A curated home base for the kidney and autoimmune community.

Patient education, peer mentorship, and clinical resources. I serve as a peer mentor and am on the Medical Advisory Committee.

Patient-focused education, research funding, and community for those living with IgA nephropathy.

The international gold-standard guidelines for kidney disease management.

Advocacy, education, and community for kidney patients and families.

Disease education with strong coverage of lupus nephritis and renal involvement.

Cross-disease advocacy and patient resources spanning 100+ autoimmune conditions.

Evidence-based clinical resources for renal nutrition therapy.

Kidney-friendly recipes, meal planning, and patient-facing nutrition tools.

Independent, citation-heavy reviews of supplements, nutrients, and interventions — the rare ad-free reference for what the evidence actually says.

Plain-English, government-maintained fact sheets on every major vitamin, mineral, and supplement.

Reliable public-facing nutrition science from one of the most cited nutrition departments in the world.

The federal evidence-based dietary guidance, updated every five years.

Cardiometabolic-focused nutrition guidance, recipes, and patient handouts.

The reference database for nutrient composition of foods — protein, fiber, minerals, and more.

Evidence-based patient resources on gut health, IBD, IBS, and microbiome science.

Clinical resources on obesity, metabolic disease, and GLP-1 medications from the physician society.

Annually updated, evidence-based standards for diabetes nutrition and metabolic management.

Pre- and post-transplant education, immunosuppression guides, and patient toolkits from the leading transplant society.

Waitlist mechanics, living donation, financial planning, and post-transplant life from the organization that runs the U.S. transplant network.

Peer community and advocacy for home hemodialysis and peritoneal dialysis patients.

Living donors and recipients showing what's possible after donation and transplant — community, mentorship, and education.

Patient-friendly explanations of the heart-kidney connection, blood pressure targets, and the new CKM-syndrome framework.

Independent, plain-language coverage of diabetes treatment, CGMs, and GLP-1 medications.

The federal research institute behind much of CKD, diabetes, and obesity science — patient pages are authoritative and free.

Free, validated mental-health screening tools and coping resources — useful for the depression and anxiety that ride alongside chronic illness.

Patient advocacy across chronic conditions — insurance, access, and policy education.

Peer phone line, patient magazine, and webinars run by kidney patients for kidney patients.

The most accurate free nutrient tracker — actually shows phosphorus, potassium, sodium, and protein in grams, which most apps hide.

Patients have a legal right to their full electronic health records under the 21st Century Cures Act — labs, imaging, and clinician notes.

Searchable registry of every U.S. clinical trial — filter by condition to find studies you may be eligible for.