Long overdue posting about my mother
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- This topic has 6 replies, 6 voices, and was last updated 13 years, 3 months ago by tnyjax34.
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July 25, 2011 at 9:08 pm #51825tnyjax34Member
Michael,
I am currently facing similar circumstances. Your mother can try TPN with a PICC line, though there is a risk for infection. How about options for a feeding tube?
Good luck…
Trevor
July 25, 2011 at 5:19 am #51824mrkvlaSpectatorThank you Lainy, Gavin, Randi, and Pam. Its day by day now, just trying to get her stronger before the next step. Thank you all for your guidance. We keep fighting and praying.
July 24, 2011 at 10:50 pm #51823cherbourgSpectatorMichael,
One of things given my Mom was an appetite enhancer called Megace. It was a liquid given once a day. It made an amazing difference and she regained and kept her weight. You may want to inquire about this medication.
I’m keeping you and your mom in my thoughts and prayers.
Hugs!Pam
July 24, 2011 at 9:10 pm #51822gavinModeratorHi Michael,
Welcome to the site. So sorry that you had to find us all here and I am sorry also to hear about what your mum is going through. I was my dads carer during his fight with CC and I so know what you are going through right now and how you feel. You have done the right thing in coming here and seeking help for your mum and I am glad that you have joined in with us. Please feel free to ask any and all questions that you have and we will do what we can to help you here. We are not doctors, but we know what you are going through right now and we care.
That is great to hear you say that both you and your mum do not want to give up the fight. And yes, as far as seeking other opinions go I agree with what Lainy and Randi have said about getting one. If your mum feels that she should get one then that is her right to do so. Please let us know how her app goes on Monday and what they say and recommend for your mum.
My best wishes to you and your mum,
Gavin
July 24, 2011 at 5:10 pm #51821RandiSpectatorMichael,
I am also in Rochester, NY and had CC treated at Strong Hospital. I was able to have a Whipple at the end of 2009 and had chemo from February – July last year. My oncologist is Alok Khorana.
While i was happy with the care that I received at Strong, I sought out a second opinion on my course of treatment from the Mayo Clinic in Rochester, Minnesota. They agreed that the right things were being done.
I would be happy to talk to you about my doctors and experience at Strong and my opinions on them and anything else that you think would help you during this time.Please feel free to write to me at randi.barrell@gmail.com (please identify yourself as Michael from cc.org (so i don’t mistake you for spam).
Hang in there
-Randi-July 24, 2011 at 3:24 am #51820lainySpectatorDear Michael, welcome to our wonderful family but sorry you had to join us. It seems that around here, the first treatment of choice is the Gem/Cis cocktail as people tolerate it fairly well. Is her ONC knowledgable about CC? We are big believers in second and third opinions. What is the hospital doing to build her up. What kind of prognosis has the ONC given her. Where is the Cancer located and what is the size. How is her LAB work? So many factors go in to this. It’s possible that she just had a bad reaction to that particular chemo. She is young enough to fight but attitude is so very important for both of you. You don’t want her using her energy negatively. She needs that energy to fight.
There is an excellent Doctor in the East, Dr. Kato and I am sure Jim Wilde will come in here and tell you about him. Also if you go to our search engine at the top of the page and type in Kato or Canady, posts will come up talking about these doctors.
When my husband was diagnosed I practiced Gut Medicine 101 and it got us though 5 years. Listen to your gut. If you feel she is not getting what she needs move her onward. I know we have had people in her position and they have bounced back. We have members who were given months and are here after years. We try to remain realistically optimistic. My bottom line after all my gibberish is that I would send all her reports and tests to Dr. Kato and see what he says. Also when you meet with the ONC you have a right to know exactly what he feels her prognosis is. Best of luck and please keep us posted.July 24, 2011 at 2:31 am #5474mrkvlaSpectatorHi my name is Michael. My mother, age 59 and in excellent health prior to illness, was diagnosed with Stage 3 unresectable Cholangiocarcinoma this past May. After reading posts on this website, I contacted Dr. Canady and a couple others, sent her scans, and all agreed that she was not, at present, a surgical candidate. She is in Rochester, NY receiving care at Strong Memorial Hospital’s Wilmot Cancer Center. I have been regularly reading the posts on this website since the time of her diagnosis. There are so many wonderful stories of hope and triumph and I have been sharing them with my mother in an effort to encourage her to fight.
She started with Gemzar/Oxaliplatin biweekly. 4 treatments were scheduled. The side effects were extreme fatigue and weakness. Also loss of appetite. After the 3rd treatment, a CT scan was taken that showed the cancer had not spread, or grown. This was, in the words of her doctor, “good news in cancer management.” A couple days later, a PET Scan showed more or less the same thing as the CT but that the cancer was “active.” Her oncologist switched to FOLFOX and she had one treatment. This past Monday, her second scheduled FOLFOX treatment, the chemo was not administered because her lab results showed a low platelet count – instead she was given a blood transfusion. On Wednesday she met with a Palliative Care doctor to deal with symptoms of incredible weakness and fatigue. He told her that her situation was “serious” and she checked into the hospital that day to “get stronger.” She is still there as of tonight. She had a procedure to help her with the ascites, which has been a problem since April. She has had four or five paracentesis procedures since May and now has a tube which allows drainage to a bag. Her oncologist paid her a visit Friday and said nothing about chemo; just that he wanted to see her get stronger. Monday she has an appointment with him to discuss the next steps. She has had no jaundice and, prior to this week, was still walking about the house, unaided.
SO – Im asking those of you that might have had similar experience to comment. We do not want to give up the fight. It seems that a major reason for her going to the hospital is her lack of nutrition and weight loss. She cries that she cannot eat and has become skin and bones. Since being in the hospital she is eating more, but still not enough. What can we likely expect? Can people realistically improve from this condition? Her palliative care doctor said that he has seen people improve… Im dreading Monday’s appointment because I feel her doctor will recommend stopping chemo. Hopefully not. That to me would signify the end is near. If thats the case, should we contact another oncologist? How much of this situation now is willpower, and within my mother’s control? Thank you all for taking the time to read this and thank you in advance for your comments. G-d bless all of you.
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