vasilikisimpson@yahoo.com
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December 10, 2018 at 6:02 am in reply to: Hello-Husband with CC struggling to recover from Whipple #97880vasilikisimpson@yahoo.comSpectator
Hi Jennifer,
So sorry to hear about your troubles and your husband’s ordeal with this wretched disease. My personal experience involves my father’s diagnosis, very recent diagnosis, of cholangiocarcinoma. Dad was diagnosed in July. Of course I realize that having him with us for the past 6 months has been a blessing. My dad lives abroad and has had some very good experience with doctors, surgeons, gastroenterologist, oncologist, internist. My dad is 71 years old, this was the year he was going to retire, start gardening, cooking, take a trip with his grandson, my 15 year old son and his best buddy. None of that happened aside from forced retirement due to the diagnosis. My dad was not a candidate for surgery due to the proximity of the tumor to the hepatic vein. We saw some of the best oncologists, biliary cancers are their specialty, they have written books on the matter, travel the world and educate the rest of the medical community. So we were advised that the surgery had little chance of success and great possibility of creating immediate and major problems for my dad, bleeding, pain, reoccurring infections etc. He initially presented with jaundice, that was our first and only indication that something was wrong. He was hospitalized, I’m backtracking now, this is before the meetings with the surgeons. He did have the metal stents set in place to remove the accumulated bile from his liver. Thank God that went well with the first attempt. Stayed in hospital for 2 weeks and then it was time to make decisions for treatment. To make a long story short, all surgeons were against the surgery, we decided on chemo for a possible extension of life prognosis and a better quality of life, if chemo indeed worked. Dad proceeded to loose weight rapidly. As soon as chemo started he lost his appetite as well. Dad has lost about 40 pounds as is extremely weak. Over the past 6 months there has been a steady, slow deterioration of body and mind (possible hepatic encephalopathy along with depression, manifesting in hallucinations). Even though the chemo was successful in attacking areas where cancer was present, it successfully attacked the lymph node spread, the tumor shrunk, the pain receded. Dad has no pain right now, but has what’s known as ascetic fluid retention. We had to have his tummy drained every couple of weeks along with continuous blood transfusions due to low platelet count. Dad has stopped chemotherapy because oncologist decided it was enough, his overall picture is of a devastated, exhausted, emaciated human being. He has no strength. He takes in very little nutrition. Please look up protein drinks and shakes to be given 3 times a day. For my dad that’s about 900 calories total, 300 calories per shake. We use a blender to make soups and creams because it helps with obviously feeding him more. We usually blend vegetables, carrots, potatos, zucchini, an onion, a tomato a bit of olive oil. Baby food, like biscuit creams blended with a banana or a blend of his favorite fruits. Yogurt, milk, jello, peanut butter. we follow the advice of a nutritionist. Please feel free to ask me any questions about nutrition. It has been an ongoing struggle. Now that he has stopped chemotherapy, doctor has introduced immunotherapy with the drug Keytruda. He does not have any accumulation of ascetic fluid for about a month now, no need for drainage, yes that is one positive. After the treatment he’s better for about 3 days and then reverts to being exhausted, continuous lack of a healthy appetite. Right now and within the space of one month, since I saw him last, he’s not able to stand on his own, hold a cup or an object. He has started developing fevers, sometimes without a virus or infection. Right now he is in the hospital again, with what appears to be a lung infection. He had a very difficult time breathing, he was in pain. Now his breathing is better. I’m taking an emergency flight overseas tomorrow to see him. I wish you all the best in your fight with this disease. It’s difficult on the patient first of course and then on all of us who love them and take care of them because it seems unmanageable for some cases. We try to provide them the best we can and that is all we can do. Stay positive and whenever you see the slightest sign of improvement, a day that he ate even a cup of yogurt tell him how good that was for him. Psychology is so important. The fact that he’s there and wants to fight regardless is an immense plus, he’s strong, be strong with him, even tell him little things like your skin looks brighter, your eyes look clear. Make sure the doctors provide you with any pain medication needed to alleviate the discomfort. Laxatives, antidepressants, very important for a psychiatrist to join in the care team. Something to help him sleep and get some rest.
Right now I need answers but they’re hard to get. How can the doctors explain how each person’s immune system may react to a load of immune cells being pumped into your body so that you can fight your disease in your own. Will they be recognized as foreign by your own cells, will these cells then be able to recognize the rogue cancer cells and attack them? For now long? Doctors say we can only tell by the looks of the patient, is there any physical improvement? Well apparently in some cases, no. So I would like to and pray at this point that my dad gets a few weeks, please god, of quality time, no treatments, no hospitals, just pain killers if need be and is his family for the holidays. to
You can also purchase vitamins, supplements and there is always CBD oil, no THE content, therefore no high, if you’re open to trying, it relaxes the patient, will be able to enhance appetite, and in some cases doctors believe it has healing properties for liver related cancers.
Good luck and God bless.
Betti
vasilikisimpson@yahoo.comSpectatorHi all,
I’m not sure if I’m posting this in the correct place (intro), hoping someone will be able to read it.
I’m the daughter of a cholangiocarcinoma patient. My 71 year old father was diagnosed with this disease in June 2018. Came on like a storm out of nowhere. Some abdominal pain, misdiagnosed as gastrointestinal issues, totally missed it on the ultrasound. Then severe jaundice came on, so obviously dad ended up in the hospital, underwent series of tests to receive the final diagnosis. Had succesful stent placement. Started feeling better. Doctors, surgeons and oncologists gave us a very poor prognosis, stage 4, inoperable, metastatic, some in the lymph nodes, some in artery and wall behind organs. Dad knows some of this information because he’s currently residing in Greece, where doctors will give minimum information to the patient in order to avoid a complete psychological meltdown where one can just pass away from hopelessness and sadness. Us, the family are fully aware. Dad has been given a time period of maximum one year. He has started chemo, has had 4 sessions that have completely wiped him out. For one he’s unrecognizable, my 6’2″ 195 pound dad is now a very fragile, frail man. Lots of weight loss and exhaustion. He sleeps all the time, refuses food, claims no appetite and pain if he eats anything solid. So, it’s power drinks, yogurt, some cream and juices he linli. Has lost interest or cannot participate in any activity, even watching his favorite shows, reading or playing on his Kindle, which he did following the first chemo session. His latest blood work showed signs of somewhat of an improvement. Oncologist told us all, including dad, that yes this is good news but due to the nature of the disease we don’t know whether these good news will reappear in the next exam. Dad is scheduled for an MRI on October 3 following his 5th chemo session. I’m just amazed at the complete collapse the treatment has caused. I was under the impression we’re doing this to give him a better quality of life and perhaps a chance of tumor shrinkage and possible surgery, I’m being very optimistic, it’s my father though so I can only hope. I currently reside in MD, in the US and am frantically looking into any clinical trials he may be a suitable candidate for.
Thank you for reading. I would appreciate any words of encouragement! I’m so glad to have been able to read many of your stories. They are comforting and inspirational.
Thank you!
Betti
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