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  FASD no obstacle for German horse riderBy Dawn Gelhart 
              
                | Sinja Gibson's accomplishments 
                  gives proof of what hard work and a loving family can accomplish. 
                  Iceberg readers may remember Sinja, a teenager with FASD, from 
                  the poem Sit 
                  and Watch written by her mother Ann Gibson, and published 
                  here four years ago. Many of you might also remember the tragic 
                  loss 
                  of her mother a year later. A few months ago Sinja's dad 
                  wrote me of Sinja's summer plans. Of course, I had to ask if 
                  they would be willing to write an article for Iceberg. Sinja's 
                  sister, Dawn Gelhart, took on the project so that you too may 
                  read about Sinja's triumph. Lastly, I have to add that I, too, 
                  believe Ann will be looking down on Sinja's race saying, "Wow, 
                  what a ride!" 
 -- Katy Jo Vasbinder, 
                  Iceberg board member
 |   Riding for Germany, Sinja Gibson will compete in the equestrian 
              events at the Special Olympics World Summer Games 2007 in Shanghai, 
              China. Held October 2-11, 2007, more than 7,500 athletes will compete 
              in 25 sports. Hamburg 2004 and Berlin 2006: 2 exciting cities, 1 fantastic event, 
              1,000 emotions – THE SPECIAL OLYMPICS! Our sister Sinja had 
              the great honour to participate as a rider in those competitions. 
              Hamburg, when she was 15 years old, was her first meeting with the 
              Special Olympics, and then two years later she was in Berlin. We 
              were so excited and proud of her. In Berlin, the big opening ceremony – with many V.I.P.’s, 
              dance and music – was the appropriate start for the wonderful 
              event. Hundreds of athletes from all parts of Germany, as well as 
              other European countries, filled the hall one after the other. In 
              the arena and in the audience you could see beaming, happy and proud 
              faces. And then the big moment: The Olympic fire was carried into 
              the hall. There was an enthusiastic cheer as it was lighted and 
              the Olympic thought was expressed, "Let me win. But if I cannot 
              win, let me be brave in the attempt." 
 Sinja and her family (Sinja is 4th from 
              the right) Sinja's participation at the games was an unbelievable success. 
              In both Hamburg and Berlin she won Gold in all her disciplines; 
              in addition, in Hamburg she had to ride out of concurrence as nobody 
              was in her class, and in Berlin she even scored 9.0 points in dressage.
 We watched as our Sinja, who could hardly read and write, stood 
              there, with a gold medal around her neck and a #1 below her. We 
              cannot fully explain how proud we were and how many tears of happiness 
              we shed.
 
 It was Sinja's 18th birthday during the Berlin games, and 2,000 
              people sang happy birthday to her at the ceremony. Afterwards, she 
              even had to sign many autographs. Who could imagine this was real? 
              At last she got the tribute she deserved for her achievements. Nobody 
              asked what was wrong with her, nobody stared at her. Here she was 
              Sinja, how she wanted to be, and it felt really good.
 Of course, we were especially happy and proud because Sinja won 
              in her competitions. But even if she had been in last place, the 
              memories would be just as good because she had the chance to shine, 
              make many friendships, and even to meet her first love at the Special 
              Olympics. All over the place we could feel the atmosphere, and often 
              those who hadn't won were just as happy as those who had. After 
              the presentation of the medals everybody – disabled or not 
              – waved their hands in the air and sang "We Will Win" 
              with all their hearts. At the Special Olympics it doesn't matter 
              whether you are physically or intellectually disabled, the only 
              thing that counts is who you are and how much fun you have. All that is left for us to say is that the Special Olympics will 
              stay in our hearts forever, and we are very proud that Sinja was 
              nominated for the German equestrian team participate at the 2007 
              World Summer Games in Shanghai. Most of her family will join her 
              as she travels around halfway across the earth to compete with other 
              riders.  We are so proud of Sinja. And we are sure that her Mum will watch 
              over her from heaven and make sure those will be special games for 
              special people from all over the world. return to top
 
 
 RECOVERING HOPE Mothers speak out about Fetal Alcohol Spectrum DisordersBy Marceil 
              Ten Eyck The DVD Recovering Hope was created about three years 
              ago by a team comprised of videographers and birth mothers of children 
              impacted by Fetal Alcohol Spectrum Disorders. The project was sponsored 
              by SAMHSA’S FASD Center for Excellence, and I think the film’s 
              approach not only educates, but also illustrates both the public 
              and personal evolution of attitudes toward mothers who drank during 
              pregnancy. I was afraid to announce that I was one of THOSE moms who drank 
              while I was pregnant because of my shame and guilt, and the anger 
              of others toward drinking moms made it much worse. But, I knew if 
              I did not share my feelings and experiences, I would not be able 
              to heal and be a positive parent.  Being approached to contribute to the Recovering Hope 
              project revived so much of my emotional history. I thought back 
              to the time when I was first in recovery and how challenging that 
              was. Then later I had to face the fact that I had caused both my 
              daughters, one diagnosed with full FAS, the other with FASD, to 
              have irreparable organic brain damage.  Because of the guilt and shame I felt when I found out that drinking 
              while I was pregnant had harmed my daughters (I had already been 
              sober for ten years at the time), I believed it was not helpful 
              to allow women in early recovery to face this horror. I thought 
              it might cause a mom to relapse, or, at the very least, to make 
              her recovery more difficult.  So, when asked to be part of a network of recovering birth moms 
              and to work on this video, I had mixed feelings. Should this information 
              be part of a woman’s early treatment and recovery? After accessing 
              my 12-step program of recovery, and realizing that I was trying 
              to control the uncontrollable, I began to understand how important 
              it would be to a family’s recovery to have information about 
              FASD, and to know how to find resources for help. Being part of the development team for this DVD was amazing. Individually, 
              the mothers had wonderful ideas, and, as a group shared experiences, 
              we were able to respect each other and work as a well-oiled team. 
              The director talked with each mom separately, asking each of us 
              what we thought should be part of the video. Then, during the process 
              of outlining the script, filming, editing and re-editing, we were 
              included in conference calls that allowed us to make corrections 
              and give fresh ideas as needed. Given that each of us is pretty 
              talkative, it speaks much about his abilities that he was able to 
              single out the important points. We were all thrilled with the finished 
              product, as it included everything we had wanted. Another important aspect of the video was that the director and 
              his team came to our homes to film. This allowed them to meet us 
              and see for themselves who we were as individuals and families, 
              not just alcoholics. For example, they happened to be in town when 
              JulieGelo was having a birthday party for one of her children impacted 
              by FASD, so the support group parents and their children were there 
              for the filming as well. When they came to our home, both my daughters 
              were there. We invited them for lunch; they joined us, and got to 
              know us as a family. This, I think, is reflected in the comfortable 
              feel of the video. Although there are families from all over the country represented 
              in this video, it was exciting for us here in Washington state that 
              many of our esteemed helpers and professionals are also a part of 
              this video. With clarity and empathy, they give information about 
              FASD, and how difficult it is to be a mom in recovery. Has this video helped to diminish anger at addicted mothers who 
              drink while they are pregnant? My brother, Tom Ten Eyck, teaches 
              addiction classes at Lewis and Clark University in Portland, Oregon. 
              He has been showing this video in some of his classes for a couple 
              of years. He told me that many of the students react to the video 
              with extreme anger….”How could any woman drink while 
              she was pregnant when she knows she might harm her child?” 
              Tom said that a lengthy discussion often follows, enabling the students 
              in the class who are not addicted to begin to get an understanding 
              of the power of addiction. He believes that the video has helped 
              some students to get in touch with their anger, to verbalize it, 
              and hopefully to begin to pass through the anger to understanding. I believe this video/dvd is a valuable addition to the resources 
              available about FASD, and it is the first available that focuses 
              on how birthmothers can incorporate their recovery with positive 
              parenting skills if their child has FASD. 
 To order free copies of the DVD, visit SAMHSA’s FASD 
              Center Web site, the database for resources, journals and information 
              about FASD.
 return to top
 
 
 Alcohol and drug hotline extends beyond 
              the phone lineBy Ann Forbes The Washington State Alcohol and 
              Drug Hotline (ADHL) started as a bare-bones operation called 
              the Alcohol Help Line 28 years ago, and has evolved considerably 
              since.  Like many of the hotline’s original volunteers, I had done 
              hours of volunteer, and later paid, phone work for Dial-a-Bottle, 
              a program funded to answer calls from those wanting resources and 
              treatment information for alcohol problems in King County, Washington. 
             When Dial-a-Bottle closed in February of 1979, I moved to the Fetal 
              Alcohol Syndrome program at the University of Washington in Seattle 
              to do phone work and training for their “5-Health Line.” 
              Helping on the FAS line was a wonderful learning experience for 
              me as a former health teacher and alcohol counselor. Though I left 
              the FAS line after a few months to start the Alcohol Help Line, 
              that experience has certainly had us incorporate a good deal of 
              training around pregnancy and alcohol/drug usage so that our many 
              volunteers can inform the appropriate callers. When we started the Help Line in 1979, we had a card table, one 
              phone line and no chairs, along with a dedicated board of directors 
              and a cadre of trained volunteers from the Dial-a-Bottle program. 
              Board members laugh now and talk about having to bring their own 
              folding chairs so they could sit during meetings. Since our grant 
              from the county was fairly small, we needed to prove our worth by 
              our call volume. We took turns having the phones transferred to 
              our homes at night, and then the first hiring we did was to retain 
              night personnel. In our 28 years of operation, we are proud that every caller has 
              connected with a live person rather than automated help. We became 
              a statewide resource with our 1-800-562-1240 number in 1982. In 
              1984, we added a generic line to maintain current information about 
              support groups and meeting times. In 1986, the county ombudsman 
              asked to include us on the jail’s speed dial to provide resource 
              information to inmates. We did this for two years, and our number 
              of callers increased by 30,000, clearly showing a need. But, since 
              there was no funding for this service and the jail’s high 
              call volume put an extreme burden on our phone volunteers and staff, 
              we very sadly had to cut this service.  In 1998, ADHL assumed the Clearinghouse contract to mail free brochures, 
              posters, videos, booklets and other printed drugs and alcohol information 
              (in a variety of languages) to those who request it. The Clearinghouse 
              distributes information at conferences, health fairs and trainings 
              across the state of Washington, and the materials and a lending 
              library are also available online at http://clearinghouse.adhl.org. 
             We now also offer an active Teen Line staffed by students from 
              the local high schools. They are all trained about adolescent resources, 
              and do some of their work via email as more teens find them on the 
              Internet. For the past three years the teens have furnished weekend 
              breakfasts for a teen shelter, preparing interesting breakfasts 
              that are healthy and fun.  Lately ADHL has been involved with Spotlight on Recovery. This 
              project aims to decrease the stigma of addiction, and provide opportunities 
              for those in recovery to be more visible role models for others. 
              Spotlight on Recovery 
              also partnered with Fairfax Hospital and the Seattle Parks Department 
              to establish a recovery garden in the White Center area of Seattle. 
             ADHL staff members are also heavily involved in outreach, joining 
              many committees in the state to promote awareness, address counselor 
              concerns and women’s issues, and assist with training and 
              educational requirements. In the area of domestic violence, we offer 
              a free group to shelters to teach women about addiction and alcoholism 
              and allow them to seek counseling while in a safe environment. We 
              bridged these two systems in 1994 and have had much success. We have also had the privilege of working with so many dedicated 
              volunteers since our conception – including one that for 16 
              years served as the Sunday afternoon phone worker. While ADHL asks 
              each volunteer for a year’s commitment following 80 hours 
              of training, we average a 3-year stint from the volunteers. We train 
              in resources, crisis work, listening skills and support groups, 
              and take them on treatment visits. Over the years, we have trained 
              more than 850 volunteers, and many are now working throughout the 
              state in a wide variety of roles. With all this success, we continue to look forward, even as we 
              look back. ADHL’s current Web initiative is “The Evolution 
              of Chemical Dependency Treatment and Services in Washington State,” 
              highlighting interviews and stories by early pioneers in substance 
              abuse treatment. The completed project will include filmed interviews, 
              timeframes and archived information mined from magazine articles 
              and other resources. Many interviews will be posted to the site, 
              including talks with Iceberg board members Marceil Ten 
              Eyck and Dr. Ann Streissguth.  Looking at the progress of substance abuse awareness and treatment 
              in our state – and within our organization – illustrates 
              the commitment and intelligence so many individuals have brought 
              to this issue. ADHL is pleased to have contributed to this progress.  Ann Forbes is the executive director of the Alcohol 
              & Drug Hotline. return to top
 
 
 A new service opens in Seattle to assess 
              for FASD in adults and late adolescentsBy Dr. Paul 
              Connor, Ph.D. For more than 11 years I have been involved in research at the 
              University of Washington’s Fetal Alcohol and Drug Unit (FADU) 
              in Seattle. I have served as project director, co-investigator and 
              principal investigator on several research grants within our unit. 
              I advanced up the faculty ladder to assistant professor in the UW’s 
              Department of Psychiatry and Behavioral Sciences and was named the 
              clinical director of FADU.  In 2006, Janet Huggins and I opened an adult neuropsychological 
              assessment service at the University of Washington’s Outpatient 
              Psychiatry Clinic, also featured in Iceberg (September 
              2006). The clinic was well received, we had many referrals and 
              we were able to see many individuals with known or suspected FASD. 
              We were happy with the services we provided and felt that we were 
              making a valuable contribution. However, operating a clinic within 
              the complex network of a university system turned out to be an extremely 
              complicated procedure, and in the end it became too difficult to 
              maintain. So, as 2006 drew to an end, we made the difficult decision 
              to close the clinic. At this same juncture in time, the grants that I had been working 
              on were ending and I found myself looking for some new challenges. 
              I knew I wanted to both continue working at the University of Washington 
              and in the field of FASD, but also felt the need to branch out. 
              With the closing of the assessment clinic and my belief that its 
              services were still needed, I decided to continue my work through 
              private practice. So, with the assistance of the chairman of my 
              department at the UW, early this year I obtained approval to both 
              work at the university and open a private practice providing adult 
              neuropsychological assessments. My practice is located in Des Moines, Washington, in an office 
              I share with three other psychologists and a social worker. In my 
              private practice I offer adults (16 years and over) a comprehensive 
              neuropsychological evaluation designed to assess cognitive function, 
              mental health status and adaptive behavior. I specialize in neuropsychological 
              assessments for traumatic brain injury (TBI), memory impairment, 
              stroke, dementia, cognitive deficits, learning disabilities, attention 
              deficits and FASD.  How is my service unique? There are many very good diagnostic clinics 
              around the country. They are very well equipped to assess and diagnose 
              FASD in children and early adolescents; however, these clinics are 
              often not as well equipped to assess late adolescents and adults. 
              Thus, the former UW clinic and my current practice fill an important 
              gap in the diagnosis of individuals with FASD. Many are not diagnosed 
              as children and live much of their lives not knowing that the cognitive 
              and behavioral difficulties they suffer from may be related to prenatal 
              alcohol exposure. As with the former UW clinic, the testing battery I use was developed 
              based on the many years of research on FASD conducted at the University 
              of Washington’s FADU. It measures intellectual functioning, 
              academic achievement, learning and memory, motor coordination, attention 
              and executive functioning. Additionally, I measure the person’s 
              adaptive functioning and screen for mental health concerns. From 
              this information, and information about prenatal alcohol exposure, 
              I am able to make an informed diagnosis of Alcohol Related Neurodevelopmental 
              Disorder (ARND), if appropriate, and make recommendations on services 
              that may be beneficial including state Division of Developmental 
              Disabilities (DDD), Supplemental Security Income (SSI), and the 
              Division of Vocational Rehabilitation (DVR).  The testing usually involves two visits to my office. During the 
              first visit, I do an interview with the person and their parent, 
              caretaker or other loved one, and then do about four hours of individual 
              testing. On the second visit, usually a couple of weeks later, we 
              meet again to talk about the results and recommendations. I can accept referrals from many sources including community providers, 
              doctors or the justice system. Referrals can also come from parents 
              and loved ones, and clients may also self-refer. Clients do not 
              have to live locally, and I have received referrals from around 
              the country to come to my offices and participate in this assessment. 
              One benefit of the private practice is that the wait time between 
              referral and the first visit can be very short. Although I do not 
              bill insurance companies for the service, clients can seek reimbursement 
              from their insurer directly.  For more information about these services, please contact me at 
              206-940-1106, download my brochure 
              , or visit my Web site at www.connorneuropsychology.com. 
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