Anastrozole Has Entered the Chat
🌼 Date: Friday, August 28, 2026
⚡ Energy: Hormone blocker round two
💗 Status: Estrogen buffet closed
🤔 Outlook: Apparently my body needed another eviction notice
Today another estrogen blocker joins the party.
Welcome, Anastrozole.
Brand name Arimidex.
Because apparently Lupron looked around my body and said, “I could use backup.”
So here we are.
Another medication.
Another tiny pill.
Another side effect list long enough to need its own emotional support binder.
Another chapter in the glamorous world of breast cancer aftercare.
Love that for me.
Not really.
We already had the discussion about how estrogen works in my body because I had not gone through menopause yet.
My ovaries were still clocking in.
Still taking orders.
Still doing their little hormone factory job like nobody told them there was a whole cancer situation happening.
Rude.
So the once-a-month Lupron shot came in and put me into medical menopause.
Basically, Lupron cuts the signal from my brain to my ovaries.
The brain says, “Hey ovaries, make estrogen,” and Lupron steps in like a bouncer at a nightclub and says:
“Nope. Not tonight, ladies.”
The goal is to shut down ovarian estrogen production so the cancer has nothing to feed on.
Because my cancer was hormone receptor positive, estrogen is not just some innocent little hormone floating around minding its own business.
In my case, estrogen is more like leaving snacks out for the enemy.
So we closed the estrogen buffet.
No more all-you-can-eat hormone bar.
No more complimentary refills.
No more midnight estrogen snacks.
But here is the annoying part.
My body is sneaky.
Even after the ovaries are told to sit down and be quiet, the body still has back door ways to make small amounts of estrogen.
Because apparently my body has watched too many crime shows and knows how to find alternate entrances.
That is where Anastrozole comes in.
It closes the back door.
So now?
Good luck, estrogen.
All entries have been closed, locked, and boarded up.
Lupron shuts down the main factory.
Anastrozole goes after the side hustle.
Together, they are supposed to reduce the amount of estrogen in my body as much as possible and lower the risk of this cancer trying to make an encore appearance.
And let me be very clear.
I do not want an encore.
No standing ovation.
No reunion tour.
No surprise guest appearance.
Cancer had its show.
The show is over.
The theater is closed.
The chairs are stacked.
The lights are off.
Security has been called.
I will continue the Lupron shot for five years.
Anastrozole is a pill I will take once a day for seven to ten years.
Seven.
To ten.
Years.
Yay.
My oncologist has me starting the pill now so that I will have experienced most of the side effects before my next appointment in about a week and a half.
Which is both logical and rude.
So, let’s talk about the side effects of Anastrozole.
Because apparently I needed another menu of possible nonsense.
The most common side effects can include joint and muscle pain.
Aches.
Stiffness.
Pain in the hands, wrists, joints, and muscles.
Wonderful.
And since I already have psoriatic arthritis, I guess I get to experience the joint pain and swelling twice.
Cool, cool.
Nothing says “you’re doing great” like stacking new joint pain on top of the joint pain you already brought from home.
There can also be hot flashes.
Night sweats.
Vaginal dryness or irritation.
Extreme tiredness.
Fatigue.
Difficulty falling asleep.
Difficulty staying asleep.
Because apparently sleeping is now considered an optional luxury item.
There can be low mood.
Anxiety.
Depression.
Mild nausea.
Vomiting.
Diarrhea.
Constipation.
Heartburn.
Headaches.
Hair thinning.
Weight gain.
Swelling in the hands or lower legs.
Wonderful list, isn’t it?
A real little pharmaceutical charcuterie board of misery.
Aches here.
Hot flash there.
A sprinkle of insomnia.
A side of swelling.
Maybe some nausea for garnish.
Chef’s kiss.
Cancer recovery is so fancy.
And then there are the more serious risks.
Long-term use can weaken bones, which can lead to osteopenia or osteoporosis and an increased risk of fractures.
Because apparently estrogen was also helping keep my bones from turning into stale breadsticks.
There can also be changes in cholesterol levels and possible heart-related concerns, especially for people who already have a history of heart disease.
Rare risks can include serious allergic reactions, severe skin reactions, or liver changes.
So basically, the tiny pill comes with a tiny warning parade.
And still, I will take it.
Do I love it?
No.
Am I thrilled?
Also no.
Am I grateful there is something I can take to help reduce my risk?
Yes.
And that is the weird emotional math of cancer treatment.
You can be grateful for the medication and still dread the side effects.
You can understand why you need it and still be annoyed that you need it.
You can know it is part of the plan and still look at the bottle like:
“What fresh hell are you bringing to the table?”
Because let’s be honest, hormone suppression is not exactly a spa day.
Lupron already shoved me into medical menopause.
Hot flashes.
Mood swings.
Sleep issues.
Body weirdness.
The whole “Welcome to Menopause: Express Lane Edition” package.
And now Anastrozole is joining the party with its own possible side effects.
Because apparently my body saw the calendar and said:
“You know what this woman needs after chemo, radiation, surgery, expanders, lymphedema, neuropathy, psoriatic arthritis, and returning to work? More nonsense.”
Thanks, body.
Very creative.
But here is the thing.
This is the next step.
This is part of the long game.
Treatment did not end when chemo ended.
It did not end when radiation ended.
It did not end when my skin stopped peeling.
It did not end when my hair started growing back.
It did not end when I went back to work.
For hormone-positive breast cancer, treatment keeps going quietly in the background for years.
Years.
Not days.
Not weeks.
Years.
That is the part people do not always see.
They see the hair growing back.
They see me dressed for work.
They see me posting pictures.
They see me laughing.
They see me looking more like myself.
But they do not see the daily pill.
The monthly shot.
The appointments.
The side effect monitoring.
The bone health conversations.
The constant trade-off between quality of life and reducing recurrence risk.
They do not see me standing in front of a medication bottle thinking:
“Okay. Here we go again.”
But here we go again.
Because I am still here.
Because I fought too hard to stop fighting now.
Because if this pill helps close another estrogen loophole, then Anastrozole can pull up a chair.
Not because I invited it.
Because it is necessary.
There is a difference.
So today, Anastrozole joins Lupron in the estrogen shutdown committee.
Lupron handles the ovaries.
Anastrozole handles the back door estrogen production.
Together, they are basically the anti-estrogen security team.
Tiny Tina’s internal bouncers.
No estrogen wristband?
No entry.
No snacks for cancer.
No buffet.
No side hustle.
No secret entrance.
Denied.
Hard pass.
Get out.
I am sure there will be days when I hate this pill.
There will probably be days when my joints hurt and I question every life choice that led me to this bottle.
There will probably be days when I blame it for everything from hot flashes to bad moods to why my knees sound like microwave popcorn.
And honestly, fair.
But today, I am trying to see it for what it is.
Another layer of protection.
Another step in the plan.
Another way of saying:
“I am still fighting for my future.”
Even if the future comes with a pill organizer.
Even if the future comes with medical menopause.
Even if the future comes with side effects, appointments, and more conversations about what my body is doing without my permission.
Cancer already took enough.
If Anastrozole helps lower the chance of it coming back for more, then fine.
Welcome to the party, Arimidex.
Please keep your shoes on, stay out of my joints if possible, and do not touch the thermostat.
The estrogen buffet is closed.
The back door is locked.
And Tiny Tina is still doing everything she can to keep cancer from getting a second invitation.
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💗 Tina –
One Badass Day at a Time
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