Jun 16
My dear cousin, Jay Mathews, passed away Sunday morning after a tortuous 3 year battle with cancer. I – and his family & friends – are devastated. He gave without asking, told the same corny jokes as my Dad, and was enthusiastic about life. He grew up on the AuSable River, as all my cousins …
Permanent link to this article: https://vickisvoice.tv/2014/06/remembering-cousin-jay/
Jun 08
I will never understand how the brain works. Or, in my case doesn’t. I still have the intelligence to know how things should be. But I have no control over how to perform the actions to make life normal.. Yesterday was a ‘good day’. What does that mean to someone with FTD? I had no …
Permanent link to this article: https://vickisvoice.tv/2014/06/today-is-a-bad-day-tomorrow-will-be-good/
Apr 12
It’s 1:39a. I’m playing games on both my PC and my iPad. Tomorrow I am hoping (praying) that I can attend our parish healing Mass. I can’t sleep. I’ve had 3 sessions of dystonia (seizure-like, muscle spasms), and everything points to my past of being unable to go outside my home. So, I take the …
Permanent link to this article: https://vickisvoice.tv/2014/04/late-night-and-parish-life/
Mar 24
When we saw it, Vicki and I each wanted to share this message with you. It captures this time in Vicki’s life so clearly.
Permanent link to this article: https://vickisvoice.tv/2014/03/ask-remember/
Jan 31
I am a diehard The Sims FreePlay gamer. I work hard on it every day because (1) I enjoy it, and (2) It forces me to think sequentially, which is the hardest part of my disease (Frontotemporal Dementia – FTD). And I am proud of the work I have done. I’ve begun posting photos of …
Permanent link to this article: https://vickisvoice.tv/2014/01/sims-design-ftd/
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