Hiya all
Found this today on the NICE website:
If we can get it and if it works for you personally, who knows?
Take care,
Marty
Oh wow, thanks for sharing…now it’s just a case of who can get it.
Jean x
My MS nurse referred me back to a consultant because Siponimod was being considered for SP. I had a consultation just before lockdown and was told Nice had rejected it so I’m very pleased they have now recommended it.
I have just had an MRI my second since diagnosis so I wait with bated breath the outcome and a further consultation. Watch this space
Jan x
Fingers crossed for you all who will benefit from the new drug.
Boudsx
It will depend on criteria, maybe even area. I’ll get excited when I’m prescribed and a little worried, I’ve managed almost 30 years without DMT’s and I would worry about side effects.
Your happy outlook inspires me Poll, keep smiling.
Jan x
I’ve just read an email from the MS trust regarding this and it say’s …if you still have relapses, or show activity on a MRI scan, so don’t think I’ll be offered it, although I will ask.
JeanX