MS-STEUNACTIE loopt van 14 januari tot 25 mei 2011 / MS SUPPORT ACTION runs from 14.JAN. TILL 25.MAY |
PLEASE NOTICE: For organizational reasons we ask those who are really coming to Brussels to fill out the form . Thanks for this.
GOAL OF THIS ACTION: MS SUPPORT ACTION : RUNS FROM 14 JANUARY UNTILL 25 MAY (MS WORLDDAY)
What has been achieved up to now:
Contacts:
Schedule for
5 May
12.30 :a.p. meeting Alexander De Croo
17 May
10 : a.p. meeting Etienne Schou
25 May (so far):
11:a.p. meeting Jo Vandeurzen (Flemish Parliament)
13.30:a.p. meeting Fadila Laanan
14:a.p. meeting Delizée
14:30 p.m. meeting with Elio Di Rupo
16:30 p.m. meeting with Petru Luhan (European Parliament)
Goal of this action :
You may know someone with MS. Or maybe you see yourself day in day out confronted with MS. In either case SUPPORT this action.
MS is a disease that although not always visible gradually makes it impossible for the patient to function normally – physically as well as mentally. MS starts in the brain. It then progressively attacks the nervous system. As it spreads throughout the body, the patient’s gait, balance, and vision deteriorate irreversibly. In the end the patient finds himself increasingly disabled and largely dependant on another person’s help.
Belgium lags behind in its fight against MS and the impact it has – socially and financially – on the patient’s life. There is no national register. Financial support remains insufficient. Not enough coverage from the media.
In order to focus public attention on this devastating disease I started this action (together with my daughter Isabella – see her picture on this page).
How to support this action:
Either visit the page on Facebook and express your support
Or Leave some comment in the guestbook on this site. The pressure must increase!
All reactions will be collected in a file. This file will be handed over to our national and European policy making authorities in Brussels on 25th of May, world MS day 2011.
The more numerous we are, the more successful our trip to Brussels will be. A special appeal to those who cannot come to Brussels: if you cannot be there please leave some words of sympathy in support of our action on the Facebook Page.
This action runs from 14 January until 25 May 2011. From the 15th of May onwards all modalities will be worked out and communicated.
Isa tells about MS – movie (Dutch spoken)
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Disclaimer: ‘MS Views and News’ (MSVN), does not endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, and procedures for your personal knowledge and to keep you informed of current health-related issues. It is not intended to be complete or exhaustive, nor is it a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly.
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