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Welcome to the "in limbo" called the disease of ambiguity, and the challenge with any early diagnosis of memory loss, delayed thinking, they are in denial and don't believe it. I'm not sure what you can do, I only know what I did in my given situation. For me, I noticed things.... my husband denied anything was wrong. So I reached out to our primary care, sent a note on the portal about what I was noticing and booked an appointment under the pretext of a 6 month visit. When we got there, I didn't mention alzheimers or dementia, but did mention that since we were care partners for one another, I was concerned since we had both been in a house with mold, which I had read could cause confusion and memory loss. She gave him a basic test in the office and then suggested when he couldn't remember the words and/or sequencing things that she wanted him to see a neurologist. You may not have access to your roommates' doctor, but all you can do is tee up the problem, to either the doctor if you have access and/or your roommate in an ongoing loving, non-defensive way. Tap into Dr. Natali, Careblazers on UTUBE, and see if there are any videos on how to have the dialogue with a loved one, about what you are seeing, so you can make them more aware, and it resonates, and they reach out for help - so key for early on treatment. I am still reluctant to say anything to my husband's friends as once they hear "something could be wrong, they "talk" through the community and walk away." I saw it happen with my neighbor; sad but true. I did talk to one of my husband's sons, after my husband started lequembe infusions for early memory loss. Believe me, I practiced a lot in how I talked to my husband early on, which led him finally to the doctors, and then what I said to the doctor once we got there to try to make the conversation positive, loving, and handled in the most dignified way. I just notice the words I pick with my husband regarding his memory loss are key - even to this day with him on the infusions - so it doesn't put him on the defense, and it looks more like we're working on "aging" together. Hope this helps in some small way. Best, Karla

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Replies to "Welcome to the "in limbo" called the disease of ambiguity, and the challenge with any early..."

@kjc48 thanks so much, Karla! You’re the first person to ever tell me they recognized early signs. Because of having no confirmation except a few remarks from my own counselors, it’s too easy to wonder if I’m losing my mind! You’re the first person to say there IS a” limbo “ stage. I do have access to his Nurse Practitioner and she’s very good. I’m sure she would find a way to recommend testing. I’m considering bringing it up with her soon, as she’s seen my friend recently. I do try to spite him respect and give affirmation (he’s actually very immature and has needed phenomenal amounts of affirmation since I met him), but I feel more and more like a caregiver. He’s commented that sometimes I treat him like he’s an old man. Afterwards while I had to tell him that I have concerns about his health. After the conversation, within hours it’s as if it never took place. I’m SURE he blames my concerns and comments on my MDD, even though I’ve been doing well. So if course then I wonder if he’s right! So I talk to a counselor and she tells me I’m doing well. She tells me that some of his changes are not normal adding. So the circle of uncertainty goes round and round.
I will reread your comment often and take your suggestions about how to see a doctor with him. (Although when I asked this time if he wanted me to come along, as a listener, he said no. 🤷🏻‍♀️

@kjc48
When I told my friends that I had early onset of Alzheimer’s I was picky who I told. Told my clergy
2 friends that don’t talk
and family told them don’t say anything to anyone.
Hope that helps
If he has a friend that does not talk spread news
and won’t leave.
I didn’t want it spread all over the place