Author: ChronicallyGratefulDeb

The body always knows what to do to heal itself. The challenge is listening and doing what your body needs. I was diagnosed with Osteoarthritis in 1997ish, Avascular Necrosis aka Osteonecrosis in my knee in 2014 and Factor V Leiden hetero, and Spondylolisthesis 2005ish Health Advocate-Health Activist-World Changer Love photography, cooking, hiking, walking ,traveling and learning to live a new normal since my diagnosis. My Links Facebook Main Profile https://www.facebook.com/debbie.briglovichandio Main Blog www.ChronicallyGratefulDebla.com Twitter - https://twitter.com/debbiea001 Instagram - https://www.instagram.com/debbiea_1962 and https://www.instagram.com/chronicallygratefulme Support Group Avascular Necrosis/Osteonecrosis Support Int’l https://m.facebook.com/groups/DeadBoneDiseaseAvn Awareness for Avascular Necrosis & Other Conditions of The Bone and Joints https://www.facebook.com/AvascularNecrosisAndBoneDiseaseAwareness/ Avascular Necrosis Awareness Day November 29 – working with elected officials to get this recognized in all states https://www.facebook.com/AwarenessByDebla/ Avascular Necrosis-Osteonecrosis Knowledge and Education https://www.facebook.com/AvascularNecrosisEducation/ Facebook Link https://m.facebook.com/ChronicallyGrateful.Me/

Thank You Proud Moment

Thank you to all of our elected officials Mayor Jamael Tito Brown Youngstown Ohio Senator Michael Rulli Ohio and Senate President Larry Obhof Ohio Congressman Tim Ryan Ohio Congressman Sean Patrick Murray of New York Governor Kim Reynolds Iowa And all the others who said yes and to the future Elected officials who also will... Continue Reading →

My Favorite Things Gift Guide Adults

Gift Guide at all price points My Favorite Things Under 100.00Tory Burch Foundation Seed Box Gift them something that gives back with Tory Burch's annual Seed Box. The limited-edition box features a curated selection of products made by female entrepreneurs—including a scarf designed by Tory Burch—all packaged in a pretty floral box so you can... Continue Reading →

HealtheVoices 2020

I am hoping to be selected for the Health eVoice 2020 conference. This would be such an honor. Avascular Necrosis needs a voice and I declined last year when invited because my cousin was very ill and later passed away. So I hope I can get the opportunity to attend this year. Here is a... Continue Reading →

Meet Julie Croner

To Our Dear Readers Often being diagnosed with a rare disease is not easy , it can often  leave you feeling alienated  exhausted and at times discouraged. We often end up having more questions than answers.   There also is very little to no public attention when you have a rare disease/disorder such as fun... Continue Reading →

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