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Cloverland Drugs, Inc. Sponsors  Cystic Fibrosis Foundation

While Cloverland Drugs, INC. products are geared towards healthy wieght loss supplements, they are also in the business of looking at other ways of helping great organztions like the Cystic Fibrosis Foundation that work to impove lives and literally add tomorrows to peoples futures. The Cystic Fibrosis Foundtion is  the world’s leader in the funding more CF research than any other organization, and nearly every CF drug available today was made possible because of Foundation support. Based in Bethesda, Md., the Foundation also supports and accredits a natio The CF Foundation is a donor-supported nonprofit organization. For more information, go to

Cloverland Drugs  is a company behind the brands you trust  offering supplements to help provide a healthy natural alternative to losing weight and maintaining a healthy life style.  Lipo-Vit by Cloverland Drugs, Inc. is a revolutionary “Green” weight loss solution.

Cloverland Drugs, Inc. Employee named Cincinnati’s Finest Young Professional

One of Cloverland Drugs, Inc. newest employees was recently named CIncinniat’s Finest Young Professional. Lisa Terry has worked in sales for 6 years as a National Sales Manager, yet in between her hectic schedule and promoting her company’s revolutionary Lipo-Vit , Lisa still found time to help where help is needed.

Terry was recently honored as Cincinnati’s Finest Young Professional  to further the mission of the CF Foundation. The Finale, which was held March 1, 2012, recognized Cincinnati professionals for their outstanding contribution to their community. The award was based on the following criteria:  volunteerism, leadership, and achievements in their career.

Terry embarked on 12-week fundraising campaign and raised over $21,000.00 for the Cystic Fibrosis Foundation to help support vital research and care programs.Terry explained why this cause is so near to her heart.  “My friend Abby has a 4 year old daughter, Emma, who was  diagnosed with cystic fibrosis (CF).  Emma is such a sweet child, I just had to do something.”

CF is a life-threatening genetic disease that affects the lungs and digestive systems of tens of thousands of people across the country.   When the CF Foundation was created in 1955, children with CF were not expected to see their first day of elementary school. Today, more than 40 percent of the CF population is over the age of 18.In recent years, medical science has made significant progress in understanding and treating CF.  Yet, Lisa Terry is hoping for more.   “The funding of CF research is working: it’s now making a real difference the lives of those with cystic fibrosis.   With the generous support of our community and others across the country, we can continue to add days to Abby’s life and to the lives of thousands of other wonderful children with this life-threatening disease.  With continued effort, I believe that one day in the near-future CF will also stand for ‘Cure Found!’ “

Terry is modest in assessing her contribution. “I’m just the organizer,” she shrugged.   “It’s the people and companies that attend events like ours that are the real heroes.  The funds they donate are fueling the research that will one day cure this disease that affects so many children in the U.S. and around the world.”