Swapna Kakani Emory Swapna Kakani was born and raised in Huntsville, AL. 1,835 Followers, 2,455 Following, 334 Posts - Swapna Kakani (@swapnaspeaks) on Instagram: "šŸŽ¤Professional Speaker/Advocate for Rare & Chronic Diseases šŸ—£Healthcare Collaborator šŸ‘©šŸ½ā€šŸ’¼Founder Thanks to members of the outpatient team I am able to fill my transplant immunosuppression specialty med. 210 Followers, 888 Following, 361 Posts - Swapna Kakani (@skakan2) on Instagram: "" The joke still inspires Swapna today and of course makes her laugh, but it taught her the importance of an extended support system. Includes free contact info & photos & court records. For 27 years, Swapna has lived with supplemental Swapna Kakani, 25, of University Heights, received a new intestine in June at the Cleveland Clinic. com · Education: Emory University · Location: Baltimore · 150 connections on LinkedIn. It is a field guide to the patient-led revolution in medical care, through a breakdown of 4 Swapna Kakani is a professional keynote speaker and advocate in the area of healthcare delivery and the patient experience. She is Swapna Speaks. In her talk, Swapna shares her After her sari ceremony and debutante ball, Swapna Kakani realizes what coming of age really means. As a second-generation Indian American, motivational speaker Swapna Kakani knows firsthand ā€œhow important it is to empower, but also increase, the patient vo 83 likes, 3 comments - swapnaspeaks on June 2, 2020: "Every aspect of my life is one of privilege as a second generation Indian American, and that includes the color of my skin, and where I live in Swapna Kakani, MPH is an award-winning, advocate, speaker, consultant, and researcher in rare and chronic disease health care delivery and Swapna Kakani Daughter of South Indian immigrants, SWAPNA KAKANI was born and raised in Huntsville. Excited to be giving a keynote at the Association for Vascular Access annual scientific meeting this Friday on the patient perspective of preserving and Swapna reconnected with old colleagues and friends from her advocacy work and enjoyed meeting and learning from several new partners in the US and the UK in chronic and rare Swapna Kakani was diagnosed at birth with a rare chronic disease, Short Bowel Syndrome. core research team member Swapna was diagnosed with SBS at birth and has lived on parenteral and enteral nutrition for most of her life. Swapna Twenty-Three years ago Swapna Kakani and her parents did not know her fate as a newly diagnosed newborn with Short Bowel Syndrome. Swapna Kakani is a nationally known speaker, and an award-winning advocate in rare and chronic disease healthcare delivery and the patient experience. Her life Swapna Kakani, MPH rare disease advocate. The operation, the latest of 54 in the life of the woman born with short bowel An influential leader in rare and chronic disease patient advocacy and a professional · Experience: The Gutsy Perspective · Education: UAB School of See Free Details & Reputation Profile for Swapna Kakani (35) in Huntsville, AL. For 27 years, Swapna has lived with supplemental intravenous So so excited to receive my order of ā€œRebel Healthā€ by Susannah Fox. Only place in town I can get it! It is such a fast and seamless Swapna was diagnosed with Short Bowel Syndrome, a chronic rare disease, at birth and for 27 years has lived with supplemental intravenous nutrition and a feeding View the profiles of professionals named "Swapna Kakani" on LinkedIn. It was my pleasure, Swapna Kakani! It was wonderful to learn more about you, your team, and your rare disease advocacy work. Learn how 3Mā„¢ Curosā„¢ Disinfecting Port Protectors and 3Mā„¢ Tegadermā„¢ CHG Dressings have helped reduce the risk of infection and improve the quality of life fo Swapna Kakani is an award-winning advocate, consultant, and researcher in rare and chronic disease healthcare delivery and the patient experience. Devi Y Hemalatha, Babu R Kakani, and four other persons are connected to 3M: Infection Prevention Patient Story: Swapna Kakani Learn how 3Mā„¢ Curosā„¢ Disinfecting Port Protectors and 3Mā„¢ Tegadermā„¢ CHG Dressings have helped reduce the risk of One of NORD's 2017 interns and #RareDiseaseDay volunteer, Swapna Kakani did a TEDx talk this year about how she found her purpose in her disease. Swapna Kakani shares her speaking engagements, healthcare advocacy initiatives, and personal insights Meet Swapna Kakani, a Short Bowel Syndrome warrior, advocate, and speaker, sharing her journey of resilience, securement, and empowerment. Interested in having me speak for your Marketing Zovi · Experience: Zovi. Swapna is currently living at 1603 Chandler Rd SE, Huntsville, AL. Marie L. com. Swapna Kakani was diagnosed at birth with a rare chronic disease, Short Bowel Syndrome. Swapna Kakani, MPH In this weekā€™s #MothRadioHour, after her sari ceremony and debutante ball, Swapna Kakani realizes what coming of age really means. There are 7 professionals named "Swapna Kakani", who use LinkedIn to exchange information, ideas, and opportunities. SBS patient. In We are thrilled for the Pediatric Intestinal Failure Research Meeting to value the community's voice as an important part of how care is delivered. She inspires people to defy all odds and to rise above their despair. By telling my story I want to educate you, I want to advocate for change, and I want Swapna Kakani, MPH I constantly wish you good health, patience, courage, determination, and all the things you need to continue the search and research to help you live more comfortably. Swapna Kakani shares her speaking engagements, healthcare advocacy initiatives, and personal insights. Registered companies at this address include K & S. 1,513 likes. If not for you Swapna Kakani, MPH,I'd still be anxious about discussing EoE, reluctant to acknowledge my disability and never would've found my specialist & the team Swapna Speaks Swapna Kakani is a sought-after professional speaker in the area of overcoming personal adversity, advocate in the area of healthcare delivery and the patient experience. Her life story shows audiences Meet Swapna Kakani, MedX ePatient 2019 and a new member of our #11Health Patient Coach Program So proud of you Swapna, thanks for all your hard work Hear about Swapna Kakani's keynote presentation titled Valuing the Patient Perspective in Preservation and Protection of Vascular Access. She was born with Short Bowel Syndrome, has required IV nutrition through In her presentation, Swapna shares parts of her 30 plus year, patient perspective on living with Short Bowel Syndrome and the key aspects she has learned to help her I learned that her name was Swapna Kakani, and not only had she undergone a high-risk transplant surgery, but she had also co-founded a powerful Swapna is an award-winning advocate in the area of rare and chronic disease healthcare delivery and the patient experience. Swapna was diagnosed with the rare disease Short Honored to serve on this project alongside incredible colleagues led by the Center for Innovation & Value Research! I thoroughly enjoyed my time on Phase I; I It was incredible to be part of this in-person meeting and this multidisciplinary team working towards forming an expert consensus around the insertion, care, maintenance, and removal of PIVCs Swapna Kakani was diagnosed at birth with a rare chronic disease, Short Bowel Syndrome. Swapnaā€™s Read the report: https://ow. Out now on The Moth Podcast! Listen to the latest episode, "A Place at the Family Table" to hear stories of finding This site is about living life to the fullest despite your circumstances and just simply, moving forward. Her Swapna Kakani's 3 research works with 5 citations and 48 reads, including: Exploring the impact of pediatric short bowel syndrome on parent wellā€being using a diseaseā€specific pilot survey Swapna Kakani shares in her talk her journey of hope, disappointment, courage and finding purpose in living with a rare disease since birth. 96 likes, 8 comments - swapnaspeaks on October 9, 2023: "Thank you Huntsville Hospital for having me present at the Advanced Practitioner Award Ceremony! I shared my story, the innovation we are 34 Swapna Kakani, MPH CEO, Healthcare Collaborator & Patient Engagement Leader/Advocacy Consultant | Rare Diseases & Public Health Researcher 2mo Edited Huntsville, Alabama Co-Founder & Researcher, The Gutsy Perspective, LLC Representing: Patients, Caregivers, and Patient AdvocatesTerm Ends: September 2027 Swapna Kakani, MPH, is an award Swapna Kakani gives the keynote speech at Asha Kiran's Ray of Hope Event. By telling my story I want to educate you, I want to advocate for change, and I want to inspire you to achieve your dreams. Today, after 40 šŸ¤ 0 šŸ“Š 102 šŸ“Ž Swapna Kakani, MPH SwapnaSpeaks Oct 14 Katie Boston-Leary giving the opening #AVASM23 keynote on the challenges of nursing today and how we individually can own 1,696 Followers, 2,249 Following, 323 Posts - Swapna Kakani (@swapnaspeaks) on Instagram: "šŸŽ¤Professional Speaker šŸ—£Healthcare Advocate šŸŽ’Living w/ Short Bowel Syndrome šŸ’šSmall Intestine Today, I am so excited to share this final report on the topic of Identifying shared patient-centered outcomes across rare diseases that are valued by the community to help streamline research When I interned at Huntsville Hospital Women & Childrenā€™s administration office before grad school, we would get report on ER admissions that required Swapna Kakani shares in her talk her journey of hope, disappointment, courage and finding purpose in living with a rare disease since birth. We are excited to Swapna Speaks. For 27 years, Swapna has lived with supplemental intravenous nutrition and a feeding Discover Company Info on SWAPNA KAKANI CONSULTING LLC in Huntsville, AL, such as Contacts, Addresses, Reviews, and Registered Agent. Listen Swapna Kakani, MPH is an award-winning advocate, speaker, consultant, and researcher in rare and chronic disease health care delivery and patient Get the details of Swapna Nimishakavi's business profile including email address, phone number, work history and more. After her sari ceremony and debutante ball, Swapna Kakani realizes what coming of age really means. ly/MHGC50QyAGb #PatientEngagement #RareDiseaseResearch #RareDiseaseData #PatientStories #RareDiseaseEconomics #HealthPolicy 1,696 Followers, 2,249 Following, 323 Posts - Swapna Kakani (@swapnaspeaks) on Instagram: "šŸŽ¤Professional Speaker šŸ—£Healthcare Advocate šŸŽ’Living w/ Short Bowel Syndrome šŸ’šSmall Intestine Alabama Rare Leadership Swapna Kakani Founder & Chief Executive Officer Swapna currently resides in Huntsville, AL where she was born and raised. Her own life story of being 2024 Research article: "Quality of life from childhood to adulthood: Perspectives from adult patients with Pediatric Intestinal Failure" in the Journal of Pediatric Gastroenterology and Nutrition. 1,511 likes. The daughter of Indian immigrants growing up in Alabama, after her sari ceremony and debutante ball, Swapna Kakani realizes what coming of age really means. View Swapna Kakani's business profile as Marketing at Zovi. She is a graduate of Randolph School, and received her Bachelors in Psychology at Swapna Kakani is a nationally known speaker, and an award-winning advocate in rare and chronic disease healthcare delivery and the patient experience. Find contact's direct phone number, email address, work history, and more.