AVM Specific Radio Show Called "AVM Live" to Premier January 10th at 8pm Central

Hi Folks,

As a few folks here know, I have been doing a morning radio show(music) for about 4 years now. My audience has grown, and it is turning into a real meaningful and successful part of my life. And I'm blessed to have a few of you that listen to it. Before my AVM I was a part-time musician, and being involved in radio has been almost therapeutic for me.

For some time I really have been trying to figure out how to best help my fellow AVM'ers in an active way. Unfortunetly like many AVM folks, I have some real physical problems, most due to the major stroke I suffered during the bleed and brain surgery. I lost use of a lot of my left side, including total loss of my left arm and hand. Hince, I type totally with my right hand. That limits me a lot, especially as related to typing much and responding a lot on this website. Traveling isn't easy too. Though I am grateful to be able to do that some, and am fortunate to have met a good number of you at our Texas AVM functions.

This brings me to my main point. I have long toyed with an AVM specific radio show for some time. Sometime in the past I had heard one, but to my knowledge, they have been more brain injury specific. And I had not been happy with the software company that you pretty much had to use, because it limits you on being able to ever play any music legally(I'm a stickler for this as I own a radio station and must stay FCC legal). So last week, I just happened to get an email from a company that offers the software that is required to do this. I signed up, and gave it a whirl, and well, it's time for me to do what I am best at, host a radio show specifically for AVM'ers. This is my calling...

The show will be called "AVM Live". It will air for now on Thursday Nights at 8pm Central. It will last two hours, and will be on my radio station "KFEE-Digital Radio & TheMorningCoffeeMix . It will be a combination of talk, interviews, and music. We will talk about things that matter to AVM'ers and their families. And It's commercial free, I'm not in this for the money. So I just wanted to let you all know. I will do the first broadcast on Thursday Night January 10th at 8pm Central. The call in number is 313-736-KFEE (313-736-5333). I will be in the chat room here on the avmsurvivors.org web site during the broadcast to make it easy to interact with you all, and as mentioned you can call in and participate by talking about the subjects at hand, and/or simply sharing what you are going through, and even requesting a song of encouragement for your AVM family. So that's it, let's do this bad boy:)

Signed,

James Larken Smith

Views: 91

Comment

You need to be a member of AVMSurvivors.org to add comments!

Join AVMSurvivors.org


Moderator
Comment by Ninibeth Ramirez on January 15, 2013 at 6:45am

That's wonderful James :-D

Comment by just call me jules-babe on January 9, 2013 at 8:52am
Rock on!

Moderator
Comment by Louisa on January 9, 2013 at 8:06am

That is fantastic James! I will put it on my calendar. You are an amazing support for the Network!

PLEASE LIKE US ON FACEBOOK AND FOLLOW BENS FRIENDS ON TUMBLR AND TWITTER AND PINTEREST

To Support AVMSurvivors.org, Click an Ad. Or Two.

Our Newest Communities

Join the Ben's Friends Mailing List

Photos

Loading…
  • Add Photos
  • View All

Blog Posts

May 2013 Community Newsletter

Posted by Ben on May 24, 2013 at 10:00am 0 Comments

Dear AVMSurvivors Family and Friends,

Celebrating Awareness Months for specific rare diseases are a great way of procuring attention to our cause. By discussing our condition and helping to educate others, our active participation creates…

Continue

confusion as symptoms mount... time for new dr?

Posted by mamaginof3 on May 9, 2013 at 3:13pm 14 Comments

Since last may, the symptoms that sent me to the neurologist in the first place are getting worse. July 11th, the MRI with Contrast found my avm, left frontal lobe. The neurologist I see right now is not concerned about the avm, and only wants to… Continue

HHT Diagnosis or Suspected

Posted by Fish on May 10, 2013 at 3:25pm 1 Comment

My husband has HHT . Daughter has been tested but no results yet. Praying God spares my children. I have two granddaughters. I have another daughter who has not been tested. We found the HHT Center in Chapel Hill after years of nosebleeds. He has…

Continue

Dreams... changing

Posted by Michael on May 2, 2013 at 3:14am 5 Comments

Hello there,

how it's for you? In my case, I have the paralysis since last october 2012. Before that I was very active with cross country running, dogsport, and so on. The good thing: In my dreams I had no Paralysis. I run in my dreams,…

Continue

One year since my bleed, more or less

Posted by tdz103m on May 2, 2013 at 5:34am 5 Comments

I don't know exactly when it happened because I slept through May 1, 2012. All day.

May 2, I was able to move around a bit. May 3 a bit more but by May 4th I was feeling in the deepness of it and told my wife to dial 911 and it was into the…

Continue

Ben's Friends Co-Founder Scott Orn Featured on Thoughtbot Podcast

Posted by Armando A. on April 21, 2013 at 8:00am 0 Comments

After being featured on a number of publications,…

Continue

Events

© 2013   Created by BensFriends.org

Badges  |  Report an Issue  |  Terms of Service