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Utter Randomness with Lulu

Utter Randomness with Lulu

By Lulu

Join me for podcasting fun! Want to know what I'm watching, listen to my Midnight Binges segment where I watch the newest shows. Looking for something new, look no further than our Under the Radar segment. Spotlight Artist places a light on artists regardless of the art they're into. Flashback Friday is just that, some nostalgia goodness. Is reading more your speed, we have a segment for that too. Our Currently Reading podcast might be your thing. Utter Randomness is just that, a segment about anything and sometimes a bit of everything! Please also consider supporting this podcast!
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Rare Disease Day and Myths and Misconceptions about Sickle Cell Anemia

Utter Randomness with LuluFeb 29, 2024

00:00
12:30
Rare Disease Day and Myths and Misconceptions about Sickle Cell Anemia

Rare Disease Day and Myths and Misconceptions about Sickle Cell Anemia

Welcome back to another episode! Join Lucy as we talk discuss myths and misconceptions surrounding Sickle Cell Anemia, Rare Disease Day, and how you can support Sickle Cell Programs within your region, or even the American Sickle Cell Anemia Association. Creative and have sickle cell anemia? Send in your artwork, photographs, stories, and more to sickletalk@ascaa.org. Your art could be featured in an episode! Sickle Talk is owned and operated by the American Sickle Cell Anemia Association and funded by viewers and listeners like you. Thank you! Support the ASCAA organization by donating today! For More Information: Website Follow Us! Facebook Instagram Twitter (X) Threads Spotify iHeartRadio Amazon Music Podcasts

The American Sickle Cell Anemia Association is a 501(c)(3) nonprofit in Cleveland, Ohio. Since 1971, ASCAA has tested, counseled, and assisted individuals, families, and the population at risk of Sickle Cell Anemia. ASCAA is affiliated with multiple major hospitals in our local area, including, but not limited to: Cleveland Clinic Foundation, Cleveland Clinic Children's Hospital, University Hospital, MetroHealth Hospital, Rainbow Babies and Children, and local clinics and community centers. Mission Statement: ASCAA is a comprehensive health organization whose mission is to connect with families, inspire hope, and improve their quality of life. We are ultimately working to create a world without sickle cell disease. Disclaimer: All information is merely for educational and informational purposes for sickle cell anemia. It is not intended as a substitute for professional advice. Please seek an appropriately qualified and licensed physician for medical advice. Should you decide to act upon any information given, you do so at your own risk. While the information has been verified to the best of our abilities, we cannot guarantee that there are no mistakes or errors. We reserve the right to change this policy, which will be promptly updated. If you want to ensure you are up to date with the latest changes, we advise you to frequently visit this page.

Feb 29, 202412:30
The Oldest (Community-Based) Sickle Cell Agency

The Oldest (Community-Based) Sickle Cell Agency

A huge shift in content ALERT!

I've been with the American Sickle Cell Anemia Association for the better part of 5-ish months. They are a 501(c)(3) non-profit that offers supportive services, counseling, testing, education, and more to individuals, families, and the population at risk for sickle cell anemia.


Sickle Talk is back! After a hiatus, Sickle Talk is making its return as a podcast. After three years since our last episode, we return to talk about the American Sickle Cell Anemia Association and how this organization got its start over 50 years ago, and the Newborn Screening Program, a federal and state program that tests newborn babies for dozens of debilitating disorders, including sickle cell anemia. Creative and have sickle cell anemia? Send in your artwork, photographs, stories, and more to sickletalk@ascaa.org. Your art could be featured in an episode! Sickle Talk is owned and operated by the American Sickle Cell Anemia Association and funded by viewers and listeners like you. Thank you! Support our organization by donating today! For More Information: Website: www.ascaa.org Follow Us! Facebook Instagram Twitter (X) Threads Spotify

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YouTube (Podcasts) The American Sickle Cell Anemia Association is a 501(c)(3) nonprofit in Cleveland, Ohio. Since 1971, ASCAA has tested, counseled, and assisted individuals, families, and the population at risk with Sickle Cell Anemia. ASCAA is affiliated with multiple major hospitals in our local area, including, but not limited to: Cleveland Clinic Foundation, Cleveland Clinic Children's Hospital, University Hospital, MetroHealth Hospital, Rainbow Babies and Children, and local clinics and community centers. Mission Statement: ASCAA is a comprehensive health organization whose mission is to connect with families, inspire hope, and improve their quality of life. We are ultimately working to create a world without sickle cell disease. Disclaimer: All information is merely for educational and informational purposes for sickle cell anemia. It is not intended as a substitute for professional advice. Please seek an appropriately qualified and licensed physician for medical advice. Should you decide to act upon any information given, you do so at your own risk. While the information has been verified to the best of our abilities, we cannot guarantee that there are no mistakes or errors. We reserve the right to change this policy, which will be promptly updated. If you want to ensure you are up to date with the latest changes, we advise you to frequently visit this page.

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Utter(ly) Random: Getting the Axe

Utter(ly) Random: Getting the Axe

It is so sad to see a favorite show get the axe...in this episode; I talk about shows that unfortunately will not return in the fall as we fly into summer. Think I missed a show or listed a show in error, reach out using voice messaging on Anchor, or find me on Twitter and Instagram. You can find a written version of this podcast here.

After my last random segment, I thought I would come up with something to warn you that while these podcasting episodes are thought out and not as random as they appear, it would be a good idea to name them, hence the Utter(ly) Random. Hope you guys like the new episodes that these have to offer!

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