The list of my issues were (this is not an exclusive list):
- poor bladder control and extreme urgency in needing to go to urinate
- inability to feel my fingers on both hands which made doing pretty much anything difficult lack of sensation on the skin of my stomach legs and feet and an altered sensation in my intestines
- worsening ability to walk straight and with the coordination
- general coordination issues
- inability to run in a coordinated fashion
- the range of my walking was decreasing so that I could walk about a kilometre at my top range with some short-term focused deficits
- some short-term memory deficits
- some word selection deficit
Considering all of these ailments and worsening disability, I felt pretty impotent in being able to do anything about it since the NHS was unable to prescribe any meaningful treatment for PPMS. I started to research around the subject and one thing kept coming up again and again.
HSCT - Haematopoietic stem cell transplantation.https://www.mssociety.org.uk/about-ms/treatments-and-therapies/disease-modifying-therapies/hsct |
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