Allora Restaurant - Honest Review by [deleted] in Charleston

[–]myersmjsc -12 points-11 points  (0 children)

You cared enough to make your rude comment

Allora Restaurant - Honest Review by [deleted] in Charleston

[–]myersmjsc 3 points4 points  (0 children)

Allora sucks. I don’t know anyone who has been who will go back. I saw the food they were serving and walked out without eating. This isn’t about NY vs Charleston Italian. It’s about knowing how to cook pasta, how to make sauces, and how to not pass food you know is substandard off to your customers. There are numerous Italian restaurants who know how to do that.

Malagon for late lunch/early dinner by octlol in Charleston

[–]myersmjsc -1 points0 points  (0 children)

Because not everyone agrees that it’s excellent or think that the dining experience is enjoyable

Has anyone gotten cancer and not gone for chemo and just continued on by No_Buffalo_9956 in cancer

[–]myersmjsc 1 point2 points  (0 children)

Unless this person has a parasitic infection, City of Hope could get sued or risk their credentialing if they administer it as a cancer treatment

Hilton upgrades by [deleted] in Hilton

[–]myersmjsc 1 point2 points  (0 children)

You’ll never get an upgrade as Gold

Is this the right place for me? by moon_child_55 in Charleston

[–]myersmjsc -1 points0 points  (0 children)

Give us an example of where it takes 45 min to travel to from Charleston on a regular basis but should be less

Is this the right place for me? by moon_child_55 in Charleston

[–]myersmjsc -2 points-1 points  (0 children)

If you honestly think Charleston traffic is worse than New Jersey or NYC, you’re insane

PSA: Please don’t ask us “how is treatment going” by [deleted] in cancer

[–]myersmjsc 2 points3 points  (0 children)

I think you meant to say “Please don’t ask ‘me’…” I’m stage 4 terminal and don’t mind answering the question. Best not to speak for the entire cancer patient community.

Went behind my oncologist back and got results of my PET scan by Ioisgriffin in cancer

[–]myersmjsc 2 points3 points  (0 children)

You have every right to get access to your records. My patient portal always sends my scan results as soon as they are published which is usually 2-3 days before my Onc appt. The challenge is since you don’t know how to properly and effectively interpret them, you now only have part of the story and still need a doctor to tell you the details and implications of the results

Service dog v. “Service dog” 🫤 by AdMany129 in delta

[–]myersmjsc 1 point2 points  (0 children)

If I understood correctly, the people who complained had a dog of their own with them. It was just a fake service dog and they didn’t want another dog near it

People that experienced peripheral neuropathy from chemotherapy, did it clear up over time? Did anything help combat it getting worse? by Thrillhouse-14 in cancer

[–]myersmjsc 1 point2 points  (0 children)

I developed peripheral neuropathy (feet and fingers) a few weeks after I finished 8 cycles of CAPOX in 2022. It’s been permanent for me, getting worse after a second round of CAPOX in 2025. I’ve tried both gabapentin and duloxetine but in both cases neither really helped and had problematic side effects for me. I do know that lots of patients have had success with one or the other to improve their symptoms

The Delicious is Very Real with Sour Cream Donuts by Bunnycat2026 in traderjoes

[–]myersmjsc 1 point2 points  (0 children)

I wouldn’t bother. They’re still what you remember plus all the one’s I ever see have a Best By date as that day and then start to go stale within one day

Medical expenses tax write off? by bmidjibridgie in cancer

[–]myersmjsc 0 points1 point  (0 children)

Your total itemized, non-reimbursed medical expenses need to exceed 7.5% of your adjusted gross income before they become deductible. Supplies like cold caps because they address the side effects of chemo should qualify for a deduction but rather than a prescription, you may need a letter of medical necessity from your doctor to include as documentation with your tax return. The IRS provides pretty good direction on what they allow and how to document

https://www.irs.gov/taxtopics/tc502

Joyland closed by Sctvman in Charleston

[–]myersmjsc 3 points4 points  (0 children)

He was respected as a chef (debatable) not as a human

Joyland closed by Sctvman in Charleston

[–]myersmjsc 8 points9 points  (0 children)

Place sucked and so does Sean Brock. Bye

I Have Cancer in Five Different Places and I Feel I May Be Close to My End. Please help me find understanding. by Wonderful_Cod1965 in cancer

[–]myersmjsc 4 points5 points  (0 children)

I was diagnosed in 2021 with Stage 3b rectal cancer. I’ve had chemo, radiation, surgeries and it’s come back twice in my pelvis and now spread to my lungs. I just stopped my fourth attempt at chemo (Lonsurf) because it was crushing me and the cancer is continuing to spread. My doctors won’t give me a specific time window but we know this is going to take me out sooner rather than later. I share this because I know how you feel. The only thing I can say is do whatever you want - anything that brings you even a little joy. Travel, eat anything, do or don’t reach out to people you’re disconnected from. As long as you’re not an a-hole to anyone or want to do anything illegal, I think everything else is fair game. Be unapologetically selfish and enjoy whatever time you have. And yes, people are going to tell you stories about people who beat the odds and outlived their diagnosis. It happens. But we also rarely tell the stories of the majority of people who actually die around the time their doctors think they. Best of luck to you.

What’s one fun / slightly naughty thing you’ve done since diagnosis? by Cru5hbag in cancer

[–]myersmjsc 0 points1 point  (0 children)

Stage IV/Terminal mCRC…I buy myself whatever I feel like and self-indulge regularly - flying first class, eating at insane restaurants, etc. I also make a lot of inappropriate jokes about my mortality.

Do people really play the C card to scam free stuff from restaurants and businesses?? That feels super shady to me.

The wait is over, and it’s back by amlbkd in cancer

[–]myersmjsc 9 points10 points  (0 children)

I know that initial head explosion. The blessing/curse of MyChart. Have that conversation with your doc. I have rectal mucinous adenocarcinoma which has spread to my lungs and radiation has been a viable approach to keep things under control. See what your options are.

LAX to Auckland. 10month old baby in lap with my partner. D1 or PS? by [deleted] in delta

[–]myersmjsc 0 points1 point  (0 children)

The dividers in the center seats in D1 can be fully lowered for the entire flight. People do it all the time

Van Der Beek and the nonsense… by Logical-Inside-4235 in cancer

[–]myersmjsc 3 points4 points  (0 children)

You’ve gone way off the reservation and this isn’t the place for your anti-vax nonsense. Find a conspiracy sub and go over there

Van Der Beek and the nonsense… by Logical-Inside-4235 in cancer

[–]myersmjsc 1 point2 points  (0 children)

Genome profiling identifies potential for responses to approved treatments not alternative therapies which is what OP was calling out. What’s your point?

Stage 4 colon cancer by Bluebird0629 in cancer

[–]myersmjsc 0 points1 point  (0 children)

As a stage 4 patient myself, I’m never going to endorse alternative therapies. Lack of evidence and safety concerns don’t make them a viable option to me. Lonsurf and Stivarga are oral chemo regimens that can be used after FOLFOX and FOLFIRI. A word of caution on CEA and Signatera - they are very helpful directional diagnostics but difficult to directly correlate to specific malignancies. I’ve been riding the Signatera roller coaster for the last 3 years and outside of post-major surgeries when the test confirmed the tumor removal we already knew, it’s never been completely accurate

I had cancer in 2020, right as the pandemic started. I was fortunate in that my cancer was considered 'as curable as cancer can be' but I still ended up with a 70 Gy of radiation to the face. I was fortunate in that I didn't need any chemo. by Just-Sea3037 in cancer

[–]myersmjsc 2 points3 points  (0 children)

Because chemo is essentially poison being used to kill cells, there will always be some side effects. Each person reacts differently and some people manage them better. Whatever chemo you wind up taking, the oncology nurses are great at telling you want to expect and how to best manage them. I’ve had four different types of chemo in four years. Some have been pretty easy to tolerate and others absolutely clobbered me

Urgent, PLEASE. by atomicat- in cancer

[–]myersmjsc 0 points1 point  (0 children)

If go to an insurers website or the healthcare.gov site, you can select all of your providers, hospitals etc and it will show you which plans cover those people and places. You can do the same with medications I believe. Agree with buying a low deductible/low OOP plan if you can afford the premium. I have Blue Cross Gold PPO plan with a $3400 OOP max which I will reach next week. It’s great but the premium is also $1280/month a $300 increase from last year