Walk a mile in the shoes of a sickle-cell warrior, one who hoped to fulfill her calling in this world. To blend in like all the normal people in the world. Almost everything she did was through survival mode; at work, at home, in school and all in all within the community. You will notice how this blood borne disease knocks her down and even makes her vulnerable numerous times as she has a brush with death. But only courage, determination and encouragement have helped her accomplish so much successfully.

Sickle Cell is a inherited blood disease that causes problems throughout ones life. These problems could be minor or even life threatening. This particular warrior puts on an unimaginable fight with Sickle Cell. Including ups and downs throughout his life that even doctor's are shocked he is still here to tell his story on how he is... "Living the Sickled Life"

Osteo what?" I thought. I was not to know that it would take me into the dark abyss of anxiety, depression, hopelessness and even bitterness. Indeed, I was in a place where I had come to learn the meaning of the word "longsuffering" ...Sometimes it looks like life has dealt you a bad hand, but what you make of it is crucial in living life to the fullest. There is no gainsaying that the road won't be easy, however when life gives you lemons, dont just make lemonade, but make smoothies, ice cream and cakes out of them. There is a strength that comes with every battle. YOU CAN DO IT.In reading this book, I hope you are inspired to look beyond your circumstances. Once you see beyond them, they will serve as stepping stones to God's purpose for your life, has planned for you.

Diary of a Little Warrior takes the readers on a journey of life living with sickle cell disease (SCD) from the perspective of a young sickle cell warrior. The young warrior provides details of what she deals with daily. As the young warrior shares her story, she is hopeful and optimistic through it all. The purpose of the book is to help educate people about sickle cell disease, raise awareness, and to empower other SCD warriors.

It's deemed the world's most common genetic disorder, but why is sickle cell disease still not fully understood in communities where it's very prevalent. The Real-Life Stories of Sickle Cell - A Global Collaboration presents stories from different parts of the world to enlighten us about the effects of this condition. Stories from sickle cell warriors, caregivers, healthcare professionals, and advocates capture these people's understanding and awareness of Sickle Cell Disease. You will read stories of hope, resilience, frustration, and sadness as we strive to bring these stories to the world. Although being the most common disorder, what this project taught us was that even people living with sickle cell disease do not get adequate treatment in most parts of the world. Sickle cell warriors are still stigmatised in different parts of the world. That sickle cell warriors would rather hide from peers or employers that they are affected, fearing the treatment they may receive. We have learned of warriors bearly getting adequate treatment because it's simply not available in their area. These stories will give you that understanding of how much we still need to do as a sickle cell community, to double our efforts to support people impacted from different parts of the world, especially developing countries.

"In Strength of a Warrior, the author sheds light not only on the nature of the disease in general, but also offers great vision into how knowledge sharing and mindset change can lead to a substantial reduction in Sickle Cell diseas 'warriors' face each day, as they go through their crises like a soldier who understands the ultimate price at war and yet still finds the courage to take up arms. This book is a significant contribution to all the warriors out there as the author shares real-life experiences with fellow warriors to inspire hope, strength and courage; as well as to impart sound knowledge to every reader regarding Sickle Cell Disease management and prevention"--Page [4] of cover.

My heart felt like it was about to explode from the pain. As the nurse quickly left the room, I then became more irate. I began beating the walls and crying "Please, please, someone help me!" At this time, someone came and closed the door to my room and by doing that made me more irate. I began to scream so loud I thought I would spit my vocals out.

Sickle Cell Anemia is a horrible disease to an outsider looking in. However, to me, it is no different than any other life-threatening disease! The only difference is Sickle Cell Anemia does not get the much-needed recognition it truly deserves. People know little or nothing about the disease because it is not seen as important like other well-known diseases are. I personally have an issue with that problem because I have Sickle Cell Anemia, and I have always been a lifelong advocate for it! Sickle Cell Anemia has affected me as well as many of my family members. There are countless other people in the world who also suffer from Sickle Cell Anemia. I decided to write my personal story because living with this disease has been quite a challenging journey for me, from my childhood until my middle-aged years. I have had both some good days and some bad ones, but God has kept me. So, I won’t complain! I feel as if I’ve been on an emotional roller coaster that has taken me on some highs and lows. It seems like I have been on this ride a million times over, and it simply will not stop. Despite experiencing some periodic turbulence, I have still managed to have some great times on this roller coaster ride! Therefore, I can honestly say, “It’s okay! I’m going to ride this ‘til the wheels fall off.” Plus, I know God will never, ever give me or anyone else more than we can handle! I have also learned how to weather the storms over the years. Early on, I lived my life worried every day because I was told that I was going to die at the age of 17. Accordingly, I lived with that expectation until I surpassed that deadline. Ever since then, I have been living my life without the constant fear of dying at such a tender age. Life is precious, and I live each day to the fullest! Sickle Cell Anemia is only a part of me; it is not the total sum of who I am!

ABC's of Sickle Cell Disease is a top educational resource for children with sickle cell disease. Parents, caregivers, and healthcare workers should have the book on hand to help explain how the condition works within a child's body. A recommended children's book for ages 5-12. It breaks down terms and concepts for children diagnosed with Sickle Cell Disease (SCD). The author simplified the information so even a child could understand how this genetic blood disorder affects the body. The book is an excellent tool for parents, teachers, healthcare workers, or caregivers to teach children.healthcare workers ABC'S OF SICKLE CELL DISEASE FEATURES: Beautiful original illustrations―Children learn more about Sickle Cell Disease using the letters A to Z. Large 8.5 x 11-inch pages. Educational and interesting―Each page effectively describes the blood disorder to young patients. Made for diverse families―The pages feature children, adults, and medical professionals from different ethnic groups because sickle cell disease affects families from multicultural backgrounds worldwide. Positive and inspiring―The book is a positive keepsake that gives young sickle cell warriors a chance to boost their confidence and creativity.