Stop Discrimination of young disabled

Signed and shared on Facebook, Lucid. Wishing all the very best to your DGD.

I have signed it. What about also doing an epetition on the government website, or getting your MP to do an early day motion?
I do not know where you live but I know my MP was involved in similar work for 25 years before becoming an MP.

Signed - hope it helps

Me too, my nephews and a niece all had ME, it's so debilitating. Mine are now in their late 20s and only the niece is left with symptoms, so fingers crossed for your DGD.

Signed - good luck with the campaign.

Lucid I'll sign, too. Let's hope that it makes a difference. Sadly, ME is still a bit of a Cinderella and, from what I've experienced, most lay people don't seem to know anything about it.

Don't want to hijack this thread, but here's a link to a comparison chart, which I've posted on a previous thread. It shows the differences between ME and CFS, which often get lumped together:

www.hfme.org/comparisonchart.htm

You might be interested in this link, Lucid, unless you already know about them. Action for M.E support them.
www.whobenefits.org.uk/page/content/front

Thanks to all for your support and for the links. durhamjen I've passed this onto my DD . DGD tried very hard to remain in college but found it too exhausting and her condition got worse. Yesterday DD went to a local college to talk about getting her on a course - they were very encouraging on the phone - but was then told they couldn't help.