December 1, 2003
Multiple Sclerosis Society
Louise McVay, a 31-year-old UK woman with multiple sclerosis, goes to Strasbourg next week to hear if the European Parliament will act on her plea for all EU countries to provide equal access to quality healthcare services for people with the most common disabling neurological condition striking at young adults.
Louise, from Loughborough, petitioned the Parliament after writing "in desperation" to the President on behalf of many of the 400,000 people with MS across Europe being denied access to proper treatment and support. The Parliament's Committee of Petitions, in cooperation with the Committee of Employment and Social Affairs, has now drawn up a report which also embraces MS research and employment issues. A motion for resolution will be debated on Thursday 18 December 2003.
It calls for:
She wrote to her MP and then to the Prime Minister, receiving "the standard reply". "In August 2001, I just sat on the internet wondering who was in a higher position than him and thought of the European Parliament.
"I went on to their website and found the name and contact details of the president and wrote explaining the difficulties of people with MS in the UK and asked for her help. I had a personal reply, saying my case was being forwarded to the Petitions Committee."
Though Louise did subsequently receive beta interferon after the Department of Health launched its risk-sharing scheme in 2002, she says has become more determined than ever to press the case for equal access to high quality treatments and services for everyone living with MS.
She told the Petitions Committee, "I am a strong person who fights hard to get what I rightfully should receive. Others are not in a position to be like this."
Also attending the debate will be Sarah Phillips, chairman of the UK
Multiple Sclerosis Society, as well as representatives of the European
MS Platform and of other national Societies.
Copyright © 2003, Multiple Sclerosis Society