Skip to content

Is it worth it to relocate for treatment at MD Anderson?!

Discussion Board Forums Hospitals & Physicians Is it worth it to relocate for treatment at MD Anderson?!

Viewing 15 posts - 1 through 15 (of 16 total)
  • Author
    Posts
  • #66276
    marions
    Moderator

    CindiS…..what a wonderful way of giving back to the community, I congratulate you on your efforts of connecting cancer patients with other individuals.
    The Cholangiocarcinoma Foundation will be rolling out a mentoring program as well. It was spearheaded by a Andy, who lost his wife to this cancer, and who saw the real value in one-to-one connections with others alike in a more intimate setting than what this board can offer.

    Congratulations on your incredible success with beating this cancer and having the heart and inspiration to help others in a most kind and caring way.

    You and your husband are wonderful people and have my greatest admiration.

    Hugs,
    Marion

    #66278
    lainy
    Member

    Dear CALicea, CONGRATULATIONS on your successful surgery! WOW! How we love the SURGERY word! Wishing you a very speedy recovery and please do keep us posted on your progress!

    #66277
    marions
    Moderator

    CAlicea….thanks for sharing this excellent news with us. Good advice coupled with personal experience is the absolute best our members can share.

    I wish for continued success and please keep the e-mails coming.

    Hugs,
    Marion

    #66275
    calicea
    Member

    Hi..I just want everyone to know MD Anderson is the best place to be… Their doctors and staff are great. I had a liver resection in September 2016. Feeling good!!! Next scan in Januay 2017.. I live in North Carolina..soon no excuses…get your research done before letting anyone touch your loved ones.. Fight the insurance companies and don’t let anything get in your way. We have a battle already with this monster… Email if you need more information…

    #66274
    cindis
    Member

    I haven’t logged on to this site in a very long time because we have just been getting on with our lives after very successful treatment of cholangiocarcinoma for my husband almost 6 years ago.

    Our surgeon at M. D. Anderson was Dr. Jason Fleming, and Dr. Javle was his oncologist.

    We live only 40 miles from the hospital, so for us it was a no-brainer to go there. However, I cannot praise the whole hospital staff enough for the whole experience. We never once felt as if we were an anonymous patient, and that we were an integral part of the whole team. We were listened to, and our thoughts and desires were always included in the process. I’m not saying we weren’t occasionally overruled, but it was NEVER a case of being talked-down to. Now that being said, I must clarify that my dad was a hospital administrator, my mother was a secretary to the dean of a nursing school at a university, my sister is an diagnostic RN, and we had a brother who was paralyzed from the neck down in an accident in the Viet Nam war and then lived at home with us for 28 years before passing from cancer himself. I have no hesitation letting medical people know this about me, and I do think it does change how we are treated. I don’t pretend to know as much as the doctors or nurses, but I do let them know I’m not totally ignorant about medical stuff and that I do my research and ask intelligent questions.

    To anyone researching any hospital for themselves or their loved ones, I would say this: research, research, research. You may have to do this very fast, so thank heaven for the internet! If you are facing a Whipple, you want the place and/or person who has performed the most, within the constraints of your budget, ability to travel to that place, and support system in place for you and your family. There will be differences in opinion and methods of treatment among these doctors, because they are different people just as we all are. You may have to ask questions – so ask!! It won’t offend them. And if it does, then decide if that matters to you.

    While the medical treatment is the primary concern, don’t overlook the support system in place for the caregiver and family. Some places are definitely better at this than others. And a caregiver who is overwhelmed and burning out from the demands now on them can’t take care of the patient well.

    Since going through our journey, Richard & I have become certified counselors with CanCare. It is a non-denominational, faith-based organization which matches a cancer patient (any kind of cancer) with someone else who has had/is still dealing with that exact kind of cancer. They may still be battling the disease, but usually are much further along the road on the journey than the patient. What they do that is so special, though, is that they will match the caregiver with another caregiver, too. It is so wonderful to have someone to talk to who has been in your shoes and is still standing! Not to mention just having someone to talk to. Your family and friends love you and want to help – and many do, in countless ways – but they can’t understand completely the path you are walking. Being able to talk to someone who has been there, and come through, is a lifesaver. CanCare is free and online at http://www.cancare.org if anyone is interested.

    I just can’t get back here as frequently as I would like, so if there are any questions I can answer for anyone, please email me at cinschmerb at gmail.com. (Written this way instead of traditional way in order to avoid scammers.)

    God bless.

    #66273
    hisprazr
    Member

    Nikki, My husband is a patient at MD Anderson currently with a very large mass that is unresectable. We kept hoping that it would get small enough to do surgery. But the chemo quit working and the amount of radiation they would have to use would have damaged too much tissue for surgery…besides there it is in both lobes and the caudate area which also makes it difficult to treat. With that said, I know that there is a clinical trial that has just gotten approval in later stages. MD Anderson is involved with MASS General in this and DanaFarber as well as a couple others. From what I can understand. MD Anderson and Mass General are leaders in the treatment of this type of cancer especially in difficult to treat cases. They have been wonderful to us and currently have his scheduled for a surgical procedure to place an alloderm spacer between the liver and stomach/small bowel to protect them while they hit him with massive doses of proton therapy. They are approaching this with curative intent and so far have found this approach to be as effective as surgery. This is the information they gave us. Personally, I like the team approach where they take the case before a whole team of specialized doctors who review and all put in their opinions on the best plan of attack in a case. What you end up with is a concensus of all of their knowledge reaching the best process for the particular patient. We love MD Anderson.
    But, we also live about 75 miles away only. So, that makes a lot of difference in these decisions too.

    #66272
    knreimer
    Member

    Nikki,

    I am currently under treatment at M.D. Anderson for CC. If you need anything at all, advice about the hospital, city, my doctor, etc.. Just let me know. It’s a wonderful place.

    Best,
    Kelly

    #66271
    lainy
    Member

    Dear Nikki, Kato/Sonneday are excellent choices. Not sure about CTCA. I don’t think either one would turn you away should they feel they want to wait to see if there are any changes. I don’t know if they can use Cyber Knife but my husband had that to shrink a tumor, although his was located in an easier place. Hoping for the best for you and soon!

    #66264
    pamela
    Member

    Hi Nikki,

    Dr. Sonnenday is the first person my daughter, Lauren saw at U of M. He is a great liver surgeon and wonderful person. Hopefully, one day Lauren will be able to have a resection. I know he will want to help your father if he can. I cannot say enough good things about him. I have heard things about Dr. Kato, but don’t feel qualified to say anything. I’m sure others will be along that can answer your questions. If you wish to ask me more questions about our experience with Dr. Sonnenday and U of M please e-mail me . All the best to you and your Dad.

    -Pam

    #66265
    nikki4470
    Member

    Thank you all so much for your kind words and welcoming. We have our appointment with Dana Farber tomorrow and will let you know how it goes. I have reached out to Dr. Kato’s office and do plan on sending him the records. I have also reached out to Chris Sonnenday at the U of Michigan. My head is spinning trying to figure out the best approach. I have also contacted the CTCA, but I am nervous because I haven’t read a lot of positive posts on this site about this treatment center. It seems as if they have a lot of different techinques that don’t seem to be offered at other places which is promising.

    I understand surgery is the way we want to go, but I do know that we need to somehow shrink the tumor enough so that it detaches itself from the hepatic artery and moves away from the blood vessels before this can happen.

    Does anyone know if Dr. Kato strickly determines whether surgery is an option at this point in time? If it’s not in his eyes because of the risk, would he tell you to consult your own oncologist and then revisit the situation with him should your situation change?

    Thank you all!
    Nikki

    #66270
    pcl1029
    Member

    Hi,
    Have you try to contact Dr. Kato for a 2nd opinion. If I were you, I would. The reason is simple, he likes to challenge himself on difficult cases.
    Surgery is the only possible cure for this disease;systemic chemotherapy and or targeted therapy are currently not.
    MD Anderson is renown for systemic treatments and clinical trials, if this is what you are looking for, then go ahead; but make sure that is what you want.
    God bless.

    #66269
    marions
    Moderator

    Nikki…a warm welcome to our site; the one no one wants to belong to and yet is glad to have found.
    I wish the best of luck with your upcoming appointment at Dana Faber. Please keep us posted. We care and we are in this together.
    Hugs,
    Marion

    #66268
    gavin
    Moderator

    Hi Nikki,

    Welcome to the site. Sorry that you had to find us all and I am sorry to hear what your dad is going through. But glad that you’ve joined us all here as you will get a load of support and help from everyone here. And I am sorry to hear that your dads surgery did not go as you all would have hoped. But unfortunately, your dads experiences of starting surgery and it having to be stopped are quite common. This cancer is very difficult to diagnose and so many people have been through what your dad has with the surgery only for theirs to be stopped too once the surgeon sees what is happening. I know that won’t make you feel better and I can so understand why the 16th October was the worst day of your life. I can still remember what I felt like when we were told about my dads CC and that it was inoperable from his diagnosis.

    Please do not give up hope now and try and stay positive if you can. No metastisis is good news and the hospitals that you are talking about are very experienced in dealing with CC patients. I know that all of this is so hard to deal with and that your head is probably still spinning right now, but you are doing an excellent job in being there and helping your dad through this. And please know that we are all here for you as well and so know what you are going through right now.

    My best wishes to you and your dad,

    Gavin

    #66267
    wallsm1
    Member

    I am not treated at MD Anderson, but others are.
    I did get another opinion at Mayo and was super impressed by them.

    Take care,

    Susie

    #66266
    lainy
    Member

    Dear Nikki, welcome to our extraordinary family but sorry you had to find us. I am so sorry about your Father’s aborted surgery. Most of the Surgeons just don’t know until they go in as to what they will really find. As for the hospitals you mentioned my own opinion is that I would go to Dr. Kato as he is so much closer. You are going through enough without uprooting to move. Honestly, the top hospitals and Doctors are pretty much on the same high level. If you go to Dr. Kato you can always decide after to send the LABS and tests to Dr. Javle for a 3rd opinion. Concentrate on the good news, NO METS! Sounds like you have done your homework as well. Please keep us posted as we truly care and I know you will get some more suggestions on the Board, soon.

Viewing 15 posts - 1 through 15 (of 16 total)
  • You must be logged in to reply to this topic.
©2019 - All Rights Reserved, Cholangiocarcinoma Foundation
Scroll To Top