Today I’m sharing a very personal story. My hope is that in sharing this story I can let others who have similar stories know that they are not alone.

My husband has recently been diagnosed with “mixed dementia”, with vascular dementia being the most prevalent. Although he has exhibited the various symptoms to varying degrees over the last several years, I – and our former primary doctor – attributed those symptoms to various other health issues.

Some of the effects of hubby’s dementia are the inability to reason, to accept facts that he doesn’t agree with, and to exhibit inappropriate behaviors. It’s not constant, but at times it seems to manifest more frequently.

We also have two dogs with various gastrointestinal issues. They both have sensitive stomachs, they both have one degree or another of lactose intolerance, and they both react when their systems are overloaded with the wrong food and treats.

For the sake of my dogs’ health status, I have to be on guard constantly. It’s impossible to convince hubby that this human treat or that human food item isn’t good for the dogs.

(I used to attribute this trait to just being “a man thing” but now I’m not so sure.)

It’s like trying to reason with a toddler who wants to share his potato chips with the family dog. That toddler isn’t old enough to understand that the family dog’s system can’t handle the chips or other human treats. And hubby’s capacity to reason has been diminished to that same level. When my calm requests that he not share those human treats and food items are met with snarkiness, it tears me apart.

All is not negative, however. A Nurse Practitioner who works at our hospital system’s Center For Successful Aging prescribed Namenda to help slow the progression of some of hubby’s symptoms. While he only started this drug last week, his mood changes already seem to have leveled out somewhat.

Now I need to work on my own stress levels. (Better sleeping habits would be a good start.) I have been doing some research, as well as subscribing to a newsletter from the Alzheimer’s organization. Additionally, family members and friends have been super supportive all along, even before our first appointment at the aging center. There is also a local support program for caregivers – called REACH – and I will be meeting with one of their folks soon.

If you deal with a similar situation, please feel free to reach out to me in the comments. Maybe we can help each other.