Lipedema is a chronic condition involving an abnormal buildup of fat—most often in the legs, hips, and sometimes the arms. It almost exclusively affects women. And here’s the part that tends to surprise people: this fat does not behave like typical fat.
It doesn’t respond predictably to diet or exercise.
It can feel painful, tender, even bruise easily.
And it often creates a distinct shape—symmetrical, with a “cuff” at the ankles or wrists.
On paper, it sounds clinical. Straightforward, even.
But in real life, lipedema is anything but straightforward.
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There’s a particular kind of loneliness that comes with lipedema.
It’s not just about living in a body that feels unfamiliar or uncomfortable. It’s about living in a world that doesn’t quite believe you.
Imagine doing everything “right”—eating well, moving your body, showing up for your health—and still watching parts of your body change in ways you can’t control.

And then imagine trying to explain that to someone.
To a friend.
To a fitness instructor.
To a doctor.

And being met with a polite nod… followed by advice that completely misses the point.
“Have you tried losing weight?”
“Maybe just more cardio.”
“It’s calories in, calories out.”

You start to question yourself.
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Not because you’re wrong—but because you’re outnumbered.
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In Canada, there’s an added layer to this story.

There is currently no specific diagnostic code for lipedema in many medical systems.
So what happens?

Patients are often given an obesity code instead.
Let that sink in for a moment.
A condition that is distinct from obesity—with different physiology, different treatment needs, and a different lived experience—gets categorized as something else entirely.

And that label doesn’t just sit quietly in a chart.

It follows the patient.
Into future medical appointments.
Into conversations about health.
Into the subtle (and sometimes not-so-subtle) assumptions that get made about their body.

​👉 Book your lymphatic drainage session here
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​Medical codes are meant to be neutral.

But they rarely feel that way.

Because an obesity label often carries an unspoken narrative:
This is your fault.
You didn’t try hard enough.
You just need more discipline.

For someone with lipedema, that narrative can feel like a second diagnosis—one that weighs just as heavily as the physical symptoms.
And over time, it shapes how people are treated.

Appointments get shorter.
Concerns get dismissed.
Symptoms get filtered through a lens that doesn’t quite fit.
And slowly, quietly, people stop speaking up.
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Here’s what doesn’t make it into the chart:

The woman who walks every day but sees no change in her legs.
The one who has tried every nutrition plan under the sun.
The one who avoids social situations because she’s tired of explaining—or defending—her body.

The effort is there.

It’s just not recognized.

And that disconnect? That’s where the loneliness deepens.
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This might be the most common question I hear from clients with lipedema.
Is it just me?
And the answer is always the same.
No. Not even close.
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But when your experience isn’t reflected in mainstream conversations about health…
When your condition isn’t clearly recognized in the medical system…
When your body doesn’t follow the rules everyone else seems to trust…
It can feel like you’re the only one living this reality.
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👉 Book your lymphatic drainage session here
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Lipedema doesn’t just involve fat tissue—it also impacts the lymphatic system.

Over time, the increased pressure in the tissues can slow lymphatic flow. Fluid can begin to linger. Swelling may increase. The body starts to feel heavier, more congested.

This is where a different approach becomes important.

Not one focused on shrinking the body.

But one focused on supporting how the body moves fluid, heals, and regulates itself.
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In my practice, I work with the body—not against it.

Using gentle, hands-on lymphatic drainage techniques, I help guide fluid out of areas where it tends to pool. There’s no forcing. No aggressive pressure. Just a listening approach—feeling where the body needs support and following that.

Clients often notice:

• A decrease in heaviness or pressure
• Reduced swelling or puffiness
• A sense of ease in their body that wasn’t there before
• And sometimes, something even more important… relief in being understood

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Because this work isn’t just physical.
It’s about being seen.
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If you’ve been diagnosed with lipedema—or suspect you might have it—I want you to hear this clearly:
Your body is not a failure.
You did not cause this.
And you are not alone in this experience.

There is a growing awareness around lipedema. Conversations are changing. And more practitioners are learning how to support this condition with nuance and care.
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If you’re in Calgary or the surrounding area and you’re navigating lipedema, I’d love to support you.
You don’t need to push harder or try another extreme plan.

Sometimes, the next step is simply giving your body the kind of attention it’s been asking for all along.

👉 Book your lymphatic drainage session here

If this blog felt familiar, you’re not imagining things.
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And you don’t have to navigate this quietly anymore.
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Helpful Resources
Alberta Lymphedema Association
 Lipedema Canada 
These organizations are doing important work in advocacy, education, and support—helping shift the narrative so fewer people feel alone in this.

That swelling isn’t in your head (or just your jeans)If you’ve ever looked in the mirror and thought, “Why do my legs look like they belong to someone else?”—you’re not alone. If your lower body feels painful, heavy, or “puffy” no matter how much kale you eat or how many steps you track, this blog is for you.
Welcome to the frustrating, underdiagnosed world of lipedema—a condition affecting roughly 11% of women, but barely whispered about in Canadian healthcare offices. Let's fix that.

So… what is lipedema, anyway? Lipedema is a chronic, progressive condition where fat and fluid accumulate disproportionately—most often in the hips, thighs, buttocks, and sometimes arms. It's often painful, doesn’t respond to diet or exercise, and can leave you feeling like your body is gaslighting you.
The tricky part? It’s not just “normal” weight gain, and not just lymphedema. And no, you’re not lazy or imagining things.

First steps when you think you might have lipedema1. Book an appointment with your doctorYes, even if you feel nervous. Bring photos. Bring a list of symptoms. And be prepared to advocate for yourself--a lot of doctors in Canada still don’t know how to recognize lipedema (don’t get me started…).
🔍 Pro tip: Ask to be referred to a specialist like a vascular or lymphatic clinic if your GP isn’t familiar with lipedema.

2. Visit Lipedema CanadaThey’ve done an incredible job gathering resources, personal stories, and medical information to help you navigate what can feel like a very isolating experience. You’re not alone. And you're definitely not broken.

3. Start working with a Certified Lymphatic Therapist (hi, that’s me)Lymphatic drainage is a gentle, non-invasive therapy that can reduce swelling, improve comfort, and reconnect you with your body in a supportive way.
At Jennifer Strukoff Wellness, I work with many women navigating lipedema—some newly diagnosed, some still fighting for recognition. And honestly? They’re some of the strongest people I know.
We develop custom treatment plans that focus on:

• Reducing inflammation and pain
• Supporting lymph flow and circulation
• Helping you feel better in your own skin

And yes, I see clients both in-clinic in Calgary and through mobile visits in surrounding areas like Cochrane, Chestermere, Langdon, Airdrie, and Okotoks.

4. What not to do when you suspect lipedema

• ❌ Don’t go on a crash diet. It doesn’t treat lipedema and often makes things worse.
• ❌ Don’t let a trainer tell you to “just push harder.”
• ❌ Don’t ignore your pain. Your body is trying to tell you something.
• ❌ And for the love of all that is lymphatic… avoid Google Images at 2am.

My experience with clients who suspect lipedema I’ve worked with women who came to me after years--years!—of being told they just needed to lose weight or “try Pilates.” I’ve seen the frustration, the tears, the disbelief when they finally hear, “Yes, this could be lipedema.”
I’ve also seen the relief. The courage. The turning point when they stop fighting their body and start supporting it.
That’s where I come in—with gentle, targeted lymphatic work, a few bad jokes, and a lot of empathy.

Lipedema awareness in Canada: we’ve got work to doCompared to the U.S. or Europe, Canada is lagging behind in both awareness and resources for lipedema—especially here in Alberta. That’s why I make education a huge part of my practice. The more we talk about this, the more women will get help earlier, and the more we can pressure the medical system to catch up.

Ready to take the next step?If something in this blog hit home, don’t wait. Book a session with me and let’s chat. You don’t need a diagnosis to start feeling better. You just need support—and maybe someone with a massage table and an excellent playlist.
Let’s take that first step together.
Because a happier, healthier you is just a session away.
👉 Alberta Lymphedema Association
👉 Lipedema Canada

As June comes to a close, so does Lipedema Awareness Month—but for those living with lipedema, the journey toward better health and mobility continues year-round.
Lipedema is a chronic and often painful condition that primarily affects women, leading to the abnormal accumulation of fat, usually in the legs, hips, and arms. It’s often misunderstood or misdiagnosed, which is why raising awareness is so critical.
One of the most effective ways to manage lipedema is by working with a Certified Lymphatic Therapist (CLT)—someone trained to address the lymphatic system’s role in this condition. As a CLT and Registered Massage Therapist, I offer support to help you feel more comfortable in your body, reduce inflammation, reduce pain, and regain control of your daily life.
How a Certified Lymphatic Therapist Can Help with Lipedema:

1. Manual Lymphatic Drainage (MLD)
   This gentle, rhythmic technique encourages healthy lymph flow and helps reduce the swelling and heaviness often associated with lipedema.
2. Compression Guidance
   I can help you find and fit compression garments that work for your unique body, which are essential in supporting tissue health and reducing progression.
3. Treatment Planning
   Every person with lipedema is different. I work with you to develop a customized treatment plan that aligns with your goals, lifestyle, and symptoms.
4. Education & Support
   Understanding your condition is empowering. I’ll walk you through the “why” behind every approach and connect you with resources like Lipedema Canada for community and advocacy.

Let’s Build Your Plan TogetherYou don’t have to wait until next June to prioritize your health. Lipedema Awareness Month may end today, June 30, but your path to feeling better can begin right now.
Book your appointment today and start planning your customized lymphatic therapy program with me.
👉 Book Now


Together, we can support your body and improve your quality of life—one session at a time.