Chronically Grateful Me by Deb Andio
Life is hard enough,don't go through life with pain that’s keeping you clutching the steering wheel. Join me as I share with you my life of living chronically grateful while living with chronic pain.
It is not just older people who are affected by arthritis, children get it too — that’s why observing Juvenile Arthritis Awareness Month in July each year is so important. Founded by the Arthritis Foundation, this campaign aims to raise awareness about this condition and share resources to help those affected by it. Did you... Continue Reading →
Understanding more about the underlying causes of pain can help improve treatments and alleviate suffering Each September, pain specialists and advocates across the country raise awareness about issues related to chronic pain during National Pain Awareness Month. Did you know that chronic pain affects more than 100 million Americans. that's 1/3 of the USA population... Continue Reading →
As an advocate for arthritis and a Facilitator to the Live Yes Connect Group and Founder of the International Support group Avascular Necrosis-Osteonecrosis Support Int’l I use Zoom a lot: as a person back in school I again use Zoom a lot: talking with family , friends and attending other meetings yep zoom again !... Continue Reading →
This is a really good app, it’s new released by the arthritis foundation just a couple weeks ago. It’s a great way to connect with others that understand what it’s like to live with pain. It provides tips to help ease the stress and anxiety that come with chronic pain. Discusses various treatments from diet... Continue Reading →
So I have been meditating for over 18 months. It has helped me learn to quiet my mind. Focus on my breathing and start taking back some control of my pain. It sure did pay off last week. I fell after another bowman lost her balance her cane went sliding and she also grabbed onto... Continue Reading →
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 →
Here’s what really stinks about having something that is called a rare disease/disorder First you probably won’t find it in any regular medical textbook or learn about it in detail in any medical school. Really ? Trust me I have looked I stumble on a paragraph here and there, but even it stinks as it... Continue Reading →
Chronically Grateful Me by Deb Andio 