Sustained federal investment drives progress in the fight against Alzheimer’s. @Ilhan @RepAngieCraig @BettyMcCollum04 @PeteStauber @Morrison4MN @BradFinstad please push for a $187.21M increase in dementia research funding at the @NIH in FY27 #ENDALZ @HouseAppropsGOP @AppropsDems
Grateful to the House for passing the AADAPT Act to train PCPs in dementia diagnosis & treatment. Now the @SenateGOP and @SenateDems need to act so the bill can become law this year. Thank you Sen. @amyklobuchar for being the Lead Cosponsor of the #AADAPTAct #ENDALZ #bipartisan💜
Kate retweeted
📰 Breaking News: The U.S. Food and Drug Administration (FDA) has cleared the third Alzheimer's blood test for individuals experiencing signs or symptoms of cognitive impairment. This is the first blood test cleared for use in patients as young as 40.
Read our full statement: bit.ly/3TZ8fBg.
Kate retweeted
Living Well with Lewy: Education, Connection and Empowerment is presented by LBDA in partnership with LBDA’s Research Centers of Excellence at Struthers Parkinson’s Center and in collaboration with @MayoClinic, Rochester, on July 28, 2026.
Register now: eventbrite.com/e/living-well…
Kate retweeted
In complement to the comprehensive U.S. Based DIAMOND Lewy™ Management Toolkit, the DIAMOND Lewy ™ Trifold is a convenient, pocket-sized resource designed to support communication and awareness in everyday health care settings.
Download now: ow.ly/uOao50ZaEC4
Kate retweeted
We are pleased to welcome incoming Executive Director of the @alzMNND Juliette Francis as our newest @mnlcoaging Delegate! #agefriendlymn #aging #mnleg
Kate retweeted
Myths related to DBS remain common, despite evidence about its relative safety. Dr. Chengyuan Wu and Dr. Delaram Safarpour discuss their recent studies on DBS risk compared to other common procedures and expert consensus recommendations for DBS referrals. movementdisorders.org/Podcas…
Proud to be back in DC with @alzMNND, @alzassociation, and @ALZIMPACT advocating for the bipartisan #ASAPAct to cover blood-based tests, #AADAPT Act to expand provider education, and increased federal investment in dementia research and support programs💜 alzimpact.org/actnow
🚨 Short videos focused on different aspects of thinking abilities that can be impacted in Lewy Body Disease, along with practical tips for daily functioning
LBDA’s latest Lewy Learning Center course, Unpacking Cognition in Lewy Body Dementia, is now available. This course will help you better understand and address the cognitive changes associated with #Lewybodydementia.
Unpack cognition at your own pace: ow.ly/3lrA50YZzWM
Kate retweeted
Join Dr. Matt Barrett of Virginia Commonwealth University for “Making Sense of Medications in Lewy Body Dementia,” to learn about commonly used medications in LBD, why certain drugs may be helpful, and which ones should be avoided.
📆 May 20 at 1pm ET
🔗 ow.ly/4oa250YXUo5
Kate retweeted
Parkinson’s is not a $50 billion problem, it is an $82 billion crisis. Economic burden means the total cost of a disease including medical care, lost work, caregiving and everyday life expenses. A new report led by the The Michael J. Fox Foundation in partnership w/ APDA and Parkinson's Foundation shows just how dramatically we have underestimated the true cost of Parkinson’s and related disorders in the United States.
Key Points:
- The total economic burden of Parkinson’s disease and atypical parkinsonism in 2024 is estimated at over $82 billion annually, far exceeding prior estimates near $50 billion.
- Costs extended far beyond medical care and included indirect costs like lost income and productivity as well as non-medical costs such as home modifications, transportation and caregiving.
- Care partners contribute substantially to the economic burden, with billions of dollars in lost wages and productivity tied to caregiving responsibilities.
My take: This is a wakeup call. Parkinson’s is not just a neurological condition, it is an economic and societal challenge affecting families, communities and health systems. We have been undercounting the true impact for years. When we include care partners, lost productivity and real world expenses, the numbers tell a much bigger story.
Here are 5 points that resonated w/ me:
1- Parkinson’s is a whole family disease and the costs extend far beyond the individual living w/ the diagnosis.
2- Non-medical costs such as transportation, housing and daily support are major drivers and have been underestimated.
3- Care partners are carrying a hidden economic burden that must be recognized and supported.
4- Government programs shoulder a large portion of the cost, highlighting the need for policy level solutions.
5- If we do not act on prevention, access and better treatments, these costs will continue to rise rapidly over the next decades.
michaeljfox.org/publication/… @MichaelJFoxOrg @APDAParkinsons @ParkinsonDotOrg
I am a constituent in Minnesota’s 5th district and I encourage Rep @IlhanMN to cosponsor HR 6130 Alzheimer’s Screening and Prevention Act (ASAP ACT) which has bipartisan support to expand Medicare coverage of blood-based dementia screening tests
@ALZIMPACT congress.gov/bill/119th-cong…
Kate retweeted
“We need ASAP A.S.A.P.” @RobertEgge in his closing remarks urges the passage of the bipartisan #ASAPAct so Medicare can cover routine Alzheimer’s blood tests. Add your voice today: bit.ly/442ieIq.
Kate retweeted
Hello #NeuroTwitter 👋
A reminder that the first MDS Young Members Town Hall will take place on March 27 | 9 AM EST!
An incredible chance for trainees to connect and get involved with the @movedisorder
See you there!
Register:
us06web.zoom.us/meeting/regi…
@AANmember @TheNewANA1
Kate retweeted
Tomorrow, more than 300 Parkinson's advocates will join us in Washington D.C. for the Parkinson's Policy Forum! Advocates are traveling from all 50 states to meet with their members of Congress, share their stories and talk about why we need our government to prioritize brain health research for the millions of Americans living with diseases like Parkinson's.
To our advocates at home, you can get involved by contacting your members of Congress from wherever you are. Visit PDPolicyForum.org for an email template and directions to get connected to your representatives.
Make sure to follow along this week to follow the action! #PDPolicyForum
Here is a look back at our event last year!
Thrilled to be back on Capitol Hill for the Parkinson’s Policy Forum! Honored to serve as the Minnesota State Lead
We urge Congress to co-sponsor the HEALTHY BRAINS Act and fund $600 million for NIH research on Parkinson’s, Lewy body dementia, and atypical Parkinsonian disorders
Kate retweeted
Lewy body dementia rarely follows a clear path. In this guest blog, @DrSamMoxon shares why uncertainty is often the hardest part for families.
Our last and important blog for our LBD focus week.
dementiaresearcher.nihr.ac.u…





























