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14 Comments
Hi Sam. Love ur site and would love to know how it was created? I’d like to do a similar thing for people with MS I’m sick of the same shit associated with people suffering and just need a good kick up the arse to get it done! I tweet about Leeds Utd , MS and work and find it a relief to vent my frustrations sometimes.
Get back when u can and take goo care of yourself!! X Mike
http://www.thebrodiefamily.co.uk
Yay! So glad I can start getting my blog fix again! Can’t believe someone would hack your site. It’s a shame you’ve lost the comments too as there were so many brilliant ones from people who have benefited from reading your blog!
Looking forward to experiencing your journey again
Mich xc
Glad to see the blog up and running again. Love reading it and it usually putting a smile on my face. Had a replapse
so got plenty time to read the ones from the beggining. Hope that idiot that hacked your site has found something better to do.
Hi Sam, glad to see your blog is back and just as amusing as ever. Keep it up! Take care! Terri xxx
Sorry to hear about your site being hacked. I’ve been reading it for a while but was too shy to leave a comment, I suppose. I’m not sure why, since I know how affable Moodiesburn folks are, being one myself
I was never diagnosed with ME, but with PVF after a flu a few years ago. For two years I did a whole lot of nothing, and some symptoms persist to date, but I’ve started to think about employment again lately. Whatever I had, there is no doubt that I drew some of the inspiration to get over it from your site and from seeing you regain much of your mobility. You are always light-hearted and humorous in dealing with the cheerless condition that is ME.
All the best!
Thanks Bart for your kind words,
All the best to you too,
Mburn all the way
Glad your site is up and running again. So funny at times and now I have an idea as to who your Celebrities friends are, makes it even better.
Understanding the problems and challenges of ME through your site is an added bonus to broaden my understanding and awareness.
Keep up the good work.
Just read your history, have you ever been checked for crohns. Yes I was diagnosed with CFS and bed ridden after 4 years turned out to be crohns. Crohns can produce similar fatigue, gut problem, temperatures and bad joints, sometimes rashes
Hi sarah,
Yeah been tested for Crohn’s
Thanks for the comment
I have no idea how many followers you have (meant to have fewer than 200), but I love your blog and find it incredibly inspirational, so I nominated you for a Liebster Award.
Rules: https://ldndiary.wordpress.com/2012/11/14/liebster-award/
My questions: https://ldndiary.wordpress.com/2012/11/20/liebster-award-part-3-my-nominees-and-questions/
Hey,
Thanks much appreciated
Hey Sam, so glad the blog is back & we can all keep up to date with your progress. It’s amazing to think how much has changed it the last few year. But as always your are super positive and thinking of others. You are proof that u can achieve anything if u put your mind to it. Now get writing cos I can’t wait to read the next blog!
Posh x
Aka Proud big sis
Hi,
xx
OMG! i just cried when i started reading your blog! I.ve had M.E for the last 4 years and have had no-one else i know with M.e, the only one who understands it to any extent is my boyfriend! But now i have you! You’re amazing and i am probably going to be addicted now
Hellooo mrs wuman!!!
Just sitting in work discussing stuff
Keep calm
Bring on tonight
Love youuuuuuuuuuuuu xxxxx