Nathalie Paravicini ND

"I have been a patient of Dr. Paravicini since 2019. I have a very complicated medical situation and with her help and guidance, she helped identify how to treat/diagnose my rare Hyper Mobile Elher Danlos Syndrome, POTS, and tethered cord, and mycotoxins mold exposure symptoms. I hezitate to share my positive experience here on a review because she is such a great doctor, and i want to keep her all to myself. Good doctors like her are rare. But my diagnosis is a rare diagnosis to have, and since good medical care is so difficult for people with rare conditions to obtain, i pray that this review will be the bridge from a disparing health situation to the path of restoration. That is what happened to me. When I first came to her I was dieing at age 28, but none of the 20 other doctors I saw were able ro help. In fact, they either ignored my plee for help or dropped me as a patient. But Dr. Paravicini always believed me. She even advocated for me at the insurance level and encouraged me to never give up, even as my health was failing me. She also manages the health of my children, who also have a very complex medical history. A few times when I was having medical crises, she allowed me to talk to her after clinic hours. She has gone above and beyond. Especially when i was having a gastric infection and couldn't afford to pay for the antibiotics that insurance wouldn't cover; she helped me advocate and find a more affordable option. Im sure at times, she even worked off the clock to see my health outcome improve. She also wrote several letters for my social security hearing, of which her medical notes were one of the cornerstones that caused the judge to approve my social security benefits. My benefits were just approved 2 days ago. Now i get to continue to heal and i have a good chance of being a mother to my kids for many years to come. I hope that if you're being cast aside/ignored by other doctors, you do not give up. The world needs people like us to help eachother find quality Healthcare so that we can remind the world through our stories of hope, that everyone, no matter their diagnosis, are worthy of being part of the human race."