lou gehrig’s disease

In this episode, it's just ME talking about LOVE :)
Here I mix it up a little and talk about what's on my heart.  This releases on Valentines Day, so talking about LOVE ... specifically 4 Easy Ways To Spread More Love.  I talk about the first few things that came to mind, Listen, Words, Time and Action.  I thought to myself, these seem so simple but realized I always need reminders, so why not share?  We all have the power to show others they are loved and not alone. There are no limits on love with those who are close or even strangers.  Listen in, open your mind & heart and reach out to someone with these in mind.  Thanks for listening and sharing with a friend.  Hugs and Love, Lorri

I am so incredibly grateful that you are here. It means the world to me! Thank you. Follow and see what's coming next: Instagram, Facebook, Twitter, TikTok, LinkedIn.

I knew I wanted to do an episode about HOPE, heading into the new year.  On December 8th we lost our friend Scott Smith and quickly I knew his words were all I needed to share.  This episode is an inspired replay.  In memory of our dear friend Scott Smith, I added a new intro,  a message from Jamie and then share my original chat with Scott and Jamie Smith.   Originally released in 2021, as they were fighting Scott's ALS, Scott and Jamie shared their hearts to encourage others.    Silver Linings, Courage Under Fire, Nothing to Lose and Riding On Hope are just a few of the topics Scott wrote about in his intimate blog, Flex On ALS.  He  documented his personal experience by sharing his fears, regrets and what he wanted us to realize before it's too late.  Scott was a personal trainer, fitness advocate and young father of two daughters Iris, 3 and Hope, 1.   Scott and Jamie shared openly about life with a terminal illness, a young family and all that came with that.  Scott's writings on flexonals.com were intended to tell the truth about one man’s journey as he walks through the fire, but trust me they will inspire you as well.  Thank you for listening and sharing with a friend as we remember Scott.  Hugs, Lorri

I am so incredibly grateful that you are here. It means the world to me! Thank you. Follow and see what's coming next: Instagram, Facebook, Twitter, TikTok, LinkedIn.

Despite a debilitating diagnosis of Lou Gehrig’s disease also known as ALS, Andrea Peet refused to let her disease slow her down.

With ALS, she has completed fifty marathons in fifty states. AMAZING!

Guy Kawasaki is on a mission to make you remarkable. His Remarkable People podcast features interviews with remarkable people such as Jane Goodall, Neil deGrasse Tyson, Marc Benioff, Woz, Kristi Yamaguchi, and Bob Cialdini. Every episode will make you more remarkable.

With his decades of experience in Silicon Valley as a Venture Capitalist and advisor to the top entrepreneurs in the world, Guy’s questions come from a place of curiosity and passion for technology, start-ups, entrepreneurship, and marketing. If you love society and culture, documentaries, and business podcasts, take a second to follow Remarkable People.

Listeners of the Remarkable People podcast will learn from some of the most successful people in the world with practical tips and inspiring stories that will help you be more remarkable.

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In honor of ALS Awareness Month, I asked the listeners, "What do you want to know about ALS & living with a terminal illness, but you're afraid to ask? "   More questions than I could imagine came in, so I asked a few friends living with ALS to help answer these tough questions.  So in this episode, I chat with  Sunny Brous, Kate Nycz, Maceo Carter and Kevin Rowland  as we go through each question submitted by listeners of this podcast.  Between us, our ALS diagnosis ages vary from 27- 47 and years living with ALS spans from 2 to 18 years, so it was great to have a wide range of experience to learn from.   I love the incredible support and curiosity for this unique episode.  We had such an amazing "round table" discussion, I decided to have 2 episodes so we could address all the questions.  In this part 2/2, we answer questions about mental strength, the grieving process, bucket list, sex/intimacy, thoughts on getting a trach, fears about what's to come, planning our own funeral and more.  If you missed part 1, we answered questions about fears of dying, mental health, survivor's guilt, what brings joy, boundaries and faith.  I hope you'll listen in and share with a friend to help us create more awareness of ALS.  Hugs, Lorri             
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I am so incredibly grateful that you are here. It means the world to me! Thank you. Follow and see what's coming next: Instagram, Facebook, Twitter, TikTok, LinkedIn.

Is your hair really BLUE? Tony Myers received a miraculous healing from ALS or Lou Gehrig's disease and then God told him to “wear the color of his healing”, he took that seriously and has been receiving puzzled looks ever since. Tony Myers is the host of the Pushing Boundaries podcast on the Charisma Podcast Network and he knows firsthand of God’s healing power. 

In this episode, you’re going to hear his powerful story of God redeeming an angry atheist and the reason why his hair is blue.

Links

https://www.tonybelieves.com/

Tony’s Testimony on 700 Club

https://youtu.be/0eCFwVeoOBA

AlongTheWay Links

http://alongtheway.media

Join My Email List

JohnAlongTheWay@gmail.com

Become a Patreon https://www.patreon.com/AlongTheWay

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AlongTheWay Links

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