The nearest neurologist and I could see was in Winchester and, after my initial diagnosis in August, I was able to see him in November. Again, he gave me a physical examination and we talked through my symptoms. He was also able to analyse the MRI scan that I had done privately. He concluded, with my age and the position of my lesions, that I most likely had Primary Progressive Multiple sclerosis.
Showing posts with label diagnosis. Show all posts
Showing posts with label diagnosis. Show all posts
Friday, April 12, 2019
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My Covid Jap Update - An Overdue Post!
I actually recorded this ages ago but forgot to post it. Hey ho! had both jabs some time back for Covid - Astra Zeneca - but had quite an a...
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One of the things I am obviously interested in is looking at each of my symptoms of MS and seeing if they, straight after the HSCT treatmen...
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My multiple sclerosis story started probably some three years ago or so. My first symptoms that I experienced were a lack of sensation in m...
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Today is the fourth day of chemotherapy and I tell you how I am feeling in the video. Whilst my body is weakening, much of this can be put ...
