I am 47 years old and have MS. I retired early at age 45 and my mobility is deteriorating. Yet my worst symptom by far is invisible central neuropathic pain.
I am therefore very moved to have learned today about a lady called Vicky, the exact same age as me, whose MS has taken a most aggressive course:
http://multiple-sclerosis-research.blogspot.com/2018/02/guest-post-argument-for-legalising.html?m=1
http://multiple-sclerosis-research.blogspot.com/2018/02/guest-post-argument-for-legalising.html?m=1
I urge you, please, to attend the house on Friday 23 February when this private members biĺl is read and vote to support.
I would be happy to meet up with you and try to explain first hand the problem of intractable neuropathic pain if that would help.
With kind regards
Ok, it was an e-mail. Probably stands even less chance of being read, let alone acted upon. But this is such a desperate tale, I urge you to do the same. Private members bills notoriously get nowhere, although this one may have a huge weight of public opinion behind it and fare better.
Ok, it was an e-mail. Probably stands even less chance of being read, let alone acted upon. But this is such a desperate tale, I urge you to do the same. Private members bills notoriously get nowhere, although this one may have a huge weight of public opinion behind it and fare better.
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