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Nutrition Tips For Healthier Families

March is National Nutrition Month and the American Heart Association is working to help kids and families live heart-healthy lives by setting healthier diet goals. About one in three American kids and teens are overweight or obese, which can lead to a broad range of health problems. You can help your child develop healthy habits early in life that will bring lifelong benefits.

Here are 10 simple tips to help you and your family on the right path to good health.

  1. Make it fun for kids to try new fruits and vegetables. Let them pick out a new fruit or vegetable in the grocery store each week, and figure out together how to cook or prepare it in a healthy way.  
  2. Whole grains are a good option! Choose whole-grain foods, such as whole-wheat bread, rye bread, brown rice, popcorn, oatmeal and whole-grain cereal.
  3. When you cook at home you have more control over ingredients and portion sizes, so aim to cook at home more often than eating out. Get great recipes and tips at heart.org/simplecooking.
  4. Ninety percent of kids eat too much sodium. Use fresh herbs can wake up any recipe, along with your taste buds, with fresh and bold flavor, without adding salt flavor. Go to heart.org/sodium and take the pledge and learn how to reduce the sodium your family eats.
  5. Watch out for added sugars. They add extra calories but no helpful nutrients. Sugar-sweetened beverages and soft drinks are the number one source of added sugars for most of us. Try sparkling water, unsweetened tea or sugar-free beverages instead of sugar-sweetened soda or tea. Add lemon, lime or berries to beverages for extra flavor.
  6. Schedule time each week to plan healthy meals. Keep your recipes, grocery list and coupons in the same place to make planning and budgeting easier. This will keep you from calling for take- out which can be high in calories and are high in sodium.
  7. Enjoy fruit for dessert most days and limit traditional desserts to special occasions. Try a delicious smoothie, a mixed berry and yogurt parfait, or a baked spiced apple or pear!
  8. Get your kids in the kitchen! They’ll be more excited about eating healthy foods when they’ve been involved. Give them age-appropriate tasks and keep a step-stool handy.
  9. Chicken, fish and beans are good choices for protein. Remove skin and visible fat from poultry. If you do eat red meat, limit it to once in a while, keep portion size small and choose the leanest cuts.
  10. Make a game of reading food labels – The whole family will learn what’s good for their health and be more conscious of what they eat. It’s a habit that helps change behavior for a lifetime.

The American Heart Association offers more resources to help your kids live a longer, stronger life. For information and tips on healthier kids including weight management, physical activity and nutrition go to heart.org/healthierkids.

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“If I Had Not Questioned the Evaluation, I Would Not Be Here Today”

I have always tried to be healthy – I go to the gym to workout, eat healthy, rarely drink, never smoked, and yet I am a survivor of heart disease.

It started years ago when I learned that I had a heart murmur. The heart murmur required no medications, but just something one lives with based on its condition.  Over the years, it was monitored by a cardiologist until one day in 2013, when my status changed.

I was experiencing chest pains due to pneumonia, not once, but twice.  This concerned me, so I went to my General Practitioner who advised that I have an echocardiogram and a consult with a Cardiothoracic Surgeon. After meeting with the Cardiothoracic Surgeon, and reviewing my echo-cardiograms and past records, I was told that I did not meet the criteria for open heart surgery which was typically performed when someone is older, less active and with a family history. Also, the surgeon said they only operate when the diameter of the aneurysm reaches 5.5 centimeters. My measurement was a 4.8. They sent me on my way – without any follow-up appointmens and was told to go back to my cardiologist.

I knew that I did have some family history of heart disease and although they didn’t feel I was a candidate – I can tell you, IF I had NOT questioned the evaluation, I would not be here today.
This is MY health and yet a small voice inside me said keep going and just live my life. If the surgeon was not worried, why should I be concerned?   I had no medical background and more importantly – NO SYMPTOMS.

The holidays came, life got busy and I put my health to the backburner.

In the meantime, my sister who enjoys doing research, looked into the John Ritter Foundation to see what else we could learn about Ascending Aortic Aneurysm.  I decided to call the Foundation and the representative asked, “Are you in Connecticut?”  I said “Yes”.  The representative said, “Do you know you have a “Rockstar” right in Connecticut at the Yale Aortic Institute?”  I had no idea!

I was grateful to learn it was Dr. John Elefteriades- commonly known as “Dr. E”.  But what is the likelihood I can meet a famous surgeon at Yale?  I saw he was having a book signing at the Yale bookstore and off to Yale we went!  The book signing was where my husband and I met Dr. E for the first of many times to come.  He was so great to listen to my situation and after hearing my story – he wanted to review my records.

For those of you who do not know Dr. E., he is one of the most accomplished aortic surgeons in the world – and created the Aortic Institute at Yale.  It was this initial meeting that I knew good or bad, regardless of the outcome, was the doctor I was going to entrust to take care of my heart.

Dr. E of Yale New Haven Hospital

After my evaluation with Dr. E., he advised me I needed surgery sooner than later. Even though he agreed with the first surgeon’s diagnosis of the anueryism, He explained that in his research/ experience the diameter of the aorta was relative to the patient’s size ( height and weight). It was just about 7 weeks later I was on the operating table with what was to become, one of the most difficult aortic dissections Dr. E. had experienced – his words – not mine.  The ascending side of my aorta was dissecting during surgery as he operated on me for a little over 7 hours.

To say I was relieved to know what it was, and have it corrected is an understatement.

At my 1 month follow up, Dr. E. asked about my siblings – knowing this heart condition can be genetic. My sister was examined and thanks to Dr. E, was found to have the same heart problem which could be corrected to save her life. And only 5 months after my surgery, she was having the same open-heart surgery and the same mechanical valve was placed.

The efforts of Dr. E and his team at the Aortic Institute, along with the American Heart Association are making great progress to fight heart disease.  There are more and more women and men being saved as a result of challenging the “typical patient” characteristics of heart disease.  Because of that, my sister and I are gratefully here today.

No one would ever choose to have a health crisis of any type, especially one which has no symptoms, is genetic, and can kill you instantly like anuerysm. And in the case of anuerysms if there is a close relative who has experienced one, you have a 21% greater chance of also having one. My sister and I are so blessed to have survived this experience.

We do not get to choose our genes, but I am here to tell you please to know yours. Learn your family history and don’t give up if that little voice in your head tells you something is off.

We, as women take care of so much for so many – whether it is a friend, co-worker, parent, child or someone else who is important to us. It is easy to ignore vague health issues which may be overshadowed by the attention and commotion of everyday life. I hope my story inspires others to take time to care for yourself. Remember, you are not replaceable.

People say to me, “You are so brave”. I saw a quote once that sums up how I truly feel: “Being brave, doesn’t mean you are not scared, it just means you go ahead and do it anyway”.

 

 

 

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The American Stroke Association receives $11.1 million gift from The Henrietta B. and Frederick H. Bugher Foundation

The American Heart Association/American Stroke Association (AHA/ASA), the world’s leading voluntary health organization devoted to fighting cardiovascular disease and stroke, announces its fifth major philanthropic gift from the Henrietta B. and Frederick H. Bugher Foundation. With its latest gift, the Bugher Foundation will invest more than $11.1 million to fund the creation of a new targeted research network in hemorrhagic stroke, a specific type of stroke that occurs when a weakened blood vessel ruptures. The announcement was made at the Association’s International Stroke Conference in Los Angeles, California. Together, all forms of stroke currently comprise the fifth leading cause of all deaths in the United States.  

To date, the foundation has invested more than $48 million in the AHA/ASA over the course of three decades, often in previously under-funded research areas. The distinctive and long-standing relationship between the foundation and the AHA/ASA continues with the development of the new ASA-Bugher Foundation Centers of Excellence in Hemorrhagic Stroke. There is a demonstrated gap in the scientific understanding of the multiple causes of this type of stroke, as well as how these serious events can best be prevented and treated. Hemorrhagic stroke currently accounts for approximately 15 percent of all stroke cases every year and these episodes have a fatality rate of nearly 50 percent in some studies. Because of the severity of this type of stroke, more than 100,000 people a year will die following a hemorrhagic stroke; especially if they do not have immediate access to highly trained medical centers who have neurosurgery expertise available.

 “Since 1984, the AHA/ASA and the Bugher Foundation have collaborated to take calculated risks and fund areas of science where there is real need; areas of science that others have often ignored. Over the years, we have built a legacy of scientific excellence that has pushed boundaries and saved lives,” said Nancy Brown, CEO of the American Heart Association/American Stroke Association. “I’m thrilled to embark on our latest collaborative initiative — new Centers of Excellence in Hemorrhagic Stroke that will put patients at the center of research in support of bold advances, while inspiring and training the next generation of interdisciplinary stroke researchers.”

 The ASA-Bugher Centers of Excellence in Hemorrhagic Stroke will employ core collaborative research, training and science. Project investigators and their fellows will build a strong network, and share their work broadly so that the scientific community at large can benefit.

 Precision medicine and data analysis will also play a key role in the research process. Specific components will include:

•Between three and five Centers of Excellence, engaging in up to three innovative research projects each, designed to make breakthroughs in prevention and/or treatment of hemorrhagic stroke;

•A centralized training structure, designing activities and engagement for fellows recruited by the Centers;

•An oversight advisory group of stroke thought-leaders to guide and oversee Center operations and to encourage approaches to specific, collaborative research questions;

•Open data sharing between projects and the greater research community using the AHA Precision Medicine Platform™, a state-of-the-art discovery portal, where researchers and physicians can quickly access and share information, collaborate on research and use precision medicine to treat cardiovascular disease and stroke;

•Development of a patient-focused hemorrhagic stroke cohort for integration into the AHA’s My Research Legacy™ initiative, a platform where people can sign up to share health, genetic and lifestyle data, to help researchers in their quest to end multiple forms of heart disease and stroke at the earliest possible time.

 As part of the My Research Legacy™ component of this initiative, the American Heart Association is currently reaching out to engage survivors and families of those affected by hemorrhagic stroke.

 An open application process for scientists interested in applying for funding as a part of this exciting research network will be announced in late 2019.

 “The blueprint for the ASA-Bugher Centers of Excellence in Hemorrhagic Stroke stands on the shoulders of our previous four collaborations with the American Heart Association/American Stroke Association,” said Bryan Adams, trustee of the Bugher Foundation. “We are proud and honored to be part of increasing focus on an area of stroke research that deserves more attention.”

 To donate and/or to fund specific programs and events visit www.heart.org/giving.  For more information about stroke, visit http://www.strokeassociation.org/.

 

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Mike’s Story

I have no recollection of the day that changed my life forever. I’ll only be able to tell the stories that I’ve been told. The evening of my sudden cardiac arrest, the doctors told my parents that I had a one in a million chance to survive. Although I’ve had many experiences that I will never forget, I will never remember the day that I went into cardiac arrest.

I was 17 years old at the time and everything seemed to be falling into place. I was a good student, had good friends, and was doing everything I could possibly do to fulfill my dream of being a college basketball player. The morning of August 24, 2006 was no different. I did my daily basketball workout in the morning, and then went over to a local basketball camp where I was a coach. I arrived at the Parks and Recreation Department, where the camp was being held, and walked over to change my shirt. That is all I remember of the day that I “died.”

From what I’ve heard I was sitting down on a bench when I just slumped over onto my knees. No one in the gym really knew what was going on. My dad, my brother, and my best friend stood there, watching. Someone called 911 implying someone had broken a bone. A second 911 was called saying a 17-year-old was on the floor and unresponsive. There was no automated external defibrillator on site.

That was when my hero’s pager went off. Luckily, he was working right next door in a different building. He left work without anyone noticing and ran over to where I was. By the time he got to me, I had turned blue and was taking my last agonal breaths. He gave me CPR perfectly, saving my life (as well as my brain).

When the ambulance arrived, they used an AED to restart my heart and put it into a normal rhythm. They still didn’t know if I would make it. I was brought to MidState Medical Center where I had a second arrest. They wanted to Life Star me to Hartford, but needed a large, specialized ambulance to hold the necessary equipment, doctors and nurses. My mom rode in the front seat of the ambulance, not knowing if I was going to live. Earlier that morning I had been battling on the basketball court; now I was battling for my life. For the next three days, I was unaware of everything. The hospital revived me, but there was still the question of whether I would have brain damage.

hospitalFinally, I started to come around and began to remember where I was and why I was there. I went through some uncomfortable tests, which resulted in the diagnosis of Hypertrophic Cardiomyopathy—a thickness of the septum and apex of my heart. After the tests, I thought I would resume my “old” life, with the exception of daily medication. I was right about the medicine, but the doctors delivered some crushing news. I would have an ICD, or a defibrillator, implanted in me and I would never be able to play competitive basketball again. At first I didn’t understand why; basketball was a big part of my life. But as time passed, I began to accept the fact that I was going to have to change many parts of my life. I felt very fortunate to be alive.

After returning home and getting my life back to normal, I felt like I needed to give back. I felt like I needed to help others. My mom contacted the American Heart Association and they welcomed us with open arms. We both became volunteers and spokespeople for them. We agreed to share our story to try to help save lives. We did lobbying in Hartford, as well as Washington D.C. We assisted in two bills being passed in Connecticut mandating defibrillators be placed in all public schools in Connecticut. It was very fulfilling to try to help save someone from going through the trauma we had experienced as a family.

As the years went on, life became more and more normal. I attended Quinnipiac University and started to pursue my new dream: to be a college basketball coach. After graduation I got my first assistant coaching job at the University of Massachusetts-Lowell. After spending a year there, I was lucky enough to get hired back at my alma mater, Quinnipiac University, as the Director of Basketball Operations. Once again, life was falling into place.

In August 2014, eight years after my cardiac arrest, it was time to get my defibrillator battery changed. Although it’s a very routine surgery, my family and I were nervous. I went in for the surgery and unfortunately, it didn’t work. They tested the device with the new battery and it did not shock properly. The doctors decided they were going to add another wire on my left side, going from the device into my heart. They went in the next day to do the surgery, added the wire, and the device worked. I went home to recover and was ready to get back to normal again.

A couple of months later, in October, the device started to get really itchy, swollen and red. I went back to the doctor and he gave me medicine, which made the device look and feel much better. Another month later, in the middle of November, I started getting sick. I was spiking fevers of 103-104 degrees. Again, my doctors had me come back to Boston thinking the device was infected.

IMG_0418Just when everything seemed so normal, life had thrown me another curve ball. After days of running blood work, doctors came to the conclusion that my implanted defibrillator had become infected. It would have to come out. The infection had entered my bloodstream, which made the need for the surgery imminent. This meant the battery and all three leads would need to be removed. We knew there was more risk associated with this surgery. They told me they were going to be prepared for any possibility. There was a 1-2% chance that while removing the leads burrowed in my heart muscle, a tear could occur. It was extremely unlikely, but if it did happen they would have to perform emergency open-heart surgery.

I went into surgery hoping for the best, but unfortunately while they were removing one of the leads, the scar tissue ripped and they had to perform emergency open-heart surgery. Twelve hours later I was brought to the intensive care unit on a ventilator. Once again there was the possibility of brain damage because my blood pressure dropped drastically during the surgery and I required eight blood transfusions.

I awoke Thanksgiving morning. The ventilator was removed and I gave a thumbs-up to my mom and my electro-physiologist. I was about to embark on two of the most physically and mentally challenging months of my life. Fortunately, I had the support of my family and close friends to help me through this time.

After recovering in the hospital and regaining some of my strength, I went home with a pic line in my right arm pumping an antibiotic into my body, and a life vest that would serve as a defibrillator until I got a new one put in. The doctors wanted to be sure the infection had left my system before putting in the new device. At the end of January, they scheduled one final surgery to give me a new device. They installed a new defibrillator (a subcutaneous ICD) and the surgery went perfectly. It was a huge relief for my family and myself.

 

This story is from Mike’s, non-profit website – http://inaheartbeat.org.  Please visit the site for more information on Mike and his amazing work.

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Super Simple Game Day Playbook

The American Heart Association | American Stroke Association set the scrimmage line on game day feasts.

 It’s time for the big game, and you know what that means! Time to grab your jersey, don your lucky socks, and grab some munchies before kickoff.

But can you keep it healthy at your game-watching bash? Yes!

Whether you’re cheering on your favorite team or checking out the game day commercials, you need to check out this heart healthy ‘playbook’ from the American Heart Association to make sure your celebration equals a touchdown. No need to bench the chili and wings.  With just a few minor tweaks, your menu can go from second string to starter while lowering your risk for heart disease and stroke, the No. 1 and No. 5 killers in the U.S.

The Food Playbook:

  1. Eat your fruits and veggies. Mom and Dad were on to something when they taught you to eat an apple a day. Fill up half your plate with these low-calorie, nutrient-rich foods that keep you satisfied. Choose veggies with hummus, salsa or other low-fat dip for a crunchy snack.
  2. Stay hydrated. Water is the best way to stay hydrated. Reach for water instead of sugar-sweetened beverages like soda and sports drinks, which add extra calories with little nutritional value. Plain water too boring? Try sparkling water or add fruit wedges to jazz it up.
  3. Put down the double bacon cheeseburger. Instead, reach for a grilled turkey burger piled high with veggies like avocado, tomato, onions and lettuce. In other words, choose lean cuts of meat and poultry without skin and extra fat removed. And add lots of veggies for an extra boost of nutrients.
  4. Hold off on the wings. A game day staple, wings are delish and often loaded with calories and trans fats. For the same spicy kick, toss grilled or baked chicken breast strips in your favorite hot sauce. You’ll barely notice the difference!
  5. Drink responsibly. Alcohol contains a lot of empty calories and can have other negative effects on your health. Watching football can mean enjoying a few beers or cocktails, but spacing them out by drinking a cup of water between each drink will help keep you on track.
  6. Toss the chips. Game snacks can be full of sodium. Along with the veggies, try a low sodium dip, unsalted nuts and seeds, and whole-grain crackers.
  7. Take your phone out. No, not to tweet. To check your portions. Portion control can help you keep track of the foods you are consuming without going overboard. For instance, a serving of chicken breast (3 ounces) is about the size of a smart phone and a medium banana is about the size of a pencil. For more portion comparisons, check out www.heart.org/PortionDistortion.

Looking for more healthy game day tips? Visit www.heart.org/GettingHealthy.

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THINK AHEAD: SAVE ON RED

You’ve surely noticed, in all those shopping trips this December, that there’s one color dominating the clothing choices: red. And in the approaching Christmas days, as you are shopping, it is a great time to look for red sweaters, tops, dresses and lights to adorn your home or business in honor of National Wear Red Day, Friday February 2, 2018.

National Wear Red Day draws attention to the fact that heart disease is the No. 1 killer of women in America – killing more women than all forms of cancer combined. Most women don’t notice the symptoms of heart disease until it’s too late. By wearing red or decorating the exterior of your home or business red, you will help share the message that heart disease is killing our mothers, daughters, sisters and friends.
For information about how you can participate in National Wear Red Day, call the American Heart Association at 413-335-9044, or email mary.ann.burns@heart.org. To learn more about your risk for heart disease and stroke, go to www.goredforwomen.org or heart.org.

 

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Alice’s Story – “Had I not called “911” I would most probably not be here”

“My name is Alice and I am a 64yr old female who is employed at Mohegan Sun

Casino. I am a shift manager at the Bus Lobby and I would consider my position to be overall moderately stressful. I mention this to alert you to the fact that not everyone displays the same symptoms and I hope by sharing my story, I can heighten your awareness.

For approximately a year prior, I had experienced heartburn on more than one occasion. Therefore I was not overly concerned. Usually I was relieved by an antacid. On that particular day, I had forgotten to take my high blood pressure medication. When I realized this, I took both and began to feel back to normal. Luckily I had the next couple of days off as part of my regular schedule. I let my husband know what happen and he said, you should have called “911”. Arriving back at work, I explained to my operational manager, Gail my recent episode.

The very next day when returning from lunch, I began to experience the same symptoms. I then relayed this to Gail and she suggested to call “911” and tell them my symptoms. When I did, they arrived and transported me to L&M in New London. Gail called my husband to meet at L&M.

The report from the EMT’s showed I needed a stent placed upon my arrival at the ER, However, they attempted the stent placement then realized I had a tear in my artery and promptly stopped the procedure. Dr. Cambi my cardiologist said if he proceeded with the procedure I would have bled to death.

Hospitalization and medication became the answer to my prayers. The doctors made it clear that had I not called “911” I would most probably not be here to tell you my story. Please be aware 80% of the people do not survive this attack and that heart attacks take many different forms and you should not ignore your body when you know something is very out of your ordinary routine.”

Alice is a volunteer for the American Heart Association and shares her story whenever possible.  If you want to know more about the signs and symptoms of a heart attack or cardiac arrest, find out more:

http://www.heart.org/HEARTORG/Conditions/HeartAttack/WarningSignsofaHeartAttack/Warning-Signs-of-a-Heart-Attack_UCM_002039_Article.jsp#.WiG7pa2ovIU

 

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RESIDENTS AND EMPLOYEES TAKE STEPS TO BEAT HEART DISEASE AT EASTERN CT HEART WALK

The American Heart Association will hold its annual Eastern Connecticut Heart Walk on Sunday, September 24 at Mohegan Reservation in Uncasville. Over 1,500 supporters and survivors are expected to attend and raise funds to support cardiovascular research and education.

 

Walk activities begin at 9:00am. Prior to the walk kick-off, participants can enjoy complimentary health screenings, a kid’s zone with entertainment, and music. The walk will begin at 10 a.m. with a ribbon-cutting ceremony followed by a walk through Mohegan Reservation – rain or shine. 

 

Those looking to start a walk team still have time to register. Registration is free. Individuals who raise $100 or more receive a t-shirt. To register as a team or individual for the Eastern Connecticut Heart Walk go to www.EasternCTHeartWalk.org, or for more information contact the American Heart Association at (203) 295-2936.

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AETNA SIGNS ON AS SIGNATURE SPONSOR OF AMERICAN HEART ASSOCIATION‘S 2017 CONNECTICUT HEART BALL

KAY MOONEY OF AETNA NAMED CAMPAIGN CHAIR

The American Heart Association announces that Aetna has signed on as the signature sponsor of the American Heart Association’s 2017 Connecticut Heart Ball. Kay Mooney, Vice President of Benefits and Well-being at Aetna will serve as the event’s chair, leading all fundraising efforts.

The Connecticut Heart Ball, the American Heart Association’s signature social event, will take place on December 2nd at the Hartford Marriott Downtown where 400 business leaders, community leaders, and philanthropists will gather to raise awareness and celebrate the important work of the American Heart Association. The elegant affair will feature dinner, dancing, and a live auction.

“I am honored to serve as chair of the 2017 Connecticut Heart Ball”, said Kay Mooney. “Aetna’s community support for the Heart Ball helps fund lifesaving research, prevention and education programs, all of which are critical to saving lives from heart disease and stroke.”
The theme for the Heart Ball is Igniting a Healthier Community focuses on promoting kid’s health and the health of Connecticut communities. Each sponsor’s support of the event will deliver a health asset in the community, such as providing CPR training kits in schools, providing recess equipment to underserved schools, and bringing awareness to congenital heart defects.  The combined efforts will be celebrated at the Heart Ball.

 

“The community-minded work that Kay Mooney has done working on our Go Red For Women Luncheon, Hartford Heart Walk, and Circle of Red makes her an inspiring choice for this year’s Heart Ball chair,” said Judy Campisi, American Heart Association, Connecticut Executive Director. “We are delighted Kay will lead this year’s Heart Ball fundraising efforts. Her unparalleled commitment to wellness, and her generosity for our cause will provide the leadership to make the evening a huge success”.

The American Heart Association is actively seeking corporate sponsorships and individual contributions toward this year’s Heart Ball campaign and event. If your company is interested in joining this campaign, or if you are interested in making a personal gift to this cause, please contact Christina Asaro at the American Heart Association at 203-303-3340 or christina.asaro@heart.org. More information about the cause and the event can be found at HeartHeartBall.heart.org.

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Nominate Someone You Know For the Stroke & Caregivers Virtual Gallery Presented by Hoffman Auto Group

Nominate Someone You Know For the Stroke & Caregivers Virtual Gallery Presented by Hoffman Auto Group

If you want to nominate yourself or someone else to be part of the Stroke & Caregiver Survivor Virtual Gallery, please read the following details, and then click on the link below share your story!

The American Heart Association has teamed up with Hoffman Auto Group to bring awareness of the risks of stroke by creating a virtual gallery of survivors and caregivers. Three stroke survivors or caregivers will be featured on virtual posters which will be posted on the social media pages of the American Heart Association in Connecticut. Each stroke survivor or caregiver’s story will be detailed on the American Heart Association’s Connecticut Blog.

The focus of the virtual posters will be to bring awareness that stroke is the number one cause of disability and number five killer in the United States. The posters will also be shared on the American Heart Association’s and Hoffman’s social media pages.

To nominate someone, or to share your story, click on the site below by September 29th to be considered. Stroke survivors or caregivers will be selected by a committee comprising of the American Heart Association and Hoffman Auto Group. Those selected will be notified by October 17th.

Click here to share your story or nominate a survivor.