Rare Tips Featured Three Ways to Get Access to High Cost Treatments Embracing Risks: How Taking Chances Enhances Life with a Rare Disease The Surprising Link Between Exercise and Myositis How is Congenital Myasthenic Syndrome (CMS) Different from Myasthenia Gravis (MG)? What You Need to Know about CMS and Clinical Trials Needle Phobia in Children: What It Is, What It Isn’t, and How to Help The Link Between Oral Wellness and Your Overall Health Five Empowering Ways to Mark Rare Disease Month Teens, Substance Use, and Rare Disease Safeguard Your Holidays: The Importance of Flu Protection Expert Advice on Managing Nutrition for Rare Disease Patients: Insights from a Metabolic Dietitian Know Rare Tips: How to Support a Friend Who’s Been Diagnosed With a Rare Disease Diagnosis and Symptoms of Autoimmune Hemolytic Anemia (AIHA) Navigating Adolescence with Rare Disease 6 Tips to Help Fight Fatigue in Rare Disease How to Manage Autoimmune Hemolytic Anemia Living With Myasthenia Gravis: 10 Things to Know Healthy for the Holidays Tips for Managing a Rare Blistering Disease Embrace your Rare Truth: Becky's Rare Tip on Finding the Right Support A Tiger Mom’s Guide for Sudden Hospitalization for a Child with a Rare Disease TargetCancer Foundation’s 5 Tips for Caregivers What Every Rare Cancer Patient Should Know In Case of Emergency: Unleash the Power in Your Pocket Protect Yourself From the Sun if You Have Bullous Pemphigoid (BP) Can What You Eat Trigger Bullous Pemphigoid, a Rare Skin Condition? 5 Things to Pack in your Emotional Toolkit Plunging is Easy, Raising Money is Hard: Lessons to Help Other Rare Disease Fundraising Organizations Four Things to Know About Rare Disease Patient Registries 5 Ways Employers Can Support Rare Disease Caregivers in the Workplace
