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Nova | nzerox2~AT~hotmail~DOT~com
Just to say thank you, I have been suffering from syptoms for I'm not sure how long now been signed off work for 3 months now and gp just did another months worth today over the phone, Fed up with tests never have I passed so many tests as I have these last few months, So tired! Dr says I should not do anything but rest for a week then do one task a day but I have a disabled son off school for the summer and a bed bound father in law to care for, Rest?

7 August, 2008 at 21:25 - Hampshire UK

Kenny McKnight | kenee~AT~btinternet~DOT~com
Thanks for the great site, I can so relate to the other peoples posts, I wish everyone well,

12 July, 2008 at 07:07 - Scotland

Rebecca | becky~AT~beckynet~DOT~net
I have been suffering in silence for about a year now, Constantly visiting my GP without any help or diagnosis, My symptoms remain as CFS ME, I did manage to get my GP to sign me off work for 6 weeks with depression, but both my employers and to a certain extent my GP were so horrible about the situation I was forced to resign,
I have not worked for over a month now, since my final resignation, and don't know how I am going to pay the rent, I have yet another appointment with my GP this afternoon and yet again remain hopeful that something will happen, It has to, My partner remains that it is all in my head and that I just need to think positively and get out and do some exercise, Haven't we all heard that before, Meanwhile I am at a loss, I can't do anything, even typing this is causing pain,

30 June, 2008 at 21:24 - UK

Angel | miss_angel_mae~AT~yahoo~DOT~com
I want to thank you for this website, As someone newly diagnosed, it's such a relief to know I'm not alone,

28 June, 2008 at 06:59 - US

oliver | ollie~AT~sandon~DOT~plus~DOT~com
i have cfs and nobody belives me

24 June, 2008 at 01:13 - england

Lucy Cox | doogle_1988~AT~hotmail~DOT~com
I just wanted to say thank you, I am suspected of having CFS and found his website to be reassuring and informative, Thank you so much

19 June, 2008 at 04:32 - England

Carolyn Brown | Dive_16~AT~hotmail~DOT~com
I was diagnosed with cfs/me in Jan this year, the hardest thing is that no-one gets it i think, i am trying to get back to work as my boyfriend suffers form severe depression and cant work so i have to be the bread winner, needless to say work aren't being great ad i feel very alone, its good to see other peoples stories and know im not alone, thank you

16 June, 2008 at 17:49 - UK

Karen Tracey | karentracey01~AT~aol~DOT~com
I have recently been diagnosed with CFS/ME after 7 months of not being able to do anything, even after sleeping uniterrupted 12-14 hours at night, i now find it difficult to walk even a few steps, the pain is so bad in my legs and hips, apart from the fact they are like jelly and go in the direction they want to, i feel ashamed that i have this syndrome as i always imagined ME to be in the head and not real, there must be something i can do to stop this, now i know different, but still find it difficult to accept, Strangley enough i am not depressed but very frustrated that i cannot do the things that i was enjoyed, will i be able to dance again, I suffered a stroke 5 years ago and lost my sight i have approx 20% vision and now feel totally peeved after getting back to normal (ha) i have to start the battle again, Im scared i wont be able to work again, how long will it take to improve? I need my life back so my 3 year old grandaugher doesn't say "why you not happy with me nan" This site has made me feel that i should not be ashamed !!!!!! Its not something ive done but i will find ways to overcome this or a least deal with it,

17 April, 2008 at 19:52 - Newport South Wales

Peter Morgan | peter_vicky~AT~btinternet~DOT~com
18 months of symptoms, 6months since diagnosis CFS / ME still waiting for some sort of help / support, About to loose job, main income, Your site seems to be giving a lot of people support & help well done and thanks,

7 April, 2008 at 20:46 - Cumbria

dawn | dragonlady1380~AT~yahoo~DOT~co~DOT~uk
hi all, im a member of a site called foggy friends and it is great for info and suport, it also has a chat room, ,
at the moment im trying to find any docs that specialise in ME/CFS in scotland, my gp has just left me to get on with it for the last 2 yrs and ive had enough

6 April, 2008 at 03:20 - scotland

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Webmaster comments :
Hi Dawn, thank you for leaving a message in my guestbook.... to date, and I have been trying to find out this information also... seemingly, there are none....

If perchance anyone has information on this subject, please feel free to leave a message....

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Linda x


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