
Be strong . Be courageous . Be hopeful.

Public Relations Director
Katie Kraning (she/her)
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Katie is a curious, lifelong learner with Communication (BA & MA) degrees. She has traveled a winding path from commercial construction communication and management, to adjunct college communication professor, to technical writer, to creative director, to homeschool mom, to e-commerce consumer liaison. Along the journey, ME/CFS became the mammoth felled tree abruptly obstructing her path. After years of chipping away at it, and all of its comorbid little friends, she has learned more than she ever imagined about something she had never heard of and that is often hidden in plain sight. She is now seeing a new way forward.
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As a person surviving through disabling, invisible, and often disbelieved or misunderstood conditions, she brings an unique angle with first hand knowledge of living with ME/CFS, as well as caring for a child with complex cares conditions. After hearing of Dr. Tam's selfless devotion to this neglected patient population, Katie felt compelled to help in whatever way she is able, when she can. She has a tenacious drive for patient advocacy and a heart to help. She is passionate about connecting with & hearing the stories of others and sharing new information to educate others. Katie truly believes that Dr. Tam has created a ripple effect that will impact people around the globe, by starting right here at home.
"ME/CFS has robbed so many people of the ability to work, learn, thrive, love, sing, travel, dance, socialize, create, live. It has shattered personal & professional relationships, stolen credibility, exhausted hopefulness & faith, made patients feel voiceless, ignored, isolated, and has devastating financial consequences & economic impacts on millions of people and their loved ones. The mission of MECFS Clinic MN is something I can support wholeheartedly in the fight to bring hope to those dealing with this every day. I still maintain hope and carry the mantle for those who have fought this for so long. I count myself a proud member of this resilient, valuable, determined community."
Fundraising Director
Jasmine McAleavey (she/her)
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Jasmine moved from Ireland to the United States in 20211 with a degree in Fine Art Sculpture from the West Wales School of the Arts and a strong sense of adventure. She worked in corporate communications and philanthropy until being diagnosed with ME/CFS and Fibromyalgia. She quickly made the hard choices and lifestyle changes required to improve her quality of life and encourages everyone to have the courage to do the same.
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Jasmine has always been involved in some form of volunteerism. It is her passion to leave the world in a better state. Since winning the diagnosis lottery with a colorful set of obscure illnesses between 2020-2023, she turned her attention to causes aligned with her new personal challenges. In addition to supporting the ME/CFS Clinic, she also runs a global Facebook support group for visible - an app and device for patients with similar chronic conditions and a local Iowa support group for patients. Food security has long been a passion for her and she helps operate a student food pantry at her job with the local community collage in her city. It brings her joy to connect people to services that can help them and improve their lived experience.
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"Rest is work. When you rest, you give your body time and space to do the hard work of repairing, organizing, fighting, and recharging. You do not need to be consciously doing anything in addition to all of this to validate your worth as a person. Give yourself permission to rest."
Nathan Horek, ND (he/him)
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Dr. Horek is a naturopathic doctor and 2011 graduate of the National University of Natural Medicine in Portland, Oregon. He has worked in private practice as well as in research at the University of Minnesota Department of Psychiatry and Behavioral Sciences.
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"With personal experience with ME/CFS, EDS, POTS and mold/mycotoxin exposure, I am volunteering with MECFS Clinic MN to help patients suffering from this debilitating condition."
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Lisa Neitge, OTR/l, CTL (she/her)
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Lisa is a licensed occupational therapists at Northfield Hospital and Clinics specialized in lymphedema/edema, post-concussion and memory care, wound care, upper extremity injuries and neuroscience. She received her Bachelor of Applied Science in Occupational Therapy at the University of Minnesota at Twin Cities in 1994, and is a certified Perrin Technique practitioner.
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"As an occupational therapist of thirty years, I truly enjoy being a partner with people as they move through unexpected life changes and managing long term conditions. I like empowering people to get back to the real layers of life through pacing and self-treatment routines. I seek to find solutions to every day problems that work for the individual and the world around them. I will often incorporate mind/body techniques into my practice, such as yoga, Pilates, mindfulness, myofascial release and lymphatic massage.
Being a part of the MECFS Clinic MN is important to me, as so many of people affected by ME/CFS and long COVID are taken out of their employment and our communities for months and years of time. These people can easily experience financial insecurity, can have limited to no options for health care and often feel lost between providers in their care. Volunteering with Dr. Tam’s clinic helps us serve this often unseen population in many ways. It also provides a network for me to keep learning and growing as a therapist.."
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