Bladder Cancer Group: Introduce yourself and connect with others
Welcome to the Bladder Cancer support group on Mayo Clinic Connect.
This is a welcoming, safe place where you can meet people living with bladder cancer or caring for someone with bladder cancer. Let’s learn from each other and share stories about living well with cancer, coping with the challenges and offering tips.
Feel free to browse the topics, use the group search to find answers to your questions or start a new discussion.
Pull up a chair. Let’s start with introductions.
What type of bladder cancer were you diagnosed with? What treatments have you had? How are you doing?
Interested in more discussions like this? Go to the Bladder Cancer Support Group.
I was recently diagnosed with Bladder Cancer Stage 2. I have had a TURBT and am now preparing for chemo and radiation treatments. I am 77 years old and a bit apprehensive about all of this. It is moving very fast (4 weeks ago had surgery. I am not even sure about the name of the cancer but will find out on Monday when I get results of PET scan done 3 days ago. Is there a real need for all this rush?
Hi Jo, thank you for your post. We are all new to bladder cancer, chemo & surgery. How was your chemo experience? How did they administer it to you? Did you have a port? Which diversion did you choose? Thank you, Jolynn
Good luck Steve. I’m 9 months out. Two turbt surgeries, 6 BCG and 3 more this past month. So far so good but this is a life long battle for many. You need to trust your urologist
Thank you for your welcome post Sue. He just had a MRI waiting on results. He had a bad fall at work where he fell backwards and hit the back of his head. He has not been the same after that fall. Waiting on a Neurologist appt. He starts January 6th with chemo. He really is confused and can’t make up his mind. Hoping to get clarity soon. But the docs still do not want to put a port in.😭
Hello @louw and welcome to Connect. My husband has dealt with invasive bladder cancer for 5 years now. Initially he had surgery and chemo to remove a small diverticulum off the bladder where the cancer was found. Lymph node removal at that time showed one positive node so the chemo was done, as well as Gemzar in the bladder. Continued recurrence and a failure on BCG and Keytruda ended up with a radical cystectomy and prostatectomy with Neobladder creation at Mayo Clinic in Rochester. He did not want a Urostomy so this was his choice. He has experienced many complications due to this surgery but now that all have been dealt with, he is happy with the outcome. He does self catheterize 3 times a day. He was 69 when he had this surgery. Others with this surgery have had better results but perhaps scarring from his initial surgery was an issue.
I recommend researching your options and forming questions for the surgeon. You want a urologic surgeon who has done many of the procedures. Referral to a large specialty center is an option. It is a big surgery with a week or more of hospitalization. It can produce a cure, though, and that is what is most important.
Welcome to Connect @jojo2059 . It has to be heart wrenching to see your brother going through so many health issues. My husband had high grade bladder cancer diagnosed 5 years ago. He has had multiple surgeries and did have chemo with Cisplatin after the first surgery. He was recommended to have a port and that worked well for him. It was removed around a year after treatment. Your brother needs help in making the decisions about treatment, but ultimately it is his decision unless he is declared mentally incompetent. Has he had neurologic testing for his potential dementia?
Hi. I was diagnosed with MI bladder cancer in June of 2024. I'm a 55 year old female. You’re right. It is scary. In the past six months I've been through 3 mos of chemo and today marks exactly 5 weeks since my bladder removal/neobladder surgery. It's certainly not easy, but you can absolutely do it, too. I would suggest allowing yourself to lean on the people around you. They will help you get through it. All my best to you!!
Hi Josephine. I had chemo (just as you described...same meds and schedule) this past summer. I had/still have a port and can't imagine doing the treatments without it. It makes things much easier on the patient in my opinion. They can do the chemo and bloodwork taken from the port and it saves your veins from all of those painful sticks. I'm glad I had one put in.
Hi @jojo2059, I'm very sorry for all your brother is going through. God Bless You All and praise God that he has you there by his side.
To answer your question, I didn't have those treatments. My treatment method was BCG, but as far as I know they're done the same way. The Nurse Practitioner administers a catheter through the urethra and into the bladder. The treatment goes straight into the bladder, which lets us avoid a lot of nasty side effects such as hair loss, and severe weight loss. Maybe someone else who has had both of those particular medicines administered and confirm the administration method. Stay strong and best wishes.
Im a 66 year old male. I have been treated with bcg for bladder cancer for a couple years now. Recently it has progressed into the bladder muscle. My urologist is suggesting I'll need chemo and bladder removal. This is all very frightening and I'm interested in how others are dealing with their bladder cancer.