hi am new just to say thanks for all your posts and honesty describing issues

[linksy]

Through reading the posts on the site I have now discovered that it is ok to mention issues that I am having with pain, brain fog, confusion and worst of all constant fatigue and I have discovered some good advice about medication and treatments. Thanks for sharing x

[Hidden]

hi linksy,my name is sue.welcome to the family(but you wont see ant horses head in this 1).iv only been a member for bout 3wks and have been so welcomed.here your going to get understanding,lots of love and most of all you`ll be heard.i was told when i was daignosed 4yrs ago that most of the symptoms id been feeling over the past 23yrs were not in my head like id been told previously.iv learnt more bout Mr fibro(the b******) in the past 3wks than i have in the past 4yrs..their all brilliant here,you`ll always get hugs...WELCOME...lv and HUGS fm me xxx

[Hidden in reply to Hidden]

I've got to ask because it's driving me crazy. What is 'ant horses head'? I don't understand what you mean.

Christine xxx

[siver52 in reply to Hidden]

see bottom of page lol xx

[Hidden]

hi and yes this is definately the place to be for a moan acry a laugh for advice weelll anything you want really and yes we are allmhere for you so come on down love to you diddle x

[Hidden]

Welcome Linksy. Thanks for posting.

I've been a member for just over one week and this is the most helpful forum I have ever joined. Everybody is here to try to help both themselves and others.

If we're feeling really bad, it's OK to have a good moan and if we are having good days, it's great to give hope to others by telling them about the good days.

Look forward to hearing more from you as we go on.

Lots of lovely hugs (((((((hugs)))))))) and welcome again.

Christine xxx

[siver52]

I am guessing the horses head is from "The Godfather". The familia, the mafia. lol xx

[Hidden]

I'm glad you said that Siver cos I didn't know lol. Sue, what are you like? LOL

Anyway, hi and welcome linsky. You can mention anything you want here and we all know what you are saying and most here have probably been through it or are going through it too.

Have you had a look at the website? It's worth reading, there's some fabulous info on there. It's on the home page under Fibro-Action, visit our website......

Hugs Sue xxxx

[Ang01]

Hi Linky, lovely to meet you, and yes, you have most definately come to the right place to get help and support, and even sometimes just to have a bit of a laugh. They do say laughter is the best medicine don't they. I'm sure we will catch up again soon, take care, Love Angela xx

[Hidden]

hi, Linky I am new too but as everyone says it is one place where people do not judge you but in the outside world away from the forum its hard for people to inderstand what we go to, I sometimes just do not bothering trying to explain to others as it can often be "oh your in pain again? and where is it now??? you know what i mean it is hard my hubby said not that long ago, so why do you still have pain when you are on a memory foam bed?

This was when he still had teeth lol.

I mean how do you explain that even when you do sleep sometimes) you wake as if you have drank a bottle of vodka as you have the hangover from hell then your hips strt screaming for some oil to get them moving and for the rest of the body well we have a round another 15 areas that hurt and then we get up go for something and stand in a trance thinking what am i looking for???? yes we all understand what that type of day is right moan over today is a motivating day am going to pack for my jollies yipeeeeee hot hot sun helps a bit with athritis.

so welcome as someone said to the family <3

[jazher]

Welcome linksy,

We have laughs, moans, rants everything you need to do. It truly is an excellent site and i would be lost without all these lovely people. hugs, kel xxx

[retiredpharm]

Hi Linksy, I am a non-chatty man, retired but have quite a few years of experiance of fibromyalgia amongst other things. This site is the best I have seen dedicated to fibro. I can't do the "facebook" or "twitter" type chatter and feel almost out of place as a fella but it is interesting to read all the comments and stuff and add a bit of my own.

Keep reading and I am sure you will find it a help.

[linksy]

Thank you all for your lovely replies and i feel at home already and free to comment on posts i hope to share laughter and moans and info with others who understand hugs to you all x