When you are diagnosed with MS (Multiple Sclerosis) it seems to come out of nowhere, even though you might have been dealing with the symptoms for a very long time. And generally, one does not understand at first the impact diagnoses will have on the rest of one’s life...
I have been disabled my whole life. I received my BI at birth. I was diagnosed with multiple sclerosis four years ago, which in itself is a brain injury. My name is Lisa Dryer and I am the host of this show. I try to have positive guests that will educate you! And inspire you, too!
I have all been going through some major life changes recently and will talk about how we handle this with disability. I also have sick parents. How do we deal with that?
Tonight I hope to talk about friendship and disability. How and why is it harder to make friends? What other challenges do we have in our communities?
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