need help for my dad
Discussion Board › Forums › Introductions! › need help for my dad
- This topic has 82 replies, 13 voices, and was last updated 11 years, 10 months ago by holly22a.
-
AuthorPosts
-
December 11, 2012 at 4:34 pm #67144lovedad09Spectator
Thanks Pamela. Yes he’s on antibiotic and on call doc said he’s on the right one. They are doing blood culture to find out more.
I feel hard to believe he’s so weak cannot take any treatment. I am not ready to lose hope yet, but doctor told me I should.
December 11, 2012 at 4:28 pm #67143pamelaSpectatorHi lovedad,
I am sorry for your pain in trying to deal with all this. I think you are doing what you need to do for your Dad already, which is be there for him. I have not been through this, but I can tell you what I would do. I would dig deep down inside and find every ounce of strength I had. You need to get hold of your emotions. I would also ask the doctor what they are doing to try and help your Dad and make sure I said to do everything possible to try and help him. Is he on antibiotics if the doctor thinks he has an infection? I’m sorry I can’t help more, but I am sending prayers and good wishes your way.
Love,
-PamDecember 11, 2012 at 3:55 pm #67142lovedad09SpectatorI got a called from Dr. Diehl and he said my dad is very weak and ill. liver function is not good, otherwise; his bilirubin would have dropped in a day or so. It’s dropping, but not dropping fast enough, means liver function damaged too much. He said my dad may have a heart detect last night. Liver function not good, my dad is weak because of the cancer. We can’t treat him because liver function is weak. On top of everything, maybe a heart detect, if not heart detect, it’s even worse means infection somewhere we don’t know. ????? Conclusion is… he doesn’t think my dad is qualify for any treatment, such as chemo or radiation. He said any chemo or radiation will kill him. He said my dad could have only days or weeks left. This sounds too crazy!!! I asked 2nd opinion with Dr. Fong. He said he’s happy to speak with Dr. Fong if he calls. I told Dr. Fong’s nurse…
I can’t believe what’s going on here…………..it’s hard for me to believe what I have heard. I don’t know how much I can trust what I heard….My dad didn’t have so many problems before he came in the hospital. Now we have so much going on. My mind is blank. I need to bring my mom in ICU tonight and my husband need to come visit. I am so upset…. I can’t believe… still can’t believe what he told me.
What should I do next??? What can I do now to help my dad? I don’t want to lose him. I love him so much.
December 11, 2012 at 2:24 pm #67141lovedad09SpectatorThanks Kris! The Sloan nurse told me if Dr. Fong sees my dad, he can also walk us to ONC. One day can see 2 doctors usually. Sounds great if we can work with someone locally, not NYC every treatment, that’ll be great.
Dr. Schreibman seems good so far. He seems very much willing to work with NYC doctors. I like it.
Right now, my dad is back to ICU, I don’t know what’s the next step is. Trying to find out more. Hospital experience sucks. Horrible place.
December 11, 2012 at 2:22 pm #67140lovedad09SpectatorMy dad was perfectly fine yesterday before I left to pick up my son. Doctor allows him to eat or drink.After I left, they changed his room. He said he’s really cold, the nurses didn’t know how to use the warm blanket…. and he chill again. The doc said breathing number not as good, sent him back to ICU again. I am so mad. Nobody calls me or explain to him what’s going on. No translator phone was used. I am still trying to find out why they moved his room last night before ICU. This place sucks!!
One good thing is my dad’s bilirubin is dropping. 18 over the weekend, 13 yesterday, 10 today. hopefully, it can drop more so that we can leave this place and seek for more treatments.
December 11, 2012 at 4:34 am #67139kris00jSpectatorThe pump delivers chemo directly to the tumor as long as there is only 1. But it was a big surgery. It is stitched into my abdominal wall. I think Dr. Kemeny is brilliant but as a person I do not like her. But there are many oncs there that specialize in hepatobiliary and gastro cancers. Dr. Fong should be able to tell you who he recommends for your father.
My trips to Sloan depend in what I’m doing. But it is a big commute. I take the train from Trenton. Hopefully you can see both docs in one day. I have only done that a couple of times but since I am inoperable I only meet with Dr. Fong every 6 months or so. And I do have another onc that I see when in treatment. He is closer and takes his orders from Dr. Kemeny. So that is an option too if your father is able to get treatment.
It sounds like Dr. S. wants to do the best for your dad. That’s important too. But you do need the best care also. I hope his bilirubin drops so you can have some options.December 10, 2012 at 7:06 pm #67138lainySpectatorCan you ask for another radiologist to take a look at the situation?
December 10, 2012 at 6:48 pm #67137lovedad09SpectatorThank you Kris! What does pump do?
How long will you spend each visit in Sloan? Can surgon app + onc app in one day? I am closer to Sloan then you are. I’ll take dad to Sloan, but he can’t get out of here yet. Hopefully, we fix it soon. It’s a hard commute to NYC no matter where people are, but I’ll do my best.
The residence stopped by again said radiologist thinks right side smaller bile branches maybe blocked so much that the bile doesn’t go to the main right duct. Radiologist doesn’t think it’s worthy to put drain or multiple drain there. Seems like radiologist gave up on draining the right side.
I asked them please talk again. We have to have a plan to do something. bilirubin 18 is still high… this seems simple but why it’s so difficult.
December 10, 2012 at 6:41 pm #67136lainySpectatorHi LoveDad, I am so very happy that Dr. Schreibman got right on it and he sounds good! He is not a downer and it seems he has renewed Hope for Dad. Wonderful that he will help you get to one of the other Hospitals. Both are good. Now if they can just get that right side working, you will be in business! All in all it is a good news day. Will wait to hear what the radiologist says.
December 10, 2012 at 6:28 pm #67135kris00jSpectatorLovedad: I understand the frustration. I see Dr. Fong at mskcc. I love him even though he keeps giving me bad news. The only thing I can say is if your surgeon is highly rated, then good. BUT Sloan Kettering is not far from you and it might be worth a trip. I doubt you would have the same mskcc onc that I have because dr. Kemeny works with her pump, but there are so many research docs there I feel it’s the best place for me.
I remember how frustrating the first few months were. From Feb 2011 until April 2011 all we did was tests. Then I switched to Sloan Kettering. April was my surgery to insert pump and then nothing but problems until late June. Then we mostly got a plan in place, although it changes monthly.
Many of us have experienced your frustration and I pray you get some kind of plan in place. But don’t be afraid to look elsewhere.
There is also dr. Kato at ny Presbyterian who is supposed to be wonderful with “inoperables”. Good luck.December 10, 2012 at 5:54 pm #67134lovedad09SpectatorSo strange… I clicked submit, but seems I lost my post. Anyway…
Today Dr. Schreibman came very quickly in the morning. He seems good, most importantly, he tells us what we should do first, control the bilirubin down to below 3, we will have much more treatment options. right now, bilirubin is still high can’t do much. Thanks God !!! Finally, there is a doc can tell me what we should do because … not I ask doc should we do this or do that? He talked to the surgeon team. They’ll find out more from radiologist since right side still not sure how’s going and bilirubin doesn’t drop/staple. To me it’s a sign that left maybe ok, but right still blocked so bilirubin stable. I asked a few times, residence came, and more waiting… Dr. Schreibman recommand Sloan and Columbia Presbyterian too. Said can help us make appointments if we need. Sounds great. He seems good so far. Hope he’ll be more in charge of my dad’s case.
The orange mucus culture hasn’t come back. STill testing. But Dr Schreibman said it should NOT be tumor spread, doesn’t go to lung usually… Thanks God!!! 1 less thing to worry about.
Hopefully, radiologist can get back to us sooner so that we can drain the right side and move on to next treatment. We got stuck in the hospital here can’t do anything. Dad is not happy with the nurses either. They don’t help much, but if family members are here, they pretended to be nicer. Some really bad, some good. We want to get out of here asap.
December 10, 2012 at 3:17 am #67133lovedad09SpectatorStill no food is allowed. Will ask about it tomorrow. I seem to have a cold too.
Going to sleep. Hopefully tomorrow can bring good news. Whatever it is as long as its good news.
Thanks!!December 10, 2012 at 3:07 am #67132lainySpectatorThis is a first for me. I have never heard of orange mucus! Have they given him anything to eat yet? Try to get some sleep tonight.
December 10, 2012 at 2:40 am #67131lovedad09SpectatorDad left ICU. We were happy for a little while and then he cough with orange mucus once. pneumonia or what??? very angry. Tomorrow, I’ll talk to all doctors/nurse about this. They are testing the culture for mucus. I hope dad is fine. Hopefully, it’s not a big problem.
This whole experience sucks!!! I can’t believe I am so unlucky one thing after another.
December 9, 2012 at 6:47 pm #67130lainySpectatorGood luck, this is the best news you have had so far. Let there be food and GO HOME!
-
AuthorPosts
- The forum ‘Introductions!’ is closed to new topics and replies.