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Celltex Client Testimonials

Condition: Dysautonomia

Kelsi, Dysautonomia and POTS

October 30, 2024

At age 14, Kelsi was diagnosed with postural orthostatic tachycardia syndrome (POTS) and dysautonomia after months of experiencing symptoms like increased heartrate, shortness of breath, and dizziness whenever she stood up. Over time, her condition worsened and list of symptoms expanded to include nausea, insomnia, brain fog, fatigue, headaches, fibromyalgia, numbness/tingling, and poor circulation. By the time she reached college, her severe fatigue, insomnia, and other symptoms made it incredibly difficult to complete a semester. That's when she and her family began looking into newer treatment options, and they eventually found Celltex. She describes her experience and incredible results below.

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McKenna, Dysautonomia and Ehlers-Danlos Syndrome

October 25, 2024

At age 15, McKenna was diagnosed with dysautonomia, a disorder that disrupts the autonomic nervous system. For years she struggled with seizures, fatigue, digestion issues, and many other symptoms that interrupted her life. She eventually found Celltex and saw life-changing results following stem cell therapy.

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Megan, Living with Dysautonomia

October 21, 2024

Towards the end of her junior year of high school, Megan was diagnosed with a rare form of dysautonomia that causes fatigue, lightheadedness, cognitive impairment, and more. At a time in her life when she was supposed to be going off to college and gaining a new sense of independence, the unpredictable symptoms of her illness restricted her from even leaving the house without her mom. A few years later, Megan found Celltex and, with the advice of her family, decided to bank her stem cells.

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Mikaela Aschoff, From Debilitating Symptoms to Thriving College Student

March 3, 2020

stem cell therapy
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Stories by Type

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Stories by Condition

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