Community-shared experiences with healthcare providers for invisible illness care
Average Rating
Felt Listened To
Avg Providers Before Dx
Recommend Current Provider
Showing 15 of 15 reviews
July 2026
Dr. Sarah M. was the first physician in over three years to actually listen to my full symptom history. She ordered a comprehensive tick-borne panel and started treatment within two weeks. I finally feel like I have a partner in my care.
June 2026
Appointment lasted only 10 minutes. He dismissed my pain as stress-related and suggested I try yoga. Did not order any bloodwork or imaging despite my worsening symptoms over 18 months.
May 2026
Dr. Maria L. diagnosed my POTS after a thorough tilt table test and autonomic workup. She created a detailed treatment plan including medication, compression, hydration protocols, and exercise guidance. Truly life-changing.
April 2026
After 14 months of post-COVID fatigue and brain fog, Dr. Robert K. was the first to take it seriously. He ran extensive labs and started a combination treatment approach. Still recovering, but finally making progress.
March 2026
Refused to test for Lyme because my initial ELISA was negative. Told me it was all anxiety and that chronic Lyme doesn't exist. Wasted months before finding a Lyme-literate doctor who properly diagnosed me.
February 2026
Dr. David W. was one of the few cardiologists in my area familiar with POTS. He took the time to explain the condition and prescribed midodrine along with lifestyle modifications. Wish he had more availability though.
January 2026
Dr. Lisa C. changed my life. After 7 other doctors dismissed me, she recognized my symptoms immediately, ordered the right tests, and started a multi-phase treatment protocol. I am now 80% improved after 6 months.
December 2025
Dr. Kevin P. was sympathetic but admitted he didn't know much about ME/CFS. He was willing to learn and ordered some basic tests, but ultimately referred me to a specialist. Appreciated his honesty.
November 2025
Comprehensive initial consult that lasted 90 minutes. Dr. Angela F. reviewed my entire medical history, ran functional labs, and created a plan combining conventional and integrative approaches. Follow-ups are harder to schedule.
October 2025
Told me that my cognitive issues were from depression, not Long COVID. Did not order any neurological testing. Prescribed an antidepressant and sent me on my way after 15 minutes.
September 2025
Dr. Patricia N. is one of the rare rheumatologists who understands ME/CFS. She spent an hour on my initial evaluation, ordered a comprehensive workup, and connected me with a physical therapist experienced in pacing strategies.
August 2025
Diagnosed my alpha-gal allergy after years of mysterious reactions to red meat. Dr. Thomas B. was familiar with the tick-bite connection and provided a thorough dietary guidance plan. Grateful for the diagnosis.
July 2025
Dr. Susan G. took a holistic approach to my Lyme treatment with herbal protocols and detox support. Results were mixed -- some symptoms improved while others persisted. She was caring but I ultimately needed conventional antibiotics too.
June 2025
Told me my heart rate spikes were from anxiety and that POTS is not a real condition. Refused to do a tilt table test. I had to drive 3 hours to find a cardiologist who would actually evaluate me properly.
May 2025
Dr. Jennifer D. runs a post-COVID recovery clinic and is incredibly thorough. She ordered imaging, autonomic testing, pulmonary function tests, and extensive labs. Her multi-disciplinary treatment plan has helped me regain about 70% of my pre-COVID function.
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Reviews are illustrative examples for demonstration purposes. Provider names are fictional and do not represent real individuals. Patient experiences vary widely and this data should not be used as a substitute for professional medical advice.