I sat down with Daniel Brown from Simon Health recently and he asked me:
"When families are overwhelmed by a diagnosis, how do you help them move past the anxiety?"
My answer surprised him.
I don't try to eliminate the anxiety. I try to redirect it.
Anxiety after a dementia diagnosis is rational. The fear is real. The grief is real.
But anxiety without direction becomes paralysis. And paralysis is the worst outcome because it wastes the time that matters most.
What I tell every family after diagnosis:
1. The diagnosis is not the disease
↳ It's information. Information gives you power.
↳ Before the diagnosis, the disease was already there. Now you can fight it.
2. Focus on what you can control today
↳ Exercise. Sleep. Social connection. Blood pressure. Hearing.
↳ These interventions work best early. Every week counts.
↳ Give the patient something to DO, not just something to feel.
3. Join a community
↳ I push families toward support groups the same way the addiction world uses AA
↳ The camaraderie of people going through the same thing is different from family support
↳ It reduces isolation, which is itself a risk factor
4. Don't wait to plan
↳ Legal and financial planning while the patient can participate
↳ Advance directives. Power of attorney. Care preferences.
↳ This is not giving up. This is giving your future self a voice.
The shift I've seen in my career:
Dementia used to be treated like cancer was in the 1970s. Nobody wanted to talk about it. Clinics were in basement corners. The diagnosis was whispered.
That's changing. And it needs to change faster.
A diagnosis is not a death sentence. It's the start of a different kind of fight.
Link to the full conversation is in the comments.
💬 If you've been through a diagnosis with a loved one, what helped most?