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1 T. pickled mango 1 tsp. fenugreek 1 tsp. fresh thyme 2 cups heavy whipping cream cup Marsala Directions: Melt butter in a heavy, large pot over medium/high heat. Add leeks and garlic and saute until caramelized, about 15 minutes. Add carrots and parsnips and cook 10 minutes.
Add vegetable stock, potatoes, parsley, turmeric, pickled mango, fenugreek and thyme. Cover and simmer until potatoes are tender. Puree half of soup in a processor. Mix puree into remaining soup in pot. Fold in heavy whipping cream and marsala. Season to taste with salt and pepper. Bring soup to simmer, thinning with additional broth, if desired. Ladle into bowls and serve.
Participating restaurants in the County Cuisine feature include Arts Tavern, blu, The Bluebird, Cedar Rustic Inn, Debs Dish, Empire Village Inn, Joes Friendly Tavern, The Manor on Glen Lake, Marthas Leelanau.
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We Finally Caught Our Limit, 'Time To Get Back To Work.' Re-Opening Friday, Feb. 17th
A mother and daughter will be traveling to New York City this month to raise awareness about a rare disease which has touched their family. Jodi Wolfe and her mother, Karol Haring of Lake Leelanau, will be in New York Friday, Feb. 24, and Saturday, Feb. 25, in preparation for Rare Disease Day on Wednesday, Feb. 29. The group will be outside the Today Show and Good Morning America, Friday and Saturday respectively, holding up signs featuring patients ghting the rare disease and others who have been lost to the disease. Jodi Wolfes son, Nate, was 5 when he was diagnosed with Langerhans Cell Histiocytosis, a disorder in which excess immune system cells build up in the body, causing tumors. Nate was taken to the doctor after complaining of knee pain. Further investigation showed that a tumor was growing on his hip, causing it to break. Its an orphan disease. This means there is no government funding to nd a cure, Wolfe said. So rare, in fact, that physicians at DeVos Childrens Hospital in Grand Rapids had not encountered it before and conferred with their counterparts in Europe before charting a course of treatment. Similar to treatment for those with
JODI WOLFE and Karol Haring of Lake Leelanau will carry signs bearing this picture of son/grandson Nathan Wolfe in New York City, Feb. 24 and 25 to increase awareness about his rare illness.
cancer, the little boy had 10 weeks of chemotherapy and radiation and hasnt looked back. I dont remember too much about it, he said. Now an eighth grader at Traverse City West Middle School, Nate is approaching his seventh year of remission. He enjoys science class and drawing and looks forward to taking hunter safety this year. Jodi Wolfe cant forget how hopeless she felt after receiving the initial diagnosis. There was little or no information. I felt so alone, she said. However, the growth of Facebook has helped her make contact with families throughout the U.S. facing the disease. Families of LCH (www.families of LCH.net) includes 35 families in Michigan impacted by the disease.