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Alison and Dave discuss the latest developments in their lives. 

Erin Taylor is our person of the episode. You can follow her at @unsteadyandready on Instagram. Erin was diagnosed with ALS at the Age of 23. 

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Our 50th episode! Hear about our amazing friend and neighbor Rajini Poth. Rajini was selected as one of the 2025 American Heart Association's Go Red for Women Class of Survivors.

Our PALS of the episode is Brian Jeansonne. He has over 12,000 Instagram followers. 

www.valentinesdaywidowoutreach.com

Instagram @prettythings.charlotte

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Alison and Dave discuss what they've been up to since the last episode. They also discuss the 5th anniversary of Angela's passing.  They discuss the latest news in the ALS community.

Thanks for listening!

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Alison and Dave discuss the devastating effects of Hurricane Helene in the mountains of North Carolina. Alison's family is from that area and her parents are very active in the relief efforts. We were able to go to the area recently and help in any way we could. 

We hope you enjoy this bonus episode. Please contact us if you want to help the people of western North Carolina. We can help channel the assistance to where it will make a real impact.

Thank you for listening!

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Alison and Dave recount the last 49 days in their lives.

• Sarah's golf event and meeting George Brett
• Post Malone
• Akron Marathon
• Randall's hankering for Jelly Belly
• Molly's big soccer outing
• Dave's teams are winning

And ALS related topics

• Molly and Carson's big award
• The ALS TDI Summit in Boston
• Touring the ALS TDI Lab/Headquarters
• Clayton Rakes takes over the nation
• My good buddy Rainer 

Dave and Alison discuss working together.

Thank you for listening! Please leave us a rating and review and tell your friends about our podcast!

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Alison and Dave discuss what they have been up to this summer. Our person of the episode is Elizabeth Them. We met her at the Guardians vs Royals game on August 26th. We also met Roseann Hickman, another ALS warrior. Randall Keen and his family accepted our ALS Ice Bucket Challenge.

Thank you for listening!

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Steve McMichael is inducted into the Pro Football Hall of Fame. He is currently battling ALS. He is our person of the episode. 

Alison and Dave talk about what they have been up to this summer....moving kids, ziplining, hiking, more weddings, traveling and spending lots of time together. 

In the ALS community we talk about Steve Gleason, Della Larsen, Sarah Nauser and Bobby Witt Jr., and Randall Keen.

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In our latest episode, Alison and Dave discuss what they've been up to this summer;

• Happy 4th of July
• The wedding of Colby and Taylor in Iowa
• Third Eye Blind in concert
• Garrett's college orientation

ALS related topics;

• 85th anniversary of Lou Gehrig's famous farewell speech
• One year of ALS for Whitford Wooten
• Recap of 100 holes and Tri State Trek fundraisers
• Brooke Eby's latest updates
• Our Ice Bucket Challenge from the Witt Wolfpack
• Download the document "Living with ALS" here  https://nap.nationalacademies.org/catalog/27739/living-with-als

Eric Graf is our featured person of the episode. His daughters Madelyn and McKenna received the Lou Gehrig Memorial Scholarship  this year. 

We play our own version of the Newlywed Game and discuss a memory of Cory and Angela.

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Amy Steins is our PALS of the episode. Check out her website at alwayslovingamy.org and on Instagram @alwayslovingamy Hear all about this wife and mom of three on our latest episode!

• Congratulations to Garrett and Hailey on their graduations
• Congratulations to Molly, Carson and friends for another successful Lemonade Stand to raise money for ALS
• Hear all about our VIP experience at Steve Miller Band in concert
•  And much more related to ALS and what is happening in our community

Thanks for listening! 

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Is this special short episode, Alison interviews her rock star nieces about their upcoming Lemonade Stand.  May 26th - June 2nd has been dedicated to Kids Quest to Cure ALS - a week for children to hold fundraisers and special events to directly support ALS and ALS Research through ALS-TDI.
Molly & Carson recorded the following segment specifically discussing their annual lemonade stand that they have held for the past 3 years to support ALS-TDI and others.  This annual lemonade stand is typically done during the late summer months with their other cousins, Mitchell and McKinley. 
This year as part of Kids Quest to Cure ALS, Molly and Carson have decided to host a special lemonade stand in their hometown of Fayetteville, NC.  They will host one this upcoming Friday and then one again later this summer when their cousins are visiting from Germany. 
If you are local to Fayetteville, NC please join the twins on Friday afternoon May 31st at 2509 S Edgewater Drive from 4pm - 6pm. If you are not local and want to help the girls raise the most money they ever have to go towards ALS-TDI - then please feel free to donate at this link:
https://fundraise.als.net/donate/kidsquest
Please include "M&C Lemonade Stand" in the Donation Notes

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