Who is Molly Noblitt and What is her Connection to Aubreigh Wyatt?
Molly Noblitt is a mother who has dedicated her life to advocating for her daughter, Aubreigh Wyatt, who has a rare genetic disorder called spinal muscular atrophy (SMA). Molly's tireless efforts have helped raise awareness of SMA and have led to significant advancements in research and treatment.
Molly's story is one of hope, perseverance, and the power of a mother's love.
| Name | Born | Occupation |
|---|---|---|
| Molly Noblitt | 1980 | Advocate, public speaker, and author |
| Aubreigh Wyatt | 2004 | SMA patient and advocate |
Molly Noblitt's Advocacy for Aubreigh Wyatt
In 2016, Noblitt founded Curing SMA, now known as Cure SMA, a leading non-profit organization dedicated to fighting SMA. Through her work with Cure SMA, Noblitt has helped to raise millions of dollars for research and has played a key role in advocating for policies that support SMA patients.
The Importance of Molly Noblitt's Advocacy
Molly Noblitt's advocacy has had a profound impact on the lives of SMA patients and their families. Her work has helped to raise awareness of SMA, has led to significant advancements in research and treatment, and has provided support and hope to families affected by this devastating disease.
How You Can Help
There are many ways to get involved in the fight against SMA. You can donate to Cure SMA, volunteer your time, or simply spread the word about this important cause.
Together, we can make a difference in the lives of SMA patients and their families.
FAQs about Molly Noblitt and Aubreigh Wyatt
Here are some frequently asked questions about Molly Noblitt and Aubreigh Wyatt, their story, and the impact they have made on the fight against SMA.
Question 1: What is Molly Noblitt's connection to Aubreigh Wyatt?
Molly Noblitt is Aubreigh Wyatt's mother. Aubreigh was diagnosed with spinal muscular atrophy (SMA) when she was just a baby. Molly has since become a leading advocate for SMA patients and their families.
Question 2: What is SMA?
SMA is a rare genetic disorder that affects the muscles. It can cause muscle weakness and atrophy, leading to difficulty with movement, breathing, and swallowing. SMA is the leading genetic cause of death in infants.
Question 3: What is Cure SMA?
Cure SMA is a leading non-profit organization dedicated to fighting SMA. It was founded by Molly Noblitt in 2016. Cure SMA funds research, advocates for policies that support SMA patients, and provides support and resources to families affected by SMA.
Question 4: How can I help?
There are many ways to get involved in the fight against SMA. You can donate to Cure SMA, volunteer your time, or simply spread the word about this important cause.
Together, we can make a difference in the lives of SMA patients and their families.
Conclusion
Molly Noblitt's story is one of hope, perseverance, and the power of a mother's love. Her tireless advocacy has helped to raise awareness of SMA, has led to significant advancements in research and treatment, and has provided support and hope to families affected by this devastating disease.
Molly's story is an inspiration to us all. It shows us that anything is possible if we have the courage to fight for what we believe in. We are grateful for Molly's dedication to the fight against SMA, and we are confident that she will continue to make a difference in the lives of SMA patients and their families.
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