Vivian Lee Foundation

Vivian Lee Foundation Nonprofit foundation raising awareness and support for cystic fibrosis. We raise funds through our Vivi's Vintage Market.

We are an organization that raises awareness and support for people living with Cystic Fibrosis. Our main fundraising event is a twice yearly market called Vivi's Vintage Market. This benefits the Cystic Fibrosis Foundation, Cystic Fibrosis Research Inc. and Vivian Lee, a 2 year old twin living with CF. All net profits will go to finding a cure for cystic fibrosis! Full details can be found at www.vivisvintage.com

Somewhere, someone in the CF community needs to see this and hasn't yet.Rise Forward applications close in two weeks, Se...
09/01/2026

Somewhere, someone in the CF community needs to see this and hasn't yet.

Rise Forward applications close in two weeks, September 15.

Two scholarships for someone living with CF and for a caregiver of a child with CF.

If this isn't for you, it might be for someone you know. Share this post. Send the link. Tag them.

vivianleefoundation.org 💜

A few spots left for Off Duty Brunch: A Morning for CF Caregivers.If you've been on the fence, this is your sign. Sunday...
08/31/2026

A few spots left for Off Duty Brunch: A Morning for CF Caregivers.

If you've been on the fence, this is your sign. Sunday, September 13 at Tavern on Kruse in Lake Oswego. A slow morning with other CF caregivers who don't need the backstory.

You don't have to be "on" for this one. You just have to show up.

RSVP link in bio.

If you've been thinking about applying, this is your sign.Rise Forward applications close in just under one month, Septe...
08/20/2026

If you've been thinking about applying, this is your sign.

Rise Forward applications close in just under one month, September 15th.

Two scholarships for 2026-2027: One for someone living with CF, age 16+. One for a caregiver of a child with CF (up to 15 years old).

You don't need a perfect story. You just need a real one.

Apply at vivianleefoundation.org 💜

Caregivers, this one is for you.Off Duty Brunch: A CF Caregiver GatheringSunday, September 13Tavern on Kruse, Lake Osweg...
08/19/2026

Caregivers, this one is for you.

Off Duty Brunch: A CF Caregiver Gathering
Sunday, September 13
Tavern on Kruse, Lake Oswego

No treatments. No schedules. Just us.

A morning to sit down with people who get it. No agenda, no need to explain what a PFT is or why you're tired. Just brunch, coffee, and other CF caregivers in the same trenches you're in. Hosted in partnership with Cystic Fibrosis Foundation, Oregon and SW Washington Chapter.

Space is limited. RSVP at the link in bio.

💜

If you've been carrying the weight of a CF journey and wondering if anyone sees it, this is for you.Rise Forward applica...
08/05/2026

If you've been carrying the weight of a CF journey and wondering if anyone sees it, this is for you.

Rise Forward applications are officially open.

Two scholarships this year: One for someone living with CF, age 16+. One for a caregiver of a child with CF.

Both include an ambassador role where you share your story with the VLF community at one of our events.

You don't have to have it all figured out. You just have to be willing to show up and be real.

Apply at vivianleefoundation.org Deadline: September 15 Recipients announced by October 1

Tag someone who should see this. Share it. Send it in a DM. 💜

Rise Forward is growing.This year, we're awarding two scholarships. Not one. Two.One for someone living with CF, ages 16...
08/04/2026

Rise Forward is growing.

This year, we're awarding two scholarships. Not one. Two.

One for someone living with CF, ages 16 and older. One for a caregiver of a child with CF up to 15 years old.

Each recipient serves as a VLF ambassador, sharing their story with our community through one of our signature events.

Applications open tomorrow, August 5.

We'll share all the details then, but we wanted you to hear it here first. This program exists because of you, because of every person who has shown up for CF families through VLF. And this year, we get to show up bigger.

More tomorrow. 💜

Today is the last day. 💜At midnight tonight, the Founding Member window for The Salt Circle closes. After that, anyone w...
05/31/2026

Today is the last day. 💜

At midnight tonight, the Founding Member window for The Salt Circle closes. After that, anyone who joins is still a Salt Circle member, but the Founding Member marker is permanent and only available today.

If you've been waiting, this is the day.

Link in bio.

To the parents of young CF-ers. 💜You become an expert fast. You learn more medical terms, medications, and treatment tec...
05/31/2026

To the parents of young CF-ers. 💜

You become an expert fast. You learn more medical terms, medications, and treatment techniques than you ever imagined.

Time is no longer your own. Treatments, appointments, and therapies fill the calendar, every single day.

You celebrate the small wins. A good spirometry number. A weight gain. A full night's sleep. They all matter.

You learn to accept help. You can't do it all, and you don't have to. Community makes the hard days possible.

You carry worry, always. It never really goes away. But love is bigger, and so is your child's strength.

And you are stronger than you know. CF changes your life, but it doesn't define your love, your purpose, or your family.

You are not alone. We see you. We thank you. 💜

05/31/2026

Salty kisses from a fresh newborn. Getting a cystic fibrosis diagnosis is always such a scary time, honestly that time is a little bit of a blur for most CF parents.

What you don’t know when your baby is diagnosed is that it will still be amazing and change your life in every way.

To all our amazing CF warriors out there not letting CF get in your way, we see you. And to the caregivers cheering them on, fighting for them, we see you too.

Address

Newberg, OR
97132

Website

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