Caregiving Perspective
Ever since Lynn became disabled, I’ve had lots of encouragement to get some help. I know I need help. My
Lynn has started a new MS medication–at least new for him. It’s Rebif, an interferon beta-1a therapy that is supposed
I have always enjoyed a good movie. It’s one of the things I miss about not being able to get
When I was trying to decide what to write about this week, I had a hard time coming up with
I follow the writings of another caregiver, Patrick, who has been caring for his wife, who has MS, for 22
If you are a caregiver for someone dependent on you for everything, you know that there is no such thing
I thought I was beyond grieving about how things had changed. …or maybe we are never completely finished grieving over
I’m going to be a grandma for the first time in June! My daughter is having a little boy, and
It is Lynn’s belief that if he accepts that he has MS, then he is allowing MS to “have” him.
When I was a child, I loved working pencil and paper puzzles. You know the ones I’m talking about? There
In 2010, I was going to work every day, and Lynn stayed home alone. At that time, he was still
As I have been reading blogs written by other caregivers or MS patients, that joke that goes around, “How many
