You are very brave for being so open about your MS - not only about its worsening (which is difficult enough) but about how you handled it all. Through you, others like you will have hope (which you should have) and courage (which you now have given them).
Kudos to you, again, for sharing your story. I wish you all the best of luck, my friend. I am pulling for you. Onward - ever onward...
Best,
Cathy
Hi Jennifer,
I think you said it just right. Try what you think might improve your life. Who could argue with that?
My health was very steady until Trigeminal Neuralgia (TN) came along. Whatever you face, you know you have the strength after learning to live with unexpected relapses.
There is beauty all around you, you have loving support, as well as support of many online frienda like me. Yes, you have hope.
Your post really got to me and i could feel for you! your are very brave.
I to have SPMS and we have to get on with the life we have and take all the help and advice 'not that that is easy for any of us MSers' Take care Jan x
Thanks for your kind comment, Jan! Dan often reminds me that those of us living with MS are a special breed and he's right, we are so lucky to have the support of friends that are perfect strangers. Understand what I mean?
All the best to you,
Jennifer