Well, that was a ‘fun’ appointment yesterday’; new (to me) GP insisted on explaining MS to me in the sort of voice some people use for speaking to a child (don’t understand why people choose a weird sing song voice for speaking with children - but I digress). Spent ages explaining what sort of symptoms I will have, the inevitable decline of motor function and so forth; and chose to give me the upbeat closer that “but don’t worry, you won’t be in any pain.”
Me: ???
GP: Pitying smile, nodding.
Me: I have been in pain with my MS since October 2013 - 24/7 365 days a year.
GP: No, MS doesn’t cause pain.
Me: (gets phone out and scrolls through contacts) Here, this is my MS Specialists’ number, he has made MS his life’s work/study, you can contact him and tell him he’s talking out of his behind where MS and pain are concerned.
GP: ?
Me: Holding out phone - please, go ahead, MS neuropathic pain is why I am on a ridiculous cocktail of drugs to control/dull the pain.
Much to and fro followed - having advised GP that I have between aware of MS for over 40 years (my oldest brother lived with it for 28 years), and I have read many, reliable research papers, including some published in the Lancet concerning MS, symptoms, medication etc. And, that I am quite aware of the symptoms that I have, because, well - I have them!
Me: Now - can you prescribe the antibiotic I need for the flipping UTI I have?!
GP: Prescription will be at the Chemist immediately.