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Hi, my name is Ogmoose!
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Ogmoose
Community member Posts: 11 Connected
My nickname anyway. Hi to all fellow sufferers. Reading some of your accounts makes me feel lucky. My diagnosis took less than 12 months thanks to a very switched on consultant at Stafford. At last I know I'm not nuts or a hypochondriac!
Comments
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Hi @Ogmoose, and a warm welcome to the community! If we can be of any assistance, do let us know.
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Hi,
Thanks for the welcome, still need to find my way round on here. Got fibromyalgia and CFS not really sure if that counts as a real disability when I see the courage of some people it seems a bit insignificant. Not ill, not dying, just aching and sleepy! -
Hi @Ogmoose, do let me know if you have any issues: our community guide may be helpful.
I believe fibromyalgia and CFS are now both recognised as disabilities- and as I'm sure you know, can massively vary in severity between different people. I have moderate ME/CFS myself and it's certainly no walk in the park! -
Thanks, that makes me feel better. I suffer from foot in mouth too. I meant my own levels not other sufferers. It's more of a hobble in the park then a short kip on one of the benches. Hope I don't seem a bit of a berk, having a bad day.
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Not at all @Ogmoose, definitely agree it's more of a hobble! Hope the rest of the day is as bearable as possible and that tomorrow is kinder to you!
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Thank you
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Hi @Ogmoose
A very "Warm" welcome to you today.
I'm part of the "community team" on the site. We are all here to help /support you in anyway!!!!
Like a number of us on here I myself have got "Chronic Pain"
This has now left me wheelchair ♿ bound.
Yes I'm classifyed "disabled" now!!!
This is no "Problem" at all.
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Thank you. I really admire all the positive attitudes you are all really uplifting!
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