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Primary Care Network offers all kinds of services for bolstering health and wellness

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The Primary Care Network offers a tremendous range of programming all geared to helping folks live their healthiest lives.

Staff at the local office, located at 5120 47 St., are excited about launching into 2022 with a spectrum of workshops from Anxiety to Calm, Happiness Basics and Moving on With Persistent Pain to Relationships in Motion, Sleep and Journey Through Grief.

Others include My Way to Health (formerly Health Basics), Strong and Steady (which focuses on bolstering one’s strength and flexibility), and H.E.A.R.T.S which has been carefully designed to help families through the loss of a child during pregnancy or shortly after birth.

Of course, due to the pandemic, programming has been virtually all online. But there has been a silver lining with that approach, explained Lorna Milkovich, executive director.

“With our group workshops, we discovered that with going online, we were able to reach some people that we may not have reached otherwise. For some, being able to attend via Zoom offered new flexibility. Others were more comfortable with that format over in-person meetings.” Moving forward, group workshops will certainly continue to be offered in-person, but the PCN will also continue with online versions as well. “That’s exciting, because it opens the door to reaching a wider demographic.

“Through the online versions, we continued to evaluate things and receive feedback, and we continue to see really amazing results. For Anxiety to Calm for example, it consistently shows that people reduce their anxiety, on average, by 50 per cent,” she explained. “It’s amazing.” As for the programs, Milkovich noted that the popular workshop Health Basics has been re-launched as My Way to Health. “It’s a very core workshop that we would encourage most people to take,” she said, adding the sessions focus on healthy living habits including weight loss, bolstering activity and assisting with chronic pain and maintaining a healthy brain through the ageing process. Essentially, participants will learn a host of practical skills they can put into action, said Milkovich.

“It’s super important that people can make changes that are meaningful to them, and that work with their lifestyles.”

There is always an emphasis on designing the workshops to be primarily skills-based, interactive and experiential. “It’s really about, how do you incorporate these skills into your life?

“With each one of our workshops, you will learn new skills that you are going to practice that week to see how they work for you. By the end, you will have four or five new skills and you’ll find those that really resonate with you; ones that work for you,” she said. “That’s what we find that really works for people.”

In a move to make the workshops even more accessible, Milkovich said many are available in both four and eight- week sessions.

“We are also starting up the workshops every month,” she said. This way, there are no lengthy waiting periods should someone miss out on signing up during a given week.

Another exciting new tool this year is the introduction of a downloadable publication called My Self-Care Journey.

“It’s a journal that is available on our web site. It was designed by several health care professionals as well as patients and other members of the community. The journal is about choosing healthy habits each day, and it helps you intentionally tune into your lifestyle choices – it provides a guide for making positive changes,” she said, adding that there are sections on mindfulness and gratitude as well. Ultimately, solid lifestyle changes typically come from making smaller, more manageable goals, said Milkovich.

“it’s more about those tiny little building blocks in your lifestyle that can make a difference. It’s also about people being kinder and gentler with themselves while building healthier lifestyles.”

“My Self-Care Journey is available to anyone – they can go online and print it off. For those who would prefer a hard copy, they can ask at their doctor’s office, or they can swing by the Primary Care Network. There is no charge.”

Looking ahead, the next Health Café is slated for March 14 and is entitled ‘Gout – Disease of the Kings’. Presented by PCN staff, folks are invited to learn more about this condition and ways to help manage it. Tune in live on the Red Deer Public Library Facebook page at 5:15 p.m. Milkovich said staff are always open to preparing Health Cafes on topics of interest to the public at large. “They can let us know – we’d be happy to hear from them,” she said. Several individual programs are available as well via the PCN, from help with diabetes, blood pressure and cholesterol to pharmacy queries to assistance with everything from quitting smoking to learning more about housing or financing. Milkovich also highlighted a relatively new program called the MINT Memory Clinic which is available with a referral from a family doctor. Folks are taken through a full assessment and provided with recommendations for ongoing care and connection with specialists.

As Milkovich pointed out, the PCN is also a hub for those seeking information about health and wellness resources in the community. Besides the workshops, health cafes and personal appointments, they can help point folks in the right direction for the best kind of assistance they may need.

“We want to help empower people to live the healthiest lives that they can,” she said, adding that it’s always so amazing to see people make terrific changes in their daily lives.

“We do get stories from people, and it is so inspiring to see the differences that have been made in their lives.”

For more about the PCN, check out reddeerpcn.com or find them on Facebook for all the latest news as well. You can also call the office at 403-343-9100.

Click here to read other stories from the Red Deer Primary Care Network.

Born and raised in Red Deer, Mark Weber is an award-winning freelance writer who is committed to the community. He worked as a reporter for the Red Deer Express for 18 years including six years as co-editor. During that time, he mainly covered arts and entertainment plus a spectrum of areas from city news and health stories to business profiles and human interest features. Mark also spent a year working for the regional publication Town and Country in northern Alberta, along with stints at the Ponoka News and the Stettler Independent. He’s thrilled to be a Todayville contributor, as it allows him many more opportunities to continue to focus on the city and community he not only has a passion for, but calls home as well.

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Ex-FDA Commissioners Against Higher Vaccine Standards Took $6 Million From COVID Vaccine Makers

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From the Daily Caller News Foundation

By Emily Kopp

Ten of the twelve former Food and Drug Administration (FDA) commissioners and acting commissioners opposed to the Trump administration’s stiffer standards for vaccines quietly disclosed ties to the pharmaceutical industry, a Daily Caller News Foundation review shows.

The FDA old guard criticized the new leadership in a Dec. 3 New England Journal of Medicine (NEJM) letter over a higher regulatory bar for vaccines, namely the expectation that most new vaccine approvals will require randomized clinical trials, arguing it could hamper the market.

“Insisting on long, expensive outcomes studies for every updated formulation would delay the arrival of better-matched vaccines when new outbreaks emerge or when additional groups of patients could benefit,” the former commissioners wrote. “Abandoning the existing methods won’t ‘elevate vaccine science’ … It will subject vaccines to a substantially higher and more subjective approval bar.”

But while the former commissioners disclosed their conflicts of interest to the medical journal — per standard practice in scientific publishing — reporters didn’t relay them to the broader public in reports in the Washington PostSTAT News and CNN.

The headlines about a bipartisan rebuke from former occupants of FDA’s highest office give the impression that the Trump administration is contravening established science, but closer inspection reveals a revolving door between pharmaceutical corporations and the agencies overseeing them.

Three of the signatories have received payments totaling $6 million from manufacturers or former manufacturers of COVID vaccines.

Scott Gottlieb has received $2.1 million in cash and stock from his position on the Pfizer board of directors, where he has advised on ethics and regulatory compliance since 2019, according to company filings to the Securities and Exchange Commission. Stephen Ostroff has received $752,310 from Pfizer in consulting fees since 2020, according to OpenPayments.

Mark McClellan has received $3.3 million from Johnson & Johnson as a member of the board of directors since 2013, SEC filings also show. McClellan also consults for the new pharmaceutical arm of the alternative investment management company Blackstone, which invested $750 million in Moderna in April 2025.

Gottlieb and McClellan did not respond to requests for comment. Ostroff could not be reached for comment.

FDA Center for Biologics Evaluation and Research Director Vinay Prasad outlined the higher standards and shared the results of an internal analysis validating 10 reports of children’s deaths following the COVID-19 vaccine in a Nov. 28 memo to staff. He called for introspection and reform at the agency.

The NEJM letter criticizes Prasad for cracking down on a practice called “immunobridging” that infers vaccine efficacy from laboratory tests rather than assessing it through real-world reductions in disease or death. The FDA under the Biden administration expanded COVID vaccines to children using this “immunobridging” technique, extrapolating vaccine efficacy from adults to children based on antibody levels.

Norman Sharpless — who in addition to previously serving as acting FDA commissioner also served as the head of the National Institutes of Health’s National Cancer Institute — consults for Tempus, a company that collaborates with COVID vaccine maker BioNTech. He has helped steer $70 million in investments in biotech through a venture capital firm he founded in November 2024. Sharpless also disclosed $26,180 in payments in 2024 from Chugai Pharmaceutical, a Japanese pharmaceutical company that markets mRNA technology among other drugs, on OpenPayments.

“I was grateful for the opportunity to serve as NCI Director and Acting FDA Commissioner in the first Trump Administration, and strongly support many of the things President Trump is trying to do in the current Administration,” Sharpless said in an email.

Margaret Hamburg, another former FDA commissioner and signatory of the NEJM letter, has since 2020 earned $2.8 million as a member of the board of Alnylam Pharmaceuticals, which markets RNA interference (RNAi) technology.

Hamburg did not respond to a message on LinkedIn.

Most signatories disclosed income from biotech companies testing experimental cancer treatments. These products could face tighter scrutiny under Prasad, a hematologist-oncologist long wary of rubberstamping pricey oncology drugs — which Prasad points out often cause some toxicity — without plausible evidence of an improvement in quality of life or survival.

The former FDA commissioners disclosed ties to Sermonix Pharmaceuticals Inc.; OncoNano Medicine; incyclix; Nucleus Radiopharma; and N-Power, a contractor that runs oncology clinical trials.

Andrew von Eschenbach, who like Sharpless formerly served both as FDA commissioner and the head of the National Cancer Institute, disclosed stock in HistoSonics, a company with investments from Bezos Expeditions and Thiel Bio seeking FDA approval for ultrasound technology targeted at tumors.

Some FDA commissioners who signed onto the letter opposing changes to vaccine approvals have ties to biotechnology investment firms, namely McClellan, who consults Arsenal Capital; Janet Woodcock, who consults RA Capital Management; and Robert Califf, who owns stock in Population Health Partners.

Califf did not respond to an email requesting comment. Woodcock did not respond to requests for comment sent to two medical research advocacy groups with Woodcock on the board. Eschenbach did not respond to a LinkedIn message.

The two signatories without pharmaceutical ties may find their judgement challenged by the FDA investigation into COVID-19 vaccine deaths, having either implemented or formally defended the Biden administration’s headlong expansion of vaccines and boosters to healthy adults and children.

David Kessler executed Biden’s vaccination policy as chief science officer at the Department of Health and Human Services, helping to secure deals for shots with Pfizer and Moderna.

Meanwhile Jane Henney chaired a National Academies of Sciences, Engineering, and Medicine report published in October 2025 that praised the performance of FDA and Centers for Disease Control and Prevention (CDC) vaccine surveillance during the pandemic — underwritten with CDC funding.

That assessment clashes with that of a Senate report, citing internal documents from FDA, finding that CDC never updated its vaccine surveillance tool “V-Safe” to include cardiac symptoms, despite naming myocarditis as a potential adverse event by October 2020, and that top officials in the Biden administration delayed warning pediatricians and other providers about the risk of myocarditis after their approval in some children in May 2021, months after Israeli health officials first detected it in February 2021. The Senate investigation named Woodcock, a signatory of the NEJM letter, as one of the FDA officials who slow-walked the warning.

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Health

RFK Jr reversing Biden-era policies on gender transition care for minors

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From The Center Square

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HHS is also working to “reverse the Biden administration’s attempt” to classify gender dysphoria as a type of disability.

The U.S. Department of Health and Human Services unveiled a multi-pronged regulatory effort Thursday to curtail gender-affirming care for minors, including gender transition procedures at hospitals.

The Centers for Medicare & Medicaid Services has drafted a rule that would prohibit pharmaceutical or surgical gender reassignment procedures from receiving federal Medicaid or Children’s Health Insurance Program funding. It’s also proposing a rule that would allow it to withdraw Medicare and Medicaid funding from hospitals that perform such surgeries on minors. HHS is also working to “reverse the Biden administration’s attempt” to classify gender dysphoria as a type of disability. If gender dysphoria were to be defined as a disability, then health care providers who don’t want to perform what the department has dubbed “sex-rejecting” procedures could be in danger of violating anti-discrimination laws.

Health and Human Services Secretary Robert Kennedy, Jr., described gender affirming procedures as “unsafe” and “irreversible,” and framed the administration’s actions as “[protecting] America’s most vulnerable.”

“Our children deserve better – and we are delivering on that promise,” Kennedy told reporters Thursday.

The department is acting on directives from an executive order from President Donald Trump’s first few weeks in office. The Jan. 28 order called on government agencies to “[defund] chemical and surgical mutilation” of children, seemingly in the manner that HHS has proposed, as well as “rescind or amend all policies” relying on guidance from the World Professional Association for Transgender Health.

The Food and Drug Administration is also taking regulatory action against some organizations that market breast binders to minors.

“Illegal marketing of these products for children is alarming, and the FDA will take further enforcement action such as import alerts, seizures, and injunctions if it continues,” said Food and Drug Commissioner Marty Makary.

Kennedy signed a declaration Thursday that gender affirming procedures for minors “do not meet professionally recognized standards of health care” and the Assistant Secretary for Health and Head of the United States Public Health Service Commissioned Corps, Admiral Brian Christine, signed a public health message stating the same.

“Evidence shows sex-rejecting puberty blockers, cross-sex hormones, and surgeries are dangerous. Providers have an obligation to offer care grounded in evidence and to avoid interventions that expose young people to a lifetime of harm,” Christine said.

The House of Representatives passed a bill Wednesday that would criminalize the act of providing gender affirming care to minors.

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