Fall 2007 Newsletter  (Click Site Map to view older newsletters) 

The Heart of It Newsletter Fall 2007 - In this Issue:
Make the Holidays a Time of Renewal
From Our Director
Family Voices of Vermont: SCHIP
Partners In Care Conference!
Thanks

Our Calendar | News & Note 

Make the Holidays a Time of Renewal

    As a child, I loved the holidays, especially the established traditions. We decorated a live tree while listening to holiday music and watched Charlie Brown find the true meaning of Christmas. Rudolph was my favorite, evoking tears every year – a little bullied reindeer who persevered despite his differences. On Christmas Eve we lit the candles that would propel the Swedish angels around, ringing the tin bells as they went. We stayed up late playing board games and pondering what might be under the tree in the morning.
Wechsler Family   As the years rolled by, I grew up, went to college and got married. My husband David  and I melded our families, religions and traditions. We would stress when we couldn’t live up to expectations, but we managed well enough. Holidays were another issue. Overburdening ourselves, we would spend too much money on too many gifts and run ragged until we collapsed. We were experiencing holiday stress.
   When our son Adam turned three, he was diagnosed with Duchenne muscular dystrophy and our lives changed forever. Now, as parents of a child with a neuromuscular disorder, we discovered real anxiety and intense stress. We were thrust into the disability world, filled with medical specialists and a quagmire of disjointed services that were difficult to understand, let alone navigate.
   To compound the stress, I also was grieving the loss of my mother, who only months earlier had succumbed to breast cancer. Our siblings spread across the country were busy with their healthy children. They didn’t know how to support us and we didn’t know how to ask for the help we needed. Devastated and scared, we turned to the Muscular Dystrophy Aassociation, which put us in contact with other parents who knew what we were going through, having walked this road themselves.
   We were exhausted and stressed from the medical and school challenges of raising a child with special needs. Just anticipating the flurry of activity with the holidays approaching would send me into stress overload. David and I decided it was time to examine our physical limitations and to modify our emotional expectations. What was our goal, after all? Mine, I decided, was simply to create a fun and relaxed holiday experience my children would recall for years to come.
   I started by simplifying decorations, holiday cards, meals and gift giving, and by making a list and sticking with a budget. I also would avoid all non-essential medical appointments and school meetings that might be stressful. I would stock up on peer support, and make time for my personal stress busters, such as walking the dogs or reading a book.
   To modify expectations, we had to be creative and be open to what flowed. I learned to appreciate that, while some relatives were supportive, others were limited in understanding parenting a child with a progressive muscle disease. I learned to be empathetic – they have holiday stress too – and to be grateful for each family member. The challenges they might offer created an opportunity to practice communication skills.
Jacob and Adam   I also resolved to stay focused on the positive things from the year, with a bent toward educating in a non-threatening, nonjudgmental way. For example, I might say, “Despite the problems advocating for school services, Adam had a great year, getting all A’s,” or “I did this really fun Walk-a-Thon. Maybe next year you’d like to join our team.” My goal became to forgive, educate and get them on board.
   Last year, for the first time in several years, we decided not to travel to visit family for the holidays. Although disappointed at first, Adam and his brother Jacob quickly embraced the decision. We hoped family would understand, but even if they didn’t, we decided celebrating at home was best for our mental health.
   We created new traditions, celebrated in intimate ways, and rested and relaxed as a family, something we don’t do often enough during the year. We lit the menorah and made latkes, decorated our tree while listening to holiday music and, as usual, I cried when Rudolph ran away from home, despondent at being ostracized for his differences. After the last candle of the Swedish angels burned, we played Monopoly and baked cookies for the anticipated “visitor” that night.
   On Christmas morning the boys lingered in their pajamas until noon, ate Daddy’s homemade waffles for brunch and assembled new toys together until dark. When they declared it was the best holiday ever, we knew we’d made the right decision
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Fall 2007 - In this Issue:
Make the Holidays a Time of Renewal
From Our Director
Family Voices of Vermont: SCHIP
Partners In Care Conference!
Thanks
Our Calendar | News & Note

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