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rachy

THANKYOU XX

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rachy

I know everyone is in the same posisition dx or not ..and i know the NHS has long waiting lists etc.. but i think its awful how when you get new symptoms/pain/numbness how we are left to deal with it until next appointment with neuro..

If it was'nt for other people to chat to on these forums etc and doing your own research i think i would be a wreck... i phoned my GP to explain about my pain/spasms have now gone and my foot is left numb.. ask if it was normal and anything i could do to help myself and was just told to keep taking meds and wait to see neuro end of month for my results.. i think its awful to leave people not knowing what to do next.. Wondering if your doing something wrong and making things worse for yourself..

 

I would like to say a BIG THANKYOU to all the new friends ive made and for all the help they have given .. :dunno:


.....................................

 

Rachy xx

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linds

and a big thankyou to you Rachy for your friendship too Love, Lindsxx


Lindsx

 

 

 

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Vegged Out
Shirl

Oh Rachy, there's an old saying, "it takes one to know one" and that is why we are all here - for each other!

 

You take care now



Shirley  "one day at a time"

 

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Jayneanne

Its great isnt it, to know that there are others out there who really understand and care

 

THREE CHEERS TO MARINA FOR STARTING THIS FORUM :dunno::wchair::bricks:

 

Hang on in there Rachy and thanks for joining us

 

Bug hugs Jayneanne xxxx


Jayneanne

We make a Living by what we get, we make a Life by what we give

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Teen

Rachy you've taken the words right out of my mouth. I feel so grateful to this forum, Marina for starting it up in the first place and to all the moderators and members for being so wonderfully supportive and understanding.

 

I have people to winge at when I can't talk to anyone in my own life and I'm grateful for that.

 

So a BIG :hehehe: from me too!!!

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Sluggish
Marina

The thanks aren't due to me at all, they're due to all of you as it's all of you who make the forum :hehehe:

 

The forum has grown into far more of a supportive and friendly forum than I ever dreamed it could and I now feel extremely proud of you all for helping to achieve that.

 

Thank YOU all :sorry::cowboy::hearts:


Marina

(belated DX in June '05, SPMS)

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Fine
WobblyGreg

Got to agree with you all the site helped a lot when i was just getting treated like some second class lost cause by my supposed health carers(still am by some TBH)here i found support and that i wasnt alone which helps.

Marina :hehehe:

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gareth

the support available here is excellent. after my diagnosis i was basically told to get on with it and apart from seeing the ms nurse once a year (who's very good), nobody seems interested or understands the daily difficulties (apart from all you wonderful people out there!) :smarty:


everybodys got to believe in something

i believe i'll have another beer

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Michelle

Cool pic! Is that you in the photo?

Michelle :smarty:

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gareth
Cool pic! Is that you in the photo?

Michelle :smarty:

 

 

that's meon the twrch in north wales near bala.

last july in all the rain we had.


everybodys got to believe in something

i believe i'll have another beer

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Oops

Another vote of thanks from here too. I read a LOT more than I post, but it's great to know I'm not alone. :penguinball:


Apologies in advance if I post then vanish for a bit - I work away from home and will be back at the weekend!!!

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linds

When I was going mad with it all at xmas you all helped so much and have done since. Like today I feel low as a visit to neuro y day was a waste of time really. He accused me of over Googling when I asked searching questions of him....like LDN.

 

Boo Hiss to the negative and come on to the postive.

 

Oh by the way he said that having ms now is not like it was 20 yrs ago when there was nothing to help...............Gee wizz i thought bring it on then..........when can we have access!!..................Love grumpy Lindsxxx


Lindsx

 

 

 

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peter

This may sound stupid but i thought that all drugs in the NHS tool box were now available to all

 

The government scrapped the postcode lottery last week

 

Peter :penguinball:


STILL LIVING ( I think )

 

DXed 2000 PPMS Wheelchair bound

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Oops
He accused me of over Googling when I asked searching questions of him....

 

ROFL...Mine does that. They hate an informed patient, don't they? :penguinball:


Apologies in advance if I post then vanish for a bit - I work away from home and will be back at the weekend!!!

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linds

Thanks Peter.I shall remind them of this.

OOpps...YES YES YES they hate a patient who pre ms ms quite academic!


Lindsx

 

 

 

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