“Let’s do the 108 Sun Salutations class on Wednesday morning!” my dear friend Nancie texted me. The special class was scheduled for the day of the summer solstice. My initial reaction was to wonder if she really knew me. After all, I’ve spent a significant part of my personal and…
Hope in Action – a Column by Kristen Wheeden
In just a few days, our son Brady will be graduating from high school as part of the Class of 2023. It feels as though my heart will be wearing a cap and gown, crossing a stage, and accepting a well-deserved diploma. On a typical day, Brady’s passing wink and…
As the mom of a 17-year-old son with erythropoietic protoporphyria and a staunch advocate for all porphyrias, I am blessed with some unexpected opportunities. These tend to happen in conjunction with international conferences organized to advance porphyria research and therapeutics. A recent trip to South Africa…
Self-help writer Eckhart Tolle once shared his belief that “awareness is the greatest agent for change.” I hope that’ll be the case as the porphyria community prepares to celebrate its annual awareness initiative on April 19. We have many stories to tell about living with or caring…
In my column, “Hope in Action,” I write about porphyria and the lived experiences of those affected by this group of ultrarare diseases. But for Rare Disease Day today, I want to take a macro view of rare diseases. According to the National Organization for Rare…
As a porphyria patient advocate, I feel blessed to have the opportunity to talk with patients every day. Some have already been diagnosed, while others are struggling to be heard. More than likely, the person on the other end of the phone has suffered terribly from tremendous pain. Or…
Last week, on Sept. 18–20, the American Academy of Dermatology Association held its annual legislative conference in Washington, D.C., where several hundred dermatologists and patient advocates gathered to discuss healthcare policy issues and advocacy. Then, on Sept. 20–22, the Coalition of Skin Diseases (CSD) held its Hill Day,…
Last week was a big deal in the world of porphyria. Some of the most brilliant minds met at the International Congress on Porphyrins and Porphyrias (ICPP) in Sofia, Bulgaria, to share their knowledge and discuss novel research. With many of the strict COVID-19 limitations lifted, researchers were finally…
Bulgaria. Honestly, until recently, I could barely place the country on a world map. Yet over the past few months, I’ve had the honor of organizing a patient day during this year’s International Congress on Porphyrins and Porphyrias (ICPP), set to take place in Sofia, Bulgaria, Sept. 4–7. Participating…
We recently returned from a college visit for my youngest son, Brady, who lives with erythropoietic protoporphyria (EPP), an ultrarare disease characterized by extremely painful phototoxic reactions to sun exposure. I can’t believe we’re already looking at college! Wasn’t I just prepping his kindergarten teacher to help manage…
Recent Posts
- FDA speeds up review of daily pill for rare sun-sensitive skin conditions
- If you’re looking for your people, they’ll be at this year’s Porphyria Palooza
- Modified drug plan aids tuberculosis patient with acute porphyria
- Living with a chronic illness like porphyria is like sleeping next to a cat
- Acute porphyria may first appear as new-onset psychosis, case shows
- Woman’s 4-year mystery illness leads doctors to suspect porphyria
- Blocking Wnt pathway may offer new treatment route for liver porphyrias
- Nerve damage persists between AHP attacks, study shows
- For young girl with fragile skin, sun protection proves crucial to care