6,503 karma · joined February 4, 2010
I guess the only other things I would want to know is what factors pushed most to switching schedules? How long do you plan to stay on the schedule? How does your employer handle this schedule change? Or are you self employed/running a business? What do you think the biggest challenges are during the switch aside from being tired at hour 10-11? What does your SO really think about this schedule? The more I think about this, the more questions I have :)
Bought some duratex roll on coating (similar to truck bed liner) and recovered it. Then went to the hardware store and bought replacement screws and bolts to reassemble the keyboard.
Can’t believe how much better it plays now. Butter smooth.
Maybe the Apple Watch is not the best fitness tracker watch but it’s plenty good for me and it’s health integration is pretty good especially with the ultra.
I use distrokid and iirc the founder posts here would like to know if there is any truth to the allegations in the video.
It’s not true. It’s grossly oversimplified. I could generate a 1hz signal that I can hear. It’s not the same as something at 400hz but it’s clearly audible with proper sound equipment.
Now as that relates to tornadoes I live in a state where there are occasional tornadoes. Every time one has been close you hear the approach.
I was diagnosed in 2020. Went to a local oncologist who said (initially) I was stage 1. We caught it early. Then they do the colon resection and I wake up to the news that I’m stage 3c. I went through a 6 month treatment which knocked it back using the standard treatment (FOLFOX) and it was undetectable. Cut to 6 months later and it was back with a vengeance.
My oncologist ordered genetic testing right at the same time I decided to go to MD Anderson. The first thing that they wanted to do was the same genetic test. Great we say. My old oncologist ordered it.
My insurance BCBS declined to pay because my old oncologist ordered it and not the current one at MDACC. We / the hospital wrote 3 protest letters and they denied the claim meaning we had to pay 5k for the test. After dealing with insurance and the testing company we negotiated a lower price but be prepared to do so.
If you can’t afford it you are sometimes able to get payment plans. And there are endowments for situations where money is tight or no insurance. None of it is fun that’s for sure. Insurance companies are not your friend.
Great point about tumor dna. It does change and the “usual” treatments become less effective. That’s when the experimental drugs are usually brought in to the treatment plan.
I am living a pretty normal life for 4 of 7 days. And honestly I’m grateful it’s only 3 days that I’m less productive or just kind of tired/ spaced out.
Another PSA- start your start up before health gets in the way. Health really is wealth and having time with energy and a clear mind is in shorter supply once health issues arise. But also balance work and life. Ok no more PSAs today :)
I’ve got stage 4 colon cancer- I see these sorts of articles passed to me from family members.
While encouraging that these discoveries are being made it’s not necessarily something that you can take to the doctor and get started with. The following needs to happen:
1- it applies to your cancer/genetics/geneticdefects 2- it’s in a stage that you can be part of testing in human trials which means usually a specialist cancer hospital. (As a side note I recommend MD Anderson as a treatment hospital. They treat me very well and advocate well with insurance fights. And if you have cancer, live in the US you will fight with you insurer) 3- Is it even ready?? Usually no. It’s just the first paper written about it and others need to reproduce the results. Then about 10 other lucky miracles happen and human trials can start. 4- don’t be afraid to go back and forth with your doctor.
I’m currently doing maintenance chemotherapy but some areas flared up and they wanted to add another chemo drug. There were 2 options and we discussed and went with the option I tolerated better.
I do HIGHLY recommend that you establish a rapport with your doctor so that you can discuss treatment options freely. The way it works at MDACC and I’m sure very similar to other cancer hospitals. Is they do all the typing and dna sequences up front. It helps them diagnose the cancer and prognosis etc. and then that lives in your chart. Typical treatment is to use traditional known chemo treatments and if they are not effective they start adding the trials that match your dna/cancer type.
Very long winded way to say unless someone in your life asks you to send these sorts of things it’s kind of like getting a lottery ticket for 10 years from now.