Spreading Awareness: Road Scholar Transport Honors Neurofibromatosis, Lupus, and Cystic Fibrosis
With a fleet dedicated to several dozen causes and organizations, Road Scholar Transport continues its mission to raise awareness for various health conditions. This May, we spotlight three significant causes: Neurofibromatosis, Lupus, and Cystic Fibrosis.
Neurofibromatosis (NF)
Neurofibromatosis is a genetic disorder causing tumors to form on nerve tissue. It affects approximately 1 in 3,000 individuals, with about 50% of cases resulting from spontaneous mutations. NCBI
Types of NF:
- NF1: The most common form, characterized by skin changes and benign tumors.
- NF2: Rarer, leading to hearing loss, balance issues, and tumors on the auditory nerves.
- Schwannomatosis: The rarest type, causing intense pain due to tumors on peripheral nerves.
In 2019, Road Scholar introduced a Children’s Tumor Foundation truck, featuring the image of President Debra Barrett’s grandson, who was diagnosed with a tumor. This initiative aims to spread the message: "Imagine the Possibilities."
Lupus
Lupus is a chronic autoimmune
disease affecting various parts of the body. Approximately 1.5 million Americans live with
lupus, with 90% being women aged 15-44. Lupus Foundation of America
Types of Lupus:
- Systemic Lupus Erythematosus (SLE): The most common form, impacting multiple organs.
- Cutaneous Lupus: Affects the skin, causing rashes and lesions.
- Drug-induced Lupus: Triggered by certain medications, symptoms usually subside after discontinuation.
- Neonatal Lupus: A rare condition affecting infants of women with lupus.
In memory of Tanitha Kulsiri, who passed away from SLE at 22, Road Scholar unveiled a Lupus awareness truck in 2013. The design incorporates Tanitha’s artwork and the message "LIVE BEYOND LUPUS," promoting the Tanitha Kulsiri Memorial Foundation.
Cystic Fibrosis (CF)
Cystic Fibrosis is a genetic disorder affecting the lungs and digestive system. In the U.S., approximately 40,000 individuals live with CF, with over 75% diagnosed by age 2. verywellhealth.com+4Cystic Fibrosis Foundation+4Lurie Children's+4
Key Facts:
- Cause: Mutations in the CFTR gene leading to thick mucus buildup.
- Symptoms: Persistent coughing, frequent lung infections, and difficulty gaining weight.
- Treatment:
While there's no cure, treatments include airway clearance, medications,
and nutritional support. reuters.com+2health.com+2thesun.ie+2
Inspired by the story of a child who referred to his condition as "65 Roses," Road Scholar designed a CF awareness truck adorned with 65 roses, symbolizing hope and the fight against the disease.
For more information on Road Scholar’s awareness campaign click here.
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