Forgetfulness

[looloo4007]

Hi everyone, It seems I have been on here before as I put my password in and got on,but I cannot remember (fibro fog ),I am 50 this year as diagnosed in Feb this year .seems like a good site .

[Hidden]

Welcome.

I'm sure you will find it helpful and get lots of support.

Good luck and best wishes.

[looloo4007 in reply to Hidden]

Thank you

[peck]

Hi and welcome to our site.Its actually better than good !!! I think you will find it very helpful and there is lots of fun.Loom forward to chatting with you . Peck.🐤

[looloo4007 in reply to peck]

Thank you

[rosewine]

Welcome hope that you find the site helpful. Any questions ask away there is usually someone around who can share their experiences. Look forward to your future posts.x

[looloo4007 in reply to rosewine]

Thank you

[TheAuthor]

Hi looloo4007

Yes,you were last on here 2 years ago when you replied to a post! So, welcome back and I sincerely hope that you are feeling as well as you possibly can be today?

Since you were last here we have merged and are no longer FibroAction but FMA UK. I have pasted you a link to our new mother site, FMA UK which hosts loads of useful Fibro information:

fmauk.org/

I want to sincerely wish you all the best of luck, and please take care of yourself.

All my hopes and dreams for you

Ken

[looloo4007 in reply to TheAuthor]

Oh really gosh my brain is worse than I thought, it's worrying, but thanks for letting me know that,and thank you for the link too,take care

[TheAuthor in reply to looloo4007]

[Pinkfinger]

Hi I am new to all this and did not even hear about Firo until a few weeks ago. However I have just about all the symptoms. I started gradually about ten years ago.

[looloo4007 in reply to Pinkfinger]

Hi there,are you now yet diagnosed then,? It's a frustrating illness and what makes me more frustrated is people can't see it so assume your ok !

[Pinkfinger in reply to looloo4007]

Well the doctor said he thinks that's what I have. I would need to have more blood tests. (I already had one about xmas that showed I had inflemation in my joints) and then said that there was nothing that could be done about it. He then asked if I wanted more pain killers.

[looloo4007 in reply to Pinkfinger]

You should ask your doctor to refer you,there are no blood tests to prove fms ....

[looloo4007]

I don't think I've replied to all on this post I can only see 5 and it says more,ill get the hang off it !!

[Hidden]

Hi looloo, welcome, I am sure you will find this place fantastic, all are very helpfull, and funny at times. Just sorry you found us with this illness. Take care

[Smiler69]

Hi welcome to our wonderful Fibro family. I look forward to speaking with you .

Jane .🌺

[looloo4007]

Thank you ,me too