There is an irony the fact that a couple of days after my last post I had the worst fibro flare up I’ve had in ages! Plans cancelled! Catastrophe!
Hey ho and never mind, we had fun anyway. As you can see we put our tree up and everything is coming up Christmassy! I’m starting to get excited about Christmas now and really looking forward to the break. Our office closes on Christmas Eve and doesn’t open again until 2010 (which is ages in the future, right?) and we’ve elected for very simple celebrations this year. On Christmas day itself we are going to the seaside (yes, I know, in England, in December, we’re insane), then I think we’re seeing family members the day after Boxing Day, going to a dinner party on New Year’s Eve at a friend-from-work’s house and who knows what in between. We’re definitely hoping for a trip to London (I want one of those Top Shop style advisor appointments before I’m too old for Top Shop) and bowling. Christmas wouldn’t be Christmas without bowling.
How about you, dear reader, what are you up to for Christmas this year?

This week I am also thankful for:-
- The writing/editing course my parents have bought for me.
- Pain medication for flare ups.
- V+ (the recording device on cable TV) which is very handy when Dave Grohl and Rhys Darby are on at the same time on different channels.
- My lovely life with Himself and the kitties (only one kitty present in the photo though!)
Learning to live with Fibromyalgia has taught me many things. And what I’m learning right now is to be kind to myself, not to expect so much from myself all the time.
Whilst I was only formally diagnosed with Fibro a couple of years ago, I’m pretty sure I have suffered on and off since I was about 17. At first they said it was “growing pains”. When I pointed out I wasn’t growing anymore they called it ME. Somewhere along the line that got changed to CFS (although I’m pretty sure they’re the same thing) and now it’s got another name! Whatever you call it, in the long run it amounts to the same thing – exhaustion, headaches, a 15 year sore throat (!!) and, coupled with the scoliosis, pretty much constant chronic pain.
Now before I go on I want to say that this isn’t a self-pity post. This isn’t a “Why Me?” lament (because, as I have said before, “Why Not Me?”). This is just a reminder of how far I’ve come.
One of the hardest things I’ve had to deal with is other people’s attitudes. ME has another name in the UK – “Malingerer’s Disease” – and I cannot tell you how many times people have said to me “but you don’t look ill”. No maybe I don’t, I’m a whizz with the make up brush but inside I feel like stir-fried ass – thanks for asking! ;p
But no matter how hard it’s been I’ve always tried to live my life to the fullest, to drag my sorry carcass out of bed and get on with things to the best of my endeavours. There have been times when I’ve had to put my hands up and admit that something is too much. I decided against a long-term dream of studying Archaeology because I knew my health wasn’t up to the 12 weeks a year in a tent in a field digging holes aspect of it all. But if I had studied Archaeology I would never have gone to Australia and I would certainly never have found out I could write.
And that’s it isn’t it, dear reader? Everything that happens, good or bad, gets us to where we are today. Yes, I may have to walk rather than run, I certainly can’t have more than one alcoholic drink without falling asleep and some days I have to drag that aforementioned sorry carcass back to bed. But on the other hand, I have gained an Masters degree, travelled the world (more than once) and worked in law in the City of London for nearly 10 years. And I also know without this I would never have become a yoga teacher. After years of practice that helped me keep my body strong enough to deal with pain and my mind strong enough to deal with the sadness the pain could bring and with the help of some fantastic teachers I realised that my limitations (for want of a better word) could help me reach out to people who wanted to know about yoga but had been too afraid to ask! As I tell my students, if I can do it anyone can.
I have days when the pain is too much, when it really brings me down. But we all have bad days. Right now I’m learning to accept the bad days and look after myself on them, because there are so many good days and I have achieved so much in my own little way.
This morning I taught my last class at The Mulberry Centre, where I teach volunteer yoga to people with/recovering from/caring for someone with cancer. As I mentioned a couple of weeks ago, my schedule has spiralled out of control and I’ve had to cut back on a few classes. I’ve chosen this particular class less because it doesn’t pay (that’s really not a huge issue) and more because it involves a nearly 2hr round trip in the car which really depletes me of spoons!
Word had got around that it was my last class and nearly everyone I’ve ever taught there turned up! It’s not a huge room so it was a bit of a squish, but we had a lot of fun and worked on pranayama and meditation. It was so incredibly moving and humbling to see so many amazing people coming to me for their yoga – and thanking me afterward for everything I had given them. Some of them had all sorts of advice/tips for living with fibromyalgia/Chronic Fatigue as well – although I’m not quite sure how that bit of information got out into the public domain!!
Speaking of the fibromyalgia, I had my follow up appointment with my GP today to get the prescription for the Lyrica (for reasons I cannot understand, you need 2 doctors say so before you can get it). I picked it up from the chemist today – although there were only 10 tablets in the whole of Surbiton and I was prescribed 84. I have to go back for the rest next week.
Because they can cause drowsiness at first I’m going to start taking them Saturday night as I’m teaching pregnancy yoga tomorrow morning. It seems somehow serendipitous that I have all of next week off in which to get used to the drowsy feeling!
So I think that’s it for today – have a great weekend everyone!