thanking the girls

[geo1888]

I would lie to say thanks to Amyloo,Heather3418,and Lulu54.
I can assure you all that i wont stop asking questions until either a doctor or a neurologist gives me an answer i can understand and explains my condition. My problem now is i have seen two neurologists, one of them an ms specialist and both of them have failed to give me any kind of answer. I realise ms is very hard to diagnose but my own gp has sent me for every test he could and they have all came back clear,what my worry is there are not many more neuros i can see in Glasgow and i cant go private. If i havnt got ms, why the mri's and the lp's they obviously thought i might have it.If it is something that mimics ms has it got a name and why treat me with ms drugs.What really anoys me is that both neurologists dont seem to care about listening to me and what my daily problems are .I know my condition is getting worse { whatever it is} but they seem to rely on their opinions and it is hard to disagree with them .Anyway the reason i havnt been on for a while is i didnt want to keep bothering you all with the same complaints and moans there are a lot of other people who need your advice more but i will  try and stay in touch and keep you all updated
Thanks again for your time and thoughts.
George

[Heather3418]

Thank you for your sweet comments.  Everyone here on the Forum are always glad to help in any way they can.

George, please know that even though you do not yet have a diagnosis, that all of us can (diagnosed/not diagnosed) learn from each member.  Each one of you bring information and questions to the Forum, that we can all learn from.

Don't be a stranger....hope that you will keep on posting and will answer questions from others in your same position.

All the Best,
Heather

[Amyloo]

Hi George,

I am always so happy when I can give any help or encouragement.  God bless you; don't give up.  And don't stop posting.  Everyone here loves to help.  Amy

[Lulu54]

You can come through here any time and moan and complain about the same things over and over and we won't care.  With my MS cog fog I might not even remember that you are repeating yourself!  :-)

The frustration you feel is obvious, and I hope you will continue to use us as a sounding board.  Its good to get it out somehow, someway.

my best,
Lulu