The second part - from under the leaves picture - that - just that ...
https://rebirthofclarity.wordpress.com/2015/08/13/i-want-to-start-a-commune-for-people-with-fibromyalgia-as-we-are-the-only-ones-that-get-it/
Thursday, 13 August 2015
Wednesday, 28 January 2015
Reblog and comment ... where next?
I just read this blog by Seeking Equilibrium (Questions but no answers yet) and yet again was struck by the similarities so many of us Fibro sufferers have in terms of our experiences with the medical community and diagnosis.
I too am at yet another of those 'umm' moments ... since my last health post here I've gained yet another unconfirmed diagnosis (PCOS - the ultrasound was clear, but bloods and other symptoms say I have it, hence not officially diagnosed), and have been referred to more than one hospital department regarding the Fibro/CFS. I've also had an MRI and EMG testing. And here comes the problem ... both those tests came back pretty much 'normal' too. In other words, at least on the preliminary inspection of the testers themselves, they didn't show up what it had been hoped/expected they would.
So I know that when I go back to see the Neurologist who sent me for the tests, he's going to do an 'umm' and pass the buck back to my GP just like the others have. My GP who's been with me the last 2 years of all this by the way has just left the practice, so it'll mean me having to break a new one in, quite possibly having to go through a years worth of bloods etc to satisfy them before getting any further.
And all the time, I'm feeling just as bad, if not worse.
All I want is a definitive answer, or at least one that won't get changed by the next person to see me. I don't even care if there's no cure at this stage.
I too am at yet another of those 'umm' moments ... since my last health post here I've gained yet another unconfirmed diagnosis (PCOS - the ultrasound was clear, but bloods and other symptoms say I have it, hence not officially diagnosed), and have been referred to more than one hospital department regarding the Fibro/CFS. I've also had an MRI and EMG testing. And here comes the problem ... both those tests came back pretty much 'normal' too. In other words, at least on the preliminary inspection of the testers themselves, they didn't show up what it had been hoped/expected they would.
So I know that when I go back to see the Neurologist who sent me for the tests, he's going to do an 'umm' and pass the buck back to my GP just like the others have. My GP who's been with me the last 2 years of all this by the way has just left the practice, so it'll mean me having to break a new one in, quite possibly having to go through a years worth of bloods etc to satisfy them before getting any further.
And all the time, I'm feeling just as bad, if not worse.
All I want is a definitive answer, or at least one that won't get changed by the next person to see me. I don't even care if there's no cure at this stage.
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