Program

Program at a Glance

WEDNESDAY, NOVEMBER 6, 2019

 

Registration
11:00 a.m. - 7:00 p.m.

THURSDAY, NOVEMBER 7, 2019

Registration
7:00 a.m. - 8:30 p.m.

Disease Overview and Introduction to the PFF
1:00 p.m. - 4:00 p.m.

Welcome reception and poster presentation
5:00 p.m. - 8:00 p.m.


FRIDAY, NOVEMBER 8, 2019

Registration
7:00 a.m. - 7:00 p.m.

Plenary Session
8:30 a.m. - 10:30 a.m.

Sessions for professionals 
10:45 a.m. - 12:00 p.m.

Sessions for patients, caregivers, those who have lost a loved one, and transplant recipients
10:45 a.m. - 12:00 p.m.

Lunch Break - Clinical Trials Innovation Series
12:00 p.m. - 1:20 p.m.

Sessions for professionals 
1:20 p.m. - 2:50 p.m.

Sessions for patients, caregivers, those who have lost a loved one, and transplant recipients
1:20 p.m. - 2:50 p.m.

Break
2:50 p.m. - 3:15 p.m.

Sessions for professionals 
3:15 p.m. - 4:50 p.m.

Sessions for patients, caregivers, those who have lost a loved one, and transplant recipients
3:15 p.m. - 4:50 p.m.

Cocktail Reception
5:50 p.m. - 6:50 p.m.

Networking Dinner
6:50 p.m. - 8:50 p.m.

SATURDAY, NOVEMBER 9, 2019

Registration
7:00 a.m. - 5:00 p.m.

Plenary Session
8:30 a.m. - 10:30 a.m.

Sessions for professionals 
10:45 a.m. - 12:00 p.m.

Sessions for patients, caregivers, those who have lost a loved one, and transplant recipients
10:45 a.m. - 12:00 p.m.

Lunch Break - Clinical Trials Innovation Series
12:00 p.m. - 1:20 p.m.

Sessions for professionals 
1:20 p.m. - 2:50 p.m.

Sessions for patients, caregivers, those who have lost a loved one, and transplant recipients
1:20 p.m. - 2:50 p.m.

Break
2:50 p.m. - 3:15 p.m.

Sessions for professionals 
3:15 p.m. - 4:50 p.m.

Sessions for patients, caregivers, those who have lost a loved one, and transplant recipients
3:15 p.m. - 4:50 p.m.

Jamberry Nails for PF

I lost my father, James Richardson, at age 59 on June 23, 2009.  He went into the quick care because he thought he had a common cold and was having a hard time breathing. They rushed him to the hospital where we sat for 4 days, not knowing what was going on, hooked up to an oxygen tank to help him breath. On the 4th day we found out that my father had idiopathic pulmonary fibrosis and due to it being in the later stages there was nothing we could do.

September is Global Pulmonary Fibrosis Awareness Month. I will be participating by wearing blue on Fridays for the entire month of September. I am also going to be donating half of any commission I make off of Jamberry for the entire month to the Pulmonary Fibrosis Foundation in honor of my father. If there was more research on IPF, it may have saved his life. He could have been able to watch his grandkids grown and enjoy all of their milestones. I am hoping that by donating we can spread the word and all breath safe! Even if you cant donate, please share my Facebook page or spread the word. Thank you all for your support and love.

Please visit my Jamberry Nails page to place your order and support the efforts of the Pulmonary Fibrosis Foundation.  If you do not need Jamberry Nails at this time but would like to support my efforts please visit my First Giving page. 

Thank you,
Janet

United States of America