About Me

Hi, I’m Christine - the heart and hands behind Early Bird Makery. I grew up in the Seattle area and now live in Utah, where I share my space (and often my fabric) with two beloved cats and more houseplants than I’ll ever admit to owning. My life these days is equal parts cozy chaos and quiet creativity, and I wouldn’t have it any other way.
I made my very first quilt when I was eighteen years old, armed with nothing but determination and the limited corner of the internet that existed twenty-plus years ago. My grandmother was a master quilter who could stitch love into every seam. Her work inspired me deeply, and even though my first quilt was far from perfect, it sparked something that has stayed with me ever since.
Quilting became even more meaningful after chronic illness changed my life’s direction. When my health ended my ten-year career as a family medicine PA and took away hobbies I adored - like playing my bassoon in community orchestras - I had to completely redefine my goals and sense of purpose. The sewing room became my refuge. Even though my body doesn’t always cooperate with long hours at the machine, the process of creating something beautiful from scraps continues to ground and heal me in ways nothing else can.
These days, I think of my personal mission as creating and curating beauty within my own little sphere - and offering encouragement wherever I can. Whether that means designing fun quilt patterns that help beginners feel confident, building community among other disabled makers, or simply cheering on a stranger on social media, I find deep joy in helping others feel seen and supported. Early Bird Makery is my way of sharing that joy: a cozy corner of the internet filled with color, creativity, and connection.
What is ME/CFS?
The most devastating illness you've never heard of.
Overview
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a serious, long-term illness that affects how the body makes and uses energy. Its most defining symptom is post-exertional malaise — when even small amounts of activity can cause a major worsening of fatigue, pain, and other symptoms that can last for days or longer. People with ME/CFS often deal with extreme exhaustion, body pain, dizziness, “brain fog,” poor sleep, and sensitivity to light or sound. The condition is usually long-lasting and can slowly worsen over time. There’s no known cure yet, and because many doctors aren’t well-trained to recognize it, ME/CFS is often misunderstood or misdiagnosed. For many of us living with it, the impact is life-changing and deeply disabling.
My Experience with ME/CFS
I developed ME/CFS in 2015 after a mild viral illness, though it took years (and a helpful suggestion from a stranger online) to finally get the right diagnosis. For a long time, I kept pushing through — working as a family medicine PA and trying to live normally — until my health made that impossible. By 2021, I had to step away from my career and many parts of the life I loved, including the home I built, the friends I saw often, and the freedom to travel or hike on a whim. It’s been a hard road, but also one that’s taught me to slow down, notice beauty in small moments, and pour my limited energy into things that bring comfort and joy. Quilting, designing, and building community have become not just creative outlets, but lifelines that help me stay connected to meaning and hope.
For More Information:
Centers for Disease Control and Prevention (CDC) — Clear, research-based overviews of ME/CFS, its symptoms, causes, and management strategies.
Bateman Horne Center — A leading U.S. clinical and research center focused on ME/CFS, fibromyalgia, and related complex chronic illnesses, offering patient education and treatment guidance.
UK ME Association — One of the largest ME/CFS charities in the United Kingdom, providing patient support, advocacy, and accessible medical information for people with ME worldwide.
Open Medicine Foundation (OMF) — An international nonprofit accelerating collaborative biomedical research into ME/CFS and related post-viral diseases, including Long COVID.
Solve M.E. Initiative — Nonprofit dedicated to funding research, raising awareness, and supporting patients affected by ME/CFS and related diseases.
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Christine@EarlyBirdMakery.com