Tell the UK government to speed up use of new treatments and tests

Share on facebook
Share on twitter
Share on email

Accelerated Access Review – UK (closes 11th Sept)

This is the UK government review on how to get newly researched treatments and tests to patients more quickly. This might have an impact on getting future M.E. drug treatments implemented and diagnostic tests for M.E. at our GP surgeries, considering the rituximab trial and all the research into potential bio-markers.

More information including and a link to a patient’s champion article to give you some ideas can be found at A Prescription for M.E.

Share on facebook
Facebook
Share on twitter
Twitter
Share on whatsapp
WhatsApp
Share on google
Google+
Share on email
Email

1 thought on “Tell the UK government to speed up use of new treatments and tests”

  1. Please help us, people with m.e., and c.f.s or whatever we are calling it at the moment we can get diagnosed and then we are left to rot basically, Ignored, there is no continuity of care for us, the pain gets worse the symptoms get worse and still nothing can be done.
    Somedays it feels like I’m in Gods waiting room for my turn to be taken and i’m not even bed bound, but hauling around a body that does not want to work in order to get things done makes life so much harder, it can be very frightening at times things happen that are never explained just added to the list of symptoms probably from your m.e. by doctors it’s not very reasurring because they dont know for sure if it is or not.
    We need alot of funding to help find out more about this disease and how to manage and control it.

Leave a Comment

Your email address will not be published. Required fields are marked *

Latest News

NHS England omits advice to apply clinical judgement re vaccine

It has come to light that a letter from NHS England and NHS Improvement to all vaccination centres and GPs in the UK has omitted advice that health professionals can and should apply their clinical judgement when placing people in group 6. Vaccination of people with underlying health conditions that put them at risk of

Read More »
Waiting for Superman Book on table

Waiting for Superman – UK Book Giveaway and Review

Do you want to win a free copy of Waiting for Superman? We have three copies to give away to people in the UK!  To enter, all you have to do is follow #MEAction UK on Instagram, like and comment on this post. The deadline is 9am (GMT) Monday 8th March! Win a copy! Thank

Read More »
#MEAction activists outside Scottish Parliament

Scottish Election! Ask your MSPs to support people with ME

If you live in Scotland, please join our campaign to ask your MSPs to pledge their support for people with ME. Email your MSPs The Holyrood elections are coming up on 6 May 2021 and we want to make sure that MSPs are aware of ME and the desperate need for support. There are more

Read More »

Help keep our work going

We rely on donations from people like you to keep fighting for equality for people with ME.

Donate

Get actions alerts and news direct to your inbox

You can choose what you want to be kept up to date on.

Subscribe
Scroll to Top