secrets of the illness and finding or developing treatments that may help sufferers. Whilst these are still the early-days for same, there is at least some hope.

*

If the reader knows a person with M.E. (PwME) within their family, friend-group, or community, please do consider volunteering some of your time &/or money to an M.E. Charity.

*

Apologies for the changes in text-size and alignment - this is not down to me, the writer, but due to issues with Blogger.

Tweets for M.E. Awareness Month

 

Regular readers of this blog are aware that I am inter alia a person with Myalgic Encephalomyelitis (pwME) and Fibromyalgia (FMS). Each May is celebrated annually as International M.E. Awareness Month due to the International M.E. Awareness Day falling on 12th May (Florence Nightingale’s birthday). This year, International M.E. Awareness Week, the week in which 12th May falls, is Monday 11th to Sunday 17th May.

[Image description: a blue equilateral triangle on a black background; above the apex the words MYALGIC ENCEPHALOMYELITIS; below the triangle base the slogan SILENCE=LIVING DEATH.]

I am categorised as having severe M.E.  For me, this means I sleep for on average 14.5 hours per day, but during the wintry weather I can sleep up to twenty-two hours in any twenty-four hour period. Additionally I am mostly bed-bound at this time of the year. My cognitive abilities are invariably worse in the cooler months. So, knowing this, I have prepared my tweets for the whole month.

Within each tweet I have placed multiple hashtags, some of which will not be appropriate at any given time, thus these will need to be deleted prior to posting.

If the reader wishes to use any of these pre-prepared tweets, you are at liberty to do so. However, please note that some may be deemed unsuitable for workplace-viewing. I leave it to the tweeters’ discretion whether or not to add the #NSFW hashtag.

After the thirty-five tweets, one will find two groups of hashtags. Again, feel free to copy and paste if wanted.

The tweets:

* tweet 1:

Computer-Usage for #pwME or other #ChronicIllnesses (2020).

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2021/03/computer-usage-for-pwme-or-other.html

* tweet 2:

Missing (2020) - a #poem reflecting on a #pwME’s personal losses due to #ME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2021/01/missing-poem.html

* tweet 3:

#PainPatches - a G_dsend! (2020) - #PainControl for a #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2021/01/pain-patches-gdsend.html

* tweet 4:

Life - Love, Lust & Loneliness (2020) - a #pwME living with the ramifications of #ME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2020/12/life-love-lust-loneliness.html

* tweet 5:

#InternationalMEAwarenessDay 2020 - a #pwME’s 100+ symptoms. #SevereME

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2020/05/international-me-awareness-day-2020.html

* tweet 6:

My #MyalgicEncephalomyelitis - My #ME (2018).

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2018/12/my-myalgic-encephalomyelitis-my-me.html

* tweet 7:

#ME (2018) - a #poem about a #pwME living with & the heartache of #SevereME

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2018/08/me.html

* tweet 8:

Possible “Class Action Against #PACE-Triallers?” (2017). #GET #CBT

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2017/09/class-action-against-pace-triallers.html

* tweet 9:

ATOS & #DWP question whether #disabled can go abroad (2017) - detailing one #pwME’s preparations for & after-effects of travel.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2017/05/atos-dwp-question-whether-disabled-can.html

* tweet 10:

#Masturbation & #ME (2017) - #sex a #pwME can engage in.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2017/05/masturbation-me.html

* tweet 11:

#DisabilityDiscrimination in #Trafford (2017) - a #pwME’s fight for #SocialCare. #SevereME

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2017/02/disability-discrimination-in-trafford.html

* tweet 12:

Tumblr & #ME (2016) - some difficulties in using websites for #pwME. #Accessibility

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2016/12/tumblr-me.html

* tweet 13:

#SevereMEDay 2016. #SevereME

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2016/08/severe-me-day-2016.html

* tweet 14:

Why I Share Personal Information Publicly (2016) - a #pwME attempts to raise #awareness.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2016/07/why-i-share-personal-information.html

* tweet 15:

Quotidian Losses: IMEAD2016 - what one #pwME lost to #ME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2016/05/quotidian-losses-imead2016.html

* tweet 16:

Art for All (2016) - making arts-venues #accessible for #disabled folk, incl. #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2016/05/art-for-all.html

* tweet 17:

And now: the Gallery… (2018) - #artworks that speak to a #pwME. NB artistic nudity!

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2016/05/and-now-gallery.html

* tweet 18:

My long-lost ability to read… (2016) - a #pwME’s fluctuating ability to read. #Aphasia #Dyslexia

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2016/04/my-long-lost-ability-to-read.html

* tweet 19:

My #Genealogy #Hobby: Researching My #FamilyTree (2016) - a possible #pastime for #bedbound #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2016/02/my-genealogy-hobby-researching-my.html

* tweet 20:

#FluJabs & #MyalgicEncephalomyelitis (2015) - #FluVaccinations for #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2015/10/flu-jabs-myalgic-encephalomyelitis.html

* tweet 21:

Coitus At Last! / "White" (2015) - working #sex round a #pwME’s #ME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2015/08/coitus-at-last-white.html

* tweet 22:

#SevereMEDay (2015). #SevereME

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2015/08/severe-me-day.html

* tweet 23:

Global Endemic Plague (2015 - so not Covid!) - #AwarenessRaising of the scale of #ME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2015/05/global-endemic-plague.html

* tweet 24:

We Live - Art for #BADD2015 - #artworks & a #poem on #disabled folk by a #pwME. NB artistic nudity!

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2015/05/we-live-art-for-badd2015-nb-nsfw.html

* tweet 25:

My MEstory: Life with #MyalgicEncephalomyelitis (2014) - short snippets extracted from almost a month’s SM posts by one #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2014/05/my-mestory-life-with-myalgic.html

* tweet 26:

#Addlement or #BrainFog (2014) - #Dyscognition, one of the main symptoms of #ME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2014/05/addlement-or-brain-fog.html

* tweet 27:

#InternationalMEAwarenessDay … 2014 - 24hrs in the life of a #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2014/05/international-me-awareness-day-12th-may.html

* tweet 28:

"This is the face" of #ME (2014) - a #poem by Sophie Turner.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2014/05/this-is-face-of-me.html

* tweet 29:

#BedsideTable (2013) - an art-project of a/cs from various #disabled folk, incl. #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2013/08/bedside-table.html

* tweet 30:

all back (2013) - a #poem lamenting the loss of one #pwME’s pre-#ME life.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2013/05/all-back.html

* tweet 31:

No Sex Please, We're... #Disabled! * (2013) - a look at the #inaccessibility of #sex for folk, incl. #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2013/04/no-sex-please-were-disabled.html

* tweet 32:

Battlers in the #MECFS Wars! (2012) - one view of the internecine squabbling btw. different factions of #pwME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2012/12/battlers-in-mecfs-wars.html

* tweet 33:

Judgmentalism of Invalids (2012) - 1st half describes #onset of a #pwME’s #ME.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2012/07/judgmentalism-of-invalids.html

* tweet 34:

#Diarrhœa (2012) - a #poem on a common issue for many #pwME. #Diarrhoea #Diarrhea

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2012/06/diarrha.html

* tweet 35:

#Pain: a #Taxonomy (2012) - one #pwME’s pain-classification.

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(11-17th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

https://crippledqueeranglo-europeanranter.blogspot.com/2012/05/pain-taxonomy.html

The hashtags:

* hashtags 1

#MEAwarenessMonth/Week/Day

#MEAwarenessMonth2021/Week2021(10-16th May)/Day2021

#InternationalMEAwarenessMonth/Week/Day

#InternationalMEAwarenessMonth2021/Week2021/Day2021

* hashtags 2

#MyalgicEncephalomyelitis #ME #MEcfs

#ChronicFatigueSyndrome #CFS #CFSme

#SEID

#G93point3 #G93

___________________________________________________________