Life’s Journey
Pressure. So much pressure. …but where does it come from? Me or “them?” This has been one of those weeks
I’ve been thinking a lot lately about respite care. I was asked to participate on a committee to look at
Do you remember when the person you care for was first diagnosed with MS? You might not have been around
Out of the blue today, Lynn asked me to write about advocacy. He said, “Please stress to your readers the
If you are a full-time caregiver, or even part-time, but the primary person responsible for someone else’s care, then you
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