Comments on: Biography http://www.konzelmans.com/konzelman Just another WordPress weblog Wed, 19 May 2010 17:20:50 -0500 http://wordpress.org/?v=2.8.4 hourly 1 By: Darien Konzelman http://www.konzelmans.com/konzelman/biography/comment-page-1#comment-148 Darien Konzelman Wed, 19 May 2010 17:20:50 +0000 http://www.konzelmans.com/konzelman/?page_id=6#comment-148 Great job Derek, and Drew! I want to point out that it's a little complicated, and sometimes doesn't work right....And how do you get to every ones biographies. Great job Derek, and Drew! I want to point out that it’s a little complicated, and sometimes doesn’t work right….And how do you get to every ones biographies.

]]> By: Danielle Wheeler http://www.konzelmans.com/konzelman/biography/comment-page-1#comment-138 Danielle Wheeler Wed, 12 May 2010 02:53:48 +0000 http://www.konzelmans.com/konzelman/?page_id=6#comment-138 Hello family, I met four of your lovely sons while they were grabbing lunch at Arby's in Medford, Oregon on their way to preform in CA. I really enjoyed meeting them and appreciated the eldest sharing your story. We have 5 children and I was there with my youngest daughter. I do not know if you ever do any fundraising events but was wondering if you lower your fees at all. I also have thought of ways to lower expenses. We have very dear friends of ours that have 3 children. Two of the 3 children have an extremely rare digenerative desease that results in death by ones late teens. They are (along with other families) part of a group of non-profit organizations that are raising funds for research. Please view their site www.hadleyhope.com There are only 500 children in the world with this desease so it is nearly impossible to get any government funding. I ask that you pray for this family and pray over whether you might want to discuss a possible future event. (There is the possibility of doing multiple shows throughout the US for this as well.) One of the families also affected by this desease has their only two children (twin daughters) suffering from this. The mother has a PR background in Reno, NV and could be a huge help in organizing a multi-tour event. Their site is www.addiandcassi.com Thank you again for your prayers and consideration. Sincerely, Danielle Wheeler P.S. continued success to all of you. Hello family, I met four of your lovely sons while they were grabbing lunch at Arby’s in Medford, Oregon on their way to preform in CA. I really enjoyed meeting them and appreciated the eldest sharing your story. We have 5 children and I was there with my youngest daughter.

I do not know if you ever do any fundraising events but was wondering if you lower your fees at all. I also have thought of ways to lower expenses. We have very dear friends of ours that have 3 children. Two of the 3 children have an extremely rare digenerative desease that results in death by ones late teens. They are (along with other families) part of a group of non-profit organizations that are raising funds for research. Please view their site http://www.hadleyhope.com There are only 500 children in the world with this desease so it is nearly impossible to get any government funding. I ask that you pray for this family and pray over whether you might want to discuss a possible future event. (There is the possibility of doing multiple shows throughout the US for this as well.) One of the families also affected by this desease has their only two children (twin daughters) suffering from this. The mother has a PR background in Reno, NV and could be a huge help in organizing a multi-tour event. Their site is http://www.addiandcassi.com Thank you again for your prayers and consideration. Sincerely, Danielle Wheeler
P.S. continued success to all of you.

]]>