r/pancreaticcancer • • Sep 14 '26

resources The Only Approved Distributor for Rasonque/Daraxonrasib Outside the USA

14 Upvotes

After talking with a Revolution Medicines representative about international access for their new treatment Rasonque, I was informed that Revolution Medicines have only one approved distributor outside the USA: Uniphar.

The Revolution Medicines web page Revolution Medicines Global Named Patient Access (GNPA) Pathway describes this program.

From the above web page:

Requests are physician-initiated and must be submitted on behalf of an individual patient. A pharmacist may submit a request where appropriate and permitted by law and regulation. Revolution Medicines cannot accept requests directly from patients or caregivers.

For participating countries, Revolution Medicines has partnered with Uniphar as the sole daraxonrasib GNPA distributor to manage individual named patient requests. Uniphar administers physician or pharmacist registration, applicable, administrative review of requests, order processing, and product fulfillment.

Additional information regarding GNPA can be obtained by submitting questions through Medical Information at [accessinquiries@revmed.com.](mailto:accessinquiries@revmed.com)


r/pancreaticcancer • • May 15 '22

To: "Worried About Cancer" Visitors

532 Upvotes

This subreddit is for patients and caregivers going through pancreatic cancer.

Here is what we tell "Worried" visitors:

  • Should you be posting in r/Anxiety or r/AskDocs?
  • You need a doctor to order the proper tests and diagnose. We are not doctors.
  • PanCan's best detection methods are MRI and EUS.
  • No test is 100% accurate.
  • If you have cancer in your family, consult a genetic counselor. [US]
  • The median age of diagnosis is 70 years old. [Graph]
  • There are hundreds of non-life-threatening conditions that are more likely and less deadly that mimic the signs of pancreatic cancer.
  • Don't waste time asking a cancer patient if they've had a symptom. The answer is yes.
  • No, we don't want to see your poop.

r/pancreaticcancer • • 8h ago

Health update (for those of you interested)

Post image
88 Upvotes

Update: Had my third post-chemo CT scan yesterday (first diagnosed stage 4 with Liver mets in March 2026) It shows no new reduction in the size of the tumors, so it seems like the Fulfirinox regimen is still working, just not as well as it once was. Now we continue treatment, and wait until the tumors start growing again, at which point we will have to look into other treatments, such as the new Daraxonrasib. It could be two months, or even two years! We just won’t know til it happens. Statistically speaking it likely won’t last that long. My cancer is still inoperable and will end my life, I just don’t know exactly when. Thank you all for your prayers and good thoughts. I wish I could spend time with you all.


r/pancreaticcancer • • 8h ago

venting Just got the diagnosis, can’t process this.

14 Upvotes

My mom is the only family I have. She lives with me and my four year old daughter. My daughters father was recently arrested and my Mom completely declined so rapidly. For the past 2 weeks she was vomiting. Urgent care insisted it was a stomach bug or gastritis. They ordered labs and sent her off. I knew something was off and so I called 911 finally. The following day an NG tube was placed, two days later TPN. Today I got the call it is pancreatic cancer, stage 3 or 4. Will my mom ever leave the hospital? I don’t know how to prepare for any of this. Any support is appreciated. This is the most devastating year of my life and I don’t know how to process this.


r/pancreaticcancer • • 11h ago

seeking advice How to process dads death…

19 Upvotes

Hi. It’s the first time I (25yo) write this. My dad (63yo) passed away on July 26th. He was first diagnosed back in May, the same day as my birthday… Since then I feel I’ve been living a nightmare, everything went downhill so fast.

He went to a normal doctor’s appointment for discomfort while eating, he was wrongly diagnosed with parasites and he got medicine, with this he lost 14 pounds in 10 days. The day of my birthday they confirmed stage 4 PANCan. They explained to us that it was almost impossible to detect it since his tumor developed in the tail of his pancreas, however he had a 10cm mass (which makes me wonder why he never had any sign if he had a huge mass) that invaded his spleen, stomach and colon, in his and multiple metastases in his liver (6cm, 3cm and 3cm), his lungs, and peritoneum. We went to 5 different private oncologists and all of them told us the hard truth… however with my mom who’s religious I decided to keep faith in that he was gonna be a miracle.

Everyone told us with palliative chemo he would have 6-12 months so it was time to make peace with everyone around him. He went through 3 infusions of FOLFIRINOX before my worst nightmare happened. JUST 3! I decided to pause my work in Germany for an indefinite period of time, took the first available flight and was his number one supporter. The mental struggle has been real. I went back for 3 weeks to Germany to catch up with work, because my dad told me he was gonna fight this!

After these 3 weeks I had to fly back home immediately because I felt it was coming, after his third chemo he stopped eating and couldn’t stand up anymore. That day he started morphine, and it went downhill. He was admitted into the ER with kidney failure, the doctors told us it was gonna be more painful for him to keep going through dialysis so they sent him home into hospice. As soon as I got there my dad had a talk with me telling me that he’s in peace with the idea of passing and that we as a family should also be prepared for it. The next 3 days I was his caregiver 24/7, I was the one to inject him with pain medication, and helping him to seat every hour of the night because he had this feeling that his body was burning from inside. When my mom went to the airport to pick up my brother who came due to the situation, my beloved and dearest dad passed away.

My mom and my siblings couldn’t say goodbye to him for 20 mins… I was the only one to comfort him. Those moments feel like a nightmare, however I remember I didn’t cry at all and my goal was to tell him in his ear how much I loved him, how caring he was and that we tried everything, but now he can rest in peace. I hope he was able to listen to those words. Now it has been almost 3 months and the grief I feel has been drowning… Next Monday of him passing away I received his mutations results where they just confirmed KRAS mutation as an opportunity for alternative therapies, so even I know it was impossible for him to be an exceptional case I prayed from the moment I woke up to the moment I was in bed.

Life feels so unfair… he never drank, smoke or had bad habits. I wonder why these awful things happen to good and caring people. I miss him every day and it’s really hard to think how to continue life without him… so far away from my mom. Is it gonna hurt this much forever? Sometimes I have moments where I have panic attacks because I realize my dad is not here anymore and I also think I would have switch places with him not even blinking once… all his pain, I would have prefer to have it by myself and protect him… I would give everything to see him or talk to him again for just 5 minutes.


r/pancreaticcancer • • 7h ago

seeking advice Please I might off myself

8 Upvotes

Hello, i just found out my mother probably has stage IV of pancreatic cancer, she can't eat properly and lost 10kg in 2 months. Tomorrow I'll learn if the tumor has reached the liver too or not. Tomorrow she will start chemio but I can't take it to see her destroy herself with such cure. I just want her to at least eat again more and regain weight. She is only 50 and I'm 20. Each time she eats solid stuff she can't digest it because of the pain. She will surely wont be able to remove the pancreas right now because of some veins close to the tumor, I can offer to take my pancreas instead in case.


r/pancreaticcancer • • 1h ago

Grandmother 84

• Upvotes

My grandmother is 84, stage 4 breast cancer, spread to her brain. She has brain cancer. She's not getting any cancer treatment right now. Lately she's had worsening back and shoulder pain, weak legs, trouble walking, and some vision loss. Pain medicine. What timeline do you expect for her to live for ?


r/pancreaticcancer • • 16h ago

Stopping Daraxonrasib

14 Upvotes

Mom (88) was diagnosed in March of 2026 after several hospitalizations and ER visits for abdominal pain. She has tumors to her liver, adrenal, thyroid and lungs but the lungs may be synchronous. In any case, she’s been relatively functional and pain free for most of the past 6 mos. With hospice support. Then heard about daraxonrasib. Started last Tuesday. Severe GI upset, 2 hours of diarrhea per day, no energy, too tired to do the skin care, too weak to do the oral hygiene. It was awful. Said she was suffering too much last night and decided to re enter hospice. I’m very relieved she’s going to be more comfortable. I know it’s new, but I still think her care team should have suggested that it may not be effective for her, given her age and advanced disease and her overall condition. I’m thrilled to see this wonderful advancement help so many, but it’s definitely not for everyone. Thanks so much for putting your experience out there, you have no idea how helpful it has been and I wish you all happiness.


r/pancreaticcancer • • 7h ago

seeking advice Pancreatic Cyst

2 Upvotes

I had an ultrasound and MRI for epigastric pain last month. The imaging found that my gallbladder is full of stones and I have two cysts on the neck of my pancreas (lobulated 4.4 cm and unilocular 1.1 cm). After another gallbladder attack landed me in the hospital this week, a GI did an EUS/FNA. The GI wrote that the larger cyst had a few compartments thickly septated. He couldn’t see the outer wall. He took out 20ml of fluid from the larger cyst. The cyst’s glucose was over 100, its CEA was under 1, and its amylase was in the 30s. The cytology listed glandular/mucinous cells and included a differential diagnosis GI epithelium vs mucinous cysts. It also contained squamous cells.

I had a surgery consult today and the surgeon thinks that the cyst is either an MCN or an IPMN. He recommended removal based on the MRI. He said that the GI who did the EUS could not tell if the cyst communicates with the duct and advised that the fluid levels are irrelevant. I’m unsure on how to proceed because I thought I’d have clarity on the type of cyst it is before any next steps were proposed.

I’m in my 40s with young kids. Wondering if anyone has any similar stories or advice for navigating this.


r/pancreaticcancer • • 8h ago

Rasonque care pack- what to include?

2 Upvotes

Hi everyone! My (32f) dad (63m) is scheduled to start Rasonque this week and I wanted to make him a care package to help feel supported through the next step of his journey though pancreatic cancer. I heard the skin side effects are the particularly difficult so I was wondering what would be the best things to include to help him with this? Thank you all in advance!!


r/pancreaticcancer • • 11h ago

seeking advice No PET scan?

2 Upvotes

My mother (64) was just diagnosed last week with pan can. It is locally advanced at least, as there is local lymph node involvement. Her next steps are another round of ct scans to the abdomen, pelvis and chest with contrast before meeting her oncology team the next day. My father had lung cancer 10 years ago and as soon as he was diagnosed, there was a full body pet scan to see if it was anywhere else. Is this not typical with Pancreatic cancer? Why a ct scan to check for mets instead of PET?


r/pancreaticcancer • • 1d ago

Good News! 37F, Stage IV, 14 months in, and doing better than I expected. Some good news for the feed 💜

129 Upvotes

Hi all, there's been a lot of heavy news here lately, so I wanted to share something on the lighter side for anyone who's newly diagnosed and scared.

How it started: I was diagnosed with stage IV pancreatic cancer (spread to liver, ovarian and distant lymph node) in August 2025 at 36. I had abdominal pain and lost 30 lbs, dropping to 82 lbs. I was on round-the-clock morphine and Creon just to get through the day. I have a germline BRCA1 mutation, which ended up mattering a lot for my treatment options.

What I've been through:

12 rounds of FOLFIRINOX (Aug 2025 - Feb 2026): My primary tumor shrank about 85%, my liver mets cleared, and my lymph nodes went back to normal.

Olaparib (Lynparza) maintenance (Mar - Aug 2026): This held things stable for a few months, then my August scan showed progression.

Now: Gemcitabine + Cisplatin (Sept 2026 - current): Day 1 and Day 8 infusions, then a week off. Honestly, I'm tolerating it really well so far.

The part I want newly diagnosed folks to hear: my pain went away after I started chemo. As the tumors shrank, I came completely off the morphine and the Creon. I didn't think that was possible when I was at my lowest.

What's keeping me going:

- I work out 5 days a week (spin, weights, hikes), then take 1-2 rest days before starting again

- I walk every single day to get some sun, even on chemo weeks

- THC helps with my appetite and my workouts, no shame

I know my story isn't everyone's, and this disease is brutal. But there are good days and good stretches, and sometimes the treatment works better than the statistics say it will. Advocate hard for yourself, ask about genetic testing, and look into trials early.

Sending love to everyone here fighting and caregiving. Hold the line 💜


r/pancreaticcancer • • 22h ago

pain management Too much pain in the intestines

3 Upvotes

My mum has too much pain in her intestines. The doctors said it is normal because there is air trapped. Everytime she moves, or tries to go to the toilet, she screams in pain. We are taking heavy drugs for pain management with the help of palliative care. We also feed her through her port. The pain though is too much. She feels her intestines will explode. Anyone has any advice ?


r/pancreaticcancer • • 19h ago

Mom just diagnosed. Need help

2 Upvotes

My mom was recently diagnosed three weeks ago after being admitted to the hosp for jaundice. Textbook, reading all your entries it seems. While in the hospital they’ve discovered enlarged lymph nodes in her chest as well as stenosis in aortic vessel in abdomen.

Trying to get clarity/answers from her myriad drs and specialists has been a nightmare. The appt we have waited for from which all other appts would come (we were told) was a sham, the pancreatic surgeon said she hated when the drs told patients that. She couldn’t do anything before the pet scan and essentially had no answers. When asked about stage she responded ‘probably three’. Chastised my mom for not reading and fully comprehending her pathology report. Said she’d have to have two rounds of chemo plus surgery and not once did anyone mention chemo to my mom. Only surgery and that it looked promising.

Then someone voided her pet scan. No answers there on who or why or when. Then the pathology report itself said ‘suspected adenocarcinoma’ and the dr can’t really do anything w the word suspected. So it feels like we aren’t even at step one yet, meanwhile thru a cat scan at the er the other day bc she now has pneumonia, they found the tumor has grown.

Time is so very critical and my siblings and I would like her to get a second opinion from Sloan or Dana Farber (and two others who’ve been recommended). But my mom says no. She will be the one to call about her body. Our point is that we will help get the ball rolling while she chases her current (useless) doctors. And she of course has not made these second opinion calls yet. So we just have to sit and wait. And it feels like we are running out of time.
Any insight/info welcome. Thank you.


r/pancreaticcancer • • 23h ago

seeking advice Mom’s diagnosed with Pancreatic Cancer, is there any advice and what to do next?

2 Upvotes

My Mom(also Breast cancer survivor) had a strange loss of appetite, drastically losing weight with sometimes back pain. So I went with her to check and the result just came out today and it’s Pancreatic Cancer(through blood test and CT scan). But the doctor didnt tell us what type, and stage of the cancer and just recommend us to either do Biopsy or Surgery(and told us with chance of 10-20% failure) by referring us to Surgeon specialist. I tried asking which option is better for my mom and the doctor just told me to discuss with my family instead of asking him with the decision leaving us with more confusion.

I’m planning to schedule for another doctor next week to get second hand opinion since all the doctors we met earlier did NOT give us clear answers. And I’m so afraid of thinking anything would happen to my mom :( I’m too young and lost. My family rely to me on what to do next

Currently shes losing almost all her appetite and her weight went down almost 8kg(in the span of 2 months) and I want to get her supplement that might help with her appetite and probably protein too but I don’t know which should I get so I might need some advice here. I also would appreciate every advice since I don’t want to miss any chance that could improve her health or anything that can help her. Thank you everyone


r/pancreaticcancer • • 20h ago

venting Insurance Denial/Pathology Error

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1 Upvotes

r/pancreaticcancer • • 1d ago

giving advice Losing My Dad to Pancreatic Cancer

22 Upvotes

My dad was diagnosed with pancreatic cancer on August 18. He passed away on October 3. Just six and a half weeks. Sometimes, I still can’t believe how quickly it all happened.

The only symptom he had was stomach pain. He went to his GP alone, never imagining it could be something so serious. None of us did. And then, suddenly, our whole world turned upside down.

As his only child, I tried everything I could to help him. He had one session of liposomal irinotecan chemotherapy, and eventually, the focus shifted to palliative care. He was hospitalised twice…once for dehydration and sepsis related to his bedsores, and another time when his blood sugar went above 600.

Both times, he seemed to get better after coming home. And both times, we let ourselves hope again. We thought maybe he would be okay for a little longer. It’s strange how even the smallest improvement can make you believe things might still turn around.

His doctor was incredibly positive, and that gave us a lot of strength. I also consulted other doctors, some were so cold, and we were often left with more questions than answers. When you’re watching someone you love suffer, you need more than medical advice. You need someone who understands how frightened you are.

Towards the end, my dad seemed to lose the will to keep fighting. He even told me he just wanted to die. I don’t think I’ll ever forget hearing that. He was in so much pain, and there was nothing harder than watching him suffer and wishing I could somehow make it all go away.

He was 82 and had always been such a strong person. He’d never really had any major health issues, so seeing him like this was something I was never prepared for. Surgery was never an option because of his age, and everything happened so fast that it feels like we barely had time to understand what was going on before we were facing the end.

Sometimes, my mom and I wonder whether his final days might have been more peaceful if he had never found out about the cancer. I don’t know if that’s the right thing to think, but the thought does cross our minds.

And then, a few days ago, something happened that really touched us.

A parrot showed up, almost as if he had come to check on my mom and me. We have been living in the same house for over a decade and have never seen a parrot before. The thing is, we had a beloved pet parrot, for 17 years. So seeing a parrot appear at a time like this felt incredibly emotional.

I know it could have been a coincidence. But honestly, a part of me wants to believe it was something more. Maybe it’s just because we’re missing them so much, or maybe these little moments really are a way of feeling close to those we’ve lost. I don’t know.

I just know that, for a moment, it brought me some comfort.

I’ve told my little one that his grandfather is a star in the sky. Maybe, in our own ways, we all need something like that to believe in. A star, a bird, a dream, or some small, unexpected moment that makes us feel like our loved ones are still around.

I also want to thank this subreddit. The resources shared here helped me realise that the end might be near, and because of that, I was able to be with my dad during his final few days. Reading other people’s experiences helped me understand how quickly this disease can progress. When everything was happening so fast, I felt less alone knowing that others had been through something similar.

To everyone who has shared their stories here, thank you. You may not realise it, but your words can make a real difference to someone who’s frightened, confused, and desperately trying to understand what’s happening to their loved one.

It’s hard to accept that someone who was such a big part of your life is just gone. I’m still trying to process it all, and some days, it doesn’t feel real.

I don’t know what happens after we lose someone. But I want to believe that the love we have for them doesn’t just disappear. That they remain a part of us, in our memories, in the stories we tell, in the stars we point out to our children, and perhaps in little moments that come along when we need them most.

Maybe that parrot was just a parrot. Or maybe, just maybe, it was a little reminder that the people we love are never really gone from our hearts.

For now, I’ll choose to believe that. ❤️🙏


r/pancreaticcancer • • 1d ago

Greetings to all the beautiful brothers and sisters from other mothers and misters.

16 Upvotes

My 74-year-old, strong, loving mom has been diagnosed with adenocarcinoma of her pancreas. The diagnosis came approximately 2 weeks ago. I don’t know how long this insidious thing has been wreaking havoc. I don’t like cancer. In fact, I hate it an awful lot.

I am keeping all the individual fighters and their friends and family members in my heart and mind.

May the universe convey ever-loving and comforting light into your hearts, minds, bodies, and souls. May you derive peace from knowing that you are not alone on your individual journeys and harness strength and power from the benevolent forces surrounding you.

My mom was recently seen here in Miami at Mount Sinai with the GI oncology department and is now scheduled for a 2nd opinion to see an oncologist at Memorial Sloan Kettering Cancer Center in New York.

Does anybody have any information to share about either of these facilities?

Please inform me on your thoughts and opinions, good and bad. I am looking forward to hearing from each and every person who has something to share. Thank you.


r/pancreaticcancer • • 1d ago

Stage 4 PDAC with weight loss

1 Upvotes

Someone close to me has stage 4 PDAC that has spread to the liver. They started chemotherapy and a clinical trial, but have lost approximately half of their body weight over the past few months. They are also refusing help from family. It’s difficult to know how to support them…

For those who have been through something similar, I have a few questions:

1) How do you balance hoping for a good response to treatment with preparing yourself for the possibility that things may not improve?

2) How do you support someone who has lost so much weight and is refusing help without making them feel pressured or controlled?

I know every situation is different, and I’m not expecting anyone to predict an individual outcome. I think the hardest part is watching someone you care about struggle while feeling unsure whether to keep hoping things will turn around or begin preparing yourself emotionally for what may come.

I’d really appreciate hearing honest experiences, advice, or anything that helped you navigate this uncertainty with someone you love.


r/pancreaticcancer • • 1d ago

Optimistic oncologist

5 Upvotes

How should I think about the optimism of our oncologist? He makes it sound like the symptoms of chemo for my dad on FOLFIRINOX will be mild/moderate. He’s in great health, but he is 75 and coming off of surgery.

He also said it’s very likely after chemo the cancer will be “cured” aka low chance of recurrence. He’s stage IIA adenosquamous which I know gives him a stronger chance since it’s early, but it sounds too easy.

Should I take the good news at face value? Or have other people felt their oncologists over promise?


r/pancreaticcancer • • 1d ago

Stage 4 pancreatic cancer, hallucinations and barely eating. Is this what the final weeks look like?

7 Upvotes

My brother-in-law was diagnosed with stage 4 pancreatic cancer in July and at the time we were told his prognosis was probably only a couple of months.

In September he spent three weeks in hospital because his pain had become so severe that they were struggling to get it under control. He eventually came home, but two weeks ago he was admitted to a hospice because his wife could no longer manage his care safely at home.

I’m posting because I would really like to hear from people who have been through the final stages of pancreatic cancer with someone they love. I know everybody is different and nobody here can tell me exactly how long he has, but I feel as though we need to prepare ourselves for what is coming.

His pain has been very difficult to control. He has been on high doses of medication through a syringe driver. He was previously receiving morphine through the driver, as well as up to five additional subcutaneous top-ups a day, but the morphine was no longer controlling his pain adequately. They have now changed the opioid in his syringe driver to oxycodone.

He is also receiving clonidine through the syringe driver and haloperidol for nausea, vomiting and hallucinations. The hospice continues to adjust the medications to try to keep him comfortable.

Since Friday, however, his hallucinations and delusions have become increasingly vivid and disturbing.

This morning was particularly awful.

At around 5am he became convinced that his wife had married the man next door. He said she had actually arrived at the hospice wearing a wedding dress to rub it in his face. He could see her there and said he could see someone's hand hiding behind the door.

None of this happened, obviously, but to him it was completely real.

He then telephoned members of the family, including his daughter, his estranged son and us, making accusations. He told us he could never forgive us because we had been hiding things from him about his wife.

There is absolutely no reasoning with him when this happens. He says these things with complete conviction.

What makes it particularly strange is that we can then telephone the hospice and ask a nurse to go into his room. When they do, he can suddenly appear completely normal. He is calm, takes his medication and says please and thank you. The nurses can walk away thinking he's absolutely fine, while minutes earlier we've been on the phone with someone who appears to be living in a completely different reality.

These episodes have been happening since Friday and seem to be becoming more intense and more upsetting each time.

The hospice has now done blood tests and neurological observations, so we are waiting to see whether they identify anything that could be contributing to the confusion.

The other major change is his eating.

He is barely eating anything now.

Yesterday, for example, he had perhaps one spoonful of his main meal and one spoonful of pudding. Then he says he's full, doesn't want it or doesn't like it.

Food has to be very soft or mashed for him, although a speech and language therapist has assessed his swallowing and apparently his swallowing function is still okay. He can also still swallow his tablets.

He is drinking water and will drink the protein milkshakes they give him, but actual food intake is now almost nonexistent.

He is also increasingly sleepy.

The hospice has said they believe we are looking at a few weeks, but when I look at how little he is eating, how frail he has become, the amount of medication he requires and these increasingly severe hallucinations, I find myself wondering how his body can continue for weeks.

I suppose what I'm really asking those of you who have sadly been through this is:

Did your loved one experience vivid hallucinations or delusions towards the end?

Did they have periods where they seemed completely confused with family but could suddenly appear perfectly normal with nurses or other people?

When they virtually stopped eating but were still drinking, how far from the end were they?

Did you see a gradual deterioration, or did things suddenly change very quickly?

And perhaps most importantly, looking back, were there signs that you now realise meant the person had moved from having “weeks” to having “days”?

I'm not looking for anyone to predict how long he has. I know nobody can do that.

I just want to understand other families' experiences because I feel we need to be prepared, particularly for his wife. She is finding the hallucinations and the things he is saying incredibly difficult, even though we know intellectually that this is his illness talking.

Thank you to anyone willing to share what the final weeks or days looked like for your loved one. I know these aren't easy memories to revisit.


r/pancreaticcancer • • 1d ago

New rasonque patient, looking for patient testimonials and experience

4 Upvotes

Hi everyone,

My father ( 63 M) was recently diagnosed with stage 4 pancreatic adenocarcinoma with metastasis to the liver 2 months ago and to say it has been an overwhelming whirl of emotions and doctor's appointments would be an understatement. He has currently undergone 5 rounds of chemotherapy with Folfirinox which he has responded to fairly well. The only major side effects he has experienced is a complete lack of appetite ( and thus significant weight loss) and fatigue, for which we are largely grateful for.

Last week, his oncologist just told us he has been approved to start treatment with Rasonque as it will help improve my father's quality of life. While ecstatic, he's concerned about the unknowns of starting a new drug and what to expect to experience while taking it. If there's anyone on it who could provide my dad, and by extension my family, some insight on what he may encounter while taking the drug I would be very grateful.

Sending strength and comfort to everyone on this path. While still new to it, I feel a very strong connection to those walking it as well.


r/pancreaticcancer • • 2d ago

No words…

52 Upvotes

My dad was diagnosed with stage 4 pancreatic cancer on August 19 at 56 years old. He underwent two rounds of chemo. His care team tried a Hail Mary to get him approved for Rasonque on September 17. We got the letter that insurance denied it on September 24. My dad died on September 28. On September 29, we got the letter that his care team had appealed to insurance on September 25. It was too late for him, but I will always wonder if he would have started Rasonque even a week before he died, could he have survived long enough to witness my sister’s wedding this month?

He was still here when I got engaged on September 19. To know that he loved and approved of my fiancé brings me so much peace. It will never take away the ache of all he will miss out on, but I find peace in what big moments in my life he got to be here for.

My heart is utterly broken, and it’s so difficult to figure out how I could ever pick up the pieces enough to live without him on earth. I’m forever changed by watching him fight as courageously and gracefully as he did.

I was privileged to be able to provide the care and support my dad needed in his last 10 days on earth. Despite how hard it was to see him so sick, I’m grateful for every moment of that time.

Knowing the intimate details of the fight against pancreatic cancer is not something I would wish on anyone. To those who are fighting or supporting someone who is fighting, I’m so sorry you understand what this disease does to a person and their loved ones. It is brutal and heartbreaking to experience.

My dad was the strongest man I have ever met. He wasn’t perfect, but some of my favorite traits of myself come directly from him. I am certain I will spend the rest of my life missing him.


r/pancreaticcancer • • 1d ago

pain management Need help with comfort options for home hospice care

6 Upvotes

Hey all. So my mom got diagnosed only last month very late and she opted to not go with treatment and all that stuff. She elected to do home hospice. She had a bad fall off her stupid bed which is super high off the ground and it really set her back. She had to get a medical bed so it could be inclined and she’s had extreme difficulty moving around and being comfortable.

She has really bad swelling in her legs and feet which prompts her to need them elevated frequently and especially while the sleeps. This whole situation has come on as such a shock to my family so we are kind of not thinking everything straight.

We’ve been propping her legs up with pillows on the bed and a pillow on the table when she wants to sit on the couch in the living room. I just feel like maybe there’s some medical device better for this ??

I looked this up and all I saw was post surgery pillows on Amazon and stuff which doesn’t look like what she needs, too many ridges and bumps. She needs something soft and simplistic

Sorry for the long winded post,

TLDR : does anybody know about any medical pillows or devices that can help with keeping the legs inclined while not having a bunch of ridges and bumps


r/pancreaticcancer • • 2d ago

Looking for advice or input

7 Upvotes

Hi all— looking for some advice or feedback, and I apologize that this will probably be rambling.

My dad, 67yrs, was diagnosed with stage 4 pancreatic cancer back in late June or early July. He’s been on chemo since late July, I want to say he’s on round 5 now maybe? I’ve heard a lot about Rasonque/ daraxonrasib and have been wanting him to get on the pill but the doctor keeps saying we have to wait until the chemo fails. Meanwhile we are watching my dad absolutely waste away day by day, he’s so frail and miserable, can’t stay awake, isn’t interested in anything at all anymore. My dad has always been the most popular, outgoing person in the room, he’s everyone’s favorite. It’s devastating seeing him live out his remaining time like this.

After reading all the articles about this “miracle drug” was so excited, then only recently read about all the serious side effects and am a bit deflated.

I’m going with him tomorrow for his labs and chemo and we are going to be able to talk to his doctor. I already asked him a few weeks ago if we could get my dad on the pill and he said explained that chemo needed to fail first, and right now it’s decreased my dads tumor by 40%. But what kind of life is this?? I guess I’m wondering if I should push more for him to be on the pill or something. I’m scared he’s going to die on chemo. There’s so much more to this story— my mom just got a double mastectomy from breast cancer and still needs surgery— we are all supposed to fly Europe in a few weeks because it’s one of my dads dying wishes and I’m absolutely terrified, oh and he doesn’t have a spleen anymore— but I’ll stop here.

Any advice or input is appreciated.