Well, cannot say I have enjoyed the best of health this past month or so, that is International M.E. Awareness Month. I have felt fairly terrible and really brain-fogged. So, writing an in-depth blog-post has not been possible. I have however managed to post on social media. Herewith I have collated some that at least give some health background and updates on my health. I would not normally post about my health, but in order to raise awareness, folk need to know what one is like when they cannot see you, as so often our illnesses are hidden or invisible.
Apologies up-front for the sight-impaired as there are no image descriptions as I just do not have the energy to do so at the moment.
Oh I know this one…
There are always folk worse than oneself to prevent one wallowing in self-pity. I am so fortunate in many ways: I have had a 'normal' life. This poor young girl has suffered terribly and is still in so much pain. Bless her & all of us with M.E.!!!
Just managed forty-five minutes out of bed, long enough to: descend stairs; eat cereal & fruit; take medications; turn on dishwasher & washing-machine; remount stairs; and, collapse back into bed. Now stiff, achey and in pain - thanks M.E.!!! %S
Well, managed a whole twenty-five minutes out of bed. Food consumed. Meds taken. Knackered. Hoping for dry & warm change to the weather…
Local weather prognostication is for rain right through to & including Sunday. So confined to my bed-cell then!!! %SSSS
So funny!!! %DDDDD
Had drink (by bed). No meds. No food. Plenty of pain. Stayed awake for about 150 mins. Now back to sleep. Bl**dy M.E.!!!! %SSS
I'm never going to recall … (another M.E. day with resulting brain-fog) …
Another nasty one: today is world #Lupus day.
Alas I do and have done officially since 1998, although I had the symptoms for years beforehand…
I shall shortly be posting from the international vigil; for those not wishing to light a candle, p'raps this status could be posted for an hour or so in support of all with invisible illnesses. Inter alia I have myalgic encephalomyelitis (ME), fibromyalgia (FMS), irritable bowel syndrome (IBS), Raynaud's syndrome, osteoarthritis (OA), a gout-like arthritis, … Only the latter gives visible symptoms when I swell up like the Michelin-man. Thanks for not judging by outer appearances. %)
Oh boy, do I know this feeling…
This is what it is like for many in the UK. I am so lucky in that the G.P. who diagnosed me supported me for some ten years. My hospital consultant is a specialist in M.E. and is totally supportive too. I truly give thanks for my good fortune having read some awful tales from fellow M.E. sufferers (PWME).
Yesterday was M.E. Day, this is also M.E. Week and Month… Awareness-raising continues! %)
M.E.Association released NOTHING for #InternationalMEAwarenessDay.
Action for M.E. released this (pdf):
My name is Colin-Roy, and I'm a spoonie!
Spoons are used to go to the loo, to think, even just breathing… %S
The M.E. scene (they call it chronic fatigue syndrome or C.F.S. in U.S.A.) from The Golden Girls. I do not recall this episode, but no doubt I must have missed the odd one or two. Susan Harris, creator and producer of the series lived with ME/CFS for many years.
By now you are probably all aware that it is International M.E. Awareness Week (part of International M.E. Awareness Month). I am grouping all my relevant blog-posts in a list below, just in case you missed one or wish to revisit one.
Another #MEstory; a day in my M.E. life - http://crippledqueeranglo-europeanranter.blogspot.co.uk/2014/05/international-me-awareness-day-12th-may.html
A personal classification of pain as I experience it - http://crippledqueeranglo-europeanranter.blogspot.co.uk/2012/05/pain-taxonomy.html
Brain-fog or M.E.-fog or fibro-fog or … - http://crippledqueeranglo-europeanranter.blogspot.co.uk/2014/05/addlement-or-brain-fog.html
A poem I wrote about the realisation of loss and grieving for my old self -http://crippledqueeranglo-europeanranter.blogspot.co.uk/2013/05/all-back.html
Finally a guest poem by Sophie Turner aka bambimax -http://crippledqueeranglo-europeanranter.blogspot.co.uk/2014/05/this-is-face-of-me.html
I have physical-, emotional-, spiritual-, sexual- and mental-health issues: how can one separate or justify segregating elements; one ought to be treated holistically.
And for those wondering how I manage to post updates & so forth: this is my way of diverting myself from obsessing about pain, anxiety & so forth and trying to refrain from creating a downward spiral.Your continued forbearance is appreciated. %)
Just need to ride it out. Apparently we're due a heat-wave for some six weeks or so. Hopefully, in that case I should ameliorate. Contacted social services, just waiting for them to get back to me about re-assessment. Once sorted I am hoping I'll calm down as should end up eating more regularly. All will be well. %)
Whoo! Managed a whole hour out of bed; now back to bed-cell. However, eaten, hydrated, medicated and did a couple of easy chores. Now exhausted & in pain again. Heigh-ho - life with M.E.
Thanks to Michelle offering me a lift to & from the polling-station, I am now able to go to cast my vote.
Not wide awake - more sort of half semi-conscious - as bones knew rain was on its way. And sure enough precipitation is falling. Heigh-ho! %S
I realise the month is not over yet; but I thought I had better do this whilst I am reasonably alert and have some energy.
Thanks to all: carers and friends; campaigners, posters and sharers; scientists and researchers; consultants, doctors and nurses; and to all those with these invisible illnesses who support each other via social media. %)