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@Mithria 

Last reply

Mithria

PpMS

Two weeks ago I've been diagnosed with PPMS, I was chosen for FenTrepid program what has scary side effects, I don't know would it help me😔 I'm not living now normal life.. Is there anyone with this diagnosis and using this treatment maybe?
8
@Lowlander
@Lowlander
 

@Mithria Hi It's still in trial, you'll have the best access to neuros along with your ms team, as for what to expect. The link below might give you some insight. https://mstrust.org.uk/a-z/fenebrutinib

1
@Mithria
@Mithria
 

Unfortunately I couldn't find help in UK,so I've moved back to Hungary for treatment. I think I'll say no for FenTrepid. Just curious how others are living with this diagnosis?