Rheumatoid Arthritis: “I’m a Nurse Not a Patient”

In this blog post, Kathleen Furbee shares her story of being diagnosed with and treated for rheumatoid arthritis and how after 10 years of treatment she is grateful for the medical advances that allow her to live a full and happy life. By Kathleen Furbee             When I was in my early fifties I came down with … Read more>>

Uterine Cancer: Why Not Me?

In this blog post, Catherine Samargo shares her story of being diagnosed and treated for uterine cancer. She reflects upon what it was like to receive a cancer diagnosis in the midst of other family tragedies and how her mindset slowly shifted from one of victimization to one of compassion for all human beings enduring … Read more>>

A Caregiver’s Guide to Understanding Dementia

In this blog post, Holly Clark offers her perspective on caring for loved ones suffering with dementia based on her professional experience working as a Community Manager for FirstCare Nursing Homes in Ireland and her personal experience caring for a family member dealing with the disease. By Holly Clark Hundreds of millions of people in the world … Read more>>

Who knew I had Glaucoma? I Didn’t.

Approximately half of the glaucoma population in the U.S. goes undiagnosed  Article by Stephanie Handler Originally published by the Glaucoma Research Foundation. On April 19, 2011, I was diagnosed with glaucoma, a serious eye disease that can lead to blindness. I made an appointment with my local ophthalmology clinic in San Francisco as soon as I noticed … Read more>>

A Clinical Trial Saved My Life

By Cynthia Pepper In this blog post, guest blogger Cynthia Pepper shares her incredible story of how she was diagnosed with inoperable cervical cancer and given little hope to survive, but a chance meeting with the right doctor saved her life. By participating in a clinical trial, she is alive today and in complete remission. … Read more>>

Christmastime Can Present More Challenges Than Cheer for Chronic Lyme Disease Patients

By Jill A. Ross This blog post shares the perspectives of members of the North Central West Virginia Lyme Community (NCWVLC), a support group for Chronic Lyme Disease patients, about how living with a serious chronic illness has affected their ability to participate in the holidays and how overextending themselves during this busy season can … Read more>>

Hyperhidrosis: More Than Just Sweating

This blog post features Molly Nair, a young woman living with hyperhidrosis. November is Hyperhidrosis Awareness Month and Ms. Nair shares how this condition has affected her life since she was in elementary school. She details what it is like to live with hyperhidrosis, the obstacles she has faced because of it, and how she … Read more>>

Jen’s Story: An Announcement – From MBC to Sarcoidosis and Beyond

In honor of Breast Cancer Awareness Month, we bring you Jen’s story… Jen is a seven-year breast cancer survivor, though she still struggles with that term. At 32, she was mistakenly diagnosed with metastatic breast cancer. She was treated for metastatic breast cancer for four-and-a-half years before her doctors concluded that she was in remission … Read more>>

Alan’s Story: I have a Rare Disease and I am Crossing Borders – #RareDiseaseDay2018

Our guest post on this Rare Disease Day 2018 comes from Alan who lives in Whales and is fighting ataxia head on. Alan is raising awareness of this disease through his blog and on social media. Connect with Alan to learn more: www.ataxiaandme.org Facebook @ataxiaandme Twitter @ataxiaandme Instagram @ataxia_and_me Alan’s Story I have a Rare … Read more>>

Susanne’s Caregiver Story: Why Do I Always Cry In Hospitals?

November is National Caregiver Month and today’s post comes from Susanne White, founder of Caregiver Warrior. She was blessed with the opportunity to care for her parents and ventured out on a journey that would change her life. She blogs about this journey on her website and shares her experience, strength and hope with others so that … Read more>>