I was diagnosed with stage 4 cervical cancer. We debated whether to go to MDAnderson in Houston, however decided it would be easier to go to UCDavis. Dr. Leiserowitz preformed a hysterectomy. He made a HUGE mistake and left 2 clips on my uretor which took 3 minor surgeries and a major surgery to repair. They sent me to Chemo every week and radiation 5 days a week. Horrible experience! They determined I was cancer free. 6 months later I had an issue. Went for tests and found cancer all over in same area only larger! I went to MDAnderson with little hope. They disagreed with UCDavis on treatment. They put me on chemo every 3 weeks. Much, much easier on my body. 6 months later they tested me ( good idea), and declared me cancer free. If you have cancer do not use UCDavis. I almost payed the ultimate price by going there.

I was diagnosed with cancer in Feb 2022. Unfortunately, I had transferred to the UCD Medical group in Mar 2022 and was assigned to Dr Gary Leiserowitz who is the a chief and administrator who has been at UCD for 40+ years. Dr Leiserowitz treats women as was common in the 1970's - you have no rights and must relinquish total control over to him. If you don', he will retaliate. I had necessary surgery scheduled and he abruptly canceled the surgery at my pre-OP appointment because I asked for him (or anyone) to explain information on a consent form. Instead of having a 5 minute conversation so I could sign the consent form, Leiserowitz abruptly canceled my surgery. His expectation was for me to blindly sign all forms and NOT have informed consent. He then lied in my medical record and said I canceled the surgery. Leiserowitz subsequently used his management position to block my treatment from any doctor. Clearly his intent was to harm or kill me, which I found, he has done to several of his other female patients. I contacted UCD patient relations for assistant and all they did was to enable Leiserowitz. Jocelyn Ward, the patient relations "manager" has no care or concern for patients; her only concern is protecting bad doctors for UCD. At the UCD Comprehensive Cancer Care Center there is no "care" , let alone "comprehensive care". If you find yourself with cancer, at UC Davis they will kill you by neglect and make your life a living hell while they are doing it.

I regret that my surgeon, Dr. Michael J. Campbell, did not put as much time and effort into my post-op care as he put into selling his skills and UCD's merits at my pre-op. I now have to go to elsewhere for cancer-care (including routine ultrasounds) because UCD lacks the resources and, frankly, the desire to help me further. I've also had to spend an exorbitant amount of time amending my inaccurate and biased medical records. My records depict conversations that never took place, statements that were taken out of context, and appointments with specialists that I never had. When I chose UCD for my cancer treatment, I thought I had found an ally in my battle against cancer. I thought UCD would have my best interests at heart and would provide me with compassionate and comprehensive care. I couldn't have been more wrong. I've spent more time and energy battling UCD (and trying to recover from my treatment here) than battling the cancer itself. On the morning of my surgery when I was having second thoughts, rather than respecting my wishes or calling a time-out to regroup, my medical team coerced me into the procedure anyway. No one noticed that I hadn't signed an advanced directive after I had requested it. They couldn't keep the oxygen mask on my face on the operating table because I was hyperventilating. The anesthesiology resident disconnected the tube from the mask and tried to push it into my mouth. I thought she was going to break my teeth and I told her that she was hurting me. That was the last thing I recall. When I awoke from anesthesia, the nursing staff chose to tell me the results of my surgery right away while I was still disoriented and then they proceeded to criticize me for crying. I had limited access to water, pain meds, and assistance with the restroom the day after my surgery because the hospital was reportedly understaffed. Other than one brief post-op appointment with Dr. Campbell, I had little to no other care, resources, or contact from UCD in the weeks after my surgery. Once I was out of sight, I was out of mind. Dr. Campbell never informed me of my cancer stage and he denied my request for a referral for radiation treatment right after he told me that I should consider radioactive iodine. As for emotional support, keep your expectations low. UCD does not practice integrative whole patient care. Dr. Campbell acted as though I was asking for something unreasonable or excessive when I requested additional time off from work at my post-op appointment to psychologically process the final pathology (lymph node metastasis) and to get a game plan for radiation treatment. UCD's Cancer Resource Center (a tiny self-serve room located inside the Cancer Center) didn't have any information on my type of cancer/endocrine disorders. The Resource Center is staffed with part time volunteers and not trained medical professionals. UCD doesn't have cancer nurse navigators. Their social worker, Jena Cooreman, will refer you back to the Resource Center if you reach out for support. UCD's Cancer Center website makes it look like they offer more resources and have more overall regard for their cancer patients' well-being than they actually do. Four years after my surgery, I'm now left on my own trying to figure out what to do with the cancerous lymph nodes I still have that can't be easily treated with surgery or radiation. Dr. Campbell told me that potential complications from further lymph node surgery could leave me disabled. He admitted that he does very few of these types of procedures, yet he couldn't (or wouldn't) refer me to another surgeon with more expertise (not even for a basic consult) and he was unapologetic about it. I have no choice but to look for cancer-care outside of the UC Davis health system and I'm left wondering exactly what part of my experience here at the Comprehensive Cancer Center was supposed to have been, "comprehensive."

The health care in Sacramento is shockingly poor. I am an RN with 40 yrs experience and I’ve seen a lot. My primary care MD At UCD was also incompetent, but that’s another story. My experience at the cancer center was poor. Had a hard time finding an RN for support but got connected through a support group. I had 4 or 5 different MDs. Surgery MD was good. But 3 medical oncologists had no bedside manner and were only concerned with the “cancer protocol”. One MD told my PCP I was depressed and needed antidepressants, because I repeatedly c/o not feeling well. After all, I had cancer didn’t I? But in the end, it was discovered I was seriously diabetic (A1c=11) and also had serious s/e from statins. They showed no interest in my s/s for over 1 yr. (was diagnosed later by other MDs). They did cancer procedures when I was having blood sugar reactions and were concerned, but completed the procedure without doing a simple blood test. Seems dangerous now. It was very disappointing, since I am a graduate of UC and wanted to support them. Wish I had explored options. It was a bad time for me.

I writing these words to let many others know about my son's experience there at UC Davis Cancer Center. My son had developed a tumor on his right leg over the course of two years. He was very stubborn and refused to receive medical attention. Finally, one day he broke down and was determined to be seen for his tumor. He was very emotional that day not knowing what he was up against. A bioopsy was done that day and days later it was official he had Myxiod Liposarcoma Cancer. Long story short a oncologist there named doctor Robert Canter saved my son's life. This doctor worked miracles and always had a way of giving my son hope like he hadnever experienced. We are fully convinced that had my son been treated some place else the story would have been much different. Doctor Canter is in our opinion a true blessing.

My son had an appointment here with hematology and this office is a joke. We never received any kind of reminder or confirmation that we even had an appointment, so we had to call and double check to see if they even scheduled it the morning of the appointment. My son's appointment was for 10:30 am. We sat in the waiting room for 45 minutes and then in our assigned room for another 30 minutes. Keep in mind they open at 8, so to be behind an hour and 15 mins is ridiculous. Also, my son is 2 and 2 year olds don't exactly like to sit and wait around for anything. It would help if they had a few toys or activities for kids seeing how it is a pediatric facility. The doctor arrived and didn't even apologize for being an hour and 15 mins late and he also didn't have any of my son's most recent labs even though our pediatrician's office said they sent them over 3 times. The doctor didn't know a thing about our son and I had to explain everything all over again. We spoke for maybe 5 minutes. I lost 3 hours of my day for a 5 minute appointment that was zero help. If you can go to another office, do it. Patients who are going to facilities like this have been through enough pain and trauma There shouldn't be any extra work and stress added because the office and doctors want to do as little work as possible.

I have been coming here for about 8 months preparing for a stem cell transplant. They have always treated me with professionalism, respect and dignity. I traveled there again today from Redding and met with transplant team. This time it looks like I am healthy enough for the procedure. I trust them and believe that they will do everything possible to make it a success.

My husband is part of an immunotherapy infusion trial in Sacramento, California. We live in Bloomington Indiana. My husband says, the entire staff from reception to his oncologist and how everything is handled there is exceptional! I have been communicating with Micaela for over a year, and she is amazing, knowledgeable, personable, and hard working with us! We appreciate her, and all she does for us!immunotherapy infusion trial in Sacramento, California. We live in Bloomington Indiana. My husband says, the entire staff from reception to his oncologist and how everything is handled there is exceptional! I have been communicating with Micaela for over a year, and she is amazing, knowledgeable, personable, and hard working with us! We appreciate her, and all she does for us!

I am having my Retuximib infusion. The nurses are Very helpful. It is not my first time for this infusion, But it is my first time receiving it here. I am a hard stick so hearing that the nurse warmed my arm in a hot towel , tried once and when she didn't get it she called for the ultrasound tech. He was able to get it on the first try. I appreciate them not having to stick me 20+ times. And being very diligent to deal with all my allergies and still proceeded with the Infusion which I greatly need. Thanks for Dealing with this Special kind of Unicorn 🦄 And Making my day a lot easier.

What incredible people. Cancer is a new journey for me and I am so pleased to be having my Chemo and Radiation Therapy at U.C. Davis. From start to finish, everyone is kind and considerate. Even so, they are extremely knowledgeable in the field and I feel very confident that they are handling my care well. If you are looking for someone to help with your treatments, this is the place.

Mallory thinks it's cute to hang up and not do her job. She has not set up major important appointments. It's the cancer center, Mallory. You have hung up on the insurance company, my mother, and myself. If you have any problems with Mallory, please report her to your insurance so we can get people who like their job and want to do their job in the office.

Very clean building and kind staff. The construction right now makes parking an absolute mess but once you're inside, it's very nice.

I have been apply for an MA job like crazy for UC Davis, I hope I get a job.

My experience, for the most part, has been very good. My doctor is Dr. Tuscano.