Hi ive just been diagnosed with this, im in my late 30s and told it is very rare. Im trying to educate myself as much as possible. But cant find lots of info out there. Does anyone else have this varient of m.s?
Hello @lynseylou235 Welcome to this forum, I have found it very helpful and comforting.
I had never heard of it and just done a quick google. I am so sorry you have had this diagnosis and I do pray you are stable.
Stay well and happy.
Welcome and I am sorry to hear of your diagnosis. There was someone recently that posted on here with the same variant so you may be able to find them through the search function. People on here may not know much about it but they are super supportive and a lovely friendly bunch 
Hey there…
Sorry I’m late to the party (blame it on the brain fog, memory issues, and extreme fatigue). I also have BCS. Diagnosed April 2024 and what an unpredictable year and ride it’s been and still going strong with full momentum through the sharp twists and turns up new mountains still being climbed only to come.out on the top of.it and plunge down hard and fast into a deep unforseen valley of the unknown and unexpected. When they say PPMS they atent kidding. There isn’t really any flat land on this train to sit back, take a breather, and relax before the “now what” phase of progressing. I remind myself it could be so much worse, I’m still here with breath in my lungs, and I need to be thankful for that and no focus on all the things I have lost and had taken from me like my hobbies, independence, career, ability to drive/travel, enjoy the sunshine and the beach, shop for myself, or remember simple things like what I wore yesterday or if I’ve took my medicine today. We are warriors and as long as we are still fighting… we are winning.
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