Topic
Rare Tips
72 articles
Rare Tips9 Things to Know After Diagnosis
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Rare TipsOrganization Spotlight: Remember the Girls
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Rare TipsNutrition and IgAN (IgA Nephropathy): A Practical, Evidence-Based Guide
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Rare TipsThe Invisible Job: What Caregiving for a Rare Disease Really Looks Like
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Rare TipsGluten-Free Doesn't Always Mean Healthy: The Uncomfortable Truth Nobody Tells Celiacs
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Rare TipsLiving with Celiac Disease: What They Don't Tell You at Diagnosis
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Rare TipsLife Hacks for Mobility Challenges: Bathroom Safety Tips and Tricks
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Rare TipsLife Hacks for Mobility Challenges: Dress with Success
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Rare TipsLife Hacks for Mobility Challenges: Get Smart in the Home
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Rare TipsLife Hacks for Mobility Challenges: Tips for the Kitchen
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Rare TipsLife Hacks for Mobility Challenges: Pool Noodles to the Rescue
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Rare TipsEmpowering Patients: The Role of Education in Rare Disease Treatment Plans
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Rare TipsCan Mind-Body Exercises Help with FSGS? See What the Research Says
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Rare TipsCan Yoga Really Help with FSGS? See What the Research Says
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Rare TipsThree Ways to Get Access to High-Cost Treatments
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Rare TipsHow Know Rare is Celebrating Pride Month
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Rare TipsEmbracing Risks: How Taking Chances Enhances Life with a Rare Disease
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Rare TipsThe Surprising Link Between Exercise and Myositis
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Rare TipsUnderstanding Congenital Myasthenic Syndromes (CMS) vs. Myasthenia Gravis
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Rare TipsWhat You Need to Know about CMS and Clinical Trials
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Rare TipsNeedle Phobia in Children: What It Is, What It Isn’t, and How to Help
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Rare TipsThe Link Between Oral Wellness and Your Overall Health
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Rare TipsFour Empowering Ways to Mark Rare Disease Month
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Rare TipsTeens, Substance Use, and Rare Disease
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Rare TipsRare Disease News Roundup
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Rare TipsSafeguard Your Holidays: The Importance of Flu Protection
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Rare TipsExpert Advice on Managing Nutrition for Rare Disease Patients: Insights from a Metabolic Dietitian
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Rare TipsKnow Rare Tips: How to Support a Friend Who’s Been Diagnosed With a Rare Disease
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Rare TipsHow Much Do You Know About Your Myositis?
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Rare TipsWhat is Autoimmune Hemolytic Anemia (AIHA)?
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Rare TipsDiagnosis and Symptoms of Autoimmune Hemolytic Anemia (AIHA)
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Rare TipsNavigating Adolescence with Rare Disease
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Rare Tips6 Tips to Help Fight Fatigue in Rare Disease
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Rare TipsHow to Manage Autoimmune Hemolytic Anemia
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Rare TipsA Celebration of Three Extraordinary Black Women in Healthcare
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Rare TipsLiving With Myasthenia Gravis: 10 Things to Know
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Rare TipsMyositis: Causes, Symptoms, and Classification
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Rare TipsWhat is IVIg (Intravenous Immunoglobin) and How Does it Work?
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Rare TipsMyasthenia Gravis: Questions and Answers
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Rare Tips8 Common Triggers for Myasthenia Gravis Flare-Ups
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Rare TipsHealthy for the Holidays
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Rare TipsTips for Managing a Rare Blistering Disease
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Rare TipsEmbrace your Rare Truth: Becky's Rare Tip on Finding the Right Support
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Rare TipsA Tiger Mom’s Guide for Sudden Hospitalization for a Child with a Rare Disease
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Rare TipsTargetCancer Foundation’s 5 Tips for Caregivers
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Rare TipsWhat Every Rare Cancer Patient Should Know
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Rare Tips"Traveling Different," by Dawn M. Barclay: A New Book for Parents of the Anxious, the Inflexible, and the Neurodiverse
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Rare TipsIn Case of Emergency: Unleash the Power in Your Pocket
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Rare TipsProtect Yourself From the Sun if You Have Bullous Pemphigoid (BP)
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Rare TipsCan What You Eat Trigger Bullous Pemphigoid, a Rare Skin Condition?
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Rare Tips5 Things to Pack in your Emotional Toolkit
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Rare TipsPlunging is Easy, Raising Money is Hard: Lessons to Help Other Rare Disease Fundraising Organizations
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Rare TipsCan Mind-Body Exercises Help with IgA Nephropathy? See What the Research Says
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Rare TipsCan Yoga Really Help with IgAN? See What the Research Says
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Rare TipsFour Things to Know About Rare Disease Patient Registries
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Rare Tips5 Ways Employers Can Support Rare Disease Caregivers in the Workplace
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Rare TipsNAC and Global Genes Publish New Guidebook for Caregivers of Children with Rare Illnesses
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Rare Tips10 Books for Families of Children with Rare Disease
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Rare TipsPlanning for Pregnancy When You or Your Child has a Rare Genetic Disease
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Rare TipsAsk a Genetic Counselor: Common Questions about Prader-WiIli Syndrome
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Rare Tips12 Impactful Books for People Facing Rare Disease
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Rare TipsFive Things to Know about Genetic Counseling and Rare Genetic Disease
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Rare TipsThree Tools for Finding an Expert in Your Rare Disease
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Know Rare Launches Its New Telehealth Solution for People With Rare Disease
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Rare Tips7 Tips For Finding a Clinical Trial for Your Rare Disease
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Rare TipsCreating a More Patient-Centric Future: Lessons Learned at the 2021 JP Morgan Health Care Conference
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Rare TipsUpdates from ASH 2020: Advances in the Understanding and Treatment of Blood Diseases
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Rare TipsAdaptive Clothing: Dress for Less Stress
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Rare TipsKnow More About: The Diagnosis of Myasthenia Gravis
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Rare TipsPreparing for the Holidays with a Rare Disease in the Time of Covid-19
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Rare TipsPlasmapheresis: Procedure Information & Potential Complications
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Rare TipsHow to Reduce Anxiety Before Medical Procedures or Treatments
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