I officially joined the club today
Today I officially joined a club that I never wanted a membership to... My doctor, from MD Anderson, called this evening with the pathology results, and I did have cancer. I actually had two masses on my right kidney. The first was 2.2cm and the second one was 8mm both were malignant, but both are now gone and I got to keep 95% of my right kidney.
I have a stage I renal cell carcinoma subtype:chromophobe. The margins were clear. The surgery was done robotically at MD Anderson on Oct 23rd 2015.
I want to thank everyone on this board for sharing their stories, fears, and wisdom. It has helped me more than you will ever know.
Comments
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Yes it was one heck of anicemantoo said:Initiation
Medic.
That was one hell of an initiation, wasn't it?
Icemantoo
Yes it was one heck of an initiation. Glad the surgery was a success and now behind you! Now you can relax and move forward with your life. Just keep up with your scans and you should be just fine.
Hugs
Jojo
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I'm very sorry you had to
I'm very sorry you had to join, but it's good news to know the surgery was a success. Stage 1 is the best pathology report someone can have, as far as I know, the recurrence rate for chromophobe is low, so wish you a long healthy life Forough
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Doctor?
Sorry to hear the C word but glad they got it out. I too am a chromy. (diagonosed in May 2015) Weird thing is my son who lives in Houston area is going in for a radical nephrectomy next week he is 36 and a father of two boys. We are very concerned. I have been told that chromies are rarely hereitary. So who knows? May I ask who your doctor is at MD? My son is going to Houston Methodist.
How soon did you get your pathology report? We are very anxious to get it because I have other children and grandchildren that will need to be checked.
Thanks
nana4life
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DoctorNana4life said:Doctor?
Sorry to hear the C word but glad they got it out. I too am a chromy. (diagonosed in May 2015) Weird thing is my son who lives in Houston area is going in for a radical nephrectomy next week he is 36 and a father of two boys. We are very concerned. I have been told that chromies are rarely hereitary. So who knows? May I ask who your doctor is at MD? My son is going to Houston Methodist.
How soon did you get your pathology report? We are very anxious to get it because I have other children and grandchildren that will need to be checked.
Thanks
nana4life
Hello Nana,
I saw Dr. Jose Karam at MD Anderson and I was so very happy he is my doctor. I live in OKC and traveled to Huston for treatment. Has your son considered MD Anderon for a second opinion? Those two hospitals are less than a 1/4 mile, if that, from each other. I stayed at the Marriott hotel that is connected to Houston Methodist. Looks a very nice place.
http://faculty.mdanderson.org/jose_karam/
It took 11 days total to get my path report back. I was warned that the path report could take a couple of weeks to hear something back. Dr. Karam actually called me himself with the path report last night at around 7pm.
Has anyone mentioned Birt–Hogg–Dubé syndrome to you? No one has said anything to me yet, but I am going to bring it up and see if I need to get tested. I have a 6 year old daughter and I wonder about her. I have no family history of kidney cancer with the exception of my great, great grandmother who died of kidney cancer at the age of 87 in 1948 so who knows...
I'm wishing you and your son the best of luck!
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Thank you. Yes I have heardmedic1971 said:Doctor
Hello Nana,
I saw Dr. Jose Karam at MD Anderson and I was so very happy he is my doctor. I live in OKC and traveled to Huston for treatment. Has your son considered MD Anderon for a second opinion? Those two hospitals are less than a 1/4 mile, if that, from each other. I stayed at the Marriott hotel that is connected to Houston Methodist. Looks a very nice place.
http://faculty.mdanderson.org/jose_karam/
It took 11 days total to get my path report back. I was warned that the path report could take a couple of weeks to hear something back. Dr. Karam actually called me himself with the path report last night at around 7pm.
Has anyone mentioned Birt–Hogg–Dubé syndrome to you? No one has said anything to me yet, but I am going to bring it up and see if I need to get tested. I have a 6 year old daughter and I wonder about her. I have no family history of kidney cancer with the exception of my great, great grandmother who died of kidney cancer at the age of 87 in 1948 so who knows...
I'm wishing you and your son the best of luck!
Thank you. Yes I have heard of Birt-hogg-dune. As far as we know no one in my family has had kidney cancer. But you never know. We are going to do some genetic testing as soon as we get the pathology report. I have already begun to getting some genetic work done. my sons Dr is Brian Miles. They are going in thinking full neph but if they can they will do partial. Take care and ILLC keep you in the loop. Us chromies are a bit different. Take Care
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Ii am new member her..
Good day to everybody,
i joined here in this site because ia am also a nephrectomy patient i was undergo operation last May 10,2015 and truly its hard to cope with this especially you knew that you have a cancer eventhough you know that the operation was a succesfully removed the cancer,now everytime i felt pain in any part of my body i was thinking it is maybe a cancer,but now when i was joined here and i read the comment maybe little by little i can cooe with in for knowing that im not alone.Thanks to all wonderful and supportive comment ive read.
God bless us all
Pearly
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WelcomeNothingtolose said:Ii am new member her..
Good day to everybody,
i joined here in this site because ia am also a nephrectomy patient i was undergo operation last May 10,2015 and truly its hard to cope with this especially you knew that you have a cancer eventhough you know that the operation was a succesfully removed the cancer,now everytime i felt pain in any part of my body i was thinking it is maybe a cancer,but now when i was joined here and i read the comment maybe little by little i can cooe with in for knowing that im not alone.Thanks to all wonderful and supportive comment ive read.
God bless us all
Pearly
Pearly,
Welcomr to the club nobody wants to join. Congrats on your first 6 months and may your now cancer free live continue forever.
Icemantoo
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Welcome Pearly!icemantoo said:Welcome
Pearly,
Welcomr to the club nobody wants to join. Congrats on your first 6 months and may your now cancer free live continue forever.
Icemantoo
I am happyWelcome Pearly!
I am happy you found us! I cannot imagine going through all of this without this wonderful and supportive group!
Hugs
Jojo
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Medic
So happy for you and your family,now you can calm done and enjoy your life and family.
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NothingtoloseNothingtolose said:Ii am new member her..
Good day to everybody,
i joined here in this site because ia am also a nephrectomy patient i was undergo operation last May 10,2015 and truly its hard to cope with this especially you knew that you have a cancer eventhough you know that the operation was a succesfully removed the cancer,now everytime i felt pain in any part of my body i was thinking it is maybe a cancer,but now when i was joined here and i read the comment maybe little by little i can cooe with in for knowing that im not alone.Thanks to all wonderful and supportive comment ive read.
God bless us all
Pearly
I had my right kidney removed ,April 2014 , now and again I get anixous when I have pain,but reading comments on here has helped me not to panic ,so i know the feeling ,but im getting better .
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Pearly,Nothingtolose said:Ii am new member her..
Good day to everybody,
i joined here in this site because ia am also a nephrectomy patient i was undergo operation last May 10,2015 and truly its hard to cope with this especially you knew that you have a cancer eventhough you know that the operation was a succesfully removed the cancer,now everytime i felt pain in any part of my body i was thinking it is maybe a cancer,but now when i was joined here and i read the comment maybe little by little i can cooe with in for knowing that im not alone.Thanks to all wonderful and supportive comment ive read.
God bless us all
Pearly
I'm so sorry you hadPearly,
I'm so sorry you had to join, who wants to? It's normal to have fear and anxiety after cancer diagnosis, it took me almost 9 months to pass it and step by step come back to the real me. If you think you need someone to listen to you , we are all here, we 've been there and truly know how it feels so please don't hesitate. A therapist,csn members,my best friend and last but not least my willing to live every minute of my remained time helped me a lot. Hope you can find yours soon.
Forough
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Sorry you had to join
I am sorry you had to join this club, there are much better clubs to be part of, but no finer people to be in club with. The support gained from this site and the wonderful people that are here make the horrible disease a little bit more bearable.
Mark
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