Jaxson’s Clayshoot for Mito CMTs
Among the various forms of CMT, mitochondrial CMT (Mito-CMT) represents a particularly challenging subset, where genetic mutations impact the mitochondria—often referred to as the powerhouse of the cell. For those living with Mito-CMT, the journey can be daunting, but there is hope on the horizon through the dedicated efforts of the Hereditary Neuropathy Foundation (HNF) and its community.
Understanding Mito-CMT
Mito-CMT is caused by mutations in specific genes that impair mitochondrial function, leading to symptoms that overlap with other types of CMT but are often more severe. These include muscle weakness, difficulty walking, and in some cases, more complex systemic issues due to mitochondrial dysfunction. For those affected by Mito-CMT, the impact on daily life can be profound, but advancements in research are paving the way for better understanding and potential treatments.
HNF’s Role in Advancing Mito-CMT Research
The Hereditary Neuropathy Foundation has been at the forefront of research and advocacy for those affected by all forms of CMT, including Mito-CMT. HNF is committed to driving research efforts that focus on uncovering the genetic causes of Mito-CMT and developing targeted therapies that could one day alleviate or even cure this condition.
Through partnerships with leading researchers and institutions, HNF is funding studies that delve into the molecular mechanisms of Mito-CMT. These studies aim to identify potential therapeutic targets and develop interventions to improve the quality of life for those living with this challenging condition.
One such story of hope comes from the Faces of CMT campaign, where the story of Jaxson—a young boy living with MTRFR C12orf65-related Mito-CMT—highlights the real-world impact of these genetic mutations. Jaxson’s journey, like that of many others with Mito-CMT, underscores the urgent need for continued research and support.
Fundraising for a Cure: HNF’s October Event
This October, HNF is hosting a critical fundraising event to support ongoing research for Mito-CMT and other forms of the disease. The 8th Annual ‘Jaxson’s Crusaders: Shotguns & Guitars’ Clay Shoot and Concert will take place on Saturday, October 12th, 2024, at the Defender Outdoors Clay Ranch located just 5 minutes from downtown Fort Worth, Texas, at 8270 Aledo Rd, Fort Worth.
The event will feature a 100-round clay shoot, followed by a live country music concert headlined by Austin Allsup. Participants will also enjoy delicious offerings from a food truck, along with beer and wine available throughout the event. This exciting day is not only about fun and entertainment but also about making a real impact in the fight against Mito-CMT.
Ticket Information:
– Single Shooter: $125
– Team of 4: $500
– Concert Tickets: $25
All proceeds from the event will go directly towards funding HNF’s research initiatives, including those focused on Mito-CMT, ensuring that the momentum in finding a cure continues.
How You Can Help
The success of this event—and the future of Mito-CMT research—depends on the support of individuals like you. Here’s how you can make a difference:
- Attend the Event: Join us in Fort Worth for a day of clay shooting and live music, knowing that your participation directly supports critical research efforts.
- Donate: If you cannot attend, consider making a donation. Every contribution, no matter the size, brings us one step closer to breakthrough treatments and a cure for Mito-CMT.
- Spread the Word: Share information about the event and HNF’s mission with your network. Awareness is key to driving support and advocacy.
To learn more about the event and purchase tickets, visit dfwclayshoot.com. For more information on Mito-CMT and the research efforts underway, please visit the Hereditary Neuropathy Foundation’s website.
To learn more about the event and purchase tickets, visit dfwclayshoot.com. For more information on Mito-CMT and the research efforts underway, please visit the Hereditary Neuropathy Foundation’s website.
To learn more about the event and purchase tickets, visit dfwclayshoot.com. For more information on Mito-CMT and the research efforts underway, please visit the Hereditary Neuropathy Foundation’s website.
Together, we can unlock hope for those living with Mito-CMT and ensure that a brighter future is within reach. Thank you for your continued support of the HNF and our mission to cure CMT.
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