Skip to main content

The Slippery Slope of Medication Overuse



Medicine Overuse. Dependency. A never ending, hard to break, cycle, pushed by medical professionals without considering the risks.

Wednesday I was diagnosed with potential medicine overuse headache, or rebound headache.

Can I say that I am at all shocked? No. Is this something I worried about every second of every day? Absolutely.

We've replaced on of my daily meds with something less potent, with a longer wait time between taking doses.

We're working to reduce how often I need to run to grab my abortive medications.

Next week, I'll be admitted to the hospital every day for 5 days, to receive IV injections of DHE, Benadryl, anti-nausea medicine, and something else. This measure is intended to stop this migraine that's been dragging on since September dead in it's tracks.

In turn, I should be able to reduce the frequency of abortive medications.

Then, I'll start my first round of Botox injections.

But, how did I get here? Me, of all people? I religiously watch the amount of medication I consume. I monitor the time between doses down to the minute to ensure medications won't interact with each other or overlap. I pay close attention to the quantity I take in a day.

I don't run out of pills to quickly. Yes, I often am due for my refill when it says I'm due for a refill and typically have other problems with pharmacies and insurance, but not because I'm requesting a refill too soon.

And yet, here I am. Victim to the very system that is meant to help me.

There are drugs out their where you can only receive x amount of pills in a month. But those aren't the medications I'm on.

So, having an intractable migraine for seven months, you end up taking pain medication. You take a dose when you wake up. Sometimes it works, sometimes it doesn't. Say it works: you may be good for the rest of the day, even if a little pain comes back, you may not take anymore medication. Say it doesn't work: you wait until x-amount of time goes by, and you take a different type of medication, because meds are a guessing game and you probably just didn't guess right on your first try.

Then you're in this cycle.  This never ending cycle where you're taking some sort of pain medication every day, sometimes twice even three times (that's the max amount you can take) a day.

But the doctors all left an important piece of information out.

These medications that have 90 days worth of medication for your 90 day supply, aren't intended to be taken every day.

These medications shouldn't be taken more than 9-10 times in a month.

9 to 10 times.

I've taken 9-10 doses this week.

Why would a medical professional give me more pills for a 90 day supply, than I'm supposed to take? Why does the prescription bottle put a daily limit but not a weekly or monthly limit on the instructions?

Thank god for my headache specialist for noticing that the amount of drugs being consumed could be having negative impacts on my health.

Thank god I keep a diary down to the minute with all this information.

But now, here I am, afraid to take any meds. I've portioned out my medication to fit into the "no more than 10 doses in a month" which equals about 2 doses a week, with an emergency dose every other week.

So my theory is that if I stop taking the medication, with the exception of my daily preventative, that after a while, the pain will go down.

I've always hated every ounce of medicine I've had to consume. I've always hated trying new medications. I've always hated counting down the minutes until I could take my next dose in hope of some relief.

So I guess I'll have to enjoy relying on blends of essential oils, coffee, and icepacks as my go to's, as for now, I don't want to touch medication.

Here's hoping next week's round of IV's and extra rest will put an end to this misery for a while.

-A

If you are using any sort of pain medicine, even regular over the counter medications such as Advil, Tylenol, or Excedrin, and you are using them more than 9 or 10 times each month, you are at risk for medication overuse as well and I would recommend reaching out to your doctor immediately.

Comments

Popular posts from this blog

It Hurts

To say I feel less than human, is probably a bit of an understatement. But I do. I've been home for a week. I've managed to pretty much lay in bed in agonizing pain the whole time. I had a half-assed attempt to see a friend that resulted in me rushing home as the nausea and aphasia set in. I successfully made it to massage therapy today. Which meant even after sleeping for roughly 2 hours, I got up at 7:30 and sat in traffic for hours to get to a less than expected appointment. Mind you, my previous massage therapist was so wonderful I'm most likely spoiled to other techniques. This lady was late, she sat in the same god awful traffic I did. We spent more time going over the woes of her morning, than we did discussing why I was there and what I hoped to achieve through various massage techniques. The massage room wasn't dimly lit, and even as the massage started, lights were still on. I found this odd, but decided to just keep my eyes closed. Then she started ...

Positive Notes

Here I go mixing things up before things have really taken off. My featured picture is intended to represent the way chronic illnesses and disabilities are only really seen in black and white. My words are intended to fill in all that grey space that is ignored. But today I needed a little color. Because at the end of the day, there's a lot of brightness and light and hope that is key component to my every day battle. So here's a sneak peak and my brand new apartment. I think I've spent the last 4 or 5 years waiting for the day that I had a place of my own. Not because I wanted freedom to do what I pleased or had the same urge to be an adult and do adult things. I in no way want to make anyone think that adulting is fun or recommended for anyone. I didn't want my own place. I needed it. I needed to not have to snarl at my parents for running the garbage disposal or cutting the grass when my head hurt too badly to get out of bed. I couldn't take one more la...

Tips and Tricks: Migraines Without Meds

We've all got that one thing that we know will make us be more comfortable, more ourselves. That little something we feel gives us an edge in whatever we're doing. It's that red pair of shoes that'll make us stand out from the crowd because there really isn't a wrong time to wear them, but they certainly aren't expected. It's that lucky pair of socks. It's the green scarf. It's our lucky pen. We want to be comfortable. But, when we've got outside forces controlling a pulsing sensation in our heads, comfort is about as far away as the sun we're desperately trying to avoid. And if you're in my position, reaching for the bottle of pain killers isn't always the right choice. To be completely honest, my pain meds scare me. Every time I get into some trance while I'm on them. Every time I feel myself coming down. Every time the pain sneaks back in. Some days I convince myself that the medication simply wore off and the br...