Sickle Cell Association of South Louisiana

Helping Break the Sickle Cycle • Follow Us on Instagram: @BRSickle and Facebook: Baton Rouge Sickle Cell Anemia Foundation, Inc.

[Sickle Cell Association of South Louisiana @BRSickle]

Did you know SCD is a group of inherited red blood cell disorders? Red blood cells are normally disc-shaped and carry oxygen. In SCD, red blood cells become crescent- or “sickle”-shaped and don't move easily. They can can block blood flow to the rest of the body.

#SickleCell

[Sickle Cell Association of South Louisiana @BRSickle]

SCASL has been serving Sickle Cell Warriors for over 47 years. We advocate for equitable health care and treatment, provide support to clients, and educate the community about SCD. Our goal is to rewrite the narrative around life with SCD. Learn more: https://t.co/xUB4XIxJhA

[Sickle Cell Association of South Louisiana @BRSickle]

Today is National Louisiana Day! We proudly serve Sickle Cell Warriors in south Louisiana by advocating for equitable health care and treatment for all people living with SCD in south Louisiana.

#SickleCellAwareness #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

Did you know around 100,000 people in the U.S. are diagnosed with SCD? SCD occurs among about 1 out of every 365 Black births, and about 1 in 13 Black or African-American babies is born with sickle cell trait (SCT).

#SickleCell #SickleCellAwareness

[Sickle Cell Association of South Louisiana @BRSickle]

Are you interested in helping the Sickle Cell Warriors in your community? Consider joining the Sickle Cell Advocates of Greater Baton Rouge! They advocate for policy changes for people living with SCD. If you want to make a difference, visit https://t.co/xUB4XIxJhA!

[Sickle Cell Association of South Louisiana @BRSickle]

Today is #NationalStressAwarenessDay! Sickle Cell Warriors should prioritize their stress stress levels. Stress can trigger a Sickle Cell Crisis. People living with SCD should try to do something that is stress-relieving every day!

#SickleCellAwareness #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

Watch the FDA's Cellular, Tissue, & Gene Therapies Advisory Committee Meeting tomorrow, Oct. 31st. The Food and Drug Administration will make a landmark decision about gene therapy for SCD. Watch Live: https://t.co/QtZbiagbMi

#SickleCellDisease #SickleCellAwareness

[Sickle Cell Association of South Louisiana @BRSickle]

Tune in to the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee Meeting on Oct. 31st. The Food and Drug Administration will make a landmark decision about gene therapy for SCD. Watch Live: https://t.co/QtZbiagbMi

#SickleCellDisease #SickleCellAwareness

[Sickle Cell Association of South Louisiana @BRSickle]

Did you know that anemia is a common effect of SCD? Sickle Cell Warriors' red blood cells die early, and there are not enough left to carry oxygen throughout the body, causing anemia. Blood transfusions are used to treat severe anemia.

#SickleCellDisease #SickleCellAwareness

[Sickle Cell Association of South Louisiana @BRSickle]

Did you know nutrition matters for Sickle Cell Warriors? Sickle Cell Warriors should eat from a rainbow of fruits and vegetables and pair them with whole grains, protein foods, and plenty of calcium-rich foods.

#SickleCellAwareness #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

Did you know joining a patient support group or a community-based SCD organization is recommended for people with SCD? We offer educational workshops for people living with SCD. For more information visit us at https://t.co/xUB4XIxJhA

#SickleCellAwareness #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

For people with sickle cell disease, ERs can mean life-threatening waits https://t.co/mlHW3uSNsC

[Sickle Cell Association of South Louisiana @BRSickle]

People living with SCD are more than just their disease. CDC's Stories of Sickle Cell aims to highlight the unique stories and diverse identities of Sickle Cell Warriors. Learn more at https://t.co/2qbdfXoakI

#SickleCellAwareness #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

People living with SCD often use coloring, drawing, and creative writing to help them through pain crises. Today is Black Poetry Day. We hope everyone takes time today to destress and create something meaningful!

#SickleCellAwareness #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

Yesterday was Global Wash Your Hands Day. Washing your hands keeps you healthy and prevents the spread of infections. Sickle Cell Warriors and their families/friends should wash their hands often because they are more prone to infections.

#SickleCellWarriors #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

Today is World Thrombosis Day. Thrombosis is a blood clot within blood vessels that limits blood flow. People with SCD are at greater risk of forming blood clots. A blood clot in one of the large veins is called a deep vein thrombosis.

#SickleCellWarriors #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

Did you know each time you donate blood you can save up to 3 lives? Many Sickle Cell Warriors need blood transfusions and rely on people donating blood. It is never to late to start donating blood!

#SickleCellWarriors #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

Today is World Mental Health Day! Sickle Cell Warriors need to prioritize their mental health. People with chronic diseases may feel sad, which can lead to anxiety and depression. Remember to take some time for yourself every day!

#SickleCellAwareness #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

Sickle Cell Disease is a lifelong illness with health implications, such as pain crises, eye problems, and infections. It is essential for Sickle Cell Warriors to build support networks of friends and family to help them.

#SickleCellAwareness #SickleCellDisease

[Sickle Cell Association of South Louisiana @BRSickle]

People with SCD can live full lives by being proactive in their care. Here are some tips to help you or someone you know with SCD stay as healthy as possible.

#SickleCellAwareness #SickleCellDisease