Podcasts about Aplastic anemia

Claire was a NICU nurse, so she had never experienced a pattient with Aplastic Anemia. Then, she became a patient herself. Find out how she learned she was stronger than she knew in this episode.

In this episode, we review the high-yield topic of⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Aplastic Anemia ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠from the Hematology section. Follow ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Medbullets⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ on social media: Facebook: www.facebook.com/medbullets Instagram: www.instagram.com/medbulletsofficial Twitter: www.twitter.com/medbullets

In this episode, we review the high-yield topic of ⁠⁠⁠⁠Aplastic Anemia⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠from the Heme section. Follow ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Medbullets⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ on social media: Facebook: www.facebook.com/medbullets Instagram: www.instagram.com/medbulletsofficial Twitter: www.twitter.com/medbullets Linkedin: https://www.linkedin.com/company/medbullets

In this week's episode we'll discuss the safety and efficacy of acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL; learn more about alternative donor transplantation for severe aplastic anemia and discuss clonal relapse dynamics in acute myeloid leukemia following allogeneic hematopoietic cell transplantation.Featured Articles: Acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL: Final efficacy and ctDNA analysis of the CLL2-BAAG trial Alternative donor transplantation for severe aplastic anemia: a comparative study of the SAAWP EBMT Clonal relapse dynamics in acute myeloid leukemia following allogeneic hematopoietic cell transplantation 

In this two-part episode, Amy DeZern, MD, MHS, with Johns Hopkins and Christin DeStefano, MD, with Uniformed Services University discuss bone marrow transplant as a first-line treatment for severe aplastic anemia, moving beyond the limitations of traditional immunosuppressive therapies for a curative treatment option. In Part II: Future Research and Care Coordination, experts underscore the critical importance of early referral and coordination between hematology/oncology and transplant centers while looking ahead at the exciting research and clinical trials yet to come. To read bios on the panelists and to access additional resources related to this episode, visit Our Site. 

In this two-part episode, Amy DeZern, MD, MHS, with Johns Hopkins and Christin DeStefano, MD, with Uniformed Services University discuss bone marrow transplant as a first-line treatment for severe aplastic anemia, moving beyond the limitations of traditional immunosuppressive therapies for a curative treatment option. In Part I: Outcomes and Equity, guests explore the benefits of haploidentical transplant, noting quicker recovery times and reduced complications compared to past methods. These advancements are particularly impactful for diverse populations, including military personnel. To read bios on the panelists and to access additional resources related to this episode, visit Our Site. 

Jenny Cape and Dr. Margolis join the WKLH Miracle Marathon benefitting Children's Wisconsin, presented by Mars Family Foundation, to share how Jenny went from being a strong, healthy athlete to suddenly being diagnosed with Aplastic Anemia. With Children's Wisconsin's quick reaction, she was back to school & playing soccer in five months!

Damian describes his story of diagnosis, treatment, and bone marrow transplant in this compelling episode.

In this week's episode we'll discuss molecular mimicry in aplastic anemia, novel experiments show that antigens associated with viral infections can mimic epitopes presented on hematopoietic progenitor cells. Then, we'll learn about prophylaxis with subcutaneous emicizumab in infants with hemophilia. Finally we'll see how hydroxyurea is associated with a significant reduction in infections among children with sickle cell anemia in Uganda.Articles featured this week:Virus-reactive T cells expanded in aplastic anemia eliminate hematopoietic progenitor cells by molecularmimicryEmicizumab prophylaxis in infants with hemophilia A (HAVEN 7): primary analysis of a phase 3b open-labeltrialHydroxyurea reduces infections in children with sickle cell anemia in Uganda

Thirteen thousand children and counting....and as you heard on our hiatus announcement, at home, moms are losing their kids, too, to the continued shock of the community. Why are we so shocked? Are we untouchable, above grief and trials from Allah? No, He's promised them to us, and we pray to pass all those tests. Ameen.One of the moms who came on before is our beloved teammate, Saira Sufi, who even recently moved us to tears at our gala when she shared the story of her son, Hadi. She is our role model, who embodies beautiful patience and imaan while facing what we can only imagine is lifelong grief. Despite losses that we would describe as "crushing," she crushed them, and instead has built a legacy for Hadi that will make those of us who never met him, truly regretful. This may be a triggering episode for anyone who has suffered immense loss and grief, so maybe listen in a group so you can support each other through this episode. Remember to pray for our sisters and families abroad who are waking up every day to the wrenching reality of an unalived child or relative. Their grief is so tragic because it was 100% manmade and 100% avoidable. Also, let's never forget to support medical research and to join minority blood registries in case we can ever help another family avoid illness and loss. This episode is for every mom, sibling, and family who's ever experienced the loss of a child, and we pray for their continued healing and reward with Allah SWT. Ameen.Links:Team Watience Website: https://www.teamwatience.com/Team Watience FB: https://www.facebook.com/TeamWatience/Team Watience IG: https://www.instagram.com/sairasufiandteamwatience/Help reach Saira's $60K research goal by donating to the Hadi Abdu Rasheed Research Fund for Aplastic Anemia: https://aamdsif.salsalabs.org/eoyp2pfundraisingcampaign/p/hadiabdurrasheedsresearchfund/index.html Be the Match and register your bone marrow with the minority registry for a child or human in need; it just takes a cheek swab, no blood! https://bethematch.org/support-the-cause/donate-bone-marrow/join-the-marrow-registry/Support the show1. Web: www.mommyingwhilemuslim.com2. Email: salam@mommyingwhilemuslim.com3. FB: Mommying While Muslim page and Mommyingwhilemuslim group4. IG: @mommyingwhilemuslimpodcast5. YouTube: https://www.youtube.com/channel/UCrrdKxpBdBO4ZLwB1kTmz1w

Dr. Roma Rajput explains the origins and treatment of hepatitis-associated Aplastic Anemia in this AAMDSIF Podcast for Patients Episode.

AAMDSIF Director of Patient Services, Leigh Clark, asks Mario about his journey with Aplastic Anemia. The conversation includes treatment and survivorship.

In this week's episode we'll report on the findings from a phase 2 trial of bone marrow transplantation as initial therapy for patients with severe aplastic anemia, discuss the utility of a PET radiomics-based model in predicting outcomes in diffuse large B-cell lymphoma, and learn more about macrophage metabolic rewiring in sickle cell disease.

I welcome my guest, Saira Sufi, to take a deep dive into the discussion of how one of her twin son's diagnoses of a rare bone marrow disorder, Aplastic Anemia led her and her remaining son to become staunch advocates for bone marrow donations. Recruiting bone marrow donors of racial minorities is important, because finding bone marrow matches for minorities and mixed race individuals is especially hard. This is why Saira works hard to raise awareness and to recruit as many people to be bone marrow donors as possible.This episode is a testament to the fortitude of a family in memory of a very special young boy.To find out more about being a bone marrow donor please visit the following website and consider being a donor yourself. It is a chance to truly change someone's life!https://bethematch.orghttps://www.aamds.org/www.teamwatience.orgYou can also watch this episode on my YouTube channel here: https://youtu.be/xgImkpUhWJgSupport the showPlease don't forget to follow me here and on social media! Click the links to keep up with my shenanigans on social media and listen to all my episodes in one place: https://www.imamuslimpodcast.com/ https://www.instagram.com/imamuslimpodcast/ https://www.youtube.com/c/ImAMuslimAndThatsOkayPodcast https://www.facebook.com/iamatopodcast/

The soul learns best by exposing us to a spectrum of experiences. My guest in episode #79, Haylee Kalani McDonald knows that truth all to well. Before age 10, Haylee was diagnosed with a rare autoimmune condition that forced her to fight for her health in a way no kid should be expected to do. But coming out of that journey enhanced and enriched, Haylee set off to become something even more. In today's chat, she shares a little more about her story. We also talk creativity, entrepreneurship, AI, marketing trends, and awakening to higher levels of purpose.

Make A Wish foundation: https://wish.org/Aplastic anemia: https://www.nhlbi.nih.gov/health/anemia/aplastic-anemia#:~:text=Aplastic%20anemia%20is%20a%20rare,way%20to%20prevent%20aplastic%20anemia.Maitreya: https://share-international.org/summary-for-new-readers/#maitreya8217s-emergenceAnthroposophic Medicine: http://www.anthromed.de/en/anthromed/anthroposophic.medicine/#:~:text=Anthroposophic%20Medicine%20is%20an%20integrative,the%20human%20being%20in%20body%2CWaldorf school : https://en.wikipedia.org/wiki/Waldorf_educationHomoeopathy: https://www.homeopathy-ich.org/about-homeopathyShare International magazine: https://share-international.org/resources/magazine/Benjamin Creme: https://share-international.org/for-news-media/who-was-benjamin-creme/Elisa's letter to Share International: https://share-international.org/resources/magazine/november-2022/#readers-letters-a-selection

In this episode, we discuss the management of acquired aplastic anemia with Dr. Amy DeZern. Here are the links to some of the key articles discussed in this show:1. Review article on aplastic anemia: https://www.nejm.org/doi/10.1056/NEJMra1413485 2. RCTs testing whether addition of cyclosporine to ATG improves outcomes in aplastic anemia:https://www.nejm.org/doi/10.1056/NEJM199105093241901https://www.sciencedirect.com/science/article/pii/S0006497120489748 3. RCT testing horse versus rabbit ATG in aplastic anemia:https://www.nejm.org/doi/full/10.1056/nejmoa1103975 4. Single-arm study of eltrombopag in addition to standard immunosuppressive therapy in aplastic anemia: https://www.nejm.org/doi/10.1056/NEJMoa1613878 5. Long-term follow up of patients treated with immunosuppressive therapy and eltrombopag:https://ashpublications.org/blood/article/139/1/34/476916 6. RACE Trial: Standard immunosuppressive therapy +/- eltrombopag in aplastic anemia:https://www.nejm.org/doi/10.1056/NEJMoa2109965 7. Clinical and molecular determinants of clonal evolution in patients with aplastic anemia:https://ascopubs.org/doi/abs/10.1200/JCO.22.00710

Devon S. Stonerock, PharmD (@DevonStoneRx) describes the underlying pathophysiology driving the development and progression of aplastic anemia, outlines treatment options based on patient specific factors and recognizes key toxicities, drug interactions, and administration considerations for patients receiving immunosuppressive therapy. For more pharmacy content, follow Mayo Clinic Pharmacy Residency Programs @MayoPharmRes or the host, Garrett E. Schramm, Pharm.D., @garrett_schramm on Twitter! You can also connect with the Mayo Clinic's School of Continuous Professional Development online at https://ce.mayo.edu/ or on Twitter @MayoMedEd. 

ENERGY PRIME TIME & MindWorks with Dr. Roxanne Daleo “I help stressed, anxious children and their parents to calm down with natural methods so they can improve their focus and just be happier overall.” The work I have to offer introduces a new paradigm for child rearing, one that understands and assumes the power within; the interconnectedness of all living things and the energy of sound frequency—what I like to call “the spiral of life” that takes us to the sacred space of our own heart and upward to a higher state of being.” Renowned clinician, leader, and pioneer in Health Psychology, Dr. Roxie has an unwavering passion for helping children discover their inner resources and realize their own self-worth. As a counselor in Pediatric Stress Management, specializing in anxious children, and parent coaching. Her training from Harvard University and the Jung Institute combine evidence-based mind/body techniques with expressive arts and anchors her work in one of the most powerful methods for awakening natural healing within. Her ground-breaking work as Founder of MindWorks for Children provides parents, caregivers and children with alternative solutions to alleviate stress and anxieties. Her use of art, music, guided imagery, and meditation programs allow children to access their own internal source of strength, love and innate gifts. https://drroxannedaleo.com/roxie/ ENERGY PRIME TIME new e-course by Dr. Roxanne Discover amazingly simple but effective "power points" in your day that will bring fast relief from chaos to calm and Connect With Your Child Like Never Before https://mystore4579.samcart.com/products/energy-prime Dr. Roxie's Guest:  Christine Berl Howland was just 13 years old when she came to Boston Children's Hospital where she first met Dr. Roxie, the Expressive Arts Therapist for the bone marrow transplant patients. Chris knew she faced a serious challenge, “when I was diagnosed with Aplastic Anemia and given 3 to 6 months to live, I immediately told to myself, ‘ I cannot die,' I never saw myself dying. I always believed I would survive. Chris is here to share her journey; she is a walking medical miracle and illustrates the potential within each of us to awaken our inner energies using mind/body techniques, such a guided imagery and to intentionally access our inner-self, the greatest source of healing. Today, Chris is a mother of three, Helen 18, Lilia 17, and Hugh 15. Over the years, Dr. Roxie offered guidance to Chris and her children. Currently, Chris works as an Educational Consultant in Upstate New York. She is a graduate of Boston College. Call In and Chat with Deborah during Live Show: 833-220-1200 or 319-527-2638 Learn more about Deborah here:  www.lovebyintuition.com

In this week's episode discuss the efficacy of rivaroxaban as antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer, learn more about the association between genomic variants and survival outcomes after hematopoietic cell transplantation in severe aplastic anemia, and discuss the long-term safety and efficacy of fixed-duration venetoclax plus rituximab in relapsed/refractory CLL.

CME credits: 1.75 Valid until: 12-08-2023 Claim your CME credit at https://reachmd.com/programs/cme/case-meet-penny-nancy-harvey-41-year-old-with-fatigue-and-aplastic-anemia/14310/ tbd

Today's episode is focusing on the highest yield facts about Aplastic Anemia. This will include the mechanism of AA, diagnostic work-up, treatment of AA, and the evolution of clones including PNH.

In honor of Rare Disease Day on February 28, Oncology Data Advisor spoke with Amy DeZern, MD, MHS, Director of the Bone Marrow Failure and Myelodysplastic Syndromes (MDS) Program at Johns Hopkins Medicine and member of the Aplastic Anemia and MDS International Foundation (AAMDSIF) medical advisory board. In this interview, Dr. DeZern explains the challenges of treating such a rare disease and shares some of recent promising updates in novel treatments for patients with MDS.

Seth is a 10 year old boy from Tasmania who is now living his best life and this is all thanks to Australian blood and bone marrow donors. Seth has a condition called Severe Idiopathic Acquired Aplastic Anemia which can be life threatening. He has endured so much testing, treatment, isolation as he was immunocompromised and way too many nights inside hospitals.  A big part of the challenge for Seth and his family is that treatment wasn't available for Seth at their small local hospital on the North-West coast of Tasmania so they were first airlifted to Hobart and then on to the "mainland" in Melbourne. To find more information about joining the Australian Bone Marrow Registry please go to: https://www.lifeblood.com.au/organ-and-tissue/bone-marrow  To learn more about Aplastic Anemia or to support Maddie Riewoldt Vision please go to: Maddie Riewoldt's Vision - Home (mrv.org.au)    

In this week's podcast, we'll talk about the long-term outcomes in patients with severe aplastic anemia treated with immunosuppression and eltrombopag, learn more about anti-inflammatory and cytoprotective effects of factor VIIa, and discuss the role of IL-1 in microbiome-induced ageing of hematopoietic stem cells in mice.

In this episode, we review the high-yield topic of Aplastic Anemia from the Heme section. Follow Medbullets on social media: Facebook: www.facebook.com/medbullets Instagram: www.instagram.com/medbulletsofficial Twitter: www.twitter.com/medbullets

In this episode, we review the high-yield topic of Aplastic Anemia from the Hematology section. Follow Medbullets on social media: Facebook: www.facebook.com/medbullets Instagram: www.instagram.com/medbulletsofficial Twitter: www.twitter.com/medbullets --- Send in a voice message: https://anchor.fm/medbulletsstep1/message

In episode 5 of "EHA Unplugged", Prof. Shaun McCann discusses HSCT in Severe Aplastic Anemia. You will hear him detail the diagnostic criteria of severe aplastic anemia (SAA) and the current therapeutic approaches for this disease. He will also characterize the results of HCT, the best conditioning options and different source of hemopoietic cells for SAA patients. What did you think of this podcast? Share your opinions with us in this short feedback survey. https://forms.monday.com/forms/d02e52896815eef59ecae09fb74dd78f?r=use1 (Provide Feedback) Would you like to receive EBAH CME credit points for listening to this podcast? Please visit the EHA Campus and finalize the quiz questions. https://ehacampus.ehaweb.org/ehailp/pages/description.jsf?menuId=1422#/users/@self/catalogues/355089/courses/392645/description (https://ehaedu.org/Campus) Subscribe, share, and review this podcast to be able to address topics you enjoy and like to listen to. Follow EHA on Instagram: https://www.instagram.com/EHA_Hematology/ (https://www.instagram.com/EHA_Hematology/) Facebook: https://e-h-a.link/facebook (https://e-h-a.link/facebook) LinkedIn: https://www.linkedin.com/company/eha/ (https://www.linkedin.com/company/eha/) Email us:  education@ehaweb.org Subscribe to receive the EHA Educational Updates via https://eha.news/subscribe?utm_medium=podcast&utm_source=bcast&utm_campaign=eha-unplugged (https://eha.news/subscribe) 

Having spent most of her youth in and out of hospital, taking on, and beating, Aplastic Anemia (a life-threatening autoimmune disease), Haylee Kalani had the chance to experience life in a new light. An auto-immune disorder where one's good cells would attack one another, from ages 8-13 Haylee became familiar with feelings of being lost, confused, insecure, and overweight during her most impressionable years. Haylee leaned into her love of creativity and that snowballed into discovering that she had the opportunity to be an Audio Engineer at a recording studio in Seattle WA (Robert Lang Studios). This is where she first found her ability and calling to help other people transform into the most creative, productive, connected version of themselves. Haylee strives to help people successfully impact others with their gifts. She now runs a successful coaching practice and focuses on life meditation, fitness, and play to keep one grounded and true to themselves. 

Haylee Kalani is a high-performance creative coach who helps mission-driven entrepreneurs create more impact, time, and abundance. Growing up, Haylee was diagnosed with Aplastic Anemia. But she wasn't defeated. Instead, Haylee chose to see life in a new light. She decided never to settle for less and to help others live a life of passion and abundance. Since then, Haylee continues to help people think outside the box, share their gifts, and expand their reach. Here's where you can find her: Her website Visit ZayZoh.com for more episodes, articles, and essays. Here's why I podcast.  

Haylee Kalani is our guest for this episode of The Small Business Show.Find our why it is important to train your creative muscle, and how to get our content marketing plan organized and batch our content creation.Haylee is a big fan of experimenting - she urges listeners to get out of our comfort zone and try something sort of “weird” and take risks in marketing.  She also recommends testing different content types to see what works best. For business owners and marketers, Haylee explains that it is important to create content about a brand's values and find a niche that represents your business. Keep it focus and specified. Don't miss this great conversation, listen or watch the videos thanks!GUEST INFO:When Haylee found out that becoming an astronaut (her childhood dream) involved a LOT of math... that's when she decided to move her love of curiosity & creativity in a different direction and  found some missing links along the way.She found that too many mission-driven professionals struggle to generate income through their content online & really connect with their core community.Creating content has been her specialty since she was a kid, snagging her parents' bulky video camera and making some rad music videos.While growing up, taking on, and beating, Aplastic Anemia (a life-threatening autoimmune disease), Haylee had the chance to experience life in a new light.The whole experience itself taught her to never settle for less & to live life as if there's no tomorrow…So she sought out to follow her passion and use her unique gifts to disrupt the current state of "typical marketing" and help brands create more impact and innovation in the world.She turns business owners, soloprenuers, and freelancers, into out-of-the-box thinkers, innovative creators, and adaptive players in this game we call marketing.So they can generate vast attention & earn more revenue for their brand to do what they do best.Help. More. People.Contact for Haylee Kalani

My guest today is Stephanie. She’s famously known for being a cast member on the hit television show 90 Day Fiance: Before the 90 Days, but she’s so much more than that. Stephanie is a YouTuber, author, dog mom and Aplastic Anemia rare disease advocate. In this episode, Stephanie talks about her time on Before the 90 Days, her battle with Aplastic Anemia and the relationship that motivated her to become independent and build her YouTube brand. To find out more about Stephanie, please follow her on social by searching @stepankamatto or visit her YouTube https://www.youtube.com/user/itsmestepanka#90DayFiancé #Beforethe90DaysPlease consider supporting us on Patreon:https://www.patreon.com/obliteratepodcastAnd follow us on social media:IG: https://www.instagram.com/obliteratepodcast/FB: https://www.facebook.com/obliteratepodcastTwitter: https://twitter.com/obliteratepodTikTok: https://www.tiktok.com/@obliteratepodcastAnd if you have any questions about the episode or want to be a guest feel free to reach out by emailing obliteratepodcast@gmail.com.

Once Haylee found out becoming an astronaut involves a LOT of math... that's when she decided to move her love of curiosity & creativity in a different direction and found some missing links along the way... She found that too many mission-driven entrepreneurs feel frantic, unfocused, stuck, and find it hard to push through new hurdles in their life/business. They often aren't performing at their highest potential and struggle to reach & connect with their ideal community. That's where her unique set of gifts come in. Thinking big, solving problems, and getting creatively efficient has been Haylee's specialty since she was a kid, finding new ways to sneak candy at night, being the go-to, "help me", friend, while constantly in the pursuit of happiness... While growing up, taking on, and beating, Aplastic Anemia (a life-threatening autoimmune disease), she had the chance to experience life in a new light. The whole experience itself taught her to never settle for less & to live life as if there’s no tomorrow… So she sought out to follow her passion & use her unique gifts to help other mission-driven, talented bad*sses become the highest version of themselves so they can create more impact & innovation in the world. She turns entrepreneurs into out-of-the-box thinkers, high-performers, and adaptive players in this game we call life… So they can reach more of the right people & increase their income in the process. Learn more at: https://www.hkalaniconsulting.com/

Seattle's Mack Bell is a 30 year-old African-American man living with Cerebral Palsy. Four years ago, it didn't look like Bell was going to make it. But today, thanks to the Seattle Cancer Care Alliance, the support and comfort from his former high school principal as well as dozens of Bloodworks Northwest blood donors he'll never know, Mack is able to tell his story of survival. And as we discover on this edition of "Bloodworks 101," Mack Bell had to come face-to-face with something we're all adjusting to - more than a year of social distancing. Part of Mack's story is the fact that as an African-American, the deck literally is stacked against him in his effort to find a suitable match as he fought Aplastic Anemia. If you'd like more information about this go to: bethematch.org/

This episode covers aplastic anemia!

Loved getting to sit down with a friend I’ve known as long as I can remember, Rebecca Syens (formerly Surita). Becca let me pick her brain about her experience of being diagnosed with Aplastic Anemia our junior year of high school. Becca explains why we didn’t talk much about it at the time she was going through it + ultimately how it completely shaped her career choice today. Her entire story is full of grit. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app Support this podcast: https://anchor.fm/carrie-schuessler/support

This episode covers aplastic anemia!

Saira Sufi joins us today to share the story of her son, Hadi, and how he remains her guide today. She has weathered innumerable losses in the last couple of years, and still holds her chin up as she advocates for her son’s disease and mom resilience. This may be a triggering episode for anyone who has suffered immense loss and grief, so maybe listen in a group so you can support each other through this episode.Also, let’s never forget to support medical research and to join minority blood registries in case we can ever help another family avoid illness and loss. This episode is for every mom, sibling, and family who’s ever experienced the loss of a child, and we pray for their continued healing and reward with Allah SWT. Ameen.Links:https://youtu.be/NrB8Iamo0OATeam Watience Website: https://www.teamwatience.com/Team Watience FB: https://www.facebook.com/TeamWatience/Team Watience IG: https://www.instagram.com/sairasufiandteamwatience/Help reach Saira’s $60K research goal by donating to the Hadi Abdu Rasheed Research Fund for Aplastic Anemia: https://aamdsif.salsalabs.org/eoyp2pfundraisingcampaign/p/hadiabdurrasheedsresearchfund/index.html Be the Match and register your bone marrow with the minority registry for a child or human in need; it just takes a cheek swab, no blood! https://bethematch.org/support-the-cause/donate-bone-marrow/join-the-marrow-registry/Web: www.mommyingwhilemuslim.comEmail: mommyingwhilemuslim@gmail.comFB: Mommying While Muslim page and Mommyingwhilemuslim groupIG: @mommyingwhilemuslimpodcast

Julie Lowe, AAMDSIF Director for Strategic Initiatives, anticipates your questions about getting involved with the Aplastic Anemia and MDS International Foundation in this recent interview.

Dr. Daria Julkowska joins the show for Rare Disease Month as the Coordinator of the European Joint Program on Rare Diseases. This organization was newly established in January 2019. Daria is of Polish origin but she has lived and worked in France for the last 18 years. She has a PhD in molecular biology and is involved in rare diseases research and management for the last ten years.The European Joint Program on Rare Diseases represents 89 partners across the EU and beyond. Internally, the partners include research funders, research institutions and infrastructures, hospitals and of course patient organizations. The program is financed by the EU and the states participating in the project.On This Episode We Discuss:Motivation to Start the OrganizationGoals for the Rare Disease CommunityCountries RepresentedRare Disease Visual PlatformAdvancing Rare Disease ResearchOngoing Research ProjectsFunding for ResearchCombating Exorbitant Costs of Treatments (Ex: Spinraza)Rare Disease Day/Month InvolvementHappy Rare Disease Month! If you are in the US you can get involved by going to the National Organization for Rare Disorders’ website, rarediseases.org. You can find ways to get active on social media and in person events. Learn more about The European Joint Program on Rare Diseases by visiting their website.Want to hear more from the rare disease community? Check out all the 20 rare disease episodes of DNA Today here! Recent episodes include #102 Seth Rotberg on Huntington Disease, #98 Lydia Seiders on Aplastic Anemia, and #95 Kieger Family on Familial Adenomatous Polyposis.Stay tuned for the next new episode of DNA Today. New episodes are released on the first Friday of the month with some bonus episode thrown in there. See what else I am up to on Twitter, Instagram, Facebook and iTunes. Questions/inquiries can be sent to info@DNApodcast.com.

This episode will set the record straight regarding cGVHD. Most cases will subside in 3-5 years. You won't want to miss this one from one of the world's leading experts on cGVHD.Dr. Steve Pavletic is an incredible resource for folks with cGVHD. Dr. Pavletic leads a chronic GVHD clinic and natural history study at the National Institutes of Health. Learn more about cGVHD, treatment updates, and his incredible opportunity for those who qualify.Dr. Pavletic will also speak about steroids, the love/hate relationship many experience with them, and much more.Did you know that some cGVHD is actually good? You will want to hear more about this too.For additional resources from the National Bone Marrow Transplant Link, visit us online at nbmtlink.org or call us at 800-546-5268.This season of Marrow Masters is sponsored by the nbmtLINK, Seattle Genetics, and our esteemed link partners.

Listen as first generation Pakistani American, Saira Sufi, shares her story about growing up as a Muslim American in in Topeka, Kansas, her Son Hadi's battle with Aplastic Anemia and how she is helping spread awareness and raise money for Aplastic Anemia research. Please be advised this episode discusses the death of a child.

35th Anniversary Podcast Series: Mary and Courtney White, family of Aplastic Anemia.

35th Anniversary Podcast Series: Ruth and Neil Cuadra, Aplastic Anemia, MDS, BMT.

35th Anniversary Podcast Series: Marissa Amuso, Aplastic Anemia, BMT.

35th Anniversary Podcast Series: Stephen King, Aplastic Anemia and PNH.

To celebrate and honor Rare Disease Awareness month (February) Lydia Seiders joins me on the show. She is a volunteer Maryland State Ambassador for NORD, the National Organization for Rare Disorders, through NORD’s advocacy arm the Rare Action Network. Her daughter was diagnosed with aplastic anemia, a form of bone marrow failure. This motivated Lydia to become an Ambassador for NORD. In this role, she leads about 200 network members across the state to raise awareness for approximately 600,000 patients affected by a rare disorder. Lydia leads educational initiatives and develops state-based campaigns to increase patient awareness. She partners with advocates nationwide to act on policy impacting the rare disease community.Lydia also works closely with the Aplastic Anemia and MDS International Foundation and the national bone marrow registry - Be the Match. She assists patients and families globally obtain reputable resources for bone marrow failure. Most recently she began collaborating with RARE Revolution Magazine, a dedicated free rare disease publication. She will help to share in the direction of the Rare Revolution movement.On This Episode We Discuss:Her daughter, known as #EmmaStrong, diagnosis of aplastic anemiaDiagnostic journeyAplastic anemia symptoms and causeNIH’s role in Emma’s treatmentCurrent research for aplastic anemiaLydia’s role as a state ambassador for NORDEducational initiatives and campaigns for the rare disease communityNORD’s resources for parents and caregiversAdvice for parents and caregivers of a loved one with a rare diseaseResources Mentioned During The Show:National Organization for Rare Disorders (RareDiseases.org)RareAction.orgWhen signing up, their system will link you to your state’s RAN by your zip codeThe Aplastic Anemia and MDS International FoundationMaryland’s Rare Action Network Facebook PageRAN is active in all 50 states, listeners can find their state to get involvedBe The Match (Emma’s Page)Learn how to join the bone marrow registryLearn more about Emma in this blog post part 1, part 2 and part 3. Stay updated with Lydia by following her on Twitter and connecting with her on LinkedIn.Don’t forget to raise awareness this month (and every month) for rare diseases, especially on Rare Disease Day which is on Thursday, February 28th 2019.Stay tuned for the next new episode of DNA Today on March 1st. New episodes are released on the first Friday of the month. See what else I am up to on Twitter, Instagram, Facebook and iTunes. Questions/inquiries for my guest, Lydia Seiders, or myself can be sent to info@DNApodcast.com.Don’t hesitate, we love hearing from listeners.

This week, we want to highlight Stacie who was nominated by her best friend, Romona. She faces certain health problems in the form of Aplastic Anemia and over the past two years, it has certainly done a number on her. Unfortunately, while dealing with this, she ended up losing her job but then got involved with Restored Hope Ministries where she got the opportunity to stay in one of their available apartments. However, there are still certain bills in the picture that she is responsible for like her car payment, insurance, and out-of-pocket medication and treatment costs. Sadly, in the midst of all of this, she ended up looking two close family members within a very short time and not to mention that her brother also is fighting cancer. Looking at her, you would never know what all is happening in her life because her positive attitude and willingness to help others is always strong. Seeing this story, we knew that we had to Make her Christmas! 

In today's episode, I take you to Pflugerville, Texas, where we attended the BBQ Benefit for Cambryn's Relentless Battle. Camryn's is a nine-year-old little girl with a rare disease. Unfortunately, she was diagnosed with Aplastic Anemia. This disease has taken her strength from her. Her body is unable to produce more blood cells to fight everyday bacterial attacks. The only way for her to survive and thrive would be a bone marrow transfusion. Camryn's father, Sgt. Kurk Anderson, with the Pflugerville Police Department, asked for assistance. As one big BLUE FAMILY, we couldn't just let this little girl go without notice. We stepped up together to perform a BBQ Benefit for her. This past Saturday, I attended the BBQ Benefit. It was enjoyable to see how law enforcement and the community comes together to help one of our own. The most important message from this podcast is to DONATE. Camryn needs to find a bone marrow donor as soon as possible. Please go to -www.bethematch.org Order your Free kit and test. https://www.youtube.com/watch?v=-tfThmXSzos

In today's episode, I take you to Pflugerville, Texas where we see the BBQ Benefit for Cambryn's Relentless Battle. Camryn's is a nine-year-old little girl with a rare disease. Unfortunately, she was diagnosed with Aplastic Anemia. This disease has taken her strength from her. Her body is unable to produce more blood cells to fight everyday attacks. The only way for her to survive and thrive would be a bone marrow transfusion. Her father, Sgt. Kurk Anderson, with the Pflugerville Police Department, asked for assistance. As one big BLUE FAMILY, we couldn't just let this little girl go without notice. We stepped up together to perform a BBQ Benefit for her. This past Saturday, I attended the BBQ Benefit, it was enjoyable to see how law enforcement and the community comes together to help one of our own. The most important message from this video: DONATE Camryn needs to find a bone marrow donor as soon as possible. Please go to -www.bethematch.org Order your Free kit and test

Daniella, co-host of the WYAF Show, shares her health journey post her nursing career as well as the difficulties balancing multiple and complex health issues.

Brendon recounts how he got into the strength and conditioning world, as well as the many unexpected that have occurred in the past few years. He is super open about becoming a parent, moving out to California, and fighting Aplastic Anemia. He talks about how these life events have changed his perspective on coaching, self care, and really life in general!

Highlights of Episode 183   "Hit the Gym with a Strength Coach" -Rhonda Catt, owner of Catt Conditioning, is on to talk about some of the lessons she learned in the Art of Coaching from the grief she experienced with the loss of her husband.  Rhonda talks about her article "Grief and the Strength Coach" and how that grief taught her to approach her clients and athletes differently.  She also goes over some of the warning signs of heart disease, especially important in someone who does not have any markers and is in good health otherwise. .    HELP BRENDON!! Time is running out to help Brendon Rearick in his battle with Aplastic Anemia, which is Bone Marrow Failure.  We set up a fundraiser for Brendon with a "Collect Moments, Not Things" T-Shirt campaign.  Please consider buying a T-shirt to help Brendon.       "Coaches Corner with Coach Boyle"- Coach Boyle talks about "Don't Look in My Window (until you talk to me first)", his videos "Downhill Lunge" and MB Overhead Rotary Throw and the article "The Truth about Achieving Excellence" and more.     Check out Coach Boyle's Functional Strength Coach 5   "Ask the Equipment Experts with Perform Better" - Erin McGirr joins us to talk about the Current Sale and the first Summit in Orlando. "The Business of Fitness with Results Fitness University"- Rachel Cosgrove is on to talk about "Dreaming Bigger". "The Functional Movement Systems Segment" Brett Jones is on to talk about "Creating Positive Responses" . "The Art of Coaching with EXOS"- Brent Callaway is on to talk about part 2 of "Forming a System in the Team Environment" . Audible.com is one of our new sponsors.  Get a FREE audiobook here.     "Subscribe at iTunes" and Get Automatic Updates If you want to save this podcast to your computer so you can import it into your Ipod or MP3 player, Right Mouse Click to Download Now (for Mac users, press Control and click)   

Highlights of Episode 182     "Hit the Gym with a Strength Coach" - Brendon Rearick, co-founder of Movement as Medicine and CFSC, is on to talk about Paying off his Student Loan at 25, having a diversified portfolio and how is program design has changed since leaving MBSC, as well as the effect of PRI, FRC, Yoga, Gymnastics and Crossfit on programming.    We also spoke to Brendon about his battle with Aplastic Anemia, which is Bone Marrow Failure, and the struggles he has had trying to get through it.  We set up a fundraiser for Brendon with a "Collect Moments, Not Things" T-Shirt campaign.  Please consider buying a T-shirt to help Brendon.       "Coaches Corner with Coach Boyle"- Coach Boyle talks about Insurance, and forum threads talking about "Why Women Want to Train", "Bench Press Technique" and "Who's a Sport Scientist?" and more.     Check out Coach Boyle's Functional Strength Coach 5   "Ask the Equipment Experts with Perform Better" - Erin McGirr joins us to talk about the Current Sale and the Triton Push Sled. "The Business of Fitness with Results Fitness University"- Alwyn Cosgrove is on to talk about "Having an Ambassador Program". "The Functional Movement Systems Segment" Brett Jones is on to talk about "The 2nd Principle- Protect, Correct and Develop" . "The Art of Coaching with EXOS"- Brent Callaway is on to talk about "Forming a System in the Team Environment" . Audible.com is one of our new sponsors.  Get a FREE audiobook here.     "Subscribe at iTunes" and Get Automatic Updates If you want to save this podcast to your computer so you can import it into your Ipod or MP3 player, Right Mouse Click to Download Now (for Mac users, press Control and click)   

Interview with Gerard Socie, from the Hopital Saint-Louis, Paris, France. Prof. Socie discusses the topic 'Severe aplastic anemia Fanconi Anemia'.The interview is led by Shaun McCann, Chair of EHATol Unit, Member of EHA Education Committee.

Interview with Gerard Socie, from the Hopital Saint-Louis, Paris, France. Prof. Socie discusses the topic 'Severe aplastic anemia Fanconi Anemia'.The interview is led by Shaun McCann, Chair of EHATol Unit, Member of EHA Education Committee.

Interview with Jakob Passweg, Prof. Hematology at Basil University, Switzerland. Prof. Passweg discusses the topic 'Severe Aplastic Anemia'.The interview is led by Shaun McCann, Chair of EHATol Unit, Member of EHA Education Committee.

Interview with Jakob Passweg, Prof. Hematology at Basil University, Switzerland. Prof. Passweg discusses the topic 'Severe Aplastic Anemia'.The interview is led by Shaun McCann, Chair of EHATol Unit, Member of EHA Education Committee.

Retrospective histologic analyses of bone biopsies and of post mortem samples from normal persons of different age groups, and of bone biopsies of age- and sex-matched groups of patients with primary osteoporosis and aplastic anemia show characteristic age dependent as well as pathologic changes including atrophy of osseous trabeculae and of hematopoiesis, and changes in the sinusoidal and arterial capillary compartments. These results indicate the possible role of a microvascular defect in the pathogenesis of osteoporosis and aplastic anemia.