Medieval Maidens will be participating as one of the many vendors at the 2012 Amazing Baby and Child Expo from 11am-4pm on Saturday August 18th in Sykesville, Maryland.

Admission is free, though all attendees are encouraged to bring a can of food for charity.

Our stand will be manned by author and Medieval Maidens creator, Lois Jarman. Stop by, say hi, and learn more about Medieval Maidens and our line of history books, dolls, and accessories.

We hope to see you there!

*All information can be found in the flyer above. Click the thumbnail to enlarge the image.

Our Medieval Maidens online store carries books detailing the lives of Gisela, Adele, Isabelle, Gevrehan, and Mary, who all lived during the Middle Ages and, in Mary’s case, the Renaissance. We also have the Gisela doll for sale as well as Medieval outfits for any 18-inch doll. Purchases can be made via PayPal or by filling out and emailing or snail-mailing our online order form. www.medievalmaidens.net/onlinestore.html

Amazon.com and Amazon.co.uk carry Gisela’s Story and Gisela’s Holiday Story.
www.amazon.com
www.amazon.co.uk

No matter what you purchase or from where, 20% of your money will be donated to CFF.

In July, Medieval Maidens will announce the total amount make the donation over to CFF.

Here’s some information on Cistic Fibrosis from the CFF website

Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that:

• clogs the lungs and leads to life-threatening lung infections; and
• obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food.

In the 1950s, few children with cystic fibrosis lived to attend elementary school. Today, advances in research and medical treatments have further enhanced and extended life for children and adults with CF. Many people with the disease can now expect to live into their 30s, 40s and beyond.

People with CF can have a variety of symptoms, including:

• very salty-tasting skin;
• persistent coughing, at times with phlegm;
• frequent lung infections;
• wheezing or shortness of breath;
• poor growth/weight gain in spite of a good appetite; and
• frequent greasy, bulky stools or difficulty in bowel movements.

About 1,000 new cases of cystic fibrosis are diagnosed each year.

More than 70% of patients are diagnosed by age two.

More than 45% of the CF patient population is age 18 or older.

The predicted median age of survival for a person with CF is in the late 30s.

Since 1955, the Cystic Fibrosis Foundation has been the driving force behind the pursuit of a cure. Thanks to the dedication and financial backing of our supporters — patients, families and friends, clinicians, researchers, volunteers, individual donors, corporations and staff, we are making a difference.

For more information, visit:
http://www.cff.org
http://www.medievalmaidens.net

Thank you for your support. Together, let’s make a difference.