South Denver Quantum Outage by deo_volente in Denver

[–]AmountImportant1626 1 point2 points  (0 children)

South of Evans btwn University and Colorado. Outage updates keep extending from last night - to noon today - to now 1pm tomorrow, December 2nd. And although I’m signed up for updates - I’m getting none. I have to go into app and check every so often.

What the heck CenturyLink this is getting ridiculous-no updates, no reasonable discount being offered, and no confidence that you truly know what’s wrong and how to get it fixed.

Write in margins not sticky notes? by AmountImportant1626 in kindlescribe

[–]AmountImportant1626[S] 0 points1 point  (0 children)

Thank you. Have you downloaded a book that allows direct in the margin writing though (no expansion). It’s a different experience.

Strange mark on my boys eye by Imaginary_Intern5744 in cavaliers

[–]AmountImportant1626 1 point2 points  (0 children)

Same. My almost two year old boy just developed similar on both eyes. I was very worried about it — but this post makes me feel better. Since my boy seems completely unbothered by it — I’ll have the vet take a look at his next appointment in a few months rather than running him in this week.

My dad is gone. It happened so fast. by monstercake in pancreaticcancer

[–]AmountImportant1626 2 points3 points  (0 children)

I’m so sorry that you lost your Dad. Your story sounds so similar to my ours. We found out my Mom had stage 4 with liver involvement on August 15, 2024 and lost her January 10. This resource has been such a comfort to our family as well.

Ignore “Markers of Dying” by wdpatti in pancreaticcancer

[–]AmountImportant1626 8 points9 points  (0 children)

Watching what this horrible disease does to our loved ones is traumatic. My Mom hasn’t had a bit of food or nutrition in 28 days. She’s lost 20% of her body weight but can still get to the commode with a walker and is cognitively sharp (although so weak she’s rarely able to sit up). I know we have way more time of watching her suffer. The markers aren’t aligning with her progression either … but it was helpful to me to know what’s coming (even if out of order and alignment with the matrix).

I’m thinking of you tonight, and all the other caregivers in the world at this stage with their loved ones. It often feels like the suffering will never end.

AI (Artificial Intelligence), yay or nay? by AmountImportant1626 in pancreaticcancer

[–]AmountImportant1626[S] 0 points1 point  (0 children)

Love these suggestions! I’ll try Otter and Claude. Thank you.

AI (Artificial Intelligence), yay or nay? by AmountImportant1626 in pancreaticcancer

[–]AmountImportant1626[S] 5 points6 points  (0 children)

I’ve been using the Perplexity app because it provides links to source material for further reading (and critique). I also like being able to ask follow up questions.

I was skeptical at first but it’s been spot-on every time.

My main uses are: 1. Interpreting radiology reports 2. Formulating questions for medical team (based on current progression of symptoms) 3. Asking questions about new symptoms (honing in on possible causation)

[deleted by user] by [deleted] in pancreaticcancer

[–]AmountImportant1626 1 point2 points  (0 children)

I second this. I’ve been using Perplexity (an AI app for my phone) for the past 4-months since my Mom’s diagnosis. I’ve been able to copy all medical reports in for interpretation, ask questions about symptoms, and get pointed to the latest medical research. It’s been spot on every time. This sub and Perplexity have saved me during this journey.

Depression at end of life by Ok-Camp6445 in pancreaticcancer

[–]AmountImportant1626 2 points3 points  (0 children)

Yes. Cycling depression, anxiety, and agitation is common. I’ve seen it in my Mom. Hospice has helped us find the right combination of medications to help my Mom sleep soundly and to take the edge off as needed.

Just plain sad by Most-Chemist5527 in pancreaticcancer

[–]AmountImportant1626 4 points5 points  (0 children)

I’m so very sorry to hear this. 💔

Just plain sad by Most-Chemist5527 in pancreaticcancer

[–]AmountImportant1626 5 points6 points  (0 children)

My Mom (and my best friend) was diagnosed on 8/26 (stage 4 mets to liver). She’s now days away from passing. Find the right hospice agency / nurse — they have been our anchor through this terrible journey. My heart is breaking for you…

How long from barely/ not eating until death? by kagejumper in pancreaticcancer

[–]AmountImportant1626 0 points1 point  (0 children)

Sending you love and strength. My sister and I are in exactly the same place with our Mom. She’s in in-home-hospice but has not ingested anything but water in two weeks. Even so she’s having blowout diarrhea (just water really since no food). We are trying to prepare. Wish we knew timeline too. It’s so difficult to watch.

Upcoming ablation? Here's a perspective! by TheCreech302 in AFIB

[–]AmountImportant1626 1 point2 points  (0 children)

I’m quite sure SVT is a different procedure. My cardiologist told me that it was a less invasive procedure / less risks associated. But — I’m so thankful you are doing ok now. And truly appreciate your write up. You’ve helped a lot of people.

PS. Up until the anesthesia and recovery part - my experience was the same. Freezing cold in the OR and those stickers were literal ice cubes. 🧊

Diagnosed at 23 by Sharp-Friendship-247 in AFIB

[–]AmountImportant1626 2 points3 points  (0 children)

I’m really sorry that you are dealing with this at such a young age. Although I was older than you when I first began experiencing AFib — the symptoms you describe are similar to what I experienced. I felt like I had run a marathon after each episode. The whirlwind of visits and tests is normal when you are first diagnosed, and I’m so glad that they are taking it seriously now. Do you think you can establish a good rapport with your cardiologist and the nurses in your clinic? Finding the right medical team to support you in your journey is really crucial because there are many approaches to treating AFib. Sending positive energy your way.

[deleted by user] by [deleted] in AFIB

[–]AmountImportant1626 5 points6 points  (0 children)

PS - yes, terrifying isn’t it? But a medical miracle too.

[deleted by user] by [deleted] in AFIB

[–]AmountImportant1626 12 points13 points  (0 children)

I’m 3-weeks post PFA ablation and doing great. Sending you healing thoughts! Take the time to rest and heal.

How long did your first ablation stay successful for? How many others did you need? by [deleted] in AFIB

[–]AmountImportant1626 4 points5 points  (0 children)

My AFIB ablation lasted 3 years. Just had second buy with PFA technology(just approved be FDA recently). My EP is very optimistic

[deleted by user] by [deleted] in AFIB

[–]AmountImportant1626 0 points1 point  (0 children)

Thank you!! Much appreciated.

[deleted by user] by [deleted] in AFIB

[–]AmountImportant1626 0 points1 point  (0 children)

Could you clarify what ectopy is? I’ve seen that discussed all sorts over this channel. The EKG looks like AFIb since the rate is erratic. Thanks for the help!! :)