Bleeding Disorders Awareness Month: CoachArt Takes the #RedTieChallenge

 In Education, Health, Inspiration, Our Mission

Join CoachArt and Take the #RedTieChallenge for Bleeding Disorders Awareness Month

Bleeding Disorders Awareness Month: CoachArt Participates in the #RedTieChallenge

Three million people across the U.S. live with bleeding disorders that can cause extended bleeding after injury, surgery or trauma, and can be life-threatening if not treated effectively.

March is Bleeding Disorders Awareness Month.  The National Hemophilia Foundation’s Red Tie Campaign raises funds and awareness to find better treatments and cures for bleeding disorders.

To share awareness of Bleeding Disorders, CoachArt is participating in the National Hemophilia Foundation’s #RedTieChallenge this month! Here’s how we did it, and how you can participate too. CoachArt uploaded a photo of our team with our best red tie look, which unlocked a $5 donation from CVS Specialty to the National Hemophilia Foundation. Join us and add your photo to show your support for Bleeding Disorders Awareness Month!

Bleeding Disorders Awareness Month: CoachArt Participates in the #RedTieChallenge

Ben, CoachArt Public Relations #RedTieChallenge

Types of Bleeding Disorders

Bleeding disorders are a group of conditions that result when the blood cannot clot properly.

  • Hemophilia A (Factor VIII [FVIII] deficiency)
  • Hemophilia B (Factor IX [FIX] deficiency)
  • Hemophilia C (Factor XI [FXI] deficiency)
  • von Willebrand’s disease (types I, II, III, aVWS, and pseudo-VWD)
  • Factor II (FII) deficiency
  • Factor V (FV) deficiency
  • Factor VII (FVII) deficiency
  • Factor X (FX) deficiency
  • Factor XII (FXII) deficiency
  • Idiopathic thrombocytopenic purpura (ITP)
  • Acquired platelet function defects
  • Congenital platelet function defects
  • Congenital protein C or S deficiency
  • Disseminated intravascular coagulation (DIC)
  • Glanzmann disease
Bleeding Disorders Awareness Month: CoachArt Participates in the #RedTieChallenge

Marci, CoachArt Social Media Manager #RedTieChallenge

Hemophilia

Hemophilia is a disease that prevents blood from clotting properly, so a person who has it bleeds more than someone without hemophilia does. It’s a genetic disorder, which means it’s the result of a change in genes that was either passed from parent to child or happened as a baby was developing in the womb. Hemophilia results from a missing or deficient protein needed for blood clotting. The two main forms are hemophilia A (factor VIII deficiency) and hemophilia B (factor IX deficiency).

Hemophilia Fast Facts

  • Hemophilia A occurs in 1 in 5,000 live male births.
  • Hemophilia A is about four times as common as hemophilia B. 
  • 400 babies are born with hemophilia each year.
  • The number of people with hemophilia in the United States is estimated to be about 20,000 individuals.

Hemophilia Resources:

KidsHealth from Nemours

National Hemophilia Foundation

Bleeding Disorders Awareness Month: CoachArt Participates in the #RedTieChallenge

Lizzie, CoachArt Program Manager #RedTieChallenge

von Willebrand’s disease

Von Willebrand disease (VWD) is a genetic disorder caused by missing or defective von Willebrand factor (VWF), a clotting protein. VWF binds factor VIII, a key clotting protein, and platelets in blood vessel walls, which help form a platelet plug during the clotting process.

von Willebrand’s Disease Fast Facts:

There are three main types of VWD and several subtypes.

Type 1 VWD is the most common and mildest form. The body has low levels of von Willebrand factor. People with type 1 may also have low levels of factor VIII, another blood-clotting protein. According to the Centers for Disease Control and Prevention (CDC), 85% of people treated for VWD in the US have type 1.

Type 2 VWD the body produces a normal amount of von Willebrand factor, but the clotting protein doesn’t work as it should. There are four subtypes of type 2 VWD—2A, 2B, 2M and 2N—depending on the problem with the von Willebrand factor. Each subtype is treated differently.

Type 3 VWD is the rarest and most severe form. The body makes little or no von Willebrand factor and has low levels of factor VIII.

Von Willebrand’s Disease Resources:

HemaAware

National Hemophilia Foundation

Bleeding Disorders Awareness Month: CoachArt Participates in the #RedTieChallenge

Melissa, CoachArt Bay Area Program Manager #RedTieChallenge

Parents of Kids With Bleeding Disorders

For parents of children with bleeding disorders, BleedingDisorders.com offers a great article “Back-to-School Tips for Parents Caring for Children with Bleeding Disorders” which includes knowing bleeding disorders basics, informing staff on how to recognize a bleed, providing staff with your child’s care plan, and updating emergency contacts.

If your child has recently been diagnosed with a bleeding disorder, it may be difficult to process and many emotional reactions are common. Hemophilia of Georgia offers a wonderful resource called The Hemophilia, von Willebrand Disease & Platelet Disorders Handbook, which includes a section for parents of children with bleeding disorders.

Join CoachArt and add your photo to show your support for Bleeding Disorders Awareness Month here.

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Making a Difference for Families Impacted by Childhood Chronic Illness

CoachArt creates a transformative arts and athletics community for families impacted by childhood chronic illness. Since 2001, CoachArt has matched volunteer coaches with kids for free one-on-one or group lessons in arts and athletics. We invite you to get involved!

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