Just Diagnosed

foxhd said:

Us OLD survivors

Just so you guys all know, Us experienced survivors have been here awhile. But we speak the truth. Making up stories would be way too hard to remember what we have said. So......having a chance to hear EIMS take on things is "fresh" and encouraging and accurate. It is all NTI. Nothing to it! Absorb all you can from our posts. It is gonna help. Good luck!

By the way, BEAUTIFUL picture Eims. Stay well for your family.

Ah Fox you old charmer!!
Eims

Ah Fox you old charmer!!

Eims x

Sable2900 said:

Just Diagnosed

Thought of another question I would appreciate your answering -- after surgery do you go to Intensive Care?  Oh more questions - do you have something going through your nose?  I understand you only get ice chips for a few days - don't care but just heard that.  Anything you can tell me about after the surgery will be appreciated.

After Surgery

My surgery was around noon on a Monday. Mine was a radical right nephrectomy. I woke up Monday night in a regular room around 7-8pm. I don't remember much of that first evening. I had some vomiting that evening, but that was because they didn't really hear me when I told them that morphine makes me sick. No tube in the nose. Only a tube somewhere else! (Catheter). The next morning they encouraged me to walk and my son helped me. I only made it to the door and back, but that was about 8 am Tuesday morning. They removed my catheter that morning. I started eating that morning (liquid diet), but was on a regular diet at lunch time. By afternoon I was walking down the hall a bit and the next day in the morning (Wednesday) I was walking around the ward. I went home on Wednesday afternoon. Because I didn't do well on morphine, they took it me off it right away and gave me tramodol instead. It worked great for me.

The biggest pain (besides in my side) from that first week was that my bowels didn't start working until Friday night. I recommend a mild stool softener/laxative (emphasis on mild) that first week. I used an over-the-counter one called Senna Plus (which I think is a natural one). The pain meds can be constipating and it takes a few days for the bowels to recover.

You will do great!

Todd

cralleycat said:

Also just diagnosed

Sable, I was also just diagnosed.(3/10/13.... thirteen thirteen!).i have a 2.5 cm tumor on my right kidney that was an incidental finding on a cat scan and confirmed with an MRI. I too am overweight, 51 yrs old and unfortunately have diabetes and a cardiac history..(2 heart attacks in the last year and 4 stents since 2001) The surgeon says I'm considered high risk for surgery so they would prefer to do the radiofrequency ablation on the tumor instead.the decision they said is mine and they would do the robotic partial nephrectomy if i choose. I'm still reeling from the diagnosis and i really want the cancer out of my body but am scared to have a surgery..but i'm afraid that if i have the ablation now and the cancer comes back that i may be in worse health later and surgery would not even be an option...the tumor was a 6mm cyst on an ultrasound in june 2009. Has anyone had the rfa treatment? 

Cralleycat

With your health history, if I were you, I would risk the surgery. You already identified the risk for future complications. The goal is to live being well in the future not compromized. If the will do the surgery, you know that they will be prepared for complications. You will be safe. That's my take.

lconno said:

Kidney cancer

I too was just diagnosed with kidney cancer, mine was found by accident thank god, I am scheduled for a kidney removal on April 30th, I am overweight also, but my drs seem to think all will be fine.   Good Luck to you!!!  Any comments are appreciated!!!  I had a hysterectomy on Feb 26th, after two weeks I was experiencing some pain that I thought was unusual, called the Dr after hours and was told to go to the ER.  Upon going to the ER a ct scan was ordered to check for infection from the hysterectomy, it was there that they found a 2.8 cm mass on my left kidney, I had a biopsy 2 days later, and was told I had renal clear cell carcinoma.  I then went to our local Karmanos cancer center, where I was given the utmost caring and kind treatment, blood work was done and my options were given to me, I was told the cancer I have does not respond to chemo or radiation, so the only option was surgical removal, I am a lil bit scared as the Dr informed me that the tumor even though it is small it is laying on top of the main artery to my kidney, so he wont know until he gets in there how much they will have to remove.  Any suggestions or opinions are greatly appreciated.  Thank you

Michigan

Iconno,

Like Garym and myself we are all from Michigan. Good to hear like Gary M and myself that your tumor is xmall and a complete recovery from the surgery alone is in the cards, Sorry you had to go thru that other stuff, but I can't help you there. As for how much they remone, partials were not none in the early years of the Century when mine was done. I understand that it is sometimes a game day decision.

 

Icemantoo

kidney cancer - just diagnosed

Diagnosed about 3 weeks ago. got a 20cm mass on the left kidney. They started me 50mg of sutent daily for 6 weeks. i was told that surgery has to be done after 6 weeks at this point. Im only 41 and have 2 small children 8 and 10 and a loving wife. I have never been so confused about anything in my life... Cant get over this pain in the chest and back....... almost unbearable. Anyone ever go thru a similar situation? 

alice124 said:

Back pain, particularly in

Finatic,

Back pain, particularly in the flank area of the back, is a common symptom of kidney cancer. With a  20 cm tumor, I'm certainly not surprised there's pain. Did your doctor start you on Sutent to hopefully prevent further growth between now and surgery? Did he tell you anything else such as what type of kidney cancer -- clear cell? chromophobe?  papillary?  A 20 cm tumor is a large tumor, and I would hope its excision in six weeks will alleviate much of the pain. If you can provide more information regarding your diagnosis, perhaps others can chime in on relevant experience.

I understand it's a frightening time for you, particularly with two young children. But kidney cancer advances have been made in recent years, months, weeks, and the outlook is not nearly as bleak as it was just a few years ago. But work on developing and charging the cancer with a positive and I CAN DO attitude; it's one of the most valuable tools you'll have in your fight.  And know that we're here to help.

 

 

Yes im on a 50mg daily dose

Yes im on a 50mg daily dose of Sutent. Started a few days ago. Im sure I was told what type it was and I want to say "clear cell". There is just so much information going back and forth it hard to keep track of everything. This is all just so sudden..... Its a large mass and the complication is that its crushing the pancreas at this time. They want to try to shrink it a bit before going in for surgery.  

 

finatic1354 said:

Yes im on a 50mg daily dose

Yes im on a 50mg daily dose of Sutent. Started a few days ago. Im sure I was told what type it was and I want to say "clear cell". There is just so much information going back and forth it hard to keep track of everything. This is all just so sudden..... Its a large mass and the complication is that its crushing the pancreas at this time. They want to try to shrink it a bit before going in for surgery.  

 

Different

WE are all different, so to speak.  I had a triple whammy (No not a Denny's breakfast either).  My tumor was big 14 cm, and I had Renal Vein invasion, plus my other Kidney is less than 100% already.  I had lights out around 10 am, and woke up around 2 am the next morning..  I did not ask before how long.. glad I didn't..  I was in the ICU for 10 days..!  This was due to the Renal Vein procedure that almost took out my remaining Kidney.  I had a tube down my throat and the Catheter.  Both tubes were put in AFTER I was out..!   Now, forget all the TV shows.. the breathing tube came out easily.. on the first day I think. No sore throat, etc.  But again due to the Renal Vein procedure the Catheter was in for most of the ICU time.  They wanted to monitor every drop that came out of me..  I won't go in to more detail there... but even that was removed easily, no pain at all..!!   I was regular the day after surgery.. and was walking on day two.  Yes I still had pain...  and a lot of fatigue.  Oh on day 12 I went home..!!  It was not bad at all... if not for the fear and the initial pain, the experince was actually pleasant, if that makes any sense.   I had a smile on my face, even when I hurt.. I made pals of the Doctors and Nurses, remember they are the ones that can bring you goodies..!  The Doctors and Nurses were so nice..  OK, so I got ice chips at first... then I asked about orange juice, nice... then one of the Nurses asked me if I wanted a Popsickle..  OH yes..!!  Popsickles are heaven..!  I was able to get a Popsickle even at 2 am..!   Then I got food...  I never went overly hungry.. and the menu had lots of healty food on it.  After like day 5, I really was ready to go home...  but as my Kidney was still in danger or failing, they kept me a long time..  Finally the numbers got in line and I never looked back..!

I hope it goes even easier for you..

Ron

cralleycat said:

Also just diagnosed

Sable, I was also just diagnosed.(3/10/13.... thirteen thirteen!).i have a 2.5 cm tumor on my right kidney that was an incidental finding on a cat scan and confirmed with an MRI. I too am overweight, 51 yrs old and unfortunately have diabetes and a cardiac history..(2 heart attacks in the last year and 4 stents since 2001) The surgeon says I'm considered high risk for surgery so they would prefer to do the radiofrequency ablation on the tumor instead.the decision they said is mine and they would do the robotic partial nephrectomy if i choose. I'm still reeling from the diagnosis and i really want the cancer out of my body but am scared to have a surgery..but i'm afraid that if i have the ablation now and the cancer comes back that i may be in worse health later and surgery would not even be an option...the tumor was a 6mm cyst on an ultrasound in june 2009. Has anyone had the rfa treatment? 

Hi Cralleycat,

I just wanted to give you the benefit of my experience with kidney cancer. I was first diagnosed in 2003, I lived in Dallas at the time. A tumor a 3.5cm was discovered on my right kidney. South Western Medical Centre offered me Radiofrequency treatment to burn the tumor. I had the treatment and obviously regular check ups, all appeared to be fine.

Fast forward 10yrs and by then living in France. I had a CT scan in 2009, it indicated a scar on my right kidney, which was assumed to be from the previous surgery. I recently had an MRI which in fact showed clearly the regrowth of a tumor, pretty much the same size as the original. I was advised that Radiofrequency was not the treatment of choice, only being used for cyst sized tumors.

I am now 8 days post op from a partial Nephrectomy robotic surgery and all the cancer was successfully removed. My surgeon informed me that had I gone this route the first time I probably would not have faced a second operation. Which was also more difficult because of adhesions from the previous surgery. I do not know if the type of treatment I had on the first occasion had any bearing on the reoccurrence of the cancer! But I am pleased to know that it has all gone now.

I hope this helps you in some way to make an informed decision and wish you all the best.

Djinnie