Daily Mail article about Michael Crawford's long slow recovery from M.E.
TBH I'm struggling to concentrate, sit up, balance, etc for more than a few minutes at a time, today. But on the whole, apart from exhaustion, nerve pain, balance and co-ordination issues that have dogged me rather this week since I took a service for a single hour the week before last, it's been a good week. The joy of friendships and the start of Lent, spring flowers, laughter and all life's sweetness makes up for the M.E.-sodden bits of life! It does for yours truly, anyway!
But I wanted to share this today. I spotted this article in the online Daily Mail (Please see link above).
It's an encouragingly honest article by actor, comedian and singer Michael Crawford, beloved by my generation as bumbling Frank Spencer on 70s sitcom "Some Mothers Do Ave Em".
Michael tells of how he was stricken by M.E. when, like many of us, overwork and getting run down (in his case the final trigger was working in a hot padded "fat" suit!) led to a virus that triggered his immune system's meltdown into M.E.
He found himself unable to pick up, even though previously so fit, after a bout of seemingly innocuous flu. That had happened to me, too in the Autumn of 2005. Well, the flu did. And the meltdown into M.E. Not the padded fat suit!
Michael had his worst period of "bust/crash" of M.E. for a whole seven years. During this time, like me, he sometimes wondered if his career was over. He retreated to complete rest and recuperation in New Zealand, allowing his body time to recover in its own way, as I'm also in the middle of doing, though I am only now just over five years into recovery. I hope by the time I get to the seventh year, I too will be back to cooking with energetic gas, like Michael, forever, or however long a "boom" of recovery I'm granted.
I'm well aware, with all the different sub-types of M.E we suffer, not all of us can achieve such a remission. Some have never had health and freedom from M.E. from a young age. I always count myself very blessed and fortunate to have been able to do so much, achieve so many of my goals before being floored by M.E.in my 40s (though it was tapping on my shoulder much longer than that, of course!).
Like many of us, Michael took the time to alter his diet to as healthy an option as possible to give his body all the help he could. I lost six stones in the time I've had M.E. (it was the debility of M.E. that slapped the weight on me in the first place of course.) One of the few "advantages" M.E. has given me is the space to sort out my Type 1 diabetes, which, although still unpredicatably erratic with unannounced hypoglycaemia at any hour of day or night, at least now is better controlled through carbohydrate counting than at any time during my adult/working life.
I bless Michael for sharing his own journey and his story all too familiar to at least some of us with M.E., those who are neither the least nor the most severely of all affected. I know some of the most severely affected find yet another story of celebrity M.E. recovery in the media is more than a little hard to swallow, and my heart goes out to all who feel this way. This is not an easy road, and the media has so long mocked and ridiculed M.E. sufferers that the resilient humour of many is tried to the limit.
Read the link and judge for yourselves.
From my personal point of view, his story inspires me. It gives me a chink of hope in the clouds of future uncertainty. In my own long, long slow miracle of painfully slow progress towards recovery, looking back on the little ways I can be useful now that were closed to me just a year ago as my career and life slipped through my grasp, I see hope that I too can dance on life's stage again, restored to some semblance of my former self!
God bless you, Michael. Be gentle with yourself and enjoy every moment of your new lease of life!
Thursday, 10 March 2011
Monday, 7 March 2011
What's in a Name?
Some days my brain is mush.
Sometimes that's thanks to being crashed from M.E.
Other days, my brain is just mush.
No excuses!
Like today.
I discovered that the plastic surface of the buttons on the door of my 5 year old microwave was getting very blistered and bubbly. When I investigated more closely, the penny finally dropped. After only five years! It's just one of those transparent plastic protectors manufacturers put over screens, meant to be peeled off immediately! Here I was, 5 years later, with the thing still in place.
Now although I bought the micro at around the same time as I was floored by my latest major bout of M.E. five years ago, I can't blame that "Duhhh!" moment on M.E. brain fog.
I can't blame comical moments like that on anything else but my slightly scatty, away with the fairies personality. I've never been that quick to grasp the plot, even with various letters after my name!
But I'm struggling now with a new "development" in the science behind M.E. Or rather the language used to provide more baffling acronyms. It's enough to induce "brain fog" in the fittest!
Circa 2008, a study claimed a link between M.E., prostate cancer and related illness, and XMRV (Xenotrophic Murine virus-Related Virus). Yes - virus-related virus. There's a good start towards clarity, eh?
Now, in March 2011, I see on various blogs, M.E. chat groups and elsewhere on the web, XMRV is going to have a name change, to HGRV (Human Gamma Retrovirus). For resultant conditions like M.E. with possible viral links, the snappy new acronym will be HGRAD (Human Gamma Retrovirus Associated Disease). One reason seems to be "Murine" refers to mice, so the new name focusses back on the humans affected, not visions of Mickey Mouse and Ratatouille!
Should we break out the champagne? (I might, if only M.E. had not also made me allergic to alcohol!). Wait! I've only recently got one friend's eyes to light up with understanding that my Type 1 diabetes and my M.E. may well both be understood one day to be autoimmune diseases, quite distinct from Type 2 diabetes and a spot of vague "T.A.T.T." (Tired All The Time).
Now we have yet more letters to juggle with! While for the general public and for many G.P.s, understanding and acceptance of the crippling, frustrating disease and the umbrella of illnesses that may or may not be related, is still a lottery dependent on personal encounters with genuine sufferers or the cynical lies propagated by the media and talking heads.
While the war of words goes on between the labels M.E. (Myalgic Encephalomyelitis, or as some insist, Myalgic Encephalopathy), C.F.S. (the much vaguer Chronic Fatigue Syndrome, which IMHO fails completely to describe 3/4 of the disabling symptoms and coddles folk into the notion that a bit of backbone would cure those contemptible malingerers!) and P.V.F.S (Post Viral Fatigue Syndrome, which unlike M.E. seems to harbour hope of a quick return to full functioning), we now find more riddling initials to addle our foggy brains!
I have so many friends at the moment struggling with a wide variety of illnesses which, like me, they simply refuse to be defined by or beaten by.
The labels, the letters may come and go. But we're here, guys, and we're not going to be filed away under T.B.A.
Keep smiling and trusting that you are certainly not alone.
Sometimes that's thanks to being crashed from M.E.
Other days, my brain is just mush.
No excuses!
Like today.
I discovered that the plastic surface of the buttons on the door of my 5 year old microwave was getting very blistered and bubbly. When I investigated more closely, the penny finally dropped. After only five years! It's just one of those transparent plastic protectors manufacturers put over screens, meant to be peeled off immediately! Here I was, 5 years later, with the thing still in place.
Now although I bought the micro at around the same time as I was floored by my latest major bout of M.E. five years ago, I can't blame that "Duhhh!" moment on M.E. brain fog.
I can't blame comical moments like that on anything else but my slightly scatty, away with the fairies personality. I've never been that quick to grasp the plot, even with various letters after my name!
But I'm struggling now with a new "development" in the science behind M.E. Or rather the language used to provide more baffling acronyms. It's enough to induce "brain fog" in the fittest!
Circa 2008, a study claimed a link between M.E., prostate cancer and related illness, and XMRV (Xenotrophic Murine virus-Related Virus). Yes - virus-related virus. There's a good start towards clarity, eh?
Now, in March 2011, I see on various blogs, M.E. chat groups and elsewhere on the web, XMRV is going to have a name change, to HGRV (Human Gamma Retrovirus). For resultant conditions like M.E. with possible viral links, the snappy new acronym will be HGRAD (Human Gamma Retrovirus Associated Disease). One reason seems to be "Murine" refers to mice, so the new name focusses back on the humans affected, not visions of Mickey Mouse and Ratatouille!
Should we break out the champagne? (I might, if only M.E. had not also made me allergic to alcohol!). Wait! I've only recently got one friend's eyes to light up with understanding that my Type 1 diabetes and my M.E. may well both be understood one day to be autoimmune diseases, quite distinct from Type 2 diabetes and a spot of vague "T.A.T.T." (Tired All The Time).
Now we have yet more letters to juggle with! While for the general public and for many G.P.s, understanding and acceptance of the crippling, frustrating disease and the umbrella of illnesses that may or may not be related, is still a lottery dependent on personal encounters with genuine sufferers or the cynical lies propagated by the media and talking heads.
While the war of words goes on between the labels M.E. (Myalgic Encephalomyelitis, or as some insist, Myalgic Encephalopathy), C.F.S. (the much vaguer Chronic Fatigue Syndrome, which IMHO fails completely to describe 3/4 of the disabling symptoms and coddles folk into the notion that a bit of backbone would cure those contemptible malingerers!) and P.V.F.S (Post Viral Fatigue Syndrome, which unlike M.E. seems to harbour hope of a quick return to full functioning), we now find more riddling initials to addle our foggy brains!
I have so many friends at the moment struggling with a wide variety of illnesses which, like me, they simply refuse to be defined by or beaten by.
The labels, the letters may come and go. But we're here, guys, and we're not going to be filed away under T.B.A.
Keep smiling and trusting that you are certainly not alone.
Thursday, 6 January 2011
One "Flu"-jab over the Cuckoo's Nest
Well, another year dawns! From my own experience and from listening to others with M.E., I know this time of year can be a tough one.
After the frantic preparations in the lead-up to Christmas, many of us can overtax our strength and immune systems before we even realise it, until the "crash" comes and makes us lay down our arms for a while! The line between "doing" and "being" is a subtle one, but an essential part of our armoury in combatting and living through this persistent, sapping disease.
Since my last blog post in October, I've certainly had my ups and downs. I was overjoyed to discover one of my short stories, "The Butterfly Wall" was to be published in the January edition of "Writers' Forum Magazine" here in the UK, and kept busy on my better days through November, when brain-fog was at a minimum, writing the first draft of my new historical novel. At about the same time I was hit by a virus which meant I was too unwell to attend my GP's annual flu jab fest. Every year it's a dilemma of "ip-dip-my-blue-ship"* as to whether I should have the jab or not.
Most years the flu jab has preceded a huge flare-up and worsening of my M.E. symptoms. So I wasn't in a hurry, once I began to pick up a little, to re-book the appointment. Even the nurse at the practice agrees it is difficult to advise what's best: as a Type 1 diabetic, I am in the "at-risk" group who are advised to get immunised, but as an M.E. patient, my immune system has ideas of its own that can make the jab less than helpful! (Solution - don't be greedy enough to have both conditions concurrently!)
However, I have now booked my shot for next week. I know at least 3 friends in our local area have been hit by severe, life-threatening Swine Flu in recent weeks, so I feel it my duty to have the jab, whatever effect it has on me, in order to protect those close to me. My mum's own health, always resilient even at 79, was compromised by the month-long saga of my failed boiler (as Facebook friends know only too well - zzzzz!) through the coldest winter in living memory, to the extent she has developed shingles in her head and the added extra side-effect of Bell's Palsy, so I refuse to put her or others at risk of catching flu from me just because the jab has adversely affected me in the past. The current jab formula claims to protect against Swine Flu, too, so perhaps it will be worth the risk this year. I hope so.
Then, the day after I finally decided to book the appointment for my jab, the national news revealed this week a shortage of the flu vaccine in some parts of the country. There's still time to race me for mine, if you're desperate - five injections a day is plenty for one body, already, if you ask me! Just call me "Pincushion"...
* The phrase "ip-dip-my-blue-ship" comes from a playground game we used to play at infant school in Yorkshire in the 1960s. The rhyme goes:
I've read about other variants since then from all parts of the country. The rhyme accompanied the counting round of the participant children's legs until the last person counted on "YOU" was out of the running for being "it" or "on" in the subsequent chasing game. The phrase is still used in my house (by me, anyway!) to express the horns of any dilemma!
After the frantic preparations in the lead-up to Christmas, many of us can overtax our strength and immune systems before we even realise it, until the "crash" comes and makes us lay down our arms for a while! The line between "doing" and "being" is a subtle one, but an essential part of our armoury in combatting and living through this persistent, sapping disease.
Since my last blog post in October, I've certainly had my ups and downs. I was overjoyed to discover one of my short stories, "The Butterfly Wall" was to be published in the January edition of "Writers' Forum Magazine" here in the UK, and kept busy on my better days through November, when brain-fog was at a minimum, writing the first draft of my new historical novel. At about the same time I was hit by a virus which meant I was too unwell to attend my GP's annual flu jab fest. Every year it's a dilemma of "ip-dip-my-blue-ship"* as to whether I should have the jab or not.
Most years the flu jab has preceded a huge flare-up and worsening of my M.E. symptoms. So I wasn't in a hurry, once I began to pick up a little, to re-book the appointment. Even the nurse at the practice agrees it is difficult to advise what's best: as a Type 1 diabetic, I am in the "at-risk" group who are advised to get immunised, but as an M.E. patient, my immune system has ideas of its own that can make the jab less than helpful! (Solution - don't be greedy enough to have both conditions concurrently!)
However, I have now booked my shot for next week. I know at least 3 friends in our local area have been hit by severe, life-threatening Swine Flu in recent weeks, so I feel it my duty to have the jab, whatever effect it has on me, in order to protect those close to me. My mum's own health, always resilient even at 79, was compromised by the month-long saga of my failed boiler (as Facebook friends know only too well - zzzzz!) through the coldest winter in living memory, to the extent she has developed shingles in her head and the added extra side-effect of Bell's Palsy, so I refuse to put her or others at risk of catching flu from me just because the jab has adversely affected me in the past. The current jab formula claims to protect against Swine Flu, too, so perhaps it will be worth the risk this year. I hope so.
Then, the day after I finally decided to book the appointment for my jab, the national news revealed this week a shortage of the flu vaccine in some parts of the country. There's still time to race me for mine, if you're desperate - five injections a day is plenty for one body, already, if you ask me! Just call me "Pincushion"...
* The phrase "ip-dip-my-blue-ship" comes from a playground game we used to play at infant school in Yorkshire in the 1960s. The rhyme goes:
"Ip-dip, my blue ship,
Sails on the water,
Like a cup and saucer,
Out goes YOU!"
I've read about other variants since then from all parts of the country. The rhyme accompanied the counting round of the participant children's legs until the last person counted on "YOU" was out of the running for being "it" or "on" in the subsequent chasing game. The phrase is still used in my house (by me, anyway!) to express the horns of any dilemma!
Wednesday, 20 October 2010
How far have we come?
Heard today, sadly, about a comment from an employer about a worker with ME who has collapsed and been ordered to take time off.
"Oh, she's the kind of person [my disgusted italics] who goes full tilt and then flops."
No, my friend, (who should know better, professing to be in the "healing" business): she's a actually a person who has contracted, to quote the World Health Organisation:
Oh, but that would be to quit peddling the patronising age-old dangerous misinformation ME patients have been suffering for decades, wouldn't it?
Sorry - long quote. Rant over.
I also smiled through my gritted teeth again at the sick but increasingly unfunny joke:
"Even the comatose can be put to work. As draft excluders."
Enough. Or I might type something I'll regret (if I could sit up for longer)!
The Father still loves me!
"Oh, she's the kind of person [my disgusted italics] who goes full tilt and then flops."
No, my friend, (who should know better, professing to be in the "healing" business): she's a actually a person who has contracted, to quote the World Health Organisation:
"a chronic, inflammatory, primarily neurological disease that is multisystemic, affecting the central nervous system, immune system and cardiovascular system, the endocrinological system and musculoskeletal system. ME can cause a wide variety of symptoms, including changes in sensory tolerance, visual problems, exertional muscle weakness, difficulties with coordination and speech, severe fatigability, cognitive impairment, problems with balance, subnormal or poor body temperature control (due to circulation issues) and severe pain which causes a varying degree of impaired mobility and disability in all cases.
Myalgic Encephalomyelitis affects the brain and spinal cord which control the body, allow thought and sensory processing, causing dysautonomia, impaired thinking and loss of internal homeostasis, the process whereby the body maintains a consistent internal environment in response to external stressors. Cellular metabolism and communication is disrupted, causing inefficiency in all biological processes. This includes the cellular mitochondria which process fuel to make energy, resulting in a deficiency of adenosine-triphosphate ATP with a chronic, severe, measurable loss of sustainable strength on exertion. A hallmark of ME is intolerance to previously trivial effort and deterioration through persistent or repeated exertion (often resulting in relapse).
Current theory suggests ME results from a persistent viral infection and/or attacks by an individual's immune system on the nervous system, musculoskeletal system, and blood vessels. It has been classified by the World Health Organisation as an organic brain disease since 1969."
Oh, but that would be to quit peddling the patronising age-old dangerous misinformation ME patients have been suffering for decades, wouldn't it?
Sorry - long quote. Rant over.
I also smiled through my gritted teeth again at the sick but increasingly unfunny joke:
"Even the comatose can be put to work. As draft excluders."
Enough. Or I might type something I'll regret (if I could sit up for longer)!
The Father still loves me!
Always something to be thankful for
This past fortnight or so, just typing at the laptop, sometimes just reaching the keyboard has made me so sick and weak I can't keep up. Let alone cooking. Cleaning out the fish. Answering door/phone to perky dead-eyed salespeople hired not to tell you what they're actually flogging. Standing and speaking at the same time. Remembering what I'm supposed to have just got ready to do. (Living, we often call it!)
My ears are ringing, my eyes feel blow-torched. Muscles jerky and painful. Breaths in and out exhausting as my chest muscles/diaphragm (3 tries to spell that by stages!) are so painful, weak, burning. Yet can't get warm even with heating on (while I can still afford to put it on!). Spirit willing? Tick. Concentration/ co-ordination? Nil.
I try to read to research and plot my novel I so want to motor on with during November's NaNoWriMo mentioned in my last post. I can't make sense of anything, even simple stuff, most of the time at the mo. Thank the Lord for the times I can get on a bit.
I try to birdwatch. My forearms quickly grow too shaky and sick to raise the binoculars. Eyes won't focus or bear the beautiful autumn sunshine. Thanks the Lord I can hear them singing though, sweet as symphonies!
My fault. Agreed to take service I promised months ago and determined to carry through with my resolve. Went to friend's funeral the same week and after a disoreintating busride, was cuddled and chatted to death by dear friends I hadn't seen since I collapsed 5 years ago, from one of my old churches. They'd missed me. I'd missed them. I made it to the afternoon and have been crashed most days since. Silly enough to have my birthday this month too. Overkill!
Doing stuff when I can. Having to put the lights out and curl up to catch up on frazzled sleep when I can't.
"Pacing!" the whispered reminder comes from the few who understand. I know, I croak. It's just that life doesn't....
Blood sugars all over place. Hypo or hyper 90% of time. (Just took me a second try to spot where the "%" was hiding on my supposedly familiar keyboard.). Sugars erratic from stressed-out immune system fighting unseen infections. Not doughnuts.
That's enough for today.
But it's something!
My ears are ringing, my eyes feel blow-torched. Muscles jerky and painful. Breaths in and out exhausting as my chest muscles/diaphragm (3 tries to spell that by stages!) are so painful, weak, burning. Yet can't get warm even with heating on (while I can still afford to put it on!). Spirit willing? Tick. Concentration/ co-ordination? Nil.
I try to read to research and plot my novel I so want to motor on with during November's NaNoWriMo mentioned in my last post. I can't make sense of anything, even simple stuff, most of the time at the mo. Thank the Lord for the times I can get on a bit.
I try to birdwatch. My forearms quickly grow too shaky and sick to raise the binoculars. Eyes won't focus or bear the beautiful autumn sunshine. Thanks the Lord I can hear them singing though, sweet as symphonies!
My fault. Agreed to take service I promised months ago and determined to carry through with my resolve. Went to friend's funeral the same week and after a disoreintating busride, was cuddled and chatted to death by dear friends I hadn't seen since I collapsed 5 years ago, from one of my old churches. They'd missed me. I'd missed them. I made it to the afternoon and have been crashed most days since. Silly enough to have my birthday this month too. Overkill!
Doing stuff when I can. Having to put the lights out and curl up to catch up on frazzled sleep when I can't.
"Pacing!" the whispered reminder comes from the few who understand. I know, I croak. It's just that life doesn't....
Blood sugars all over place. Hypo or hyper 90% of time. (Just took me a second try to spot where the "%" was hiding on my supposedly familiar keyboard.). Sugars erratic from stressed-out immune system fighting unseen infections. Not doughnuts.
That's enough for today.
But it's something!
Friday, 8 October 2010
ME patients blood donor ban
"A pint, that's very nearly an armful!" as Tony Hancock lugubriously put it in his classic "The Blood Donor" sketch.
I'm off this morning to give blood. Just in connection with the usual round of tests for my Type 1 diabetes. Not as a donor, ever again, it seems by today's BBC headline. Today my blood was officially declared unfit to grace the veins of anyone but myself!
Click to read "M.E. PATIENTS FACE UK BAN ON DONATING BLOOD"
M.E. doesn't make the news every day. When it does, the invisible community of M.E. patients often breathes a collective sigh of dread, if they are up to it. We wonder, what will the media manage to mock in the latest headline?
-Will there be a new way of getting a laugh out of "Yuppy Flu"?
-Will there be a new raft of arguments about the research required to get to the root of M.E.'s neurological causes?
-Will XMRV (xenotropic murine leukemia virus-related virus) be thumbs up or thumbs down as the culprit this time?
-Or will we shudder with impotent grief at another wave of generalised attack aimed at real benefit bludgers, who, of course, some misinformed angry people will see as including all those hardworking, taxpaying members of society who from this devastating illness and others find themselves forced to claim invalidity benefit reluctantly, completely against their nature or aspirations?
Blogging for a few minutes on a good day or preaching for an hour a month does not, believe it or not, constitute the abilty to work full or often even part time. If only! I know, because year after year before diagnosis I drove myself back to working again and again before another complete collapse.
It got to the point when I was so obviously ill to all my colleagues and parishoners around me, they used to beg me to leave late meetings early. I so hate letting people down that I was thrown into despair at how to do all I was obliged and delighted normally to do while my body and mind were unable to stay upright, too sick with disorientating exhaustion to sleep, caught in crippling pain, uncoordinated, feverish, spaced out, dizzy and nauseous and increasingly unable to perform all the work I so love, or indeed, any work consistently.
Today the headline leaves no doubt. M.E. is real. So real that the health authorities are banning all M.E. patients, in a crash or in remission (i.e."cured" enough to function for a period, hopefully indefinitely or permanently, in "boom" after "bust"), from giving blood. One day soon, we will know exactly what virus or gene is triggering this hellish disease and be in a position to conquer it. (Though cancer and the common cold give us less optimism to hold our breath for that in our lifetimes!). I'm an optimist, though, and I have to believe these headlines are little beacons on the way.
Meanwhile I will go on doing what I can to pace myself into another period of remission. My prayer is that when it comes, it will be forever. My determination is that on that day, I will not be sucked into the arrogance of the "cured" which harangues those still gripped by the illness to "do what I did, and look, I'm fine".
If I had done that every time in my life when I too appeared "cured" when in remission, I would have hurt and possibly destroyed the hope and joy in many with whom I can now empathise.
Together, one day, we will dance in the sunshine and have our full lives restored to us and be more than overjoyed to graft gleefully in the valleys where we are needed.
Maybe one day, too, we will be able to give "very nearly an armful" again to save our neighbour.
I'm off this morning to give blood. Just in connection with the usual round of tests for my Type 1 diabetes. Not as a donor, ever again, it seems by today's BBC headline. Today my blood was officially declared unfit to grace the veins of anyone but myself!
Click to read "M.E. PATIENTS FACE UK BAN ON DONATING BLOOD"
M.E. doesn't make the news every day. When it does, the invisible community of M.E. patients often breathes a collective sigh of dread, if they are up to it. We wonder, what will the media manage to mock in the latest headline?
-Will there be a new way of getting a laugh out of "Yuppy Flu"?
-Will there be a new raft of arguments about the research required to get to the root of M.E.'s neurological causes?
-Will XMRV (xenotropic murine leukemia virus-related virus) be thumbs up or thumbs down as the culprit this time?
-Or will we shudder with impotent grief at another wave of generalised attack aimed at real benefit bludgers, who, of course, some misinformed angry people will see as including all those hardworking, taxpaying members of society who from this devastating illness and others find themselves forced to claim invalidity benefit reluctantly, completely against their nature or aspirations?
Blogging for a few minutes on a good day or preaching for an hour a month does not, believe it or not, constitute the abilty to work full or often even part time. If only! I know, because year after year before diagnosis I drove myself back to working again and again before another complete collapse.
It got to the point when I was so obviously ill to all my colleagues and parishoners around me, they used to beg me to leave late meetings early. I so hate letting people down that I was thrown into despair at how to do all I was obliged and delighted normally to do while my body and mind were unable to stay upright, too sick with disorientating exhaustion to sleep, caught in crippling pain, uncoordinated, feverish, spaced out, dizzy and nauseous and increasingly unable to perform all the work I so love, or indeed, any work consistently.
Today the headline leaves no doubt. M.E. is real. So real that the health authorities are banning all M.E. patients, in a crash or in remission (i.e."cured" enough to function for a period, hopefully indefinitely or permanently, in "boom" after "bust"), from giving blood. One day soon, we will know exactly what virus or gene is triggering this hellish disease and be in a position to conquer it. (Though cancer and the common cold give us less optimism to hold our breath for that in our lifetimes!). I'm an optimist, though, and I have to believe these headlines are little beacons on the way.
Meanwhile I will go on doing what I can to pace myself into another period of remission. My prayer is that when it comes, it will be forever. My determination is that on that day, I will not be sucked into the arrogance of the "cured" which harangues those still gripped by the illness to "do what I did, and look, I'm fine".
If I had done that every time in my life when I too appeared "cured" when in remission, I would have hurt and possibly destroyed the hope and joy in many with whom I can now empathise.
Together, one day, we will dance in the sunshine and have our full lives restored to us and be more than overjoyed to graft gleefully in the valleys where we are needed.
Maybe one day, too, we will be able to give "very nearly an armful" again to save our neighbour.
Wednesday, 6 October 2010
Ebb and flow
I was talking last week on the phone to a friend whose grandson, now in his 20s, has had M.E. since his teens. Our experiences are similar in that when a period of relative "boom" comes in the M.E. energy rhythm, we tend to attempt too much and face "bust" again with almost immediate effect. He tries to climb mountains, then collapses again before he can complete it - he hasn't ever had chance yet to be the man he dreamed he'd be.
The lad's mum has funds enough to send him abroad to the greatest experts in the field. Even they can do little more than tell him what we all know in our hearts. Sleep does not refresh our batteries and our bodies aren't recharged by rest to be "fit for purpose". Once the body is sufficiently drained and exhausted, the pain levels, the muscle co-ordination, the brain's recall, the autonomic systems are in meltdown in ways we cannot predict or prevent.
Walking across a room can still be a mountain or marathon to me! I've had a life of fulfilment, challenge and exploration; my heart goes out to those who have never had enough respite from M.E. to recognise themselves well in the first place.
My little goals are more modest these days, of necessity. Attempting to be as useful as I can, WHEN I can, dreaming of returning to my ministry one day, unable to fulfil the 24/7 vocation of a minister or most days even getting by with basic tasks since my most recent collapse, I've offered to take one service every month or so in the churches of our local Circuit. It sounds so little. But this time last year I could not have offered even an hour a month's voluntary local preaching.
Last Sunday was one of those occasional services. The steward picked me up and drove me to his church a few miles from my home. Even the journey itself, crunched into the car with its twists and turns on the highway is disorientating enough!
It now takes me so crazily long to prepare for one brief session in the pulpit and aisle. This is what I do! Why does it cost me so much now to do it? So long to recover afterwards. But it's the joy and privilege it always was, and perhaps even more precious for what it takes me now to offer it.
People in these churches who knew me "before" are touchingly delighted to see me "facing the wrong way round" again, even if only for an hour. They often say how well I look. Does that just mean "standing up" these days? They see me holding the sides of the pulpit (how it hurts to grip with sore, jerky fingers!) and don't realise that it's sometimes only that which keeps me upright till I can sit down during some quiet hymn or song or reading so the room will stop booming and spinning jerkily, all blare and blaze.
Most don't realise that what I used to do "on the wing" I now need extensive notes for, to keep everything in my head, so we can take the collection in the right slot or remember the punchline to a "spontaneous" illustration. Maybe they think at 49, I've always had this collapsible stick hidden in a closet somewhere, waiting to produce to keep the rubbery pavements from throwing me off kilter! Maybe they are just being kind!
I still chuckle to remember at my hastily-arranged "farewell" service, as other colleagues celebrated their time here and went on to new parishes and challenges elesewhere, as I was reluctantly forced to become a reclusive shadow, one dear lady from another denomination leaned across to me and stage-whispered with a horsey commiseratory pat that set my raw muscles alight with pain:
"I'm so sorry to hear you're jacking in the church!"
I've never "jacked in" my calling and I never will. It hasn't jacked me in, either, or at least God through the grace of his Spirit in Jesus never ever will! But a very different course has to be plotted with Him, now, moment by moment. Trusting in His strength, with no fear of mistakenly thinking my own is sufficient!
Since my hour leading worship on Sunday, I haven't been able to function much. I had rested up to be ready. Afterwards my body had had more than enough. For days now I haven't really had the strength to cook or read or concentrate for more than a few moments at a time.
I once had sessions with an Occupational Therapist, who was slowly learning from M.E. patients why the psychological "treatments" didn't work when the illness was patently all too real and neurological/immune system based. Through the brainfog, swollen glands, untrustworthy vocal cords, in a darkened room with muted light so my eyes could bear it, I told her:
"To me it's a bit like a tide coming in. Moving towards recovery is like waves lapping up the shore; the breakers drag you back a little down the beach before being drawn back up again, gradually towards the strand."
I've had glimpses of high tide and I truly treasure them. Today I'm somewhere wandering among the rockpools, and do those limpets nip!
The lad's mum has funds enough to send him abroad to the greatest experts in the field. Even they can do little more than tell him what we all know in our hearts. Sleep does not refresh our batteries and our bodies aren't recharged by rest to be "fit for purpose". Once the body is sufficiently drained and exhausted, the pain levels, the muscle co-ordination, the brain's recall, the autonomic systems are in meltdown in ways we cannot predict or prevent.
Walking across a room can still be a mountain or marathon to me! I've had a life of fulfilment, challenge and exploration; my heart goes out to those who have never had enough respite from M.E. to recognise themselves well in the first place.
My little goals are more modest these days, of necessity. Attempting to be as useful as I can, WHEN I can, dreaming of returning to my ministry one day, unable to fulfil the 24/7 vocation of a minister or most days even getting by with basic tasks since my most recent collapse, I've offered to take one service every month or so in the churches of our local Circuit. It sounds so little. But this time last year I could not have offered even an hour a month's voluntary local preaching.
Last Sunday was one of those occasional services. The steward picked me up and drove me to his church a few miles from my home. Even the journey itself, crunched into the car with its twists and turns on the highway is disorientating enough!
It now takes me so crazily long to prepare for one brief session in the pulpit and aisle. This is what I do! Why does it cost me so much now to do it? So long to recover afterwards. But it's the joy and privilege it always was, and perhaps even more precious for what it takes me now to offer it.
People in these churches who knew me "before" are touchingly delighted to see me "facing the wrong way round" again, even if only for an hour. They often say how well I look. Does that just mean "standing up" these days? They see me holding the sides of the pulpit (how it hurts to grip with sore, jerky fingers!) and don't realise that it's sometimes only that which keeps me upright till I can sit down during some quiet hymn or song or reading so the room will stop booming and spinning jerkily, all blare and blaze.
Most don't realise that what I used to do "on the wing" I now need extensive notes for, to keep everything in my head, so we can take the collection in the right slot or remember the punchline to a "spontaneous" illustration. Maybe they think at 49, I've always had this collapsible stick hidden in a closet somewhere, waiting to produce to keep the rubbery pavements from throwing me off kilter! Maybe they are just being kind!
I still chuckle to remember at my hastily-arranged "farewell" service, as other colleagues celebrated their time here and went on to new parishes and challenges elesewhere, as I was reluctantly forced to become a reclusive shadow, one dear lady from another denomination leaned across to me and stage-whispered with a horsey commiseratory pat that set my raw muscles alight with pain:
"I'm so sorry to hear you're jacking in the church!"
I've never "jacked in" my calling and I never will. It hasn't jacked me in, either, or at least God through the grace of his Spirit in Jesus never ever will! But a very different course has to be plotted with Him, now, moment by moment. Trusting in His strength, with no fear of mistakenly thinking my own is sufficient!
Since my hour leading worship on Sunday, I haven't been able to function much. I had rested up to be ready. Afterwards my body had had more than enough. For days now I haven't really had the strength to cook or read or concentrate for more than a few moments at a time.
I once had sessions with an Occupational Therapist, who was slowly learning from M.E. patients why the psychological "treatments" didn't work when the illness was patently all too real and neurological/immune system based. Through the brainfog, swollen glands, untrustworthy vocal cords, in a darkened room with muted light so my eyes could bear it, I told her:
"To me it's a bit like a tide coming in. Moving towards recovery is like waves lapping up the shore; the breakers drag you back a little down the beach before being drawn back up again, gradually towards the strand."
I've had glimpses of high tide and I truly treasure them. Today I'm somewhere wandering among the rockpools, and do those limpets nip!
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