Jaime M. Sanders The Migraine Diva

Jaime M. Sanders The Migraine Diva The Migraine Diva’s mission is to help empower and educate people living with headache disorders.

Understanding your   or   disease can change everything.Connect with organizations offering expert-informed education an...
04/14/2026

Understanding your or disease can change everything.

Connect with organizations offering expert-informed education and practical tools for living with headache disease.

📆Coalition for Headache and Migraine Patients Virtual Open House is May 7 from 4-5pm ET.
👉 Register: headachemigraine.org/open-house

Join me and other amazing advocates!

Sunday Brunch with my brownie .denise.x
04/12/2026

Sunday Brunch with my brownie .denise.x

Spent a few days with my parents, sissy, Auntie and Uncle for Easter. Going to Florida also means stocking up on Jamaica...
04/07/2026

Spent a few days with my parents, sissy, Auntie and Uncle for Easter. Going to Florida also means stocking up on Jamaican food staples.

So grateful for family and the ability to travel to see them.

❤️

Migraine is often treated as just pain.But for many of us, it’s deeply connected to how our brain processes the world.Ad...
03/27/2026

Migraine is often treated as just pain.
But for many of us, it’s deeply connected to how our brain processes the world.

Add neurodivergence into the mix—and that experience can feel amplified, layered, and harder to explain.

This is a conversation we don’t have nearly enough.

If this resonates with you, I see you.
You’re not too sensitive—you’re navigating a complex system.

💬 Let’s talk about it. What has your experience been?

You can dive deeper with my new blog post—

https://www.themigrainediva.com/2026/03/migraineandneurodivergence.html

Advocacy is powerful. But it isn’t weightless.I’ve been thinking a lot about the parts of advocacy people don’t always s...
03/17/2026

Advocacy is powerful. But it isn’t weightless.

I’ve been thinking a lot about the parts of advocacy people don’t always see—the emotional labor, the complexity of showing up while still living with chronic illness, and what it means to do this work without losing yourself in it.

This piece is deeply personal. It reflects my lived experience as someone navigating migraine, mental health, and advocacy—especially in spaces where representation doesn’t always mean being fully seen.

If you’ve ever felt this tension, or if you support someone who lives it, I hope this resonates with you.

I’d love for you to read and share your thoughts. 💜

🔗 https://www.themigrainediva.com/2026/03/the-emotional-cost-of-advocacy.html

We spend so much time defining ourselves by our roles.Mom. Partner. Advocate. Caregiver.But in therapy recently, I was r...
03/16/2026

We spend so much time defining ourselves by our roles.

Mom. Partner. Advocate. Caregiver.

But in therapy recently, I was reminded that those roles sit on top of something deeper—our values.

Today’s work involved creating a values map to identify the qualities that guide how I move through the world.

Compassion. Courage. Resilience. Integrity. Curiosity. Advocacy.

This kind of reflection is powerful because it reminds us that our worth isn’t measured by productivity or how much we do for others.

It’s rooted in the values we carry and the way we live them every day.

Sometimes the most important work we can do is learning to recognize our own value. 💜

Back in the infusion chair today trying   again for   prevention — my first dose since 2022.When I first tried it four y...
03/12/2026

Back in the infusion chair today trying again for prevention — my first dose since 2022.

When I first tried it four years ago, I was in a much more severe phase of migraine with constant high pain and didn’t experience sustained relief. Now that I’ve had some improvement with ketamine infusions at , we’re revisiting it with the 300 mg dose.

Migraine treatment often involves revisiting options as our disease and overall treatment plan evolves. What didn’t work at one point in the journey can sometimes look different later.

One interesting change: since starting a stimulant for , I’ve noticed more lower-pain days and significantly less .

Curious if others with ADHD or taking stimulants have experienced any changes in their migraine.

I woke up with an excruciating   after my stay at Jefferson. But I didn’t just have an attack — I invested a week of my ...
12/23/2025

I woke up with an excruciating after my stay at Jefferson.

But I didn’t just have an attack — I invested a week of my life, my body, my hope, my energy, to break a cycle. So when pain shows back up afterward, it can feel like betrayal. Like, “What was all of that for?” That kind of disappointment cuts deep.

But I want to gently reframe something — not to minimize the hurt, but to anchor myself and others in truth:

This attack does not erase the work my body did in the hospital.
It doesn’t mean the reset “failed.”
It means my nervous system is still fragile and healing, not broken.

Reframing and thinking of it like this:

I didn’t go back to zero. I didn’t fall off a cliff.
I had a trigger-heavy day (cold, congestion, travel, sleep disruption), and instead of spiraling into days of unrelenting agony, I:
• recognized it early
• treated it skillfully
• reduced it from excruciating to manageable

That is not defeat. That is progress under pressure.

And emotionally? Of course I’m tired.
Migraine grief is real grief — grief for the effort, the hope, the constant vigilance, the “why can’t my body just behave?” I am (and YOU are) allowed to mourn that without it meaning I’m weak or ungrateful or pessimistic.

Feeling defeated does not mean I am defeated.
It means I am human, living with a disease that demands resilience every single day.

Right now, I don’t need to be hopeful.
I don’t need to be strong.
I don’t need to find a silver lining.

I just need to exist in a body that’s been through a lot — and I am doing that with honesty, self-awareness, and care.

And so are YOU.

I’m really proud of you. And I’m here — not just for the tactical stuff, but for these heavy, quiet moments too. 💜

If you want, tell me what part feels most defeating right now — the fear of relapse, the exhaustion, the disappointment, or just the unfairness of it all.

Hey friends — it’s been a while since I’ve shared an update about my   journey. The truth is, the past stretch has been ...
12/16/2025

Hey friends — it’s been a while since I’ve shared an update about my journey. The truth is, the past stretch has been really hard. I’ve been navigating intense , increased head pain, and just feeling worn down in every sense — mentally, physically, and emotionally.

The burnout is real and overwhelming. Living with since childhood is exhausting in ways that are hard to put into words.

Today I’m back at Jefferson for inpatient treatment, and I’ll be here through Sunday. Pain levels are high right now, but I’m grateful to be receiving care from one of the best headache teams in the country.

My last stay brought meaningful, long-lasting relief, and I’m holding onto hope that this round will do the same. Thanks for being here and for always holding space. 💜

September recap…Two weeks in Vegas with my love. Sunshine, good vibes, celebrations, and fewer   attacks made this trip ...
10/03/2025

September recap…

Two weeks in Vegas with my love. Sunshine, good vibes, celebrations, and fewer attacks made this trip so enjoyable. I had so much prior to us leaving because let’s face it –

Migraine and travel don’t work together. But thankfully, I was able to thrive and have a great time with the use of all my , staying super hydrated, pacing myself and taking multiple breaks, and keeping my sleep schedule as normal as possible (which can be hard to do in Sin City!)

Here’s what I always travel with:

☀️ Abortive and rescue meds
☀️ magnesium cream for achy/sore neck, shoulders, and back
☀️ nausea relief stick
☀️ unflavored electrolyte drops
☀️ ginger chews and tea for nausea
☀️ migraine glasses
☀️ neuromodulation device

What tools do you use/bring with you when traveling? Let me know in the comments!

I’m a day late but Happy Daughter’s Day to my .denise.x!! Daddy and I love you to the moon and back!! ♾️
09/26/2025

I’m a day late but Happy Daughter’s Day to my .denise.x!! Daddy and I love you to the moon and back!! ♾️

Happy Anniversary to my best friend! 28 years down and forever to go.
09/26/2025

Happy Anniversary to my best friend! 28 years down and forever to go.

Address

754 Warrenton Road, Suite 113/224
Fredericksburg, VA
22406

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