Jun 212017
 

The Longest Day is finally here and my excitement is at fever pitch! All of the planning and hard work has come together, and I know it will be another fun and successful event. My team is certainly ready to make the most of this special day.

Why do I fight Alzheimer’s on The Longest Day, year after year? It is because my wonderful husband Warren is courageously living with Alzheimer’s.

This is my fourth year as team captain and I’m proud to say that each year has gotten better than the year before. In my “rookie” year, my team raised $12,000, and in my second year of participation, I added an auction and raffle to my event and raised $34,000. Last year was a big year for my team, equaling a whopping $43,000 in donations!

I am proud and truly astonished by all my team has accomplished, and today is the day to celebrate. We all know that in order to find a cure and support families facing this disease, we need more funding, so every dollar we raise is a step closer. Knowing we are a part of that drives us even more!

I feel blessed to be part of the St. Louis Bridge Center, surrounded by hundreds of people that support me and care about this cause. Besides playing bridge all day and evening, we will have a silent auction and multiple raffles. There will also be t-shirts available for sale that will help all of us “go purple!” We have raised more than $25,000 so far and look forward to adding much more throughout the day today.

There are a lot of longest days in the life of a caregiver; there are days when I am exhausted and wonder how I’m going to get through this experience. But then I remember how much Warren needs me. Thankfully our family, friends and our support group are a major part of helping me cope. They help make the longest days seem a little less long – and days like today a lot more fun!

Participating in The Longest Day is my way of saying “I love you, Warren” while helping the millions of others that are living and struggling with this disease. I wish the best of luck to everyone celebrating today, no matter how you are participating. Have fun, and remember: the fight must go on!

 

About the Author: Linda Powers and her family and friends are participating in Alzheimer’s Association The Longest Day®. Linda is captain of the St. Louis Bridge Center team and plays as a member of the American Contract Bridge League (ACBL). Click here to visit Linda’s team page.

Jun 202017
 

Today we have honored the life of my aunt Jeanine Brown.

This incredible woman was responsible for my first-ever public dance moment. It was her wedding reception, there was a Soul Train dance line…and I was paired up with my grandmother.  Needless to say, it was quite the night!

Aunt Jeanine was far too young to have been taken from us by Alzheimer’s disease this past January. Not long after her passing, my wife Daisey struck up a conversation with one of our long-time dance students at the Arthur Murray Dance Studios; we learned that she was a board member of the Northern California and Northern Nevada Chapter of the Alzheimer’s Association. She told us about how the Association is leading the fight to end Alzheimer’s.

As business owners, making a donation here and there of course seems like the right thing to do.  But to us – with our close connection to Alzheimer’s disease – that simply didn’t feel like it was enough. We needed to do more. That is how we became participants in The Longest Day, which provides us an opportunity to do what we love – DANCE! – and raise funds and awareness to fight this disease at the same time.  It feels like the perfect match.

My wife and I are competitive about the things we’re passionate about, and we’re very passionate about The Longest Day. Being affected by the disease firsthand is why we decided to lead the charge within our dance community, and our community has responded! Today, members of our staff have each donated the proceeds from the dance classes they love to teach, and everyone around us is showing their love. We have honored Jeanine and everyone in the Arthur Murray community touched by this disease – and millions more.

The thought that people around the world are joining together today to make sure that this generation will be the last generation affected by Alzheimer’s is astounding. For our part, we have danced all types of ballroom dance to support Jeanine. While it isn’t quite the same as that Soul Train line I joined so many years ago, we are all dancing with that same kind of joy in our hearts.

This may be our first year participating in The Longest Day – but it is the first of many more to come!

About the Author:  Chris Lynam, his wife Daisey and family and friends of the Arthur Murray Dance Studio are participating in Alzheimer’s Association The Longest Day® on June 21, 2017, to raise awareness and funds for Alzheimer’s care, support and research. Chris and Daisey are captains of Team Arthur Murray in Redwood City, California. To date, the Arthur Murray group has raised over $40,000 for The Longest Day.

Jun 192017
 

Our Longest Day is spent playing golf, my husband Mickey’s favorite sport, which he grew up enjoying with his dad.

In 2013, at age 55, Mickey was diagnosed with early-onset (also known as younger-onset) Alzheimer’s disease. Our family wanted to find a way to fight back, and we wanted to include Mickey in whatever we did. A golf tournament in his honor on The Longest Day was the best – and most obvious – choice! 

Today marks our third annual “Mickey’s Mania” Golf Classic. Our friends will come from far (and not so far) to join us for a great day of fun, laughter, food and libations. Everyone is here because they know that even after Mickey is gone, there will be people who need caregiver support and resources from the Alzheimer’s Association – and we raise funds and awareness in honor of his amazing fight.

We started the day by setting up signs acknowledging our donors and supporters; as the players make their way through the 18 holes, they will see all the people who were crucial to putting this event together – and there are so many.

Players arrived bright and early at 7 a.m. to pick up their goody bags – of course wearing hats monogrammed with our “Mickey’s Mania” logo – and then enjoyed a breakfast assortment of traditional San Antonio breakfast tacos; these delicious essentials are crucial to powering through the long day ahead! As the players lined up, I reminded them that we are here to rejoice in life – making this day, The Longest Day, the best day ever.

Mickey has almost been in tears as he greets old friends he hasn’t seen in some time, along with people we don’t even know who showed up to play golf today and support the fight.  He asks: “Is this all for me?!”  I tell him yes, it is – for him and the millions of others living with Alzheimer’s disease.

As each team finishes their round, they make their way to the silent auction. Then The Kimberly Dunn Band entertains us through lunch, as they’ve done for the past two years.

Shortly, the top three teams will be awarded prizes and the winning team will be awarded the coveted monogrammed “Purple Jacket”, much in the style of the green Master’s tournament jacket given to the pros. As the players eat, our family will stop at each table, thanking everyone for coming. We are already a little sunburned, but it has all been worth it!

My favorite part of The Longest Day is driving in the golf cart and seeing each team as they play. Some people have run up to hug me or introduce themselves, and as always, this day will result in so many wonderful memories and photos. Mickey really enjoys looking at the pictures from the last two years of the event on our wall at home even though he can’t remember the celebrations. I am lucky to have my memories from each of those amazing days.

We won’t have the final numbers for few days, but our hope is always to raise more than the previous year. To date, our efforts have raised more than $50,000 for the Alzheimer’s Association; we hope that the numbers this year will exceed that, making it a record year for Mickey’s Mania.

Alzheimer’s is a cruel disease, and we wonder if Mickey will be here for next year’s tournament, which we are already in the midst of planning. As scary as that thought is, what we don’t have to wonder about is our commitment to this cause. Our family will continue to raise funds until our task is finished, and a cure is found – eradicating Alzheimer’s disease for good.

About the Author: Together with her family and friends, Jane Wakely is participating in Alzheimer’s Association The Longest Day® on June 21, 2017, to raise awareness and funds for Alzheimer’s care, support and research. You can visit Jane’s team page here.

Alz.org main site  |  Research  |  Advocacy  |  Care and support  |  Message boards  |  Disclaimer  |  Donate  |  Contact us  |  Sign up for e-news
© 2011 Alzheimer's Association | Blog Suffusion theme by Sayontan Sinha