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October 26, 2022

Major news for patients this week. As of Monday, TRICARE has dropped nearly 15,000 community pharmacies from its network, leaving nearly 400,000 patients to find a new pharmacist.

 

The health care program that offers coverage for military service members, retirees, and their families, previously included independent pharmacies in its network. But new contracts with its contracted pharmacy benefit manager, Express Scripts, mean fewer pharmacy options for patients.

 

This puts military patients, especially those living in rural areas, in a tight spot. It takes away a patient's choice in where they get their prescriptions filled, which may mean having to drive past closer pharmacies to reach the in-network pharmacy or even having to leave town.

 

News stories like this are why we advocate to protect patient access and defend the pharmacist-patient relationship. We dive into this story and more on this week’s podcast episode.

 

In The News

Is your pharmacy among the 15,000 leaving the Tricare network? With just days before 15,000 community and independent pharmacies will leave the Tricare retail pharmacy network, questions remain about the impact on patients' ability to get their medications. (Federal Times)


Family Caregivers Find Support on #dementia TikTok. Jacquelyn Revere moved back home at 29 to care for her mother, who had Alzheimer's disease. She spent six years as a caregiver and shared her experiences on TikTok, building a large following on her channel, "Mom of My Mom." (KHN)

 

 
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Geri

My name is Geri @everydaylivinglupus and I am from NYC. I was diagnosed with #lupus in July 2017 when I was 27 years old.

In the beginning, my joints were hurting but I just thought it was part of getting old and I sort of shrugged it off. But soon the joint pain got unbearable. Just walking down the stairs was a struggle.

My Story

 
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On this Friday’s Halloween edition of the podcast, we talk about the latest health policy news and hear patient horror stories about insurance delays, the high cost of care, and so much more.

 

We are sad to announce that this is the final show for our field correspondent, Kate Pecora. But to honor her time spent speaking with patients and caregivers in the Patients Rising community, we are sharing her story this week.

 

Kate lives with spinal muscular atrophy (SMA), which requires her to use a wheelchair. But getting medical devices covered by insurance is not always easy. Here’s a preview of Kate’s story.

 

Kate Pecora: “I can't tell you how many phone calls I had to make specifically to the insurance company, and then to the durable medical equipment company and to my doctors. I think in total I probably spent a week's worth of working hours on getting this chair, and that is the experience of nearly everybody that I have talked to that has ever had to go through this process, specifically of getting anything of greater value than $5,000.

 

So I can tell you my chair is an ultra-lightweight manual wheelchair and so for me, off the shelf it would've cost around $6,000. Some of these wheelchairs can cost up to 30, 40 thousand dollars depending on the type of equipment they have, the functionality, whether it's a standing chair or something like that. So, you know, insurance companies are gonna drag out this process as long as they can to say something isn't medically necessary.

 

I think for me, the biggest kind of joke was when I received the first denial of my wheelchair and in context, I've used a wheelchair since I was around 10 to 12 years old is when I really started using it for daily use. My particular insurance company said that it was not medically necessary for me to be choosing a wheelchair. It’s ridiculous, and so that started the whole appeal process, which lasted the full 30 days, so that was a whole month.”

 

Kate shares her full story and the fight to finally get the wheelchair she needs in this Friday’s episode.

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Before you go, a big piece of news for caregivers. Medicare is proposing severe cuts to home health care, which is a critical service for so many families.

 

I talk about how this will impact caregivers and family members all across the country on the STAT First Opinion Podcast. Patients deserve reliable home health care to keep them healthy and comfortable. And family members deserve the peace of mind that comes with it.

 

Thank you for spending your Wednesday with us, keep an eye on your inbox next week for more health policy headlines, patient resources, and health advocacy.

 

Sincerely,

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Terry Wilcox

CEO & Founder
Patients Rising

     
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Patients Rising, 700 12th Street NW Suite 700, Washington, District Of Columbia 20005, United States, 202-751-1186

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