Katee Yang, PsyD

staffing issues, you could be on hold for a appointment for a very very long time.
Jun 6th, 2022

Feb 23rd, 2022

I've been a patient there since 6 months old #THEBEST
Feb 8th, 2022

STAY AWAY! My wife was diagnosed last Summer for Huntington's Disease by HDSA Duke University. Came here for continuation of care because we moved to Philly. They said my wife doesn't have HD because she doesn't have the movements. Not all patients with Huntington's experience movements in the first stages! They are using outdated material on HD. It used to be called "Huntington's Chorea", but over time the name was changed to "Huntington's Disease". My wife has cognitive symptoms and a CAG repeat of 42. We met a total of 3 doctors and all had horrible bedside manners because they didn't even introduce themselves- Dr. Amalia Peterson (fellow doctor), Dr. Sarah O'Shea, and another doctor who we think was Karen Marder (doesn't help when she didn't introduce herself). Lastly, we met with a social worker named Deborah Thorne via video call. She told my wife, You look great, I cant tell anythings wrong with you, be happy about that." She just insulted every individual who has a disability. Not every disability is VISIBLE!!! And is she saying that if my wife looks great, that people in their later stages of HD look horrible?!?! Huntington's Disease isn't seen visually 100% of the time, every patient is different. Find a clinic where you don't have to educate the doctors on the disease. Find an HDSA Center of Excellence where they've actually seen HD patients and have updated material. My wife posted our experience on her Facebook support group and they were all horrified, but not surprised. STAY AWAY! My wife was diagnosed last Summer for Huntington's Disease by HDSA Duke University. Came here for continuation of care because we moved to Philly. They said my wife doesn't have HD because she doesn't have the movements. Not all More
May 19th, 2022

Mom arranged to donate her brain for study upon her death. At the time, family asked to be given the full autopsy report and were told it would take 6 months, but we would get it. After 8 months, we were told that it was delayed due to Covid, but would be available soon. After 10 months we were told it never takes this long and would be available after the pathologist signed off. No one ever kept us up to date with what was going on. It's now more than a year since her death and we have heard nothing. Is it Incompetence? Lost specimen? Commercialization of her remains? Insensitivity? Would definitely recommend AGAINST dealing with this group. Mom arranged to donate her brain for study upon her death. At the time, family asked to be given the full autopsy report and were told it would take 6 months, but we would get it. More
Nov 24th, 2021