Brigid Freyne MD

Reviews

• CT

  Carmen Thompson-Gibson

  Jul 28, 2026
  5.0
  Dr Freyne is a blessing. If I'd had her treating me from the beginning I don't think I'd be falling apart now. She's thorough, to the point and thinks ahead. The staff has been friendly. The Dr is timely and quick.
• CK

  Connie Katsikaris

  Jul 1, 2026
  5.0
  Great experience. Staff is professional.
• LW

  Laura Walker

  Jun 9, 2026
  5.0
  Quick service.
• RB

  Rebecca Byrd-Chamorro

  Apr 20, 2026
  2.0
  I’m giving 2 stars because the office staff was super friendly. I did not experience a long wait time either. That said, Brigid seemed nice but was not very engaged. I tried to reason with myself that maybe she’s on the spectrum and that’s okay. She dismissed my complaints as “fibromyalgia” and literally tossed my lab results aside saying “false positive”. I’m from Maryland, so I called a friend at Johns Hopkins who works in rheumatology. They were appalled at the dismissal of my labs and symptoms and the fact that a rheumatologist would diagnose fibromyalgia on the first visit. They immediately referred me to another rheumatologist who saw me almost immediately. That doctor ordered a menagerie of bloodwork. That bloodwork confirmed not only do I not have fibromyalgia (I mean, maybe I do but that’s not the main complaint) but that I have overlapping lupus and Sjogren’s. The new doctor also ordered X-rays and MRI’s at my first visit along with additional bloodwork so we can monitor progression of these diseases. If you go here, go with caution. If you feel dismissed, get a second opinion.
• KJ

  Kara Jones

  Mar 13, 2026
  1.0
  I went in to make sure my symptoms were solely CRPS, (women commonly develop autoimmune problems with this awful disease) & treatment. My nervous system is also really broken, I can't even regulate my body temperature anymore. I know CRPS is a rare disease, but I had my hopes up for finally getting treatment, as most "specialists " around here are cash only & charge up to 100k$. I expect Drs to not know anything about this disease, it's rare, and many don't..but to completely ignore me, not even write down my CRPS dx, also in my medical records(dx by several specialists over the last 3 years), to only give me muscle relaxers and label me as fibro...I'd give anything for that dx, I'd be in less pain and wouldn't need the loads of meds from pain management. The only meds that truly help is a specific steroid that settle down firing nerves. Then just telling me no, no steroids. I get damn near suicidal during flareups..even the ERgives me a huge dose when I'm at my limit for extreme pain. /I shouldn't expect medical treatment after 3 years of being passed around..but this is the 1st time I've been completely ignored. I respect the Drs that tell me they don't know how to treat me, at least they don't waste my time & money. Due to lack of treatment, my bloodwork is always a mess, and it has spread to full body. My stomach, heart, face/ 1head, literally everywhere. It feels like I'm on fire with broken bones...I've broken 7 teeth from subconsciously grinding them during flareups. I have a wheelchair, because if I do to much, I literally can't walk. You actually recommended exercise..I'd end up hospitalized or dead from over heating...My toes are crooked from extreme nerve damage left untreated. You know how horrible it feels to be dismissed, and that dx was really disrespectful for what I (and others) have to live with. It's called the suicide disease for a reason..Does this look like fibromyalgia to you(pics below)??? My limbs turning dark purple was the dead give away for CRPS..my foot was obliterated by an 8k lb forklift.. I've been in severe pain since the night of the accident over 3 years ago... Sorry for the long review...but I give up. Only the wealthy have access to care...12k for ketamine...exact same treatment, different doses, for depression, 1k...Between this and bad genetics, I'll be lucky if I live to see 50 anyways...