Tag: Neurological Illnesses

+

MS News: April 2017

The latest MS news about clinical trials, research, treatments, mental & emotional health, diet and lifestyle, including highlights from Barts MS Blog

MS News: March 2017

Highlight still on American Healthcare Act, the replacement plan for the Patient Protection and Affordable Care Act (ACA) released by Congress on March 6, 2017 Society Releases Statement on American Health Care Act National MS Society Urges Lawmakers to Oppose American Health Care Act Reducing Out-of-Pocket Cost Barriers to Specialty Drug Use Under Medicare Part D: Addressing Researchers find patients’ annual financial burden under … Read More MS News: March 2017

MS News: January 2017

Go red to Kiss Goodbye to MS campaign! Supporters in County Donegal asked to Help Kiss Goodbye to MS Supporters in county Longford asked to Help Kiss Goodbye to MS Co Leitrim people are being asked to help ‘Kiss Goodbye to MS’ Highlight! The top 10 drug launches of 2017 The year in new drugs

200 days

“To many, life with MS can seem like a book where letters have been replaced by numbers or where the cover can be too hard or too soft for its content. Because of this, I don’t want them to see what MS can turn into. I refuse to show them that there is no cure, I refuse to give them a reason to give up on me. In my view, it is very much a case of the illness being mine, but the tragedy theirs if I let them.”

10 years: a lot to be thankful for

“MS itself? It took my job, but it doesn’t own me. MS doesn’t get praise for having me. No matter how bad MS treats me in the future, I am its CEO instead. I will never lose is the knowledge that I conquer MS every single day of the year. Perhaps not physically, but mentally I am stronger than MS.”

Ten happy MS years

A milestone like no other. A curious, strange one indeed. Ten years of living with MS. Ten. In fact, ten years and one week. Reality suddenly became a very different kind of living. As strange as it sounds, it became a more fulfilled life, a happier one also.

Positive MS News: September 2014

It has been a big and very busy September for researchers, clinical trials and pharmaceutical companies. Early this month, the Joint ACTRIMS/ECTRIMS Meeting took place in Boston. For more, please check the extensive website of the conference.

MS in numbers

“Instead of going into the possibility of ending their life in a wheelchair, I refer to the opposite side of the scale. When they say “But 25% of people with MS will end up in a wheelchair!” I say “Perhaps, but that means that 75% of people with MS will not end up in one at all!”

Game, set, relapse!

“In short, if I’d have to sell myself with these words, I still wouldn’t receive a Booker prize. I could post “Another MS Relapse” award on the fireplace mantel, but they’re just a waste of space. I thought of referring to a relapse as something you just have to get your teeth in, but I don’t want to steal Luis Suárez’s limelight.”

Volunteering, a worthy cause

“In fact, for anyone interested in volunteering, research shows it can be beneficial in improving mood, self-esteem and quality of life, and in reducing stress, pain and depression. It also shows that ill people who volunteer, become better at managing their own illness in turn and volunteering can strengthen their immune system.”

%d bloggers like this: