Fibromyalgia Action UK
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Anyone had dynamic MRIs done on NHS to check for PC3? Thanks

Hi there, has anyone had success getting an NHS referral to check for PC3? I am not claustrophobic and have had many regular MRIs done. I was diagnosed with fibromyalgia years ago and have never been happy with the diagnosis. I can't look up without pain and I'm convinced that it is compression which is causing my CNS work up and widespread pain. I'm feeling pretty desperate.

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HI LADYMARMALADE, I HAVE PASTED YOU THIS FROM YOUR POST SECTION SO THAT YOU WILL SEE THIS.

GOOD LUCK

KEN

TheAuthor Volunteer

Hi Ladymarmalade

I sincerely hope that you are feeling as well as you possibly can be today? I have pasted you a previous link from FibroAction about PC3 MRI and it would appear that the chances are of this are not good I am so sorry to say.

healthunlocked.com/fibroact...

I want to wish you all the best of luck with this, and please let us all know if you do succeed in this?

All my hopes and dreams for you

Ken

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Hi ken, I've got it now so I'll look at it, thanks. I've had a bad month but am up to looking at this stuff again. It's a bit overwhelming. I've done nothing about the benefits I asked about. I never thought I'd ever be looking at this stuff :-(

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Hi Ladymarmalade

I understand only too well how difficult this must all be for you. If you need any help or advice with your disability forms, please contact Mdaisy, who is the forum administrator. I have put her email address below:

info@fibroaction.org

Take care and I want to wish you all the best of luck.

Ken x

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