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The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.message sent
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What It Is Like to Have a Rare Disease. How Clinical Trials Changed My Life?
When I was about 1, I started walking with a stiff gait and stumbling quite a bit. Soon after my parents noticed that I stopped meeting childhood milestones. Worried, they took me to the doctor to learn more. A month before my younger brother was born, my parents discovered why I struggled: I had SMA and it was ultimately a fatal condition.
At the time, there were no real treatments and little research being done on SMA. My parents felt devastated and hopeless. But they turned their fear into action and helped create the SMA Foundation to fund research and encourage better treatments.

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