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July Teen Hangout 2020

Screen Shot 2020 07 28 at 6.47.13 PMJoin the FARA Ambassadors for a hangout for teenagers, 13-19, with ataxia (of any form). FA Teen Hangouts are hour-long web-based hangouts. If you don't have ataxia, you are not allowed to participate in the hangout. This is simply a place to meet and talk to other people who may be going through struggles and good times similar to you. There will also be at least three adult FARA Ambassadors present. The adults will be there to help keep the conversation safe and going.

Join our Thursday night hangout this month in a discussion lead by FARA ambassador Kyle Waterman about "Tips and Tricks" that make living with ataxia easier Tell us what you do, learn what other teens do. Help other teens (and FARA Ambassadors) by sharing your life hacks. Join us to talk or just listen. We are sure you'll find you aren't alone! It is just a relaxed conversation...the theme gets us going, but we definitely don't stick to it! It isn't counselling.

Brett Davis

BrettName: Brett Davis

Age: 38

Where do you call home? Fayetteville, NC

Education degree(s): Associates degree in computer programming

Who do you live with? I live by myself.

What's a typical day for you? I try to exercise somehow every day. I like to play a little chess with the FA friends and take care of myself.

How long have you known you are living with FA? I was clinically diagnosed when I was 12, so 26 years ago. It wasn't confirmed in a test until I was 15.

Are there any others with FA in your family? No

July Teen Hangout

Screen Shot 2020 07 09 at 4.05.52 PMJoin the FARA Ambassadors for a hangout for teenagers, 13-19, with ataxia (of any form). FA Teen Hangouts are hour-long web-based hangouts. If you don't have ataxia, you are not allowed to participate in the hangout. This is simply a place to meet and talk to other people who may be going through struggles and good times similar to you. There will also be at least three adult FARA Ambassadors present. The adults will be there to help keep the conversation safe and going. Join our Saturday hangout this month to talk with Kate Walker and Madelyn Fredrick about having a YouTube channel. They each have FA YouTube channels. So, let's talk to them about how they do it, how it helps others, and how it helps them. Join us to talk or just listen. We are sure you'll find you aren't alone! It is just a relaxed conversation...the theme gets us going, but we definitely don't stick to it! It isn't counselling.

Jennifer Gasner

Jennifer GMy name is Jennifer Gasner. My FA diagnosis came nearly 30 years ago, at 17. It was genetically confirmed when the test became available. I have a BA in English and a Masters in Recreation. I grew up in Wisconsin. In 1999 I started using a wheelchair and began working with Independent Living Centers, (ILC's), an important resource for people with disabilities that I knew nothing about. That experience changed my perspective on disability so much. It led to being proud to be disabled, which I had been avoiding referring to myself as. I also felt comradery with my disabled friends, regardless of their diagnosis. I had only briefly met one other FA'er and felt very alone. It was great to discover commonalities and people who had experienced things I hadn't as FA progressed.

Matthew Jordan Penman

MatthewName: Matthew Jordan Penman

Age: 35

Where do you call home? Calgary, Alberta. Canada.

Education degree(s): I have a diploma in Professional Counseling, Certificate in Addiction Work and I am currently working on my Masters in Counseling.

Who do you live with? I am living with my wife, my father, who lives with us, and our fur babies, Fergus (Husky/German Shepherd), and Charli (Purebred Boxer).

What's a typical day for you? Currently, I am working in a harm reduction facility for seniors and working on my portfolio for my RPL to get into a master's program. We are trying to buy a house right now, and it's our first, so it's very time-consuming.

Subcategories

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!


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