Erev King’s journey with LAM hasn’t been easy—but it’s one of strength, determination, and advocacy. She first noticed shortness of breath in her 30s. At the time, she had a history of atrial fibrillation, and her symptoms were often brushed aside. Over the years, the breathing issues persisted. She was eventually referred to a pulmonologist, and after abnormal PFTs and a chest CT, she received a diagnosis that changed everything: LAM.

By then, Erev had already been through early menopause and hysterectomy. She immersed herself in research and made her way to the Cleveland Clinic.

Though her case is believed to be sporadic LAM, her doctors are also exploring connections to tuberous sclerosis (TSC).

Erev brings a unique perspective—she’s a PhD in biostatistics, a trained orthopedic surgeon turned researcher, a wheelchair user due to a spinal cord injury and primary progressive multiple sclerosis, and a proud mom of three. She’s also a para-archer on Team USA and now a fierce advocate for LAM patients, especially those diagnosed later in life.

“The LAM Foundation gave me connection and hope,” she says. “It’s a lifeline—offering resources that help guide my care and reminding me I’m not alone.”

To those who donate to TLF, Erev offers a heartfelt message: “Your support powers research that lets us live fully with LAM. We are your sisters, mothers, and daughters. Thank you for standing with us.”

Erev’s story is a powerful reminder: strength lives in every breath—and in every patient’s voice.