Don't be frightened....I have managed to fight back against SPMS , with a lot if exercise, I am physically better now than the point where transition started. As you have no relapses coming up, you can plan your life better. I know I am lucky, and SPMS won't be the same for everyone. Best wishes, keep in touch if you need..
@2ptayor
Not certain why you beleive SPMS has less pain,. Pain and intensiity of pain can and does varies from person to person regardless of having RRMS, SPMS and PPMS . You;re very fortunate that you no longerbhave pain.
That's what I have and the Flare-ups can be scary but as long as you have a Good Strong Support System ❤️ and a Faith it will help Greatly.😉
If you are not already aware of this to help you with regaining your walking.......
I highly recommend that anyone with MS should join The MS Gym. Trevor is the first therapist that I have seen who truly understands the unique problems that we encounter because of MS. He has specific exercises that address foot drop, spasticity, balance and all of the special challenges that we face.
He has also just recently developed a specific program, along with a very powerful message, for those who are walker or wheelchair bound.
https://www.facebook.com/groups/TheMSGym/
@A MyMSTeam Member
Ocervus is only approved by the FDA for treatment with RRMS and PPMS... not SPMS. Additionally insurance and Medicare will only cover it for RRMS and PPMS... not SPMS.
The question posed by the originator of the thread had to do withb SPMS and not PPMS , Therefore there's no reason for her to ask about Ovrevus.