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The MS Society has been campaigning for this but they really NEED US, the people with MS, to help strengthen the campaign by writing to our local politicians and putting pressure on them with our personal MS stories and how the heat affects us. The more of us who can get involved the quicker this will happen.
Without us and our personal stories it will fall on deaf ears as it's just the society lobbying for it without support from sufferers'. Together we can make it happen though!!
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