Been having a nose around on here and finally decided to say hello as you don't seem to bite the "newbies"

Bit of a long story, but it seems that everyone who has this seems to have similar agonies getting their GP's to diagnose this.
I've suffered with (supposedly) spondylosis since an accident in my early teens, which just tended to flare up periodically. Flared up big time in January this year, leading me off to the GP after a couple of weeks as my usual remedy of ibuprofen didn't seem to be working. Got fobbed off by the emergency doctor with a prescription for co-codamol and told to take things easy. Two weeks later, I'm back in the surgery again feeling even worse, with pains in both legs and my arm! Managed to see my GP this time and got my a change in tablets to diclofenac after he suggested that the inflamation in my shoulder had probably trapped a nerve!!
Two weeks later I was back again, pains getting worse and tablets not helping despite the shoulder being much better. Now my friend has recently been diagnosed with FMS and swears blind by now that my symptoms are so much like hers that she's sure I've got the same thing. Can you hear my GP laughing at this suggestion, cos that what he did


So this time I leave the surgery with tramadol to add to the diclofenac and a referal to a physiotherapist. And so the cycle repeats itself, back and forth to the doc for 2 months with him insisting I've merely trapped a nerve in my back/neck. Seven weeks I waited for physio!! but he was well worth the wait, six sessions later and my neck and back are feeling better than they've felt for years, really improved posture ..... the works!!! Apart from one thing ... I've still got legs that feel like dead weights, and periodic pins and needles, arms that keep going numb and cramps in my fingers (sound familliar anyone???)
Doctors visit number ?? (I've count by this time) results in a slight change of track, now he wants me to see an orthapaedic consultant .... just to see what they think. Roll on another 2 weeks wait, and off to the appointment with a very nice, very helpful orthapaedic practitioner who, after running a few tests decides to send me off for an MRI. Another wait, another fortnight sees the MRI being done, followed by another visit to see Mr Nice Helpful orthapaedic man three weeks later. By this time I've been off work for 11 weeks, I'm getting really peeved with the pain, really, really fed up of daytime telly (there's only so much Jezza K a "sane" woman can take) and slightly stir crazy. How relieved was I when he said that my MRI was completely clear, absolutely no damage to my neck whatsoever woooooo hoooooo!! So what the b****y hell's been causing all this flipping pain then, his suggestion ..... Fibromyalgia

So finally, last week I go back to see the doc, he's not had the MRI results yet so I tell him what's been said about the MRI and then finally



So long and short of it is, another blood test to rule out anything else it might possibly be, a new prescription for amitriptyline to add to my others, and if the bloods come back negative, he'll refer me to a rheumatologist for them to confirm his diagnosis!!!!!!!!!
So not quite there yet, but I think I've finally managed to stop banging my head against a brick wall.
Sorry it's such a long rant, but after almost 6 months of grrrrrrrr with my GP, i think it's acceptable

Simi