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A Shout Out to all SPMS Patients out there
Now that I’ve somewhat recently joined the Secondary Progressive (SPMS) crew, any medicines that could possibly help us get my full attention. There’s not a lot!
New drug foralumab [Improvements Continue in Second SPMS Patient Given Foralumab | Multiple Sclerosis News Today/] has miles of road testing before it would become available in any of our MS service stations. It does this: ‘Six months of treatment with foralumab nasal spray led to significant functional improvements in the second patient with non-active secondary progressive multiple sclerosis (SPMS) who received treatment under a single-patient expanded access program’.If it makes it through – the delay to us in the UK will be far longer. Hey-ho
If you have SPMS let me know how your journeys have been going. I ask as someone whose GPS isn’t quite sure of the road ahead. What have your experiences been?
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