Society – Mov Soc Fri, 11 Jun 2021 18:39:04 +0000 en-US hourly 1 Society – Mov Soc 32 32 Herbalife Nutrition Education Scholarships awarded by the American Society for Nutrition and the Academy of Nutrition and Dietetics Fri, 11 Jun 2021 18:27:00 +0000

LOS ANGELES–(COMMERCIAL THREAD) – Herbalife Nutrition, a leading global nutrition company, in partnership with leading professional nutrition and dietetic organizations, the American Society of Nutrition (ASN) and the Nutrition education for the public (NEP), a dietetic practice group of the Academy of Nutrition and Dietetics, has awarded its annual scholarships to support the research, education and / or clinical training of promising students passionate about nutrition and intending to become a registered dietitian (RD).

“Dietitians are at the forefront of teaching Americans the principles of healthy eating and how to use nutrition to achieve their health goals and we are proud to support them on their educational journey,” said Dr. Kent Bradley , director of health and nutrition at Herbalife Nutrition.

Now in its third year, the $ 5,000 Herbalife Nutrition Fellowship is awarded by ASN to Registered Dietitians (RDs) or those intending to become dietitians, and was awarded this year to Mr. Alan Dawson, MS, RD, CSSD, LD, from Florida State University.

ASN is the first national scientific society dedicated to the advancement of research in nutrition and its clinical applications. Each year, the ASN Foundation distributes nearly $ 100,000 in prizes, travel grants and scholarships to students and young researchers to support their academic efforts. The ASN Foundation strengthens the Company’s efforts by fostering the development of the next generation of nutrition scientists and practitioners.

The scholarships awarded through the NEP, a dietetic practice group of the Academy of Nutrition and Dietetics, were three $ 1,000 scholarships in 2020 and 2021 to support student research and / or dietetic education training at promising students enrolled in an accredited dietetics program at the junior or graduate level. The NEP scholarship recipients included Kayla Parsons and Leigh Neptune, both from the University of Maine, while the third recipient will be named in the fall of 2021.

In addition to the financial support given to each scholar, they will each receive an all-expense paid trip to Herbalife Nutrition headquarters in Los Angeles, California at a later date.

About the American Nutrition Society

The American Society for Nutrition (ASN) is the premier professional organization for nutrition researchers and clinicians around the world. Founded in 1928, the company brings together the best nutrition researchers, physicians, policy makers and industry leaders to advance our knowledge and applications of nutrition. ASN publishes four peer-reviewed journals and offers training and professional development opportunities to advance research, practice and education in nutrition.

About NEP

Nutrition Education for the Public is a dietetic practice group of the Academy of Nutrition and Dietetics. NEP provides services to over 900 members who are committed to helping individuals understand and use vital nutritional information. The NEP has set itself the overarching goal of improving the communication and teaching skills of its members.

About Herbalife Nutrition Ltd.

Herbalife Nutrition (NYSE: HLF) is a global company that has changed people’s lives with great nutrition products and a proven business opportunity for its independent distributors since 1980. The company has been delivering high quality products backed by science , sold in over 90 countries. by entrepreneurial distributors who offer one-on-one coaching and a supportive community that inspires their clients to adopt a healthier and more active lifestyle. Through the company’s global campaign to end hunger, Herbalife Nutrition is also committed to bringing nutrition and education to communities around the world.

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Arab universities stifle research and failing society, scientist says Fri, 11 Jun 2021 06:53:02 +0000

Faced with the drop in funding, researchers are forced to orient their projects towards what can be described as attractive themes.

The problem is exacerbated by the lack of regulatory frameworks and a culture that hinders opportunities for cooperation; each researcher works according to his own vision, or according to the orientations of senior professors. Some may justify this by fear of overlapping specializations or the tyranny of one field over another.

The result is the absence of the “research team” as an effective concept in universities and research centers.

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Personally, I think this has led to a drop in patent applications and the failure of universities to support entrepreneurship and to cooperate with industry in order to contribute to development plans. Most Arab universities show an institutional failure to develop the visions of researchers and their methodological tools and to improve the working environment.

How can we overcome all of this?

I believe, first of all, that a new academic culture is necessary to support young researchers and women in particular and thus help to create an environment which encourages the introduction of innovative ideas without restriction or stereotype. In addition, donors should be encouraged to fund all disciplines and subjects in order to produce a balance between different fields and to contribute to real, ongoing and well-established activities that use research to develop societies.

Amal Amin is Assistant Professor of Nanotechnology at the Egyptian National Research Center and founder of Women in Science Without Borders Initiative. See a recent profile of her in Al-Fanar media here: “Amal Amin: An Egyptian Scholar Seeks Equity for All in Research and Science”.

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PatientsLikeMe Partners with Huntington’s Disease Society of America to Create Integrated Online Community for Patients and Caregivers Thu, 10 Jun 2021 13:00:00 +0000

BOSTON–(COMMERCIAL THREAD) – The world’s largest integrated community, health management and real data platform, PatientsLikeMe (PLM) today announced its partnership with the Huntington’s Disease Society of America to launch a virtual community for people living with Huntington’s disease (HD) and for those caring for people living with HD. This tailor-made community will focus on education and knowledge sharing among peers. This community will serve as a catalyst to expand researchers’ knowledge of the disease through analysis of patient-generated data. This collaboration will support patients and families struggling with HD and allow them to make their voices heard, to learn from others who have had the same experiences as them and to accelerate the development of treatments and cures through the participation in research. Through this partnership, PatientsLikeMe and the Huntington’s Disease Society of America aspire to improve health outcomes and quality of life in the HD community.

PatientsLikeMe’s mission is to improve the lives of patients through new knowledge derived from experiences and results shared in the real world. The mission of the Huntington’s Disease Society of America is to improve the lives of all people affected by Huntington’s disease and their families.

“The partnership with PatientsLikeMe is an exciting new step in our work to help families affected by Huntington’s disease come together to support each other, find vital resources and share their journeys so that HD care is better. as quickly as possible, ”said Louise Vetter, President & CEO of the Huntington’s Disease Society of America.

Brad Hornback, Chief Community Officer at PatientsLikeMe, said, “We are delighted to partner with the Huntington’s Disease Society of America. PLM’s vibrant community and robust health tracking tools will provide increased support to help individuals navigate their HD journey.

“This partnership is exciting in many ways, but the most exciting thing for us is that we continue our mission of raising the voice of patients to the level of evidence while focusing on Huntington’s disease,” said said Dr Kate Burke, Senior Medical Advisor for PatientsLikeMe. “As we involve more and more people in research and empower them to share their stories and experiences with HD, we can help researchers discover new treatments and cures faster. ”

About PatientsLikeMe

PatientsLikeMe is the world’s largest integrated community, healthcare management, and real-world data platform. On PatientsLikeMe, members can put their illness experience into context and find answers to their questions. They can easily come into direct contact with limbs that have the same conditions, have the same symptoms, or have used similar treatments. Data generated by the members themselves is systematically collected and quantified while also providing an environment for peer support and learning. The site allows members to monitor symptoms of their condition (s), share their experiences with the disease and the results of their treatment, and learn how to improve their care through peer interactions. These data capture the complex temporality and competing influences of different life choices, socio-demographics, conditions and treatments on a person’s health. Everything members share empowers the community for personal action, making PatientsLikeMe a clinically sound resource with demonstrated impact, including over 100 studies in peer-reviewed medical and scientific journals. To learn more about PatientsLikeMe, visit

About the American Huntington’s Disease Society

The Huntington’s Disease Society of America is the premier nonprofit organization dedicated to improving the lives of everyone affected by HD. From community services and education to advocacy and research, HDSA is the global leader in providing help today and hope for tomorrow for people with HD and their families. To learn more about Huntington’s disease and the work of the Huntington’s Disease Society of America, visit or call (800) 345-HDSA.

About Huntington’s disease

Huntington’s disease is a fatal genetic disease that causes the progressive breakdown of nerve cells in the brain. It deteriorates a person’s physical and mental abilities during their first few years of work and has no cure. Each child of a parent with HD has a 50/50 chance of inheriting the defective gene that causes HD. Today, there are approximately 41,000 symptomatic Americans and more than 200,000 at risk of inheriting the disease. The symptoms of HD are described as having ALS, Parkinson’s disease and Alzheimer’s disease – simultaneously.

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The Recorder – Historical Society of Greenfield will not open a museum in 2021 Wed, 09 Jun 2021 19:51:38 +0000

Posted: 06/09/2021 15:40:54 PM

GREENFIELD – The Historical Society‘s board of directors has decided not to open the museum on Church Street for the 2021 season.

“We don’t have the staff, and we don’t have the airflow, in terms of meeting COVID restrictions,” said Meg Baker, company secretary. She added that although state restrictions were recently dropped, the building is not designed to allow adequate air circulation, nor is it well designed to accommodate one-way traffic or have disinfectant stations for hands.

Although closed to the public, the Historical Society of Greenfield still aims to bring the museum to the community in new ways, Baker said, whether through Facebook Live, hosting Zoom speakers, or connecting with other historical societies. Across the country.

“We are looking to make collections accessible to people in new ways,” she said.

For people who wish to access a particular collection – for research or other purposes – the company can accommodate “very limited visits, by appointment,” she added.

“We are taking this opportunity to do general building maintenance,” Baker noted.

Some outdoor events will be taking place throughout the summer, including an Ice Cream Social on August 7 (with a rain date of August 14).

While the building itself will be closed, Baker said the company still welcomes contributions of historical artifacts.

“We’re always interested in talking to people about what they think is historically relevant,” Baker said.

The company is particularly interested now in learning more about how the COVID-19 pandemic has impacted the lives of local residents, she said. Already, the museum has collected a roll of toilet paper – a reminder of the early days of the pandemic – from Baker Office Supply, and a canceled jury summons.

“It’s that kind of thing that we’re really interested in collecting,” she said. “How has COVID and the past year affected your life? … The story begins yesterday.

The best way for people to contact if they think they might have an artifact of interest is by emailing

“We’re not in the building all the time, so we might not hear a phone call, but we’ll still get an email,” she said.

Monetary donations are also always welcome, Baker noted. People can donate either online through the Paypal link on the website,, or by sending an email and setting a time to deposit money or a check.

“We are very excited to open next season,” she said. “In any way people want to contact us, we can’t wait to do so.”

Mary Byrne can be reached at or 413-930-4429. Twitter: @MaryEByrne

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Haverhill Accountant joins the Board of Mass. Society of CPAs as vice-president Wed, 09 Jun 2021 04:00:42 +0000

A Haverhill chartered accountant who works at Waltham was recently elected to the board of directors of the Massachusetts Society of Certified Public Accountants.

John D. Geraci, Managing Partner at LGA in Woburn, will be Vice Chairman of the Board of Directors and Chairman of the Audit Committee for the year 2021-2022.

The MSCPA Board of Directors is a 19-member elected group that sets policy, manages programs and oversees activities that benefit the 11,000-member organization and the accounting profession in Massachusetts.

“The MSCPA Board of Directors is a remarkably diverse group of individuals who play a vital role in shaping the priorities of the Society and are committed to improving the profession,” said Amy Pitter, President and CEO . “I am delighted to have John on the Board of Directors and look forward to seeing how his leadership will continue to benefit the Society, the community and the profession over the coming year.

Geraci has extensive experience assisting clients in areas related to mergers and acquisitions, due diligence, budgeting and forecasting, coaching and leadership. His previous experience includes 12 years working for a large regional accounting firm in Boston.

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Fayette County Cancer Society Meets and Reviews New Nominations | New Tue, 08 Jun 2021 10:00:00 +0000

The Fayette County Cancer Society held a monthly meeting on May 24 in the conference room of the First Baptist Church.

President Judy Collier opened the meeting with prayer. Twenty-four members and four guests answering the call.

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Westport Humanitarian Company Gets New X-ray Machine Mon, 07 Jun 2021 16:24:54 +0000

WESTPORT – When a pet is sick or injured, it is a scary time for the animal and for those who care for it. And the Westport branch of the Connecticut Humane Society has seen its share of sick animals, said Theresa Geary, the organization’s director of operations.

Not only does the humanitarian company provide medical care for animals destined for adoption, it also provides veterinary care at a reduced price for pets whose owners might not be able to afford a traditional clinic. Sometimes these animals need an x-ray, but until recently the Westport branch of the Humanitarian Society did not have its own x-ray machine.

Now the Westport branch has its own x-ray machine, thanks to a $ 53,000 grant from the John T. and Jane A. Wiederhold Foundation, a Torrington-based organization that aims to help animals of all kinds.

Animals suspected of bone fractures and other problems previously should have been taken either to a local clinic that had a relationship with the humanitarian society or to the humanitarian society’s Fox Memorial Clinic. Geary said she was grateful to have access to the machine in Newington, but bringing animals there could be stressful and prolong the diagnosis.

“The sooner you get a diagnosis, the faster the animal can be treated,” Geary said.

Geary said the new machine was purchased and installed a few weeks ago, and made a huge difference. She said the x-ray machine “can be used for all kinds of things”, not just breaks or fractures.

For example, Geary said, if an animal is vomiting or has a lack of appetite, an X-ray may be needed to determine if the animal has swallowed a foreign object.

While Humane Society staff were happy to take the animals to the Newington Clinic when x-rays were needed, Geary said it was a relief to be able to streamline the process.

“Whatever is in the best interest (of the animals), we will do it, but if we can reduce the stress – which the x-ray machine will do – we want to do it,” she said.

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UAH CON faculty and staff volunteer to support Tyrosinemia Society – Yellowhammer News Sun, 06 Jun 2021 19:00:20 +0000

Faculty and staff at the University of Alabama at Huntsville (UAH), part of the University of Alabama system, give back to their community and the world by supporting the Tyrosinemia Society and its new partnership with an organization called PatientsLikeMe.

The Tyrosinemia Society is a nonprofit organization dedicated to helping members of the tyrosinemia community. Tyrosinemia is a group of rare genetic disorders that prevent the breakdown of the amino acid tyrosine. Usually detected in early childhood by newborn screening tests, tyrosinemia occurs in one in 50,000 to 100,000 births worldwide. Left untreated, the disease can lead to liver failure, but with early detection and lifelong management, people with tyrosinemia can develop normally and lead healthy lives.

UAH faculty and staff got involved in society when they saw the chance to make a real difference in the lives of people with this disease.

“The faculty of the Faculty of Nursing has seen the need for a not-for-profit advocacy organization to meet the needs of families and patients affected by the four types of tyrosinemia,” says Dr. Elizabeth Barnby, Professor clinical associate at CON and president of the company. “The Tyrosinemia Society supports patients and families with all four types of tyrosinemia: transient tyrosinemia, tyrosinemia type 1, tyrosinemia type 2 and tyrosinemia type 3. Types 1, 2 and 3 are inherited diseases. rare caused by enzyme deficiency on the tyrosine catabolic pathway. Transient tyrosinemia is more common, but only a transient condition that occurs most frequently in babies born prematurely. The most serious type of tyrosinemia is type 1, and it is a life-threatening condition that can claim the life of a child very early in life, but if identified and treated it can develop into a manageable disorder.

This year, the Tyrosinemia Society partnered with PatientsLikeMe (PLM), the world’s largest integrated community, health management, and real-world data platform. This collaboration will give visibility to the company and its members, allowing them to learn from their peers living with tyrosinemia, and provide an opportunity for the tyrosinemia community to share their lived experiences by providing patient-generated data. . These data will ultimately be used to increase researchers’ knowledge of the disease through a natural history study.

“All types of tyrosinemia will benefit from a natural history study to improve our understanding of the basic pathophysiology of the disease,” says Dr. Barnby. “I am very grateful that my colleagues at UAH and other institutions across the country and the world have chosen to donate their time and energy to make the nonprofit Tyrosinemia Society possible. Their efforts are truly selfless and compassionate and will improve the lives of children and caregivers affected by tyrosinemia and related disorders. “

The company’s partnership with PLM represents an important step towards providing a robust set of data that would otherwise be difficult to obtain on this relatively rare disease, greatly benefiting families affected by tyrosinemia. Developing an online community to support tyrosinemia patients and caregivers marks the first time that a pediatric rare disease community has partnered with PLM, laying the groundwork for other rare disease communities to follow .

Along with Dr Barnby, other UAH volunteers who support the company include Board Member, Dr Jerome Baudry, Webmaster Hunter Cowing, Board Chairman, Dr Kader Frendi, Board Member , Dr Angela Hollingsworth, Secretary Preston Miller, Vice President and Treasurer Dr Mark Reynolds and Chair of the Medical / Scientific Advisory Board, Dr Darlene Showalter. Dr Gordon MacGregor and Dr Casey Norris, former UAH professors, will also continue to serve. Volunteers have become essential to support this cause by performing a multitude of tasks and services.

“These volunteers voluntarily donate their time, talents and hearts to the cause and accept no reimbursement,” notes Dr. Barnby. “They really are the most wonderful thing about the Tyrosinemia Society. They are making a huge difference for children around the world! They build a non-profit family support structure with financial grants from key stakeholders. They create web pages, answer questions, educate the public about tyrosinemia, and network with the National Institutes of Health (NIH), the Genetic and Rare Diseases Information Center (GARD), and the NIH / Office of Rare Disease Research ( NORTH) to improve results. for patients with tyrosinemia. Some even translate, because people from all over the world regularly contact the Tyrosinemia Society. We are a leader in the treatment of tyrosinemia and do what we can in our spare time to help. And none of this would have been possible without the support of the administration of the UAH College of Nursing. “

The Tyrosinemia Society is a community of advocates, caregivers and healthcare professionals dedicated to educating and inspiring individuals to improve health outcomes and advocate for adults and children with tyrosinemia and disorders related. The company has gained a global reputation for transforming healthcare outcomes for those affected by this disorder through education and research in collaboration with universities and healthcare industry professionals. To learn more about the company and its mission, please visit

PatientsLikeMe allows its members to monitor symptoms of their disease, share their disease experiences and treatment results, and learn how to improve their care through peer interactions. Members can put their illness experiences into context and find answers to their questions by connecting easily and directly with members who have the same conditions, people who have the same symptoms or have used similar treatments. For more information on PatientsLikeMe, visit

(Courtesy of UAH)

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Genealogical Society Welcomes Swedish Researchers | News, Sports, Jobs Sun, 06 Jun 2021 05:55:01 +0000

Janet Wahlberg and Jack Ericson are pictured part of the research book they used to document the genealogy of Swedish families locally.

CASSADAGA – Janet Wahlberg and Jack Ericson were the guest speakers at the recent Chautauqua County Genealogical Meeting held at the Cassadaga American Legion Hall on Maple Avenue.

Both speakers spoke about the number of Swedish immigrants traveling to America during the years 1866-1868 due to the potato famine, smallpox vaccination and population growth in Sweden. At one time, Jamestown had the largest Swedish population in the eastern United States.

They have many resources to help the family with their research. The important part Ericson said is having the person’s name and the birthday. Obituaries, Ericson said, are like “gold mines” because they have so much family history. Ms Wahlberg said they are located at Hall House, 73 Forest Ave., Jamestown.

Much of the information was found in the 25 counties and 91 parishes of Sweden. Complete registers were kept by the parishes. Ms Wahlberg said people doing research should contact them to find out how to use the records.

Gail Dash is the president of the company, with Ruth Nichols as vice president. Wayne Leamer is the editor of the newsletter and we thank Leamer for his excellent work with the recent edition. Debbie Kotar is the treasurer. The company has a research room in the Fredonia Barker Library which stores many family stories.

For more information on the Genealogical Society, write to POBox 404, Fredonia, NY 14063. New members are welcome.

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Hardin County Ag Society releases June Board meeting minutes – WKTN Fri, 04 Jun 2021 18:17:47 +0000

The Hardin County Agricultural Society met on Wednesday, June 2, 2021 for its monthly board meeting in June. Eleven directors and eight guests were present.

Corey Ledley, Chairman of the Board, opened the meeting.

Tori Korian, of Hardin County OSU Extension, said she would take a new job in Hancock County. She also said all livestock records were due this week.
Tim Striker, Hardin County commissioner, said commissioners were given a large sum of money and were looking for projects in the county that it would be used for. They ask organizations to submit projects to them.
It has been noted that Bob Fish, former Director of the Board of Directors and former Chairman of the Board of Directors has passed away today.

It was noted that an executive committee meeting is to be scheduled soon to consider the demands of the superintendent of the land.

Corey Ledley said he is working on a new 2 year gas contract, as our current gas contract ends July 31, 2021. The board voted to have Gammon’s Tree Service cut 8 large oak trees in the park exhibitions for $ 200 an hour, 8 hours of work. A working day to paint the roofs of the racehorse stable has been set for Saturday, July 24, with a start at 7:30 am. Work continues with County Commissioners for the paving and tracing of the new parking lot.

Craig Stump, campground co-chair, said he’s working on a national Cushman contract, with that event slated for next year in June. And, another event is in the works for next year in September after the fair. It was noted that there are still a few campsites available for this year’s fair.

Rob Wilson, president of entertainment, said he was working on securing an inspirational hour speaker and music for the service. It was noted that an updated contract is required for the All American Petting Zoo. Rob will work on securing this contract.

Cattle judges are still needed for dairy and beef. The dairy beef feeders were weighed on May 29 and 104 feeders were weighed and labeled. Sheep weighing is scheduled for Saturday June 12 from 8 a.m. to 10 a.m. and goats weighing is scheduled for the same day, Saturday June 12 from 10 a.m. to 11 a.m. Jack McBride noted that if an exhibitor chooses to bring their animal home, the 840 tags cannot be cut from the animal – this is a federal offense. Paul Ralston, chairman of the poultry committee, said the book of fairs indicated that poultry were not required to undergo pullorum testing this year, but IT IS REQUIRED this year and a date will be set for testing.

It has been noted that if anyone wishes to have a supplier spot at the Hardin County Fair 2021, they must go to and complete a contract request form under the dealership / supplier tab. All contracts are done online this year.

Sherri Beale, Jr Fair Board Advisor, said she continues to look for an art judge in high school. She also requested that on the working day, during lunch, the committees stay with their senior director of the show board and review the floor plans, etc.

Judi Cronley, said there are a few organizations that haven’t paid for this year’s sponsorships. Reminders will be sent to them. It has been decided that the show brochures will not be printed this year, as the show will have a new app with all the information and there will also be big screen TVs located around the fair grounds with information about the events. of the day. There will be around 650 people in the community who will receive a postcard, indicating how to view the Premium Fair 2021 book.

Kolt Buchenroth said Big Screen TVs, I Phones and I Pads for Doors and other miscellaneous. items have been purchased. Kolt also said that sponsors will receive thank you cards for being a 2021 sponsor.

Under former profession:
Doormen are still needed for Fair Saturday and Fair Wednesday morning.
Open class judges are always needed for wine, HS art, woodworking, photography, and flowers.

In the context of new business:
It has been noted that the Ohio Department of Agriculture receives $ 50,000 for each Ohio fair. Judi indicated that the Q2 newsletter will be sent out soon. It was also noted that 3 major family events chose to cancel in July, due to the COVID pandemic. The next fair’s board meeting is scheduled for Wednesday July 7 at 7 p.m. in the Arts / Crafts building.

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