By Brian LeBlanc
When I was diagnosed with Alzheimer’s disease in 2014, I could’ve never guessed the path ahead. Crazy. Amazing. Uncertain. Scary. Rewarding. All rolled into one. All I knew was that I felt a calling toward dementia advocacy and to help others on similar paths with education and resources.
Fast-forward a few years, and I was absolutely honored, humbled and inspired to receive the Rhoda L. Jennings Distinguished Older Advocate Award from the Southern Gerontological Society. (OK, so Maureen jokes that seeing me “humbled” isn’t something everyone can say, but it’s true … 100% humbled to tears.)
The awards ceremony was held April 7 in Panama City, FL. The banquet hall was packed with so many wonderful people in the world of gerontology (a big, fancy word for aging), of which Alzheimer’s and dementia care is just a small part. So there were doctors, scientists and researchers, university professors and other educators, advocates, influencers – all spanning different disciplines and areas of expertise across the whole South.
It was almost too much! Although, if you know me, the more people to chat with the better! (But again with my nasty habit of digressing.)
It was an honor to be considered a peer – even if just for a day – and to have my longtime efforts acknowledged toward Alzheimer’s and dementia advocacy and education. When I went up to receive the world, it was the best feeling ever to turn back around and see these great folks standing and applauding.
And on a side note, I was so happy to be able to attend so soon after my recent pacemaker procedure.
Dementia Advocacy Through Outreach and Education
But more important than all that? The mission. #WeAreDementiaStrong has been steamrolling with the dementia advocacy mission. Maureen and I have always worked so hard to produce educational content, and we’ve been very blessed that so many organizations have offered us platforms to speak and/or write as guests.
In the past 18 months, there’ve been some awesome developments:
- #WeAreDementiaStrong now has 501(c)(3) status, allowing us to receive grants and donations to scale this awesome mission and reach more people.
- Both #WeAreDementiaStrong and Caregiver Support and Resources, LLC now have new websites that are regularly updated with new informative content to help persons living with dementia and their care partners.
- We’ve produced a new magazine – “What To Do After A Dementia Diagnosis” – available in both downloadable PDF and hard-copy formats.
- We’re launching the new #WeAreDementiaStrong podcast to reach greater audiences in the digital realm.
- We’re producing new on-demand Continuing Education Credit opportunities with Inspired Memory Care for social workers, nurses, patient advocates and other professionals who serve roles in the continuum of dementia care.
And we’re happy to say, there are even more irons in the fire! More education. More partnerships. More avenues for community outreach.
#WeAreDementiaStrong Is Here For YOU!
We walk this dementia path together. Maureen, the love of my life, is the absolute best care partner, life-care planner and Patient Advocate anyone can ask for. And we sincerely hope our lived experience – the good, the bad, the funny, the sad and the ugly – helps you in some small way.
We’re honored for the recognition. But there’s so much more work to do – while I still have breath in my lungs and perhaps a few healthy brain cells left to say what needs to be said.
Much love.
Peace,
-B
Congratulations on your recovery from surgery, on this award, but mostly on your continuing efforts on behalf of everyone affected by dementia.
I’d like to advocate for the Association to develop a specific fund to provide grant money that would allow help with respite care so caregivers could have assistance giving them the opportunity to delay facility care for the person they are responsible for. It’s something I feel the Association hasn’t seriously addressed as part of their Caregiving Arm. It should look like the work being done by Seth Rogan’s charitable organization is doing. With the massive funding from the government and donations from the public and businesses, I think it’s time to offer more than in-person and virtual support groups, online and in-person seminars and courses, a 1-800 number, or online tips. A fund for support group leaders or local chapters to offer respite services through a home care agency or local facilities may help ease the enormous stress of daily caring so that fewer people with later stage dementias are moved into facilities and remain at home as caregivers are afforded an opportunity to have periods of rest.
Would you consider introducing this suggestion to the Association or including it in your platform of advocacy?
Thaks, Deborah Gregson
Amazing Grace Caring Guidance
Greensboro, NC
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what an honor-and well deserved. Congratulations and Godspeed
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