The Heartbreaking Realities of Being a Caregiver with HD

These days as my father’s Huntington’s disease progresses and I take on more and more, I have learned how quickly being a caregiver can consume my life. Yes, he is still living two hours away and I don’t take care of his day-to-day needs, but I do everything else for him from paying his bills to booking doctor appointments, following up on every detail, and making sure his supplies are stocked. When he became suddenly ill after a routine vaccination and ended up in hospital, I was at his bedside advocating…Read More

You May Also Like…

0 Comments