Guest guest Posted September 4, 2008 Report Share Posted September 4, 2008 Hi All, Last week I passed on some information about grants possible to go to the conference. I went in to fill out the grant today and they are no longer taking applications. They said they had over 500,000 request. I just thought I would pass that info along to all of you. Sue Subject: IMDSA Conference 2009 To: mosaicds Date: Wednesday, September 3, 2008, 5:27 PM Hello IMDSA Families! I’m Rowe and the Family Assistance Coordinator for the 2009 Conference being held in Cincinnati, OH July 10-12, 2009 . I volunteered for the job because I want to help as many families get to the conference as I can. First of all, for those of you who do not know me, I’m a single Mom to two great boys, Trey age 8 with ADHD and Austin age 5 with MDS. I had no prior knowledge of Austin’s MDS or even DS before his birth. There were no signs from sonograms and I was too young to have an amnio done. So when Austin came at 36 weeks, weighing in at just 5 pounds 2 ounces and 18 inches long (after only 3 hours of labor!) it was a shock to my then husband and me of the diagnosis of Down syndrome. From that time until the spring of 2007 I had always thought Austin had a “milder” or “lighter” form of DS not knowing at all about mosaicism. In the spring of 2007 I was a full time college student taking an English class and was required to do a research paper. I did it on Down syndrome and thus found out about Mosaic DS and IMDSA. I became a member and went to the conference in Richmond, VA (we live near Lexington, VA) in the summer of 2007 and it was there that I had Austin tested for MDS and to an accuracy of 96% Austin has MDS. I have been involved with IMDSA ever since and even though I’m raising two boys alone, and a part time college student (studying for my Nursing degree), I try to help out any way I can. So when the opportunity to help with next year’s conference presented itself I jumped on board. My job is to help families get to the conference by any financial means possible. There are local and long distance organizations, grants, and corporations willing and able to donate money for this cause and it’s my job to contact them on your behalf. I will be the sole contact person between them and you (and of course IMDSA’s Board of Directors and committee chairpersons for the conference), all you have to do is say; “YES WE WANT TO COME!!!” Please send me an email at becky@... with the following information.. 1. Name of Family (initial contact first/last name) 2. Number of Family members attending conference (and ages) 3. Name of Family Member with DS/MDS (and age) 4. Email & physical addresses, phone number(s). That’s all…I do the rest for you (how easy is that?!) I know some or most of you are thinking this is charity or a handout, please don’t think that, for that is not what it is. A lot of clubs (such as Lions, Rotary, Kiwanis, etc), corporations, have money set aside for non profit organizations such as IMDSA and are willing to give us their money! All I have to do is ask for it (on yours and IMDSA’s behalf of course!) All you have to do is let me know that you and your family want to come to the Conference it is that simple I promise. Please note that there are no guarantees that each family will get this assistance, however, this is the first step in attempting to receive the assistance. Please feel free to contact me at anytime should you have any questions, God Bless, Family Assistance Coordinator International Mosaic Down Syndrome Association (home) (cell) Blessings Abound, (Becky) Rowe Mom to Trey (8 ADHD) & Austin (5 MDS) ________________________________ Family Assistance Coordinator www.imdsa.org or becky@... Help Team Austin @: http://teambrats08.chipin.com/team-austin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2008 Report Share Posted September 4, 2008 Thanks Sue, I had saved that information to look into further. Thanks for the update! G'night ya'll!!! Blessings Abound, (Becky) Rowe Mom to Trey (8 ADHD) & Austin (5 MDS) ________________________________ Family Assistance Coordinator www.imdsa.org or becky@... Help Team Austin @: http://teambrats08.chipin.com/team-austin IMDSA Conference 2009 To: mosaicds Date: Wednesday, September 3, 2008, 5:27 PM Hello IMDSA Families! I’m Rowe and the Family Assistance Coordinator for the 2009 Conference being held in Cincinnati, OH July 10-12, 2009 . I volunteered for the job because I want to help as many families get to the conference as I can. First of all, for those of you who do not know me, I’m a single Mom to two great boys, Trey age 8 with ADHD and Austin age 5 with MDS. I had no prior knowledge of Austin’s MDS or even DS before his birth. There were no signs from sonograms and I was too young to have an amnio done. So when Austin came at 36 weeks, weighing in at just 5 pounds 2 ounces and 18 inches long (after only 3 hours of labor!) it was a shock to my then husband and me of the diagnosis of Down syndrome. From that time until the spring of 2007 I had always thought Austin had a “milder” or “lighter” form of DS not knowing at all about mosaicism. In the spring of 2007 I was a full time college student taking an English class and was required to do a research paper. I did it on Down syndrome and thus found out about Mosaic DS and IMDSA. I became a member and went to the conference in Richmond, VA (we live near Lexington, VA) in the summer of 2007 and it was there that I had Austin tested for MDS and to an accuracy of 96% Austin has MDS. I have been involved with IMDSA ever since and even though I’m raising two boys alone, and a part time college student (studying for my Nursing degree), I try to help out any way I can. So when the opportunity to help with next year’s conference presented itself I jumped on board. My job is to help families get to the conference by any financial means possible. There are local and long distance organizations, grants, and corporations willing and able to donate money for this cause and it’s my job to contact them on your behalf. I will be the sole contact person between them and you (and of course IMDSA’s Board of Directors and committee chairpersons for the conference), all you have to do is say; “YES WE WANT TO COME!!!” Please send me an email at becky@... with the following information.. 1. Name of Family (initial contact first/last name) 2. Number of Family members attending conference (and ages) 3. Name of Family Member with DS/MDS (and age) 4. Email & physical addresses, phone number(s). That’s all…I do the rest for you (how easy is that?!) I know some or most of you are thinking this is charity or a handout, please don’t think that, for that is not what it is. A lot of clubs (such as Lions, Rotary, Kiwanis, etc), corporations, have money set aside for non profit organizations such as IMDSA and are willing to give us their money! All I have to do is ask for it (on yours and IMDSA’s behalf of course!) All you have to do is let me know that you and your family want to come to the Conference it is that simple I promise. Please note that there are no guarantees that each family will get this assistance, however, this is the first step in attempting to receive the assistance. Please feel free to contact me at anytime should you have any questions, God Bless, Family Assistance Coordinator International Mosaic Down Syndrome Association (home) (cell) Blessings Abound, (Becky) Rowe Mom to Trey (8 ADHD) & Austin (5 MDS) ________________________________ Family Assistance Coordinator www.imdsa.org or becky@... Help Team Austin @: http://teambrats08.chipin.com/team-austin Quote Link to comment Share on other sites More sharing options...
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