I created this blog 21 years ago - this month. Hard to believe it's been that long ago. If it were a person, it could walk into a bar and order a drink in all states!
Anyway, in those 21 years I've rarely posted about politics. I believe I've only posted about them twice. Once when a republican was running for office in Texas and his only platform to run on was that his opponent wrote romance novels, which he called porn. He said it made her a sexual deviant and unfit for office. I believe it was a midterm election and may have been the first midterm election I ever voted in. She beat him, by the way! The other time was in 2024 when I explained why I was voting the way I was, even though the person on the ticket wasn't in my top 10 of who I wanted to see as president. Aside from those two instances, I don't think I've talked politics here.
I also don't think I've ever talked about any serious illnesses I was dealing with because I was always focused on getting through them and didn't want it to impact how anyone treated me.
But, today, I'm going to discuss both of those things here, for a reason.
In December 2013 I went in for a routine mammogram. It came back abnormal and so I had to go back for an ultrasound, followed by a biopsy, which resulted in me getting told in early January 2014 that I had breast cancer. There are very vivid memories from the day I was told that resonate to this day. The fear. The shock. The disbelief. Not necessarily in that order. But, that's not really what this post is about.
I don't remember the specifics about when I was told what kind of cancer it was and what it meant. I was diagnosed with HER2 positive breast cancer. I also don't remember how I learned more about it because I do know that there was a point early on where I decided that anything I learned would come from my oncologist. I may have done some internet searching before I came to that decision but I know that throughout my actual treatment, I refused to look up anything online. So I don't know if what I came to know about it came from a quick search before I decided the internet was to dangerous for me at that time, from my oncologist or searches after treatment. But, essentially, HER2 positive cancer is a very aggressive cancer. I was diagnosed at stage 1A but was treated the same as if I was diagnosed as stage 4. The only difference was that I had an end date for treatment and stage 4 patients do not. There was a time when someone coming in at my stage would be told to get their affairs in order because it was very hit and miss if chemo helped with it and the odds favored the patient dying rather than beating it.
I asked the hospital where I was being treated to pair me with someone who had gone through the treatment plan they had me going through because I really needed to talk to someone who could fully understand what I was going through and it truly helped. She told me about an online support group for HER2 positive patients that she said helped her. More on that in a minute. I don't think I ever went there until after my treatment had ended - again because of the online fear factor thing.
One of the drugs used to treat HER2 positive cancer is herceptin. My insurance was charged $13,000 for each infusion of it and I got it every three weeks for a year - it's not cheap.
The person I had been partnered with had been diagnosed at stage 3. She was considered a dead woman walking when she was diagnosed. Dr. Dennis J Slamon had worked for years on herceptin and had to fight tooth and nail to get funding for his research. (There is a movie about it called Living Proof starring Harry Connick Jr.) It became a game changer in treating HER2 positive cancers. The person I had been partnered with got treated with it because they figured that since was dying anyway, they had nothing to lose in letting her get the treatment. It was considered an experimental drug at the time and only available to stage 3 or stage 4 patients. But, as she went through treatment, scans proved that it was dissolving her tumors. At the time we were paired together, it had been about five years since she'd been treated and she was still cancer free.
Just the few years later that I was diagnosed, herceptin was standard of care for all HER2 positive cancer patients. I didn't have to go through a trial or let them give me an experimental drug - it was tried and true by that point. And for that, I am grateful.
Now back to the online support group. Once I was done with treatment, I started spending a LOT of time on the message board, reading people's stories and commenting on new comers. After a while, I felt like an old timer and grateful to be able to share with others who might be coming in scared, like I had.
But then, notices started coming in about people who had been on the board for forever that were having recurrences or dying, years and even decades after they had been living with no evidence of disease. It was scary and I decided that for my own peace of mind, I had to stop frequenting the message board and just be grateful that I was healthy-ish.
There were several people on the board that I became close to and we kept in touch, sometimes through the board and sometimes through personal emails.
There was this one woman that we were communicating via the private message system on the board. She was a later stage and was experiencing severe side effects from the treatments she was getting. Herceptin wasn't enough and she was one going into trials and getting experimental drugs. I hadn't heard from her in a while and feared the worst. I didn't know how to get in touch with her outside of the message board so there wasn't a lot I could do.
Then, a couple of days ago, out of the blue, I was notified that she had sent me a private message. She said she hadn't been on the board for years but that she had gone for a clinical trial of a new drug hoping to target HER2 positive cancers and that she had been off the drug for three years now and that she was no longer having symptoms, her cancer was stable (not gone apparently but stable is good!) and she was doing well enough that she had even been able to return to work part-time. I was so excited to hear all that and to know she was doing well, or at least definitely better than before.
But then I got pissed. And this is where the politics come into my post. I probably wouldn't be alive today if not for the work of Dr. Slamon. The woman I had been partnered with wouldn't have survived to be partnered with me without his work. The woman that sent me the message the other day wouldn't have a decent quality of life today if not for the work of other medical professionals trying to find cures for cancer. Yet, we have someone sitting in the White House that feels that funding research for deadly diseases is a waste of money. He can find money for illegal ballrooms and to put his name on everything he can think of and to pay insurrectionists for their work on January 6, 2021, but finding cures for deadly diseases is a waste of money to him and it makes me angry. This one hits close to home too. There's always a chance my cancer will come back and I haven't reached the point - even almost 13 years later - where I take my cancer free status for granted. And if it comes back, will I miss out on a groundbreaking drug that would ensure it would never come back because of who is in the White House, because he cares about no one but himself?
I've read articles about people who supported Trump and championed his policies - until they affected them personally. An example is Milo Yiannopoulos who supported Trump and was all for deporting people - until he got deported himself. Now he's "ashamed" of his past support for Trump.
I've never supported Trump - ever - and I will never understand anyone who does. I voice my complaints but don't really do anything about it. And now I'm looking at something that could have a direct impact on me and I'm mad. And motivated.
Right now, all we have is our voice and our vote. I've been struggling getting registered to vote back in Texas because I haven't updated my license since I moved back. The changes Trump has made in government, you have to have appointments to go anywhere and it's hard, if not impossible, to get through to them via phone or email to set that appointment up. It wasn't this hard where I was living but here, it's been challenging. I had been thinking I would have to sit this election out but one message from someone I was afraid we had lost got that fire going again. We have to vote to put a stop to Trump's agenda - that only benefits himself, not every day Americans - and get some oversight back in congress. It can't happen soon enough!