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Sickle Cell Oregon Newsletter October 2025 | Myth-Busting & Trait Info

Sickle Cell Oregon Globe – October 2025 Newsletter

Welcome to the October 2025 edition of the Sickle Cell Oregon Globe! This month we’re setting the record straight on common myths about sickle cell disease, sharing critical information about sickle cell trait that could save lives, and issuing an urgent call for blood donations to support our community.

In This Month’s Newsletter:

Setting the Record Straight: Myth-Busting About Sickle Cell Disease

Misinformation about sickle cell disease can be harmful and even dangerous. Executive Director Pastor Marcia Taylor addresses two of the most persistent myths about SCD that need to be corrected:

Myth #1: Only Black People Get Sickle Cell Disease
The truth is that sickle cell disease does not discriminate based on ethnicity or skin color. Anyone of any ethnicity can have SCD. The disease is also found in people of Indian, Middle Eastern, Hispanic, and Mediterranean backgrounds. Whether children are born with SCD depends only on their parents’ genetic status, not their ethnicity or race.

Myth #2: Sickle Cell is a Contagious Blood-Borne Disease
SCD is a genetic condition present at birth, inherited when a child receives a sickle cell gene and an abnormal hemoglobin gene from each parent. It is not possible to get infected with SCD from someone else’s blood. Sickle cell disease is not contagious—you cannot “catch” SCD.

Understanding Sickle Cell Trait: What You Need to Know

An estimated 2 million Americans have sickle cell trait (SCT), yet many don’t know it. Understanding sickle cell trait is crucial not just for your own health, but for family planning decisions. If two people with sickle cell trait have children together, their child could be born with sickle cell disease.

What Is Sickle Cell Trait?

Sickle cell trait means you have inherited one sickle cell gene from one parent and one normal gene from the other parent. While most people with SCT live normal lives without symptoms, some carriers with a high percentage of sickle cells can experience serious complications under certain conditions, including dehydration, cold temperatures, stress, low oxygen levels, infections, or surgeries.

Critical Information for Sickle Cell Trait Carriers

If you have sickle cell trait and have experienced pain episodes, hospitalizations, or complications—your experience is real and valid. Some SCT carriers do have problems, and you deserve proper medical care. Don’t let anyone dismiss your symptoms.

Warning Signs That Require Immediate Medical Attention

If you have sickle cell trait and experience any of these symptoms, seek medical help immediately:

  • Severe, unexplained pain
  • Extreme fatigue
  • Shortness of breath
  • Blue-tinged nails or lips
  • Sudden weakness
  • Swollen hands and feet

Essential Tips for People with Sickle Cell Trait

  • Avoid high altitudes (can be life-threatening for trait carriers)
  • Avoid extreme temperatures
  • Stay well hydrated at all times
  • Know your sickle cell percentage
  • Tell ALL your doctors about your SCT
  • Get genetic counseling before pregnancy
  • Know the warning signs of complications

Urgent Need: Blood Donations Save Sickle Cell Lives

Blood transfusions are one of the most critical treatments for sickle cell patients, but less than 10% of Americans donate blood. Sickle cell patients benefit most from blood transfusions from people of the same race or similar ethnicity, yet only 5% of blood donors are of African ancestry. Help make a difference for SCD patients in Oregon and the Pacific Northwest by pledging to donate blood this month.

Read the Full October 2025 Newsletter

Sickle Cell Oregon Globe – October 2025

Click here to download the October 2025 newsletter.

About the Sickle Cell Oregon Globe

The Sickle Cell Oregon Globe is the monthly newsletter of the Sickle Cell Anemia Foundation of Oregon & PNW. We serve families affected by sickle cell disease throughout Oregon, Washington, Idaho, Alaska, and Hawaii with support groups, educational resources, awareness events, and community connection.

Contact Us:
Sickle Cell Anemia Foundation of Oregon & PNW
4566 N. East 87th Ave
Portland, OR 97220
Phone: 503-249-1366
Email: info@sicklecelloregon.org
Website: www.sicklecelloregon.org

Keywords: sickle cell trait Oregon, sickle cell myths, SCD misconceptions, blood donation Portland, sickle cell disease prevention, genetic counseling, sickle cell awareness Pacific Northwest, SCT complications, high altitude risks sickle cell

The Sickle Cell Oregon Globe Newsletter 09-25

Sickle Cell Oregon Globe – September 2025 Newsletter

Welcome to the September 2025 edition of the Sickle Cell Oregon Globe! This month brings exciting news for the sickle cell community in Oregon and the Pacific Northwest, including a major breakthrough in bone marrow transplant treatment, new pregnancy guidelines from the WHO, and important fall health tips.

In This Month’s Newsletter:

Major Breakthrough: New Bone Marrow Treatment Shows 97% Success Rate

Medical centers across the country, including Johns Hopkins and Vanderbilt, have achieved remarkable success with a new bone marrow transplant approach for sickle cell disease. This innovative treatment uses “half-matched” donors such as parents, siblings, or children, making it accessible to virtually everyone. With over 97% success rate in adult patients and costs significantly lower than gene therapy, this breakthrough offers new hope for sickle cell treatment options.

WHO Releases New Pregnancy Guidelines for Sickle Cell Disease

The World Health Organization has published important new guidelines to help pregnant women with sickle cell disease have safer pregnancies. These guidelines emphasize the need for specialized prenatal care, including extra folic acid and iron supplements, more frequent check-ups, and careful pain management planning. Women with SCD thinking about pregnancy are encouraged to consult with their healthcare providers early.

Upcoming Events & Support

  • Sickle Cell Live! Awareness Dinner – Thursday, September 25, 2025, 6-8:30 PM at Crowne Plaza Hotel, Portland
  • Monthly Support Group Meeting – Thursday, October 17, 2025, 7:00-8:00 PM (Online via Zoom). Join fellow sickle cell warriors to learn, share stories, and receive support. Register at https://tinyurl.com/scdgroup

Staying Healthy This Fall Season

As temperatures drop in Oregon and the Pacific Northwest, people with sickle cell disease need to take extra precautions. This newsletter includes essential tips for managing your health during cooler weather, including staying warm to prevent pain crises, getting your flu shot, maintaining hydration, and keeping up with medications like hydroxyurea.

Quick Pain Management Tips

Learn practical strategies for managing sickle cell pain at home, including heat therapy, gentle exercise, hydration, and breathing techniques. The newsletter also provides guidance on when to contact your doctor if pain worsens.

Important Drug Safety Update

Critical information about Oxbryta (voxelotor) and its removal from the market by Pfizer in September 2024. If you were taking this medication, please consult with your healthcare provider about alternative treatment options.

Read the Full September 2025 Newsletter

Sickle Cell Oregon Globe – September 2025

About the Sickle Cell Oregon Globe

The Sickle Cell Oregon Globe is the monthly newsletter of the Sickle Cell Anemia Foundation of Oregon & PNW. We serve families affected by sickle cell disease throughout Oregon, Washington, Idaho, Alaska, and Hawaii with support groups, educational resources, awareness events, and community connection.

Contact Us:
Sickle Cell Anemia Foundation of Oregon & PNW
4566 N. East 87th Ave
Portland, OR 97220
Phone: 503-249-1366
Email: info@sicklecelloregon.org
Website: www.sicklecelloregon.org

Keywords: sickle cell disease Oregon, SCD treatment breakthrough, bone marrow transplant, sickle cell pregnancy, patient support Pacific Northwest, sickle cell awareness Portland, SCD pain management, hydroxyurea treatment

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