← Return to Medicare Coverage for Exams following Mastectomy

Discussion
justlucky avatar

Medicare Coverage for Exams following Mastectomy

Breast Cancer | Last Active: 1 day ago | Replies (15)

Comment receiving replies
Profile picture for justlucky @justlucky

@prarysky - Thank you for your comments and understanding.

You are so right! Never did I ever think I needed to learn about ICD-10 and CPT codes! I should have tracked how many hours I've spent on this one claim so far. It's enormously time consuming. Just this week I've probably logged 4-5 hours. I turned 75 last year and the day will come when I can no longer handle research and follow-up - for this or any other medical situation.

That's interesting feedback about the program you attended. I'm single and I learned a long time ago I need to be my own advocate for everything because no one else will be. Plus I don't have $495 (the amount of the 2023 denied claim) or $223 (the current denial) to just throw away. So I push.

Regarding the current provider....I thought I had found a needle in a haystack when I connected with her. After I moved, I must have contacted a dozen MDs, trying to establish a relationship. Although I was not in need of immediate care, I didn't want to wait to find someone when/if something happened to my implants. It was the internet version of picking an MD out of the yellow pages. Not the best way to pick an MD. I spent many hours on the internet calling every plastic surgeon in the area who does breast surgery. My requirements were not extreme. I needed someone who 1) took insurance (of any kind - some I learned do not), 2) accepts Medicare, 3) has solid credentials, and 4) accepts patients who do not need surgery or other cancer treatment currently (remember my reconstruction was done in 2005). When I did stumble upon my current MD within the same health system of my other providers (hence, all records were available), her first opening was 10+ months later. Only with the assistance of the Dir. of Patient Relations did I net an appointment that was "only" 4 months out. I felt extremely lucky. Therefore, the idea of going in search for another provider would be a last resort.

I tell you this (and all others reading my sad tale) only because it should be a consideration for any survivor who is planning a move outside of the geographic area where she originally received treatment. I don't live in the boondocks. It's not the major metro area I came from but it's not the sticks either. Little did I know finding a new provider would be one of the challenges of relocation that I would face!

Jump to this post


Replies to "@prarysky - Thank you for your comments and understanding. You are so right! Never did I..."

@justlucky
Such good advice! I am also 75. Although we'd long dreamed about moving to the wider open spaces beyond a metropolitan area, those are now fantasies. I've read of retirees moving to towns in Arizona or Colorado only to find doctors are reluctant to take on more Medicare patients in areas of high Medicare enrollees.

That is no surprise given the relatively low Medicare reimbursement rates to many doctors, especially those in primary care fields. We also have had to rely on the emergency room more than when we were younger, so now appreciate that we are close to good hospital emergency rooms.

There are many troubling issues with health care access bubbling up and already here. There is maldistribution by specialty and geography. There has been for decades but it seems worse today. There also seems to be a bottleneck in training programs, e.g., a lack of nursing programs.

In case this may be useful, here's a link to Triage Cancer. They provide all kinds of useful information and it is not just limited to cancer, though that has been a primary focus:
https://triagecancer.org