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FARAFARA Cure FA

FARA Ambassador Program

FARA Ambassadors are a united team of patient volunteers living with FA who are committed to supporting FARA in the search for treatments and a cure.

The Ambassadors are a service team within the FARA organization. Participants in the FARA Ambassador Program are passionate about building and upholding relationships within the FA community. Together we seek to know more about the research and pharmaceutical pipelines being developed through FARA in order to be better prepared to represent the FA community when opportunities arise to educate the medical community and potential donors. When meeting with scientific groups, pharma partners, and the FDA, our purpose is to promote awareness of the patient perspective of living with FA. We believe our dedicated support is key to continued success toward our ultimate goal of treatments and a cure.

FARA Ambassador Program Mission Statement:

The FARA Ambassadors are positive, supportive, peer representatives for the FA community, actively raising awareness and funds for FARA. To learn more about the FARA Ambassador Program or to have a FARA Ambassador speak at your event, please contact: info@cureFA.org.

The Ambassador Blog

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This blog is a vehicle for the voice of the FARA Ambassador Program and features posts from Program participants and friends from the FA community on a wide range of topics.

The blog features posts about FARA events, articles about living with FA, spotlights on individuals throughout the FA community, weekly interviews to “Meet the Community,” and more. We hope that you will be inspired, uplifted and encouraged through the FARA Ambassador Blog!


 

USF Scientific Symposium and FARA Energy Ball 2014

The 6th annual FARA/USF Health Scientific Symposium took place at the USF Health Center for Advanced Medical Learning and Simulation (CAMLS) in Tampa, FL on Thursday, September 4, 2014. Researchers, clinicians, patients and families gathered together to hear upcoming research, possible treatments and patients’ inspiring stories of living with Friedreich’s Ataxia. This year’s focus was “what a difference a year makes” and all these three components were touched upon.

The FARA Energy Ball is an event held to benefit funds and research for FARA and USF Ataxia Research Center. $1.8 million was raised for research on Saturday, September 6th! Please read below for personal experiences shared by those living with FA...

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Read more: USF Scientific Symposium and FARA Energy Ball 2014

Ashley Dodson

Name: Ashley Dodson

Age: 30

Where do you call home? Alabama

Occupation/Employment: I'm a wife and I clean my house, that is my job. :)

How long have you been living (or known you are living) with Friedreich's Ataxia? I was around 8 when I was diagnosed. My teacher noticed my writing was shaky and I couldn't keep up during a spelling test, and when my sister would cut my bangs and I'd shut my eyes, I would loose my balance.

Do you have any known family history of similar symptoms to FA? No (not that I know of).

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Read more: Ashley Dodson

11th Annual Fuzzy Buzzy Golf Tournament

Sunday, September 7, 2014 was the 11th Annual Fuzzy Buzzy Golf Tournament. I am amazed every year at the length this tournament has been going. When the Fuzzy Buzzy started, there were not many other FARA fundraisers, but looking at the calendar these days, it’s a packed schedule. Once again, this year, was a great success. We raised $20,000 for FARA and even more awareness! This brings the 11 year total to $125,000, furthering research to find a cure for FA.

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Jason and Alex Dagley

Name: Jason Dagley

Age: 29

Where do you call home? Frisco, Texas

Education: Some college

How long have you been living (or known you are living) with Friedreich's Ataxia? I have known I have FA since I was 10. My symptoms started around the age of 4-5. I was having difficulty in gym class doing aerobics. My coordination was off. The teacher suggested that I see my doctor. The doctor did some assessments in her office. She suggested that I have further tests done at Scottish Rite Hospital. After a thorough neurological test they really didn't know. In my medical record, it states that it couldn't be FA because my parents are only related by marriage. In the middle of all this we moved to Baton Rouge, Louisiana. We were hooked up with a neurologist at children's hospital in New Orleans. She conducted more tests, nerve and muscle biopsy, EMG, nerve conductions, an MRI and a spinal tap. They even tested my parents with some these. Nothing was conclusive.

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Sam Brown

Name: Sam Brown

Age: 14

Where do you call home? Allen, Oklahoma

Education: 8th grade

How long have you been living (or known you are living) with Friedreich's Ataxia? I was eight years old and in second grade when I was diagnosed.

Describe your transition from walking to walker/wheelchair. My chair has made it so much easier getting around - kinda made me lazy. Although, I do wish I could keep my legs straight with a walker. I started using a chair full-time before I was 10. I really don't remember much about that time.

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Read more: Sam Brown
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