Several years, I released a free ebook called “After the Diagnosis.” The booklet included tips and suggestions from family caregivers on how to manage after a family member’s diagnosis as well as information about navigating the health care system.
I’m updating the ebook and would love to hear your suggestions in order to make the resource truly helpful. What kind of information, if any, did you and your caree receive? What kind of information would have been helpful for you to receive the day off the diagnosis? What did you need in the days and weeks afterward? Which resources would have been helpful for you to have?
Please share any thoughts and requests in our comments section, below.