Porter and Adeline were born Feb 27th 2017, seven weeks early. They fought all odds and after a month of being in the NICU, they got to come home. On July 4th, I awoke to find my sweet Adeline had passed away in her sleep. This girl, let me tell you, was a certified diva from day one. She was perfect in every way and had a pacifier that even said future president. The 4th of July will forever be the most horrific day of my life and I have no reasons as to what truly happened to my baby girl. The unknowns and what ifs haunt me today, as they did from day one. I started this team, not only to honor Adeline, but to raise money for research of SIDS. I would never wish this heartache on anyone and if I can do anything to help to potentially prevent a person, down the road, from experiencing this, then I will stop at nothing short of trying to doing so.

Buckout held in memory of rowlyncashkeyser.

In honor of Adam Lee Smith (March 24, 2009 - May 14, 2009). His wings were ready but our hearts weren't!!

On January 30th 2018 SIDS took away our healthy and happy angel Adam James. At 3 1/2 months our time with him changed from creating memories to only remembering them. Adam brought us joy and happiness! He was a sincerely jovial spirit, with an intoxicating and entertaining personality. One giggle or smile from him would melt your heart and hug your soul. Our Adam will be forever in our hearts and we will live our lives with his happiness and his love in our actions every day. Help us to educate others about SIDS and bring about a cure or solution that may protect others from the heart ache and sorrow we have endured.

Beautiful Adriana passed away 6/27/19 at just two months old. We love and miss her dearly. She will forever be in our hearts. Our beautiful angel girl.

Emma Louise Andrews was taken at 3 1/2 months old on June 4th, 2019. Her death is a SIDS account that no medical reasoning can explain. There wasn’t an accident, there wasn’t suffocation. My sweet angel took a nap one morning and didn’t wake up. Losing a child is hard, but losing a child for no rhyme or reason is unbearable. I hope to raise money so hopefully one day, no family will have to experience this again.

Alexis passed of sids on may 5th 2015 and was born march 6th 2015

My family + I use the power of music, creativity, + love to generate a beautiful festival to honor my daughter's life.

Amir Clyde Starnes 1/6/22-5/14/22 Fly High Baby Boy🕊 You are loved & missed every second of everyday💙

Avery's Quest was started in 2007, just a few months after the passing of sweet Avery. 14 years later we are still raising money for a much needed cause.

If love Could Have Saved You,You Would Have Lived Forever!

Coming together to make difference

Our beloved Isabelle Grace only spent six weeks on this earth before she passed suddenly from Sudden Infant Death Syndrome (SIDS) on March 17th, 2020. In honor of her, we would like to raise funds to advance research into the causes of SIDS. Any amount is appreciated, and prayers are welcome, too. Our little Saint Isabelle Grace, pray for us! All funds will be donated to the American SIDS institute which funds research, education, and support. Please see www.sids.org.

Brooks Grey Miller was the light of our lives, and taken way too soon. Forever 3 months old, and forever my baby. ❤️

Adventure with Cam. On January 5th 2021 my wife and I lost our precious baby boy Cameron Jackson Buenger to SIDS. Our world was shattered that day and has been ever since. In devastating times the power of human kindness and rallying together can ease the burden, even if only temporary. @CamLivesOn on Instagram is a page dedicated in memoriam to take pictures w/ our engraved wooden keychains of Cam's feet to travel w/ Cam. Use the #CamLivesOn & #WhereCamAdventures when you take a picture and post to your social media platform. Keychains are available for purchase on the IG page. Also, if you would like to make a contribution to the American SIDS Institute we’ve created this page in honor of Cameron and to spread awareness. Every dollar counts as we raise funds to continue to research the cause and especially the reason why this happens to our little ones. Please help out this incredibly good cause so no other parents have to endure the pain of losing their baby.

We are a dance studio who would like to bring awareness to SIDS. Our studio is named after our studio owner, Marquita Felton’s deceased older sister, Lakeisha “Kee” Felton.

Philly law firm

Remembering our sweet boy who gave us 5 beautiful months before becoming a sleeping angel.

Ellie Olivia came into our lives on August 16, 2012 and was the sweetest little baby. She had the most awesome smile with her tongue always sticking out and she had the craziest hair <3 She left our world WAY too soon on December 6, 2012 and has been changing lives ever since. This team will honor the life of Ellie while supporting SIDS research and raising awareness to others.

Emily Brooke Berube 8/9/20-2/13/21

Our hope, above all else, is to open the lines of communication. While we seek to, one day have no worries about our children, we are determined to access resources and support for our community. This is our first step outside our comfort zone and we take this step for all those who know the agony of living beyond their precious and heaven sent child/children.

Some people only dream of angles, we held one in our arms . Our mission is to help fund SIDS research and awareness.

Finn was a fighter from the moment he was born so it is only appropriate we keep fighting for him. He is loved and remembered by his whole family who pray some day no one will have to endure the pain we did. We Are Finn's Fighters! Until we meet again my sweet boy, may God hold you in the palm of his hand.

We are raising money in honor of Gabrielle Doreen-Marie Maloney who was born to two loving parents on 10/21/2008 and who was taken way too soon on 01/23/2009.

There are many misconceptions about SIDS. In the US, there are about 4,000 sudden infant deaths each year, and about 1/2 of these losses are due to suffocation or other causes. Grace's case fell into the other category: Sudden Unexplained Infant Death. There was no clear cause of Grace's death, which is why it is so crucial to support the American SIDS Institute. Grace's tissue is being used by Dr. McEntire and all of the other tireless researchers at the institute who are working to prevent other families from experiencing such loss. Many families are unaware that they are able to donate tissue to the American SIDS Institute after the loss of their baby. The researchers need more resources and more advocates in order to continue their work. The world will never know another Grace Margaret, but it is our hope that her legacy will be one of generosity and love. Please consider supporting the American SIDS Institute.

I am proudly representing Hailey's Angels in memory of my daughter, Hailey Anne Giagnacovo, who passed away from SIDS in May 2006. She was 10 months old and it was her very first day at her new babysitter's house when she passed away. She was put down for her last nap and never woke up. Sudden Infant Death Syndrome (SIDS), also known as cot death or crib death, is the sudden unexplained death of a child less than one year of age. Diagnosis requires that the death remains unexplained even after a thorough autopsy and detailed death scene investigation. SIDS usually occurs during sleep. This is my 5th year of participating in this fundraiser and I'm SUPER happy and proud to be part of it. Anything and everything you can give would be more than appreciated. Hope is always about finding a cause and then a cure as to what took my daughter and so, SO many other little ones. It's devastating and life altering and it just plain sucks, so... whatever you can do, please know I will always be grateful Please feel free to pass this around too! I'll be gifting one donor a baked good basked on May 17th by picking a name out of all those that donated (randomly). All the goods will be baked with love so it will be a nice thank you!!! Thank you in advance!!! You guys rock!!!

Heather's Headache is an alternative/top 40 rock band based in Northern Virginia. The band has been performing for over 15 years, with 3 albums, and a number of notable live appearances to their credit. Lead singer, Brandon Heiner and his wife Rachael, lost their two month old son, Brady, to SIDS in 2004.

In July of 2021 our family was devastated by the loss our son Liam, who died of SIDS. Liam never lived to see his first Christmas and we, as a family, have decided to fill his stocking every year in support of SIDS research, to commemorate and honor the four months that we were able to spend with him. This, and every, Christmas join us and support our efforts to save other families from suffering the same tragedy. Please donate in order help us reach our goal of eliminating SIDS.

Zumbathon

In Loving memory of Taisha Starr Sampson, who we unexpectedly lost on Sunday September 25, 2021, please consider donating to the American SIDS Institute. Sudden Unexpected Infant Death prevention is a cause that was close to Taisha's heart, having tragically lost her own daughter Mecca Starr Sampson when Mecca was only three months old. Your support will help honor both Taisha's and Mecca's lives while funding research and resources that support prevention and a cure. In the fight to save lives no contribution is ever too big or too small. Thank you for helping ASI save babies and thank you for honoring our Starrs...our beloved Taisha and Mecca Sampson..

Tristen Keoni Reyes passed away from SIDS on June 16, 2008. He was 5 months old. Even though it has been 10 years there is not a day that goes by that we do not think of him. We want to help people who have gone through this as well as try and prevent it from happening to others.

Issabellas Army is dedicated to bring SIDS awareness and to end SIDS.

The team is in memory of my brother Jason.

My family sponsors events in remembrance of Jared Ryan Sigle, son of George Sigle & Jenn Bender, grandson of George and Paula Sigle. Gone from our arms but never from our hearts. We hope in some small way our donation to research at the American SIDS Foundation, will help find answers to this devastating disease and another family will not have to go through the tragedy we did that fateful day 15 years ago.

Jenika was born 8/6/08 as a happy and healthy 7 lb, 7 oz sweet baby girl. On the morning of 9/9/08, my husband and I woke up to find she had gained her Angel wings and flew home during the night. She was our firstborn and brought us nothing but pure joy in those 34 days. It’s been almost 15 years and during the 5000+ days we’ve spent here without her, there has been not ONE single day that she has not been thought of and missed. She meant everything to her family and we will fight every day to help bring an end to SIDS in her memory ♥️

In our quest to keep Kash’s memory and smile alive, we’re asking every one of you, both near and far, to help us celebrate April 1st by wearing buffalo plaid and doing 2 acts of kindness (in honor of him turning 2) and sharing using the hashtag #kashskorner Then, join us as we ‘blow bubbles to heaven’ to our sweet boy that evening. Also, if you would like to make a contribution to the American SIDS Institute we’ve created this page in honor of Kash. Every dollar counts as we raise funds to continue to find clues and reasons as to why this is happening to our precious littles. From the bottom of our broken hearts Thank You! We look forward to hearing the stories of ways you’ve spread a ‘Kash Smile’ and seeing everyone in their buffalo plaid ❤️🖤

Our team is made up of Cayden's family, extended family, and dedicated fan club. We lost Cayden suddenly on September 1, 2015. Although he lived just a short time, we are AMAZED at how many lives he touched. Please join us in supporting research for Sudden Infant Death Syndrome. We are raising money for the American SIDS Institute in memory of Cayden Bennett Cox.

Hi friends and family! Thanks for visiting our page. This year, 2020, we are hosting a virtual, on-your-own 5K in honor of Louisa, in hopes of helping the American SIDS Institute get the funds it needs to continue education, research, and support for SIDS families. You can make your $31 donation above ("Donate Now" button) and then do your 5K (3.1 miles) in parts or all at once. Walk, run, hike, skip, shimmy. . . whatever mood strikes you. Let us know know you're done and you'll get a little something in the mail as a thank you. July 31st is the deadline. So much love! Beth and Derek

September 11 is a date that strikes fear and sadness into the hearts of Americans, but for our family this heartbreaking date means the nightmare in which we lost our Blaise to SIDS. Our amazing supporters rallied behind us, and together we are a team of family and friends dedicated to keeping the tiny life of Blaise "alive" in our hearts. Our goal is to celebrate Blaise by spreading awareness about Sudden Infant Death Syndrome throughout our community and by educating all caregivers about current SIDS research and ways in which the risk of SIDS may be reduced.

We are trying to raise awareness for SIDS and host a memorial walk in her name. Beautiful and healthy baby girl when she came from the hospital! No family should have to endure such pain!

Madailyn Eve was born a perfect healthy baby girl to a loving family full of love and happiness. Madailyn died sleeping just 2 months and 19 days after she came into this world. Ever since then her mom has made it her mission in life to help walk the other mothers who lose a child through the difficult life they will live after losing their greatest love. 2010 was the year everything changed for our family. 9 years later we are all continuing to live our lives through her. Her short time has shown us life is too short and helping others is the greatest way for her story to be heard.

Matthew passed away November 12, 2016. He was only 6 months old. We put him in his bed, he went to sleep and never woke up again. The pain I felt is indescribable, I'll always wonder why? Why my baby? His cause of death was ruled as SIDS. I miss him more and more everyday. Now I want to do anything and everything I can to raise awareness and to help raise money for research so maybe one day SIDS can be prevented. So I'm asking you to donate to Matthew's Purpose so we can maybe have some answers to the why's. Every little bit helps. It is greatly appreciated. Thank you, Amanda Haughton

Mia Rosalinda Oviedo passed away in her bassinet on February 23rd 2021. She was only 18 days old. Mia was the light of our lives and we miss her more than words can describe. Mia will never be forgotten, her legacy lives on every single day.

Losing a family member is never easy but losing a little person, a child is a lot worse. We often think why? what has this innocent child done to have his life taken so suddenly? Whether you're religious or lean on scientific belief , our hearts still break when we hear of an infant's death. Marcus Alexander Roberts Jr. was born May 11, 2017 and for 5 months he was a joy to anyone who met him. Tiny hands, fat cheeks and a precious smile, nicknamed Mj and/or Jr this little person was a true blessing. October 26,2017 Jr. was pronounced dead, cause of death Sudden Infant Death. Parents ask questions, people cry, family asks for prayers during this hard time but the elephant in the room is SIDS how can we have a name for something when we hardly understand or know what it truly is? Family and friend of Jr. have taken an oath to raise money and donations to help the American SIDS Institute research, educate and prevent SIDS.

Baby to left Michael John Myers died of SIDS 12-27-1994 this is my nephew and baby to the right died of Sids on 11-10-2018. This is my great nephew I can’t lose any other family member to sids so help raise money so this stop. Both baby were just 3 moths old and my great nephew was 2 month old

Hey there, Im Sgt Nop3. and here is a little about me. Father.Husband.Brother.Son.Gamer.Streamer. Youtuber.Friend.Veteran. Ok, so a little more in depth on these facts is I have 4 kids (3boys and 1princess) I'm married to a wonderful woman who supports everything I do (that's right I'm the lucky one). Have many many siblings (3bros and 3sis's) and some really awesome parents 2dads and 2moms. I love streaming a variety of games so you'll see plenty on this channel. I spent a few years in the Army and then worked in Alaska as a fisherman. Now I work for one of the greatest companies in the world Southwest Airlines. Love my job. I lost my brother in 1985 to SIDS and am now in the position to host an awesome event in his name!

On July 3rd 2016 we woke up to find Our very healthy 6 month old baby girl unresponsive, I rushed her to the hospital where she was given chest compressions nonstop for an hour straight, they were able to resuscitate her once but shortly after her little body stopped fighting and our little Paisley grew her wings. I had no idea so many were affected and I most certainly didn't think that this would happen to us. I realized We need to raise more SIDS awareness. I know my precious angel has a great purpose and I believe maybe this is "Paisley's Purpose"! Together WE can and will make a difference!

Payton's Peeps are raising funds in memory of Payton Krumwiede. Payton was born on July 8th, 2008 and earned his angel wings on September 8th, 2008. We are focused on raising funds to help research SIDS that takes our babies way too soon. If you complete the virtual 5k please email me your address so we can send you a little gift! Charper26@hotmail.com

Our angel Drayla was born August 21 2019 and left us September 2 2019. She had the most beautiful smile. She was our “Pinky”. Forever in our heart. I miss her so much.

Nala Rebecca Mitchell was born on Thursday February 28, 2019 and she gained her wings on Friday April 5, 2019.

This team is to support Quintine Schmidt's life. He was born March 2010 and gained his wings October 2010!

In memory of my precious grandson, Kylar Joel Chauvin

In memory of Ricky lee Dodson 12-7-2015 to 3/13/2016

Hello! Run for Research is a team training for Grandmas Marathon, a race that takes place in Duluth, Minnesota! We are running for all families, for all loved ones, that have been effected by SIDS. Our goal is not only to bring awareness, but to raise as much money as possible for research, so we can better understand SIDS. Any donation is a step in the right direction. It will help get us closer to the ultimate goal, and that is to cure SIDS. T-Shirts and Bracelets are being figured out, so stay tuned for more details regarding that! Run for Research thanks you so much! Updates will be happening regularly, with events coming up in the future! Once again, thank you!

My family would like to start an event in honor of my nephew who passed away from SIDS. We would like to do it yearly to honor my nephews memory and the beautiful short life he had

SHANA JA'NELLE THE DAUGHTER OF MARTHA JANE WALLACE & At the time of her death had 1 sister Crystal. Since then 1 more sister Desiree' & 1 brother Drew & 1 niece with another nice on the way & 1 unknown right now. Shana was VERY LOVED FOR A VERY SHORT TIME!! And as her mommy it made me mad there was NOT alot of funds for S.I.D.S. SO I AM NOW GOING TO TRY & HELP OUT IN THE RESEARCH OF SUDDEN INFANT DEATH SYNDROME BY SELLING ITEMS AT SCHOOL ACTIVITIES IF THE SCHOOL ALLOWS ME TO. NOT A DAY GOES BY THAT I DON'T STILL MISS & GRIEVE MY BABY!! BECAUSE OF HER DEATH I NOW HAVE PTSD & HOPING BY DOING THIS I HELP MYSELF TOO!!

In memory of Shannon Eileen Mayo, 6/29/13 - 9/18/13

I am a single mother who lost my youngest son on March, 23rd, 2017 to SIDS, 14 days after his first birthday. I have wanted to get involved and do something so badly and I finally see that the opportunity is POSSIBLE!!! I want to contact companies and have coffee cups, t-shirts, bracelets, key chains, anything else we can get...pens, pencils, necklaces, anything at all from local and any sort of company that makes items such as those so for example fund raising companies that do personal labeling, local t-shirt printing companies, there are so many places that make these items personalized and I want this to be BIG!!! Just like breast cancer awareness has grown to be an international symbol and month of dedication... I will not give up until SIDS is honored and recognized nationwide as big as breast cancer awareness and even bigger!!! Our society does not talk about this like they should. As a parent who lost a child to SIDS you feel like you did something wrong, and you are ashamed that you could have done something, the education, knowledge, and the attention it deserves is not out there and it needs to be!!! I am very committed and I owe this to my son to make it happen. I could contact all these companies that develop the items we could sell as a fundraising and awareness item and have proceeds donated and we could have the blue and pink SIDS bow made, millions and dispersed, we can grow this into something huge so it gets the research and funding it needs and helps the awareness of this terrible life ending problem. This can be huge!!! I will make it huge. I am part of a very generous church that is huge and Nationwide and between the help from them not only volunteer wise but financial donations we are talking a lot of money which in turn will save lives...SIDS does not just take the life of the child, it takes the soul of the family with it left with no answers and it took me almost a year to get motivated and get excited to do this and open my eyes and my heart to the world again!!! My friends, church members, and social media together can do this...please give me this opportunity I will not let you down and this will become one of the most well known foundations in history!!! I am 30 weeks pregnant with my last baby. After losing my son I didn't think I could ever have another child and I planned not to, however heavenly father had another plan for me. I am scared to death to put my unborn baby girl down for a nap when she is born, I don't know how I will do it. My anxiety is through the roof, but with this as my project and knowing I am doing something amazing I know I will have the strength to be the best mommy ever to my unborn daughter and I look forward to the future of future SIDS Awareness and Prevention Month!!!!!!! I want fun runs, sports tournaments, news coverage, people standing on the roads all over town with nets on a stick like the firefighter do taking donations, I want neighborhood fairs and potlucks where a percentage of proceeds go to the foundation, I want pink and blue SIDS balloons, everyone wearing SIDS shirts for the activities especially what I want to call the SIDS Run...a let's say 3 mile run where all proceeds to register are donations and given to the foundation and the runners wear the shirts. I want huge gathering there...food trucks, novelties for sale with SIDS Awareness and colors on them, auctions from local company donations, tickets sold for drawings to win prizes also donated by local companies and all proceeds to the foundation...and when I say local I will start it here and spread it across the states. I will find a way to be at every event and coordinate it and I guarantee as I am sure you also know that hundreds will step forward to volunteer as well...this is what I was meant to do in life, now I know it for sure...I want to do all of this...Go BIG or Go Home!!! I have hundreds of ideas of events that could be held in that one month of Spring to raise funds and most importantly spread awareness and education. I have an amazing group of people that will help me start this if I can have some leads and assistance from you and the go ahead to get started...through social media alone I can make this huge...I promise to not let you down. Since we are already running into summer I say that May because of Mother's day and the great weather should be SIDS awareness month. We can start other fundraisers in the meantime and acquire ideas and volunteers over the next few months and by May 1st, 2019 we will have ourselves a full blown nationwide SIDS awareness month and so many different things to represent it, support the cause, raise money, get people involved, businesses, and educate...I know this can be done, thank you for your time I am so excited to hear from you!!!!!!!

We are a non for profit women’s group. We have done numerous things for the community. We are so proud to be apart of this organization. We are dedicated to keeping family close.

My name is Kathi Murtagh, I stumbled across the Spring for SIDS website several years ago and signed up to participate. Our team SoulBabies has raised between $1200 - $1500 each year for the past few years. I am a "Subsequent Parent", and I cannot express in words the heartache these losses have caused over the years. On Oct. 2, 1985 I gave birth to my son Christopher, he passed on Dec 30, 1985. I really had never heard about SIDS, or as they called it "crib death", and was angry that no one could tell me what caused this mysterious thing that took my son from his father and me. We were very young at the time and all the stages of grief affected us in different ways. Two years later, I learned I was pregnant again. After an extremely difficult pregnancy, I gave birth to our daughter Heather on Dec. 17, 1987. I called her my miracle child because of the difficulties of my pregnancy and having lost our son, she was a miracle to me. Unfortunately, that was short lived. My baby girl was gone. She passed away on Jan 18, 1988. Again, we had to lay a child to rest. No reason other than SIDS was given. How could this have happened again? Many, many years had gone by, yet I still hadn't really dealt with the loss of not one, but two children. This wasn't something that I would just talk about. Only those who were close to me knew of my losses. No matter how hard I tried, I could not allow myself to believe there was nothing I could have done to save them both. The typical denial, non-acceptance and guilt were at times unbearable. So many questions, yet no answer, was always weighing on my mind. When I spoke with my Grandmother the first year I signed on to SFS, I told her I needed a team name. She suggested SoulBabies. She said my babies’ souls are in heaven now. I loved the name, not just because it made sense but because my Grandma, a woman I have always admired, chose it. Today, all these years later, I still get the case of wondering what Christopher and Heather would be like now. What would they be doing. Would they be like their older sister? Would they have their own families? Participating in Spring for SIDS has helped me tremendously. I know I can talk about my SoulBabies now. I know they are above watching over our families. I know they know how much they were and are loved and missed every day. We have two very special SoulBabies guarding us. I am so grateful I found the SFS site that day, and grateful that I have the ability to help contribute to the research for the baffling, mysterious syndrome that's claims the lives of all our SoulBabies. I did not join this cause for just my own children, but in honor of all those lost to SIDS. I pray that answers are found in my lifetime, and we can all know more about the cause and hopefully a preventive measure to ensure no more parents, siblings, families or friends have to endure something so devastating. No one truly understands the loss of a child, unless they experience it themselves. No one understands what a surviving sibling goes through. That is not a burden I want other parents to endure. I hope that next year there is a way to memorialize not just one child on our page, but for us Subsequent Parents, a way to honor our other children as well. For not once, but twice, we endured heartaches that forever change our lives. Thank you everyone at The American SIDS Institute, Spring for SIDS and all the teams and their members for their dedication to this research. May we all have peace of mind and success and one day find the answers we so desperately seek. I look forward to participating every year in SFS Thank you for reading my story and teaching me that we are truly not alone in our quest for answers. God Bless you all! Kathi Murtagh Team Captain, SoulBabies

Having a bowling tournament along with selling shirts It will be held at Lucas Lanes in Blackwell Ok, 74631

Swing Phi Swing Social Fellowship, Inc.® is a non-profit organization dedicated to community service, promoting and achieving academic excellence, and enhancing community and cultural consciousness. Our specific purpose is Supporting Women In Need of Growth, which facilitates the attainment of goals that are necessary for personal and professional growth. Swing welcomes diversity, encourages individuality, and offers a haven for women who feel a strong connection with their ethnic heritage. Our vision is to promote leadership, academic excellence, community involvement and civic and cultural consciousness. We strive to embody a Sisterhood through fellowship of women of all creeds.

Team Ashley Nichole is in memory of my Angel Ashley Nichole, it was inspired to help raise awareness about SIDS and through community involvement raise money for research.

Remembering Ayden Michael Hisquierdo 02/04/2015 - 03/18/2015

In celebration of Brendan's upcoming birthday and SIDS awareness month, I wanted to set up an event and try to help raise money to support SIDS research and prevention. SIDS is a silent killer and you a lot of times there is not enough information available or parents aren't fully given the statistics so they are aware how real this is and how it can happen to any baby but especially premature baby's 1 in every 10 girls and 1 in every 3 boys from 3-6 months old the more information we can get the better we can protect our babies ❤️❤️

Our Angel Carter passed away when he was 1 year and 2 weeks old. He was our baby and forever will be. We hold this charity dear to our hearts bc we don't want anyone to suffer the way we have after losing our precious baby boy. Carter still lives in our home his pictures are all over our walls and his spirit surrounds us. We have been blessed with two more kids after him and we are now a family of 7 plus an angel in the sky.

Raising money in honor of Damire Rogers for his 1st heavenly birthday.

This team has been created to show SIDS awareness 💙 in honor of my handsome son Elias Daniel who passed away from SIDS💙

My grandmother-in-law told me when I was sobbing the most, "God needed a little Angel and he chose Isaac". I have kept that in my heart ever since. This was the hardest thing I have ever had to deal with in my life. Would I like an explanation? Yes! As would many other mothers. I decided that determination is the only way to ever get explanations. And, most of all, if I can help in any way to never let another mother have to deal with losing their child then I am happy!!

On July 14th 2008 we were blessed with identical twin boys, Kaleb & Kenley. Although they came 5 weeks early they were strong and perfect! On September 15th 2008 a curve ball hit our life, that still haunts us to this day. We woke up to find Kenley wasn't breathing. I immediately began CPR and called 911. At the hospital the doctors broke the news that they were unable to revive my baby boy. We lost a part of us that day that we will never get back. When I discovered the Spring for SIDS foundation in 2010 it gave the loss of my son new meaning. Since then I have dedicated myself to spreading awareness and raising money each year to contribute to the mission of finding a cause and cure for SIDS. Until answers are found I will continue to stand up and remain hopeful that one day we will know how to stop this and one day put an end to the pain SIDS has caused us. https://youtu.be/dZcop1f060c

Team LHQ is a dance team from Agawam Ma. We compete in 4 regional competitions and 1 national competition yearly. This year we are dancing at the Power of Dance compeition. Where Dance Studios Across America join The Power of Dance to raise money fot their chosen charitie! We have choosen SIDS in memory of Miss Connie's Granddaughter Londyn May Abbate who passed away September 13, 2018 from SIDS at only 5 weeks old. We as a team will be raising money in her honor.

We lost my baby nephew before he turned 2 months old. He brought so much joy to our lives and this team and march is in his honor.

The picture is my daughter Malaysia .. She was born a preemie and when she passed due to SIDS her actual age was 9 months but adjusted was 6 months.. It all happened so fast and we would just like to do anything we can to bring SIDS awareness to everyone's attention.

On June 5 2011 our family was blessed with Samuel. He was a happy baby who lit up a room when he was in it. On August 26 2011 our family lost Samuel to SIDS. It became our goal to help fight back against this disease and bring infant loss out of the taboo. Together we are making a difference.

Brianna Plaster and her baby sister Valentines 2005

Texas Students for SIDS Awareness (TSSA) is a group of students at the University of Texas at Austin dedicated to hosting events to raise awareness for Sudden Infant Death Syndrome (SIDS), promote safe sleeping environments for infants, and raise money for SIDS research.

This is a senior project. We will be hosting a 5k in Hutchinson, Ks on November 13, 2021.

US Foods-Manassas-Engagement Team

Team Wallace Warriors is a parent duo who has chosen to run a virtual 5k for SIDS (Sudden Infant Death Syndrome). We as a team will be raising money for this cause in hopes to raise awareness for SIDS, promote safe sleeping environments for infants, and to further advance its research. Our son stopped breathing in his first week of life, but we were very lucky to catch it in time and save him after several CPR compressions. However, we know many have not been. We hope to continue to do our part for this cause to help others as we embark in our 3rd Annual Fundraiser/5k this year on March 30th, 2023! We have raised $4,000 through our first two years and hope to raise more. Thanks to all who contribute!

A group of loved ones who are running for a cause to fight SIDS, always remember our Zander and hope that this does not have to happen to any other families. We are still hurting and thinking of him everyday. Please help us raise money for SIDS research and come celebrate the life of one perfect baby boy 💙