Podcasts about sickle cell awareness month

This episode is being released in honour of Sickle Cell Awareness Month. It features a conversation with Ufuoma, an alumna of the 1834 Fellowship and founder of the Sickle Cell support organization, NotJustYou. Ufuoma discusses the impactful work her organization does and how her involvement with the 1834 Fellowship opened doors for her to advocate for the sickle cell community. This advocacy includes a meeting with Canada's Prime Minister and participation at the UN Permanent Forum on People of African Descent in Geneva, Switzerland. Ufuoma also shares advice for Black young adults interested in exploring policy and social change by engaging with non-profits.Host: Iyanu Soyege------Connect with the 1834 Foundation and its initiatives below:Instagram (1834 Fellowship): instagram.com/1834fellowship Twitter (1834 Fellowship): twitter.com/1834Fellowship LinkedIn (1834 Fellowship): linkedin.com/1834-foundation Instagram (1834 Global): instagram.com/1834global Twitter (1834 Global): twitter.com/1834global

Ryan Gorman hosts an iHeartRadio nationwide special featuring John Drikell Hopkins, founding member of the Zac Brown Band, who joins the show to discuss his fight to find a cure for ALS through his Hop on a Cure foundation. Also, Dr. Courtney Fitzhugh, Sickle Cell Disease Expert with the National Heart, Lung & Blood Institute, checks in for Sickle Cell Awareness Month to explain the disease, its impact on life, and the latest treatments. Finally, Dr. Christine M. Crawford, Child Psychiatrist & NAMI Associate Medical Director, discusses rising concerns of parents and caregivers who are struggling to navigate children's mental health.

September is Sickle Cell Awareness Month. In this Cancer Matters podcast, Dr Bill Nelson, the Director of the Johns Hopkins Kimmel Cancer Center, speaks to Dr Rick Jones and Dr Robert Brodsky about treating sickle cell anemia, an inherited disorder where mutations in the globin gene cause the red blood cells to take on a sickle shape, leading to severe pain and organ damage. They discuss and compare the types of bone marrow transplants currently used to treat the disease and highlight the significant improvements in reducing complications, such as graft-versus-host disease and graft rejection.

On today's show, we discuss a new report on the status of maternal health in Arkansas. Also, new treatments are being introduced as we recognize Sickle Cell Awareness Month. Plus, the Red Ball is rolling through northwest Arkansas.

In this episode of *Sickle Teller*, we dive deep into the world of sickle cell anemia, a genetic blood disorder that affects millions worldwide. Learn about the science behind the crescent-shaped red blood cell and if you're looking to understand more about this condition or seeking information to help a loved one, this episode provides crucial insights into sickle cell anemia and its impact on lives.

In this episode of Sickle Teller, we explore the origins of Sickle Cell Awareness Month, a dedicated time each September to shine a spotlight on sickle cell disease. We delve into the history of this important observance—how it began, and the importance of raising awareness daily. But why is Sickle Cell Awareness Month so vital? We discuss the importance of educating the public, dispelling myths, and advocating for better healthcare and research. We highlight how awareness can lead to better understanding, support, and ultimately, a brighter future for those affected by sickle cell anemia.Join us to learn how you can be a part of this movement and make a difference in the fight against sickle cell disease.#SickleTeller #SickleCellAwarenessMonth #HealthAdvocacy #PodcastEpisode #HealthcareEducation

It's Sickle Cell Awareness Month, so it's only right that we shed light on the disease and share information. This week we are joined by Denice, who talks us through her experiences of living with Sickle Cell. 00:00 - Introduction 03:25 - Milan Fashion Week 25:18 - Sickle Cell - What, Where, When, How and Who! @denicekoduah Sickle Cell Charities: https://www.sicklecellsociety.org/ https://oscarbirmingham.org.uk/ https://www.letstalksicklecell.co.uk/ Give blood here: https://www.blood.co.uk/ You can watch the episode here https://youtu.be/472Kozpz6cg If you want more, join us on Patreon for extra exclusive episodes: www.patreon.com/styleandcitydiares You can find us here... Instagram: @Styleandcitydiaries / @prinnyraee / @amberleaux / @prinnyxamber Twitter: @Stylecitydiary / @prinnyrae / @amberleaux Tiktok: @Styleandcitydiaries / @prinnyraee / @amberleaux Youtube: Prinny and Amber Email: info@styleandcitydiaries.com www.styleandcitydiaries.com Learn more about your ad choices. Visit megaphone.fm/adchoices

And then there were two... Dr. Karen & Dr. Tiffany discuss the importance of balancing work and personal life both during and "after" the pandemic.  Dr. Zanetta is taking hiatus from our usual schedule but will be back!September is Sickle Cell Awareness Month. Sickle Cell is a hereditary blood disorder that causes the red blood cells to form in a sickled or banana shape instead of the normal round shape. This change in shape makes it difficult for the red blood cells to function properly, including carrying oxygen to cells. Sickle Cell presents in two ways: Sickle Cell Trait (SCT): genetic carrier of the disease, but usually does not exhibit symptomsSickle Cell Disease (SCD): experiences symptoms such as anemia, swelling in hands and feet, pain episodes, frequent infections, or vision problemsSCD and SCT impact African Americans at disproportionate rates. Sickle Cell affects 1 million to 3 million Americans and 8 to 10 percent of African Americans. This is because SCD and SCT are an evolutionary trait that people developed in response to help protect them from malaria. As such, this condition is common in large parts of Africa. People whose ancestors are from other regions where malaria was common are also at a higher risk of inheriting SCD or SCT, including people of:Mediterranean descentMiddle Eastern descentSouth and Southeast Asian descentCentral and South American descentCaribbean descent RESOURCES:Sickle Cell VideoSickle Cell Disease.org Join the Conversation! Follow us on social media!3 Black Docsfacebook.com/3blackdocstwitter.com/3blackdocsinstagram.com/3blackdocsDr. Karen Winkfieldfacebook.com/drkarenwinkfieldtwitter.com/drwinkfieldinstagram.com/drwinkfieldDr. Zanetta Lamarfacebook.com/drzanettainstagram.com/drzanetta

The American Red Cross issued an urgent call for action this week, warning of a critical shortage in the national blood supply that poses a significant threat to the healthcare of patients across the country, particularly those in the Black community who rely on life-saving blood transfusions to manage sickle cell disease.  With the blood supply dwindling by nearly 25 percent since early August and a series of natural disasters in recent months, the situation has become increasingly dire, according to a press release from the organization. The Red Cross reports a surge in blood drive cancelations and a substantial decrease in blood and platelet donations in regions affected by recent catastrophes. August witnessed a big decline in donor turnout – a staggering 30,000-donation deficit for the month. September is also designated as Sickle Cell Awareness Month, drawing attention to the importance of raising awareness about the more than 100,000 people in the United States grappling with the disease. The majority are of African descent and depend on regular blood transfusions to manage their condition. The Red Cross is now launching a campaign titled "Joined by Blood" throughout September and October. The initiative involves collaborations with prominent organizations within the Black community, including 100 Black Men of America and Kier's Hope Foundation.  One in three African-American blood donors is a compatible match for individuals with sickle cell disease. For more information on how to donate blood or get involved in the "Joined by Blood" campaign, head to the American Red Cross website. Learn more about your ad choices. Visit megaphone.fm/adchoices

So, let's talk about the pain experienced by individuals with sickle cell disease… When is the last time you've been to a hospital? Living life with an ‘invisible' disease, many sickle cell patients endure pain and discomfort that frequently goes unacknowledged and unnoticed. Many of these people are hospitalized an average of 3-6 times per year. However, due to the lack of visible symptoms, they often go undertreated. It's disheartening how patient care for this remains overlooked even though sickle cell disease is the most inherited genetic disorder in the United States. But that needs to change, and so I'm here to shout from the rooftops today. Join us as we start the National Sickle Cell Awareness Month with an episode talking about the life our sickle cell patients have to deal with every day. Why you need to check this episode: Understand the life a lot of sickle cell patients deal with, especially with this ‘invisible' disease; Recognize the importance of not undertreating the pain experienced by sickle cell patients and believing them when they report pain, even when no visible signs are present; and Gain awareness as to what pharmacological and non-pharmacological ways are there to help patients deal with the pain and discomfort brought on by the disease “We need to not only recognize our patients with sickle cell disease, but we need to respect our patients with sickle cell disease; we need to trust our patients with sickle cell disease. All of these things need to happen if you are going to be the best healthcare provider you're going to be. We can't wait for the month of September to be talking about like, ‘Hey, let's look out for our sickle cell patients'. Because again, sickle cell patients don't only come to the hospitals in September.”– Dr. Berry Pierre Notable Quotes: “If a disease has a whole month dedicated to it, it is of importance; it is something that we need to keep very good track of.” – Dr. Berry Pierre “It (the sickle cell disease) is the most inherited genetic disorder. Now, if I told you a disease was the most inherited genetic disorder, you would think that everyone would be on red alert when they're taking care of these patients. But that, unfortunately, is not the case, and there is still a lot to learn especially from a patient care perspective.” – Dr. Berry Pierre “It's important to understand that your patient is there and needs to be taken care of by you. You can't allow any preconceived notion or patients you might have dealt with to affect you from taking care of the patient in front of you.” – Dr. Berry Pierre “The pain of sickle cell patients—treat it like you will be treating family. We are not in the position to undertreat the pain of our patients anymore. And if you ever needed any thought to say like, ‘Alright, is this sickle real? Is this something I should be worried about?' Again, I repeat, it is the no.1 genetically inherited disorder.” – Dr. Berry Pierre Sign up at www.listentodrberry.com  to join the mailing list. Remember to subscribe to the podcast and share the episode with a friend or family member. Listen on Apple Podcast, Google Play, Stitcher, Soundcloud, iHeartRadio, and Spotify Resources: My thoughts on Netflix's Painkiller The pain of sickle cell disease with Dr. Berry Pierre | Lunch and Learn Lunch and Learn with Dr. Berry Episode 51: Discussing Sickle Cell Disease

To listen to the full episode, check out our Patreon Page - http://patreon.com/theyellowpillpod To leave a comment at any point during your listen, here's a link you can use - https://bit.ly/typs10e4 # About the episode  In continuation with the theme of our previous episode and in recognition of Sickle Cell Awareness Month, this episode explores the complex issue of medical ethics and family responsibilities through "My Sister's Keeper (2000)".   Inherited or congenital illnesses can often be a source of difficulty and turmoil for families, as this movie portrays.   However, the deeper lesson for us as young adults is about the tough choices we may have to make in life, many of which we may be unprepared for and undeserving of.   When faced with decisions relating to life and death, we never truly know who we will become. . . . Before you go, here are a few ways to support the podcast! Become a TYP Patreon ♥️ - http://patreon.com/theyellowpillpod Leave us a review where you're listening right now!

Did you know that September is Sickle Cell Awareness Month?  Sickle cell is a genetic trait affecting red blood cells — and it causes intense pain and anemia.  Sickle cell disease occurs among one out of every 365 African American births. But some health care providers miss sickle cell symptoms or don't take seriously people who have the condition. To learn more about why, guest host Tim Nelson spoke with Rae Blaylark and Dr. Stephen Nelson. Rae Blaylark is the President and CEO of the Sickle Cell Foundation of Minnesota. Dr. Stephen Nelson is a pediatric hematologist oncologist and Chief Medical Officer at the foundation. Use the audio player above to listen to the full conversation.  Subscribe to the Minnesota Now podcast on Apple Podcasts, Google Podcasts, Spotify or wherever you get your podcasts.   We attempt to make transcripts for Minnesota Now available the next business day after a broadcast. When ready they will appear here. 

During this episode I share information about sickle cell disease in honor of National Sickle Cell Awareness month. History to ExploreNigeria has a population of 112 million people. About 25% of adults there carry the sickle cell trait  (source). According to the World Health Organization, more than 300,000 babies with severe hemoglobin disorders are born globally each year, but 75 per cent is said to be found in Sub-Saharan Africa (source).African ProverbHe who is sick will not refuse medicine. ~ Nigerian ProverbsPlease tweet us using the #cleverlychangingpodcast to tell us what this proverb means to you or leave us a voicemail and let us know what you think this African Proverb means.Word of the EpisodeIn the Gambia Dutu means Mango.  Order a Clever Homeschool Kit: Don't forget to order one of our exclusive Clever Homeschool Kits. The value of each individual kit is $175 USD, and the first 25 people who sign-up for a kit will receive free-shipping. Kits ship in early October and will include: t-shirts, games, stickers, a planner, and more.Register for your clever homeschool starter kit here.Let's Connect!Want to be a guest on an upcoming show? Just fill out this form, and we will send you an interview link when your request is approved.We're bringing back Cleverly Cultured Kids! We want to feature your kids on Cleverly Cultured Kids, so please complete this Interview form for kids, and we will send you an interview link once your request is approved.You can call us directly now. Please leave us a voicemail and let us know how you enjoy the show or share your questions.Grown Folks Talking About National Sickle Cell Awareness monthElle Cole empowers moms and advocates for children with sickle cell disease. She is a mom of twin daughters, one of whom is living with Sickle Cell Disease and Type 1 Diabetes. In 2020 she was awarded the Advocating for Another WEGO Health award. She is the author of four children's books: A Sickle Cell Coloring Book for Kids, ABCs of Sickle Cell, and The Ultimate Sickle Cell Activity Book. She is a writer, speaker, and Podcast Producer. Feedspot named the Cleverly Changing Podcast #3 on the Top 20 Homeschooling Mom Podcasts list. She also produces the VitaminSC3 Podcast which is a new podcast that shares real stories about families battling sickle cell disease. The podcast is powered by the Sickle Cell Community Consortium. She's been featured on NPR, ABC 7, BBC World Service Radio, and many podcasts. Her website CleverlyChanging.com discusses wellness, personal finance, and parenting.Connect with Elle Blog

September is Sickle Cell Awareness Month. Dr. P and Quannecia, a “Community Queen” in Houston, TX discusses her life with Sickle Cell and her passion for educating her community and raising her two sons, both with the sickle cell trait. 

Shout to 36 mafia (100.3beat)and Nicalina for her time and knowledge on today's segment of sickle cell awareness --- Send in a voice message: https://anchor.fm/gwen-dickerson/message

In support of Sickle Cell Awareness Month, Provokin' Dialogue will be doing a two-part episode dedicated to the struggles of managing sickle cell pain.Part 2 continues with R.E.M.E. detailing his journey toward understanding his body and how to recover during a crisis. R.E.M.E. opens up about his struggles due to the lack of resources provided to the sickle cell community. Shaquan questions why there is a lack of awareness around the disease and why drugs are pushed to patients over natural pathways.For more sickle cell disease resources, please visit:Your Fellow Sickler - R.E.M.E's YouTube channel documenting his journey with sickle cell diseaseSickle Cell Disease Association of America - General sickle cell disease info Find Us OnlineInstagram: instagram.com/provokindialogueFacebook: facebook.com/provokindialogueTikTok: tiktok.com/@provokindialogueCreditsCo-host: R.E.M.ECo-host: Shaquan Smith About UsIt's time to bridge the gap from debating opposing sides to having conversations while respecting one another's perspective, or what we call Provokin' Dialogue. Explore the conversations of two brothers in completely different stages of their lives, but come together to offer you new insights to everyday topics. From careers, relationships, and politics, to family, superpowers, and the meaning of life. See how R.E.M.E's witty outlook on overcoming hardships and younger brother Shaquan's curious ecocentric spirit strengthen each other's perspectives to find you leaving every episode with a refreshingly new point of view.

Regina Hartfield is CEO and president of the Sickle Cell Disease Association of America. Hartfield served on the association's board of directors for three years, including as chair of the fundraising committee. Previously, she managed federal, state and commercial contracts for CVP, an information technology consulting firm in Virginia and Maryland. Hartfield was a community affairs professional in the nonprofit arena in New York for more than 25 years where she gained experience as a leader in nonprofit organizations. She graduated with honors from Lehman College of the City University of New York with a Bachelor of Arts in community outreach. Servio Astacio was born in the Dominican Republic with sickle cell anemia and experienced symptoms from an early age. His condition prevented him from pursuing his dream of military service, but he remains driven to growing in other areas of his life. Now 25 years old, Astacio lives in Miami, owns a business and pursues interests in finance and technology. He advocates for sickle cell awareness and research and has spoken at conferences, symposia and roundtables.

Sickle Cell Awareness Month

September is Sickle Cell Awareness Month, and this week RP is talking to the amazing Sophie Lavarin-Leconte. Sophie is a sickle cell warrior, happily married with two beautiful children. Tune in as she shares her journey with sickle cell and some words of encouragement for those living with sickle cell. According to RP is available everywhere you enjoy your podcasts. Follow us on social media @Accordingtorp and Blackivymedia

In support of Sickle Cell Awareness Month, Provokin' Dialogue will be doing a two-part episode dedicated to the struggles of managing sickle cell pain.Part 1 begins with R.E.M.E. discussing his experience managing sickle cell disease and revealing the many side effects of the drugs he's used to cope with sickle cell pain. Shaquan reflects on the memories of R.E.M.E in the hospital and is left surprised by an untold story R.E.M.E has never shared with him.For more sickle cell disease resources, please visit:Your Fellow Sickler - R.E.M.E's YouTube channel documenting his journey with sickle cell diseaseCenters for Disease Control and Prevention - General sickle cell disease info Find Us OnlineInstagram: instagram.com/provokindialogueFacebook: facebook.com/provokindialogueTikTok: tiktok.com/@provokindialogueCreditsCo-host: R.E.M.ECo-host: Shaquan Smith About UsIt's time to bridge the gap from debating opposing sides to having conversations while respecting one another's perspective, or what we call Provokin' Dialogue. Explore the conversations of two brothers in completely different stages of their lives, but come together to offer you new insights to everyday topics. From careers, relationships, and politics, to family, superpowers, and the meaning of life. See how R.E.M.E's witty outlook on overcoming hardships and younger brother Shaquan's curious ecocentric spirit strengthen each other's perspectives to find you leaving every episode with a refreshingly new point of view.

8.29.2022 #RolandMartinUnfiltered: Jim Crow voting law upheld; Black Duke volleyball player called n-word; Tabitha Brown fires back The 5th U.S. Circuit Court of Appeals is upholding a voting law it knows is steeped in racism.It's an1890 Jim Crow law that white supremacist state leaders designed to disenfranchise Black voters. I'll be talking to one of the lawyers from the Mississippi Center for Justice who is fighting to change it.  The only black Duke University volleyball player was called racial slurs during a match against Bringham Young University. Her father will be joining me tonight to discuss how both schools responded and how his daughter is handling the situation. BYU said Sunday that  Internet sensation Tabitha Brown says take her as she is or don't take her at all. We'll be talking about code-switching and how some entertainment leaders want us to tone down who we are to make others comfortable.  And September is Sickle Cell Awareness Month. We will be talking to the Senior Advisor of Black Women's Health Imperative about  Pfizer's $5.4 billion investment in one of the more promising drugs to treat the disease.   Support RolandMartinUnfiltered and #BlackStarNetwork via the Cash App ☛ https://cash.app/$rmunfiltered PayPal ☛ https://www.paypal.me/rmartinunfiltered Venmo ☛https://venmo.com/rmunfiltered Zelle ☛ roland@rolandsmartin.com Annual or monthly recurring #BringTheFunk Fan Club membership via paypal ☛ https://rolandsmartin.com/rmu-paypal/ Download the #BlackStarNetwork app on iOS, AppleTV, Android, Android TV, Roku, FireTV, SamsungTV and XBox

Neglected and overlooked by the clinical foundation all through the greater part of its set of experiences, sickle cell disease remains one of the most common (and commonly misunderstood) hereditary conditions on the planet. In this episode, the crew will touch on this topic to get more Familiar with Sickle Cell so join us and We are so honored and thrilled to be joined this episode by not one, but two incredible guests! You'll hear first from Jessica and Lickson, who share with us some of their firsthand experiences living with sickle cell disease. Also you can check out Jessica's Youtube channel "Get Cozy with the Colzie's" we have a QR code on the flyer. #liveatthebarbershoppodcast #sicklecell #sicklecellawareness #podcast --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app --- Send in a voice message: https://anchor.fm/live-at-the-barbershop/message

September is Sickle Cell Awareness Month! As I celebrate my one year anniversary of this podcast, I think this is a great topic to discuss for this special month. You will be able to gain some great insight about sickle cell including what is sickle disease, who is at risk,  and possible treatments. In addition, you will learn more details about sickle trait and is it considered  synonymous with sickle cell disease.  Thanks to all of my awesome listeners and please continue to share the podcast with others and continue to leave your positive reviews.  Your continued support is truly appreciated.    Below is link to share with family/friends/colleagues for quick access to Refine Your Health Facebook page please like and follow for great content and includes links to choose a preferred podcast streaming platform. Refine Your Health Podcast  https://linktr.ee/refineyourhealth Website links referenced in episode:  Facts about Sickle Disease - https://www.cdc.gov/ncbddd/sicklecell/materials/factsheets.html Sickle Cell Disease Association of America, Inc. - https://www.sicklecelldisease.org/get-involved/events/national-sickle-cell-awareness-month/#

We are still celebrating Sickle Cell Awareness Month, and in this BONUS episode of Silent Podcast, Ijeoma and Christina connect with Maya Bloomberg, a board certified Family Nurse Practitioner. She specializes in hematology and is passionate about the sickle cell patients she treats. The trio discusses advocacy, patient rights and care, and how racial disparities play a role in this life-altering disease. Not only is this episode super inspiring, it's a wealth of information for sickle cell patients and advocates alike. In our opinion, there is no better way to end sickle cell awareness month than with this episode of Silent Podcast. You can connect with Maya Bloomberg on Instagram at @thehemenp. Silent Podcast is sponsored by The Ruby Ball Foundation where our goal is to create a voice in the silence by promoting awareness while empowering and improving the quality of life for individuals living with sickle cell disease around the world! For more information, visit www.therubyball.org. You check out this episode of SILENT Podcast on YouTube at https://youtu.be/70T-8pAnpLE. --- Send in a voice message: https://podcasters.spotify.com/pod/show/the-ruby-ball/message Support this podcast: https://podcasters.spotify.com/pod/show/the-ruby-ball/support

September is Sickle Cell Awareness Month, to promote our sickle cell initiative blood drive at Fellowship Missionary Baptist Church 3355 N 4th St, Minneapolis. Saturday, September 25, 2021

How bad is banana-shaped blood? We always knew we'd do an episode about sickle at some point down the line, so why not give it a go during Sickle Cell Awareness Month? And why not do our first full outside-the-studio recording too… in Birmingham! In this week's episode we're gonna feel. Shyarntai, a 19-year-old student, talks to us about her experience of living with sickle cell and Jenica Leah, a Sickle Cell Activist and Expert, comes through with some heartfelt lines on how she is trying to help people with the disease. So, whether you know all about it or wanna hear a bit more, this one is for you. Hosts: De-Graft Mensah & Roshan Roberts Producer: Jack Suddaby Sound Designer: Jack Suddaby Editor: Sam Bonham 00:00 A warning from Shan 00:15 B-Town 01:04 "I feel like I can't move" 01:55 Intros 03:08 Speaking with Shyarntai about A LOT 10:36 Reflectionsssss 11:01 Evan's story 12:20 Chatting with Jenica Leah at a Blood Donation Centre 18:11 Shan and DG talk it all through 18:50 Thanksssssssss

In support of Sickle Cell Awareness Month, Provokin' Dialogue will be doing a two-part episode dedicated to elevating the voices of the sickle cell community.Part 2 continues R.E.M.E's story of him being kicked out of the hospital and having to think on his feet to make it through a severe crisis. Later, Shaquan and R.E.M.E go into a Q&A segment to discuss questions ranging from the difference between sickle cell trait and disease, figuring out if there is a cure, to R.E.M.E identifying as a werewolf. Yes, I said werewolf!To learn more:Follow R.E.M.E's journey with Sickle Cell Disease on YouTubeCheck out the CDC website for general info

Sky sits down with Ameer Campbell, CEO of Until We Find A Cure, to discuss sickle cell. We talk about the disorder, how it effects the body, mind and how family members can be helpful.

Dr. Corey Hebert is here to elevate our thinking and brings to our attention that there is a new medicine for the treatment of sickle cell anemia. Learn more about your ad-choices at https://www.iheartpodcastnetwork.com

Each September, Children's of Alabama honors Childhood Cancer and Sickle Cell Awareness Month. This two-part, Inside Pediatrics Podcast series features two physicians from the UAB Division of Pediatric Hematology, Oncology and Blood and Marrow Transplantation. In episode one, Dr. Matthew Kutny, director of the Leukemia, Lymphoma and Histiocytosis (LLH) Program, reveals how the new generation of treatments is more customized for each patient and targeted for each type of cancer.

In support of Sickle Cell Awareness Month, Provokin' Dialogue will be doing a two-part episode dedicated to elevating the voices of the sickle cell community.Part 1 begins with the question "What is sickle cell?" R.E.M.E and Shaquan discuss the attributes of having Sickle Cell Disease (SCD) and their perspective on living with someone with SCD. R.E.M.E opens up about his struggles and with the disease, before revealing a story you don't want to miss!To learn more:Follow R.E.M.E's journey with Sickle Cell Disease on YouTubeCheck out the CDC website for general info

Indira is the Vice President of Operations and Co-director of Life and Family Foundation/ Living With Sickle Cell inc and co-founder of POSH- People of Sickle Cell Hope.

September is National Sickle Cell Awareness Month. We invited teen entrepreneur, Nazhi Forrest, to share insight on how to pursue goals while facing challenges in life. . Featuring special guests Nazhi Forrest @nazhitheebakerllc and Dr. Charlie Ware @healingblendsglobal Fundraiser Severely Sick Sickle Cell Sisters https://gf.me/u/yuqwca For more inspirational programs, please follow @TFG365TV Yannick Jackson Executive Producer TRAINING FOR GREATNESS, INC. A holistic approach to professional and business development. VIRTUAL EVENT: SICKLE CELL AWARENESS WATCH PARTY @TFG365TV | FACEBOOK & INSTAGRAM . Training for Greatness hosted a virtual event in support of Sickle Cell Awareness Month.

We are taking a pause in our season 2 programming to acknowledge Sickle Cell Awareness Month. We will hear letters and reflections from those with the disease, this weeks reflection is from Jemela, read by our host, Taylor Camille. Jemela's Spotify Pain Relief Playlist can be found here (https://open.spotify.com/playlist/1AErVDWjtW5lNgfHl8sWaP?si=p974KzMtTje5QNiAOVJICg). Sickle Cell Anemia News: Awareness month events (https://sicklecellanemianews.com/2020/09/01/national-sickle-cell-awareness-month-events-underway/) Follow Beyond Our Cells on Instagram (https://www.instagram.com/beyondourcells/) Twitter (https://twitter.com/beyondourcells) Follow host, Taylor Camille (https://www.instagram.com/tayllure/)

I’m humbled to be a part of the Trav Market Media network of travel podcasters. Have you had a chance to listen to our network? We share informative travel information for travel agents. Take for example my podcast where I share informative information for travel agents especially when working with clients with special needs! Check us out on Trav Market Media! In this episode, I’ve had the pleasure of speaking with Elle Cole, a traveling and fearless travel mom, and medical advocate! I invited Elle to be on my podcast today to talk about a very unique travel special consideration...okay well actually two! Elle’s daughter has Sickle Cell Anemia and Type 1 Diabetes and you will be surprised to learn that Sickle Cell affects more people than you may have learned about in health class. Sickle Cell Anemia is described by Elle in this episode and she shares about how she is able to travel and her advice about working with a travel agent when planning a vacation. In particular, there are things to consider such a flying for individuals with Sickle Cell that affects oxygen levels when flying. Elle's daughter also has Type 1 diabetes. This type of diabetes currently has no cure and medical professionals still do not understand why it occurs. We also discuss how Elle manages her daughter's diet and keeps her insulin to help better support her during their vacations. In this episode, we dive into traveling with Sickel Cell Anemia and Type 1 diabetes and things you really need to consider before traveling. I know this episode has been released at the end of the month but I wanted to emphasize that September is also Sickle Cell Anemia Awareness Month. Sickle cell disease is a genetic condition that affects the body’s red blood cells. It occurs when a child receives two sickle cell genes—one from each parent. In someone living with this disease, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle”. In this episode, we’ll chat about how it affects travel and what you can do to better support your clients or disclose this information to your travel agent so they can better understand and help you plan an unforgettable trip. A program called Be the Match helps those with Sickle Cell Anemia and Cancer receive a bone marrow transplant match to find a cure. Unfortunately, black people only represent 4% of the registry. By joining people would sign up to send in a cheek swab to join the registry so they can be matched in the future. Right now, bone marrow and stem cell transplants are the main ways that people with sickle cell and cancer are being cured. September is both Sickle Cell Awareness Month and Childhood Cancer awareness month. To find out how you can help visit Be the Match Donor or - Text "SC3Carley" to the number 61474 or visit join.bethematch.org/SC3Carley for more information. Guest: Elle Cole is a mom of twin daughters, one of whom is living with Sickle Cell Anemia. She serves as a health advocate for Sickle Cell Disease and Type 1 Diabetes. She is an ambassador for St. Jude Children’s Research Hospital. And raises awareness about Sickle Cell Disorders to help make the quality of life for people living with genetic disorders and autoimmune diseases better. Elle is also the author of "A Sickle Cell Coloring Book for Kids". This book seeks to simplify and explain the symptoms of SCD. When raising a child with a genetic disorder such as SCD there is so much to learn, so the author simplified the information so even a child could understand how this genetic blood disorder affects the body. The coloring book is a great tool for parents or caregivers to color along with the child. Book - "A Sickle Cell Coloring Book for Kids" Elle's Links:Website: CleverlyChanging.com Instagram: Instagram.com/CleverlyChanging Youtube: Youtube.com/CleverlyChanging Facebook: Facebook.com/CleverlyChanging Twitter: Twitter.com/CleverlyChangin Are you considering a vacation? Reach out to me and let me know how I can help you plan your next trip! See omnystudio.com/listener for privacy information.

We are taking a pause in our season 2 programming to acknowledge Sickle Cell Awareness Month. We will hear letters and reflections from those with the disease, this weeks reflection is from Sabah, read by Sabah herself. Sickle Cell Anemia News: Awareness month events (https://sicklecellanemianews.com/2020/09/01/national-sickle-cell-awareness-month-events-underway/) Follow Beyond Our Cells on Instagram (https://www.instagram.com/beyondourcells/) Twitter (https://twitter.com/beyondourcells) Follow host, Taylor Camille (https://www.instagram.com/tayllure/)

The 2020 Playoffs are here... "wubble-style". Also, the W crowns her most valuable with a lil' trophy drip. _________________________ September is Sickle Cell Awareness Month. Patients all over the world batter through crippling pain and it's our responsibility to know about Sickle Cell Disease (SCD) and how we can help. For more, check out 'The Sickle Cell Podcast' or on IG @SickleCell101. Blood and bone marrow donations are life-saving to SCD patients. To find out if you're a match, please visit www.BeTheMatch.org for a kit or donate today at your local Red Cross. Visit www.RedCross.org. Thank you for listening! >>>>>>> Find us on social: IG: @FromTheSidelinesPodcast FB: @FromTheSidelinesWNBA @mosdev_ @sweetshe0421

We're sharing stories, responses and discussing the theme of this year's Sickle Cell Awareness Month, "Sickle Cell Taught Me..." Current event links: Black Blood Matters: https://www.wavy.com/news/health/red-cross-black-blood-matters-for-some-with-sickle-cell-anemia/ Sickle Cell Patients Should Have Medical Exemption in the UK: https://sicklecellanemianews.com/2020/08/19/uk-nhs-medical-exemption-petition/ Millions of Americans carry the sickle cell trait, many without knowing it. Could they be at risk for severe Covid-19?: https://www.statnews.com/2020/09/03/millions-carry-sickle-cell-trait-could-they-be-at-risk-for-severe-covid19/ When Actions Speak Louder Than Words — Racism and Sickle Cell Disease: https://www.nejm.org/doi/full/10.1056/NEJMp2022125 --- Support this podcast: https://anchor.fm/thesicklecellpodcast/support

Hey lovies in honour of Sickle awareness month I decided to do an episode covering the topic so we can all have a general information on the topics. The links below are information for further readings :https://ghr.nlm.nih.gov/condition/sickle-cell-disease, https://www.mayoclinic.org/diseases-conditions/sickle-cell-anemia/symptoms-causes/syc-20355876, https://medlineplus.gov/sicklecelldisease.html. Subscribe to my podcast so that you can get an instant update when I release an episode. Thank you guys for your continued support I really appreciate it. If you wish to share your views on the topic my social media is IG: chinanna96, twitter: Chinanna_.

We are taking a pause in our season 2 programming to acknowledge Sickle Cell Awareness Month. We will hear letters and reflections from those with the disease, this weeks reflection is from Princess, read by Princess herself. Sickle Cell Anemia News: Awareness month events (https://sicklecellanemianews.com/2020/09/01/national-sickle-cell-awareness-month-events-underway/) Follow Beyond Our Cells on Instagram (https://www.instagram.com/beyondourcells/) Twitter (https://twitter.com/beyondourcells) Follow host, Taylor Camille (https://www.instagram.com/tayllure/)

Single elim's are coming up... and they suck. But first, let's talk about the Top 8 teams who've made it to this year's Playoffs in the wubble. Oh, and Deon's back! ---------------------- Hey, September is Sickle Cell Awareness Month. Patients all over the world battle through crippling pain and it's our responsibility to know about Sickle Cell Disease (SCD) and how we can help. For more, check out 'The Sickle Cell Podcast' or on IG @SickleCell101. Blood and bone marrow donations are life-saving to Sickle Cell patients. To find out if you're a match, please visit www.BeTheMatch.org for a kit or donate today at your local Red Cross. Visit www.RedCross.org to give!

September is Childhood Cancer and Sickle Cell Awareness Month. In this episode of the Inside Pediatrics Podcast, Dr. Jeff Lebensburger shares an update on sickle cell disease – early detection and treatment, bone marrow transplants, current pain therapy and promising research for a cure within the first few months of life.

Great news, this is a life changing episode. Episode 40 is a bonus release issued to help celebrate Sickle Cell Awareness Month. This conversation is all about saving lives in the black community. Sickle Cell Disease is a genetic disorder that can affect any ethnicity or nationality, but in the US it disproportionately affects people of African descent. During this episode, I spoke with a long time friend Ebere who joined Be the Match's donor registry many years ago and later donated her bone marrow, which helped save someone's life. Listen to her experience and if you are willing to join the donor registry text SC3Carley to 61474 or visit https://join.bethematch.org/sc3carley.INTRO (00:00)WORD OF THE EPISODE (3:00)GROWN FOLKS TALK (3:50)WE NEED YOU TO SHARE THIS PODCAST AND SUPPORT USTell a friend or two about the Cleverly Changing podcast. While we love having a conversation with each other, the podcast will only be able to exist if more people are listening. If you know someone who has children, our tips and tricks are beneficial to parents who homeschool and those who are interested in supplementing the education of their children.Furthermore, wherever you are listening to this podcast, please leave us a review.In addition, to keep the podcast going consider becoming a monthly supporter through our Patreon page visit our secure page: https://Patreon.com/CleverlyChanging.CONNECT WITH OUR GUEST: Ebere, a health care professional and bone marrow donorInstagram: https://www.instagram.com/mizebbstarPlease share this conversation with a friend and join the Be the Match Registry. https://join.bethematch.org/sc3carley★ Support this podcast on Patreon ★

Mimi Update... Supermom Culture... Pop Culture Update... What Mimi is watching... Sickle Cell Awareness Month. Follow me @mimicutelips everywhere on social. Share your thoughts on the episode on social using the hashtag #MimiSaidWhat Email mimi@mimicutelips.com

This week, Dev flies solo while Deon is away caring for one of our biggest fans. Hey, September is Sickle Cell Awareness Month. Patients all over the world battle through crippling pain and it's our responsibility to know about Sickle Cell Disease (SCD) and how we can help. For more, check out 'The Sickle Cell Podcast' or on IG @SickleCell101. Fellow WNBA Fans, take 2 seconds to send up some positive words for Kiera, our SCD Warrior!! Thank you! Blood donations and bone marrow are life-saving for Sickle Cell patients. To donate, please visit www.BeTheMatch.Org for a kit and find a local Red Cross at www.RedCross.org to give blood today!

We are taking a pause in our season 2 programming to acknowledge Sickle Cell Awareness Month. We will hear letters and reflections from those with the disease this weeks reflection is a short and sweet account from Jay, as read by host, Taylor Camille. Sickle Cell Anemia News: Awareness month events (https://sicklecellanemianews.com/2020/09/01/national-sickle-cell-awareness-month-events-underway/) Follow Beyond Our Cells on Instagram (https://www.instagram.com/beyondourcells/) Twitter (https://twitter.com/beyondourcells) Follow host, Taylor Camille (https://www.instagram.com/tayllure/)

What exactly is professionalism and why are underrepresented minorities more harshly policed? Dating as a medical student, Sickle Cell Awareness Month, Vice Presidential Candidate Kamala Harris, and black hair in the hospital.

We are taking a pause in our season 2 programming to acknowledge Sickle Cell Awareness Month. Later this month we will hear letters and reflections from those with the disease and are starting off the month with a reflection from host, Taylor Camille and a special guest. Sickle Cell Anemia News: Awareness month events (https://sicklecellanemianews.com/2020/09/01/national-sickle-cell-awareness-month-events-underway/) Follow Beyond Our Cells on Instagram (https://www.instagram.com/beyondourcells/) Twitter (https://twitter.com/beyondourcells) Follow host, Taylor Camille (https://www.instagram.com/tayllure/)

Being that September is Sickle Cell Awareness Month and with the unfortunate passing of Chadwick Boseman from colon cancer, the topic of genetic history needed to be addressed. It’s been a while but this topic and the passing of Chadwick was something I was moved to speak about. I hope you found this episode somewhat informative!

September is Childhood Cancer and Sickle Cell Awareness Month. In this episode of the Inside Pediatrics Podcast, Dr. Girish Dhall shares exciting news from the Pediatric Hematology-Oncology team, including new collaborations and clinical trials available to patients, research and fellowship training opportunities, and a significant jump in the division's U.S. News & World Report ranking among the top programs in the country.

Hi everyone! First of all, thank you so so so much for all the support and love that was sent my way after the first episode, it was overwhelming! Thank you so much for clicking on this episode! In honor of Sickle Cell Awareness Month, I talked to the stunning girls of the Kyha Foundation - Iggie AIkhomu & Karimat Karim. They cleared up common misconceptions about sickle cell, shared their tips and tricks for handling critical situations, and spoke on their experiences with starting fundraisers and juggling their lives. I learnt a lot during this episode and I'm sure you will too. Enjoy! P.S. I apologize in advance for the poor audio quality, I recommend you listen with earphones. Let's connect! https://www.instagram.com/nyerepod/ Kyha Foundation Instagram: www.instagram.com/kyhafoundation/ --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app --- Send in a voice message: https://anchor.fm/nyere/message

September is Sickle Cell Awareness Month and in this episode we speak to Isowa, a sickle cell warrior and founder of IsoWarrior. Isowarrior is a foundation that helps to raise funds through various programs and initiatives, with the aim of creating awareness for and supporting patients who suffer from sickle cell disease. Isowa shares her life story and the plans she has for her foundation. Sickle cell disease is a group of inherited red blood cell disorders. There is currently no known cure, other than bone marrow and blood transplants, however there are multiple ways of managing the symptoms. In some parts of Africa, the prevalence of SCD ranges from 20% to as high as 45%! Visit Isowa's web page at www.isowarrior.com and learn how you can contribute.

It's sickle cell awareness month so this week we caught up with entrepreneur Caleb Boaz in Weho to learn more about sickle cell disease, its origins and how what he does to mitigate the genetic disease. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app Support this podcast: https://anchor.fm/brotherly/support

Junior speaks to us about the great strides that have been made and he also talks about his foundation Kier's Hope. Learn more about your ad-choices at https://news.iheart.com/podcast-advertisers

It's Sickle Cell Awareness Month! Francene Marie interviews Dr. Yvette Miller - Red Cross Executive Medical Director and member of Delta Sigma Theta and also the amazing Maya Franklin - External Communications Manager and Biomedical Field Marketing and Communications for the American Red Cross. Join us from 10 am to 3:30 pm at the Omegas of Charlotte Fraternity House along with the Red Cross, located at 3301 Statesville Ave, Charlotte, NC 28206. The goal is to collect 80 units of blood It's hosted by the Delta Sigma Theta & Omega Psi Phi on September 21, 2019.

The gang is back with another episode to MELANTE YOUR PALATE and FEED YOUR SOUL!!! num num num We discuss Sickle Cell Awareness Month and what we NEED to do to get NY State Legislators to support the 2019 Sickle Cell Treatment Act A6493 and S2281 ***Special Guest*** Ginger Davis She is the spokesperson for Sickle Cell Disease, the Coalition of Inherited Blood Disorders, and Rare Diseases. She is also a member of the NAACP Brooklyn Branch. For more information about sickle cell disease, and links to resources, visit https://sctpn.net. Look at the Events page to see the listing of activities, and check out the Media page to see news clips, and read the Blog. The Sickle Cell Thalassemia Patients Network (SCTPN), in collaboration with Candice’s Sickle Cell Fund (CSCFI), Queens Sickle Cell Advocacy Network (QSCAN), and the NYS Sickle Cell Advisory Consortium are hosting a press conference on the steps of NY City Hall on Monday, September 9, 2019, 10:00 am, in recognition of the City Council’s adoption of the State Legislative Resolution (SLR 335). The Sickle Cell Thalassemia Patients Network is located in Crown Heights, Brooklyn. The listeners can call (347) 533-8485 to speak with a Community Health Worker about their concerns.

Do you know your genetic status in regards to Sickle Cell Anemia? Knowledge is power and this episode is a reminder to any and everyone who may be unsure. As we begin Sickle Cell Awareness Month, it is important to we start by just knowing where we stand so we know where to start our journey. The month will be dedicated to getting this message across to everyone as well as how teach other why it is important to be informed of your status. Thank you and enjoy

In honor of Sickle Cell Awareness Month, host Taylor, candidly talks about her life living with Sickle Cell Anemia and all the challenges she faces.

During this month of September which is Sickle Cell Awareness Month, join me in this important discussion with Tosin as she shares her experiences living with sickle cell anemia and the incredible strength she demonstrates every day despite the challenges and pain that come with this illness. Her website is sicklecellwarriors.com and the Facebook group is Sickle Cell Warriors. 

September is National Childhood Cancer and Sickle Cell Awareness Month. Dr. Kim Whelan talks about the Alabama Center for Childhood Cancer and Blood Disorders, and its impact on patient care in the state of Alabama and across the country. Together, the University of Alabama at Birmingham (UAB) and Children's of Alabama are one of only 19 sites nationwide to participate in the Children's Oncology Group phase one and two consortium which allows our families to have access to the newest drugs and promising clinical trials without having to travel out of state. Each year, more than 1,500 children come to our center for care, and more than 300 dedicated pediatric healthcare professionals provide exceptional patient care, education and research. We are committed to finding a cure for all children – down the street and around the world.

September is Sickle Cell Awareness Month, and our guest for Episode 11 has a compelling story about how she learned about the disease. Elle Cole is a writer and founder of CleverlyChanging.com, a lifestyle blog that focuses on “Empowering the Total Person.” Elle and her husband have two daughters—twins. One of them has sickle cell disease, so the ups and downs of this genetic disorder are well known to them. As an advocate and blogger, Elle hones in on sharing educational information the disease, the trait--which her other daughter has, how both are inherited, and about symptoms and treatments. She also talks about the importance of empowering her daughter to advocate for herself as a patient. Read more at https://planetnoun.com.

It’s Monday and Uncle Steve opens up the show with a special type of happiness because The Browns did not lose. Nicki Minaj and Cardi B. are beefing right now. Barack Obama voices his opinion of President Trump. Serena Williams shows how champions handle themselves at all times. CLASS. Miss Carla has her Power Update as she talks about the finale. Junior talks about Sickle Cell Awareness Month. The crew talks about Sunday’s NFL game and Pimpin’ chimes in. Closing Remarks for today has a special message of staying on the wall and more! Learn more about your ad-choices at https://news.iheart.com/podcast-advertisers

  Welcome to 4 Your Health Radio w/ Marsha Thadison. This health show is designed to inform everyday people about the benefits of healthy food for our mind, body, and soul. On this show, people will learn how to prepare meals, to be for medicine and much more. This radio show will help put the power of good health back into the hands of the people.  Tamika Moseley talk about  Sickle Sell Seminar and Sickle Cell Awareness Month. https://www.ssnaturalhealing.com http://www.yesterdayskitchen4today.com https://www.facebook.com/Yesterdays-Kitchen-4-Today-228600220519293/?ref=hl (To all my 4 Your Health Listeners this program/radio show advises all that the information presented here is for the purpose of information, and education only. It should not be construed as offering medical advice or the diagnosis and or treatment of any illness, injury, condition or prevention for any health problems the viewer should consult licensed physician or health care practitioner for proper diagnosis and /or treatment.)

Conquering the Curve, Inc's Chad Leonard returns to Marvel&Friends continuing to educate us, and inform us about the organizations continued mission regarding Sickle Cell Awareness. As a recap of Sickle Cell Awareness Month, Mistah Marvel and Chad discuss health, social implications, and catch up on times since they last sat down together picking up from the death of Mobb Deep's Prodigy.

Tonight, on It's Real Talk Radio, we'll be recognizing Sickle Cell Awareness Month, which is September for those who don't know. Ms. Sha', It's Real Talk Radio co-host, has the Sickle Cell Trait and has a child who has the actual virus which is passed on genetically. Millions of people carry the trait and millions live with the actual illness and it's important to recognize and educate ourselves on this deadly disease, which claims the lives of countless people including Hip Hop legend, Prodigy. Sickle Cell patients live with great discomfort and pain and there is no cure for it. When you have it, you have it for life. Some of you probably have a family member who has this illness and you yourself may carry the trait and not even know it. There is so much to be educated on when it comes to Sickle Cell Awareness and there's no better suited person to learn from than Ms. Sha', because she has been dealing with this disease for years! There are organizations that help and support Sickle Cell patients, including the Sickle Cell Society, the Children's Sickle Cell Foundation and others which we'll get into on the show. So make sure you listen in because there will be a lot of valuable information you can learn and pass on to friends, family and loved ones. It doesn't get much realer than this! Topics like this are what It's Real Talk Radio is all about. Spreading knowledge and making a voice for the people. #ItJustGotReal Call In # 347-838-9540

Why does it seem so many young people are dying from violence? This week we dedicate the show to all the families of victims of violence. In Longview there have been 11 homicides in 2015. The ones unsolved are those of black people. The community has had enough, but the lack of trust amongst the people and police has stifled the arrest process. This issues is not exclusive to Longview, Tx. All over the country there have been problems with solving crimes in particular sections of the community. We will discuss all the aspects of this problem and kick it off as always with black history. Since it is Sickle Cell Awareness Month, we have a little something about that too for you.

The Black History often forgetten always kicks off the Show. We will discuss the NAACP Journey for Justice March that culminated in Washington D.C. this week. We'll take a close look at how drugs and violence have impacted the communities of color in the past decade. On behalf of Sickle Cell Awareness Month will share facts on the disease. As always we encourage the listening audience to tune in by dialing 347-855-8118 so that you can add your seasoning to the pot we've got cooking. After all that, we hope to inspire you into action for the betterment and advancement of your neighborhood and more.

Tonight we are experiencing some technical difficulties. Hopefully, they will be corrected soon. We apologize for the inconvenience. September is Sickle Cell Awareness Month. We will talk about how this deadly and debiliating disease impacts the community of color and lesser known group in the world significantly. We will also talk about how your local community can make some changes to impact violence and build unity amongst law enforcement and the neighbors. As always we will go back in history using research Jerry Mitchell gathers for the Clarion Ledger of Jackson, MS. We will dedicate a portion of our show to how we can pull ourselves out of poverty with a little grace and mercy from our Father. Lastly, we will put all these issues in the pot and let it simmer so you can digest what we are serving. 

Special Guest Jonette Jordan stops by TSS and educates the crew about Sickle Cell in honor of Sickle Cell Awareness Month, the crew talks about an open letter to white gay men, and then ends the episode on Back In The Day.Support the show (https://paypal.me/TheShiznitShow)

In this episode, Black Hollywood Live hosts Nick Perdue and Megan Thomas interview special guest Drew Sidora. Drew Sidora hails from Chicago, Illinois. Drew will next be seen playing Tionne "T-Boz" Watkins in the VH1's Crazy Sexy Cool: The TLC Story premiering October 20th on VH1. Drew is best known for breakout roles in The Game, That's So Raven, and the original Step Up. Drew recently produced her first feature film Blessed and Cursed with Deitrick Hadden, starring Sheryl Lee Ralph Drew also launched her own record label, Record Breakers Music Group. The label serves as a platform to showcase young artists and music producers. As a child, T-Boz was diagnosed with Sickle Cell Anemia, and this encouraged Drew to become a spokesperson for Sickle Disease Association of Illinois. September is Sickle Cell Awareness Month and you can see this link for more information: http://sicklecelldisease-illinois.org/. Drew Sidora was the Host of the 2013 Real Men Cook in Chicago, promoti

In honor of Sickle Cell Awareness Month, we will discuss this critical issue and the plight of the African-American community. Sickle cell anemia (uh-NEE-me-uh) is a serious disease in which the body makes sickle-shaped red blood cells. “Sickle-shaped” means that the red blood cells are shaped like a "C." Sickle cell anemia affects millions of people worldwide. The disease has no widely available cure. However, there are treatments for the symptoms and complications of the disease. Bone marrow transplants may offer a cure in a small number of cases. Due to improved treatment and care, people who have sickle cell anemia are now living into their forties or fifties, or longer.