I am a caregiver to my 59 year old husband, dx with LBD in 2015. I started a new blog to be able to share some of the stories about what life is like with this disease. If there is a way for you to share it or post it, I would be grateful. We are three years in, and people have no idea what to expect–really expect. The few blogs that were active, after their LBDA people passed, they stopped writing. main page

An example of a story:

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I’d appreciate whatever you can do. I wish I had someone writing about these things. You just cannot be prepared enough to deal with what this disease brings.

Best always–
Houston, TX

Please do not post the attached letter. It is for your authentication of my blog only. Thank you.

Jane D.Ward

Feb 06, 2019