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Tuesday 10am - 6pm Wednesday 10am - 6pm Thursday 10am - 6pm Friday 10am - 3pm

Medacare Skin Clinic, 96 Grey Street, Gladstone, Invercargill (2026)

20/04/2026

THIS IS FOR TRANSFORMATION SEEKERS

This programme is not a series of single treatments. It is a sequenced, compounding clinical system — each phase building on the last, each session amplifying what came before. It is designed for people with real skin concerns who want real, lasting change.

- If single treatments haven't been enough.
- You've tried individual treatments and seen temporary results.
- Results faded before your next appointment.
- Your skin has plateaued and isn't responding the way it did.
- You're ready to invest in a programme that creates structural, lasting change.
- You want skin that stays clear — not just improves briefly.

BUILDING THE FOUNDATION YOUR SKIN NEEDS

IPL is not just a pigmentation treatment. Across 6 sessions, it performs a biological reset of the dermis — resetting gene expression toward youthful patterns, normalising vascular reactivity, priming fibroblasts, and creating the structural foundation.

A Stanford University study published in the Journal of Investigative Dermatology found that after a course of IPL, 1,293 of the 2,265 genes associated with skin ageing shifted back toward the expression patterns of young skin. These weren't cosmetic markers — they included key regulators of cellular longevity, proteasome function, cell-cycle integrity, and the suppression of cellular senescence.

"The researchers concluded this may represent functional rejuvenation — not a cosmetic imitation of youth. Your skin isn't being made to look younger. Its underlying molecular activity is being reset toward a younger state".

This gene expression shift builds with each session. You need the full 6-session course to accumulate it. Clinical studies also show skin treated regularly with IPL over years continues to improve — meaning consistent maintenance doesn't just maintain results, it compounds them.

WHAT IPL ACTUALLY TREATS

IPL is a multi-target technology — each session addresses multiple concerns simultaneously. You are not treating one thing at a time. You are running parallel repair programmes in the same tissue, in the same session.

- Pigmentation
- Vascular Conditions
- Acne & Active Skin
- Aging & Collagen
- Barrier Dysfunction
- Gene Expression Reset

SESSION BY SESSION — The Compounding Effect

Results do not accumulate in a straight line. They compound. Each session amplifies what came before because the biological momentum is still running when the next session arrives.

SESSION 1
Initiation:
- Photothermal stimulus initiates wound-healing cascade
- Surface pigment begins fragmenting (20–30% improvement)
- Inflammation begins decreasing. Some vessels start closing
- Collagen synthesis initiates. Gene expression begins shifting

SESSION 2 (2–4 weeks later)
Momentum Doubles:
- Session 2 arrives while Session 1 collagen synthesis is still active
- Addresses deeper vessels and pigment Session 1 softened
- 40–50% visible improvement. Skin cell renewal cycle completes

SESSION 3
Exponential Acceleration:
- 60% improvement in vascular and pigmentation. Texture improving
- Wrinkle reduction measurable — 24% at this point
- Skin staying clearer between sessions

SESSION 4
Structural Change:
- Deeper structural changes visible. Pore refinement noticeable
- 70% improvement in redness and pigmentation

SESSION 5
Optimum Reached:
- Wrinkle reduction reaches 33% (vs 24% at Session 3)
- 25% skin tightening and pore improvement reached
- 80% improvement in vascular and pigmentation
- Barrier fully competent

SESSION 6 (Transformation Complete)
Maximum Results — Phase One Foundation Set:
- Maximum collagen density achieved. 85–95% clearance of pigmentation and vascular lesions
- 33%+ wrinkle reduction locked in and stabilised
- Barrier fully restored.
- 1,293 ageing-related genes reset toward youth
- Fibroblasts biologically younger — Phase Two begins on this foundation if deeper collagen or scar remodeling is needed (Microneedling).

By the end of Session 6, your skin has been biologically reset. 1,293 ageing-related genes are expressing closer to their youthful patterns. Fibroblasts are more numerous, more responsive, and more capable. The collagen achieved through IPL is not the end result — it is the starting platform for best foundational results.

Microneedling builds a different type of collagen, through a different mechanism, reaching deeper tissue, producing results IPL structurally cannot reach if further treatment is needed for aging skin.

WHAT IPL BUILDS

- Indirect collagen via chromophore heating
- Strongest in upper to mid dermis
- Gene expression reset across 1,293 ageing-related genes
- Vascular, pigmentation, and barrier normalisation
- Fibroblasts biologically primed and reset
- Much much clearer, healthier skin.

WHAT MICRONEEDLING AFTER IPL CAN ADD

- Direct mechanical injury — separate, additive collagen pathway
- Reaches reticular dermis — deeper than IPL
- Mechanically disrupts fibrotic scar tissue
- Progressive shift toward Type I collagen (mature, structurally strong)
- Measurable laxity improvement IPL alone cannot produce

Microneedling asks your fibroblasts to do a great deal of work. IPL has spent 5–6 months making those fibroblasts younger, more numerous, and more responsive. The mechanical signal from microneedling lands in tissue that is primed to act on it — not fatigued, aged tissue working against its own biology. IPL-rejuvenated fibroblasts produce better collagen. New collagen deposited after microneedling can remain in place for 5–7 years.

Microneedling intervals are 6-8 weeks, so more time between sessions in this phase.

WHAT THIS MEANS FOR WRINKLES — The Most Important Number in This Programme

Wrinkle reduction matters most to the majority of clients. IPL alone delivers 33%+ wrinkle reduction across 6 sessions — that is the documented, research-backed figure from clinical trials, and what I see in clinic. That is Phase One.

Microneedling through a completely separate pathway — direct mechanical injury stimulating new collagen type I, III, and VII, tropoelastin, and dermal reorganisation — independently produces a further 25–50% improvement in wrinkle severity scores, confirmed across systematic reviews. This is additive. It is not the same collagen, triggered the same way, in the same tissue depth.

The combined result across the full IPL - microneedling programme is not 33%. It is 33% as a starting point, with a further 25–50% improvement compounding on top of it through Phase Two — on IPL-primed fibroblasts that are biologically younger and more productive than they were before Phase One began. This is why completing both phases matters.

IMPORTANT!!

Before or straight after your first IPL session — and every day throughout the entire programme — you need to apply Retinaldehyde Vitamin A morning and night. This is the most important thing you can do at home. Sunscreen is second. Vitamin A is first.

Vitamin A controls between 350 and 1,000 genes responsible for cell proliferation, differentiation, angiogenesis, and neocollagenesis — the exact biological processes that IPL and microneedling are activating. Without adequate Vitamin A at the tissue level, the genetic programme these treatments are trying to run cannot complete. The stimulus lands. The response is diminished.

IPL and microneedling are the signal. Vitamin A is what makes the cells capable of receiving and acting on it. Starting straight away means every one of your treatment sessions lands in tissue that is gene-primed to respond.

Why Retinaldehyde — because its' one conversion step from active Retinoic Acid, and the most potent form of Vitamin A available without prescription. Unlike retinol (which requires two conversions) or prescription tretinoin (which causes inflammation and barrier disruption), Retinaldehyde is sun-safe, non-inflammatory, and suitable for use throughout an active treatment course. It is encapsulated in a patented liposomal delivery system that drives it into the dermis — not just onto the surface.

I will recommend the right formula (the correct formula and potency for skin concern) and give you 20% off your first bottle before or at the time of your first session.

01/04/2026

SCHOOL HOLIDAYS — IPL EDIT

The kids are home. That means you finally have a window.

Half Face IPL + Dermalux LED (Worth $275) → $149
Full Face IPL + Dermalux LED (Worth $375) → $249

Plus take home a free 15min post-care mask with vitamins (Worth $51) after your first session (Between 6th-17th of April).

Book one, or lock in a course.

Autumn is the best time to start treating skin damage with IPL — and I am making it easier to start.

Successful skin treatment is not just a science — it's an art.
Medacare specialises in advanced IPL using the Anthelia, a physician-grade system that delivers a level of precision, control and clinical outcome that standard IPL simply cannot match. In skilled hands, this is one of the most effective treatments available for transforming the skin.

Each session can precisely target:

Your Sun Damage
Unwanted Pigmentation
Visible Red Veins
Ongoing Acne & Rosacea
Unrefined Texture, Pores & Hydration
Declining Collagen
Lost Skin Firmness
Downregulated Youth Genes (1293 Of Them)

Dermalux Tri-Wave LED is included in every session to accelerate repair, reduce post-treatment inflammation and amplify your results.

Two treatments. One appointment. One outcome.

Available during April school holidays only. Slots are limited.
To lock in a course, continued sessions must be pre-booked at the end of your first session.

No consult required if you've been seen at Medacare before. New to the clinic? Book via the link and we'll confirm IPL is right for your skin before we begin.

Book at www.medacare.co.nz

Tuesday – Friday, Invercargill

25/02/2026

There's a reason some people with eczema never fully respond to standard treatment - and once you understand it, everything starts to make sense.

For a lot of people, the usual approach works. Moisturise. Reduce inflammation. Protect the barrier. Done.

But for others - maybe you - it doesn't. And that's not a failure of willpower, or bad luck, or not trying hard enough.

It's because atopic dermatitis isn't one condition. It's two distinct pathologies that look identical on the surface but have completely different drivers underneath. And treating the wrong one is exactly why so many people stay stuck.

The Barrier-Driven Type

This is the one medicine understands well. The skin barrier - your body's physical wall against the outside world - is genetically weak. It can't hold moisture. It can't keep irritants out. Things get in, the immune system reacts, inflammation follows.

Treat the barrier. Calm the reaction. This approach works here.

The Immune-Driven Type

This is where things get more complex - and where conventional treatment consistently falls short.

In this type, the problem doesn't start at the skin. It starts with an immune system that is fundamentally dysregulated - specifically, a Th2-dominant immune response that has become hypersensitive and chronically overactive.

Here's what that actually means:

Your immune system is overproducing specific inflammatory chemicals called cytokines - particularly IL-4, IL-5, IL-13, and IL-31. These aren't just causing surface inflammation. They are actively suppressing production of your key barrier proteins: filaggrin, loricrin, and involucrin - the proteins responsible for holding your skin together.

So your barrier isn't weak because of genetics alone. Your barrier is being actively dismantled from the inside by your own immune response.

IL-5 specifically drives the production of eosinophils — specialised white blood cells associated with allergic inflammation. Elevated eosinophils on a blood test are one of the clearest signals that this immune-driven type is what you're dealing with.

Why Elevated Eosinophils Matter

Eosinophils aren't passive bystanders. When activated, they release toxic proteins - eosinophil-derived neurotoxin and eosinophil peroxidase - that directly damage your skin barrier. They create microscopic breaches that bacteria exploit. And paradoxically, despite being immune cells, they are ineffective at killing Staphylococcus aureus — the bacteria most commonly colonising eczema-affected skin.

Elevated eosinophils correlate with more severe atopic dermatitis, higher IgE levels, greater infection risk, and — critically — a better response to immune-modulating therapies rather than barrier repair alone.

The Spiral That Keeps People Stuck

Once immune dysregulation takes hold, a self-perpetuating cycle begins:

Overactive Th2 immune response → IL-4, IL-5, IL-13 released → barrier proteins suppressed → skin barrier breaks down → Staphylococcus aureus enters and colonises → bacteria form biofilms → immune system escalates response → eosinophils activated → more barrier damage → more bacterial entry → cycle repeats.

This is why short courses of antibiotics fail. A 7-day course kills surface bacteria. It does not pe*****te biofilms - protective bacterial colonies that are up to 1000 times more resistant to antibiotics than free-floating bacteria. When the antibiotics stop, the biofilm releases its colonies and reinfection follows. Minimum 14-21 days is typically required just to begin disrupting biofilm structure.

The Cell Danger Response - Why It Never Fully Resolves

Your body has a built-in healing sequence called the Cell Danger Response. It runs in three phases: defend against the threat, repair the damage, then resolve the inflammation and return to baseline.

In chronic immune-driven atopic dermatitis, this sequence gets interrupted. The body never reaches phase three. It stays locked in defence mode - perpetually sensing danger, perpetually inflamed, perpetually reactive.

Think of it as an oversensitive alarm system where the original event set the sensitivity so high that almost anything triggers it now - cold air, chlorinated water, soap, humidity changes, airborne chemicals, even physical friction.

Why Environment Hits This Type So Hard

Your immune system doesn't just react to pathogens. It reacts to multiple categories of signals: (Here's two)

DAMPs - Damage-Associated Molecular Patterns - triggered by things like chlorine in water, dry cold air, chemical exposure, and physical trauma to the skin.

PAMPs - Pathogen-Associated Molecular Patterns - triggered by bacteria like Staphylococcus aureus.

In immune-driven atopic dermatitis, Pattern Recognition Receptors on your skin cells are chronically upregulated. They are scanning constantly. The threshold for triggering a full immune response is extremely low. This is why environmental factors that wouldn't affect most people - indoor heating dropping humidity below 30%, formaldehyde off-gassing from furniture, VOCs from cleaning products, hard water with elevated chloramine - can send the skin into a flare. Every one of these is being read by your immune system as a threat signal.

What This Changes About Treatment

If your atopic dermatitis is immune-driven - elevated eosinophils, recurring infections, diminishing returns on steroids, failure to respond to barrier repair - then the treatment approach needs to shift fundamentally.

Barrier repair still matters. But it cannot lead. Because your immune system will continue breaking that barrier down faster than any topical can rebuild it.

What needs to happen simultaneously:

Immune modulation - calming the Th2 overresponse.

Nutrients I commonly prescribe include perilla, quercetin, omega-3 fatty acids (high ratio of DHA to EPA, not the other way around like most supplements), vitamin D and zinc and here's why.

Perilla is the most potent natural eosinophil suppressor available. It potently inhibits IL-5 production at transcriptional level, it directly suppresses eosinophil activation, degranulation, and chemotaxis, it reduces eosinophil survival signals and suppresses IL-4 and IL-13 (other Th2 cytokines). This leads to a 30-50% eosinophil count reduction, 20-40% IgE reduction, 40-60% IL-5 reduction, and effects are measurable within 4-6 weeks (faster than omega-3 alone)

Omega-3s shift the immune response away from Th2 dominance. High dose DHA decreases IgE and Th2 cytokines (IL-5, IL-13) and reduces eosinophil count reduction by 30-50%, improves barrier function by 20-30% and reduces itch intensity and flare frequency.

Vitamin D directly regulates immune function and supports barrier protein production. It directly suppresses Th2 immune responses and IL-5 production (the cytokine creating eosinophils). Vitamin D receptors on eosinophils signal reduced activity and D is essential for barrier protein production and infection resistance. By addressing the inflammatory driver that is actively damaging the barrier from within, eosinophils are reduced.

A zinc deficiency associated with elevated eosinophils and Th2 dominance. Supplementation helps normalize eosinophil counts.
Zinc is essential for immune regulation (shifts away from Th2 responses), critical for barrier integrity and protein synthesis, and
required for wound healing.

L-histidine is an essential building block for filaggrin synthesis (key barrier protein - Th2 cytokines actively suppress filaggrin production). Histidine is 48% of Natural Moisturizing Factor (NMF) in stratum corneum. It converts to urocanic acid (UV absorber, immunomodulator) and normalizes skin pH (alkaline pH worsens eosinophilic inflammation).

How they can work together:

Triple eosinophil suppression: Perilla (IL-5 inhibition) + DHA (pro-resolving mediators) + Vitamin D (Th2 modulation)

Dual barrier support: L-Histidine (filaggrin substrate) + DHA (lipid matrix) + Zinc (protein synthesis)

Mast cell-eosinophil axis disruption: Quercetin (stabilizes mast cells) + Perilla (prevents eosinophil response)

Immune rebalancing: Vitamin D + Zinc + DHA (shift from Th2 dominance)

With therapeutic supplementation, testing, correct dose and form is individual to each case and can be prescribed after a consultation. I work only with practitioner grade, high quality, excipient free supplements, free from unnecessary additives and many common allergens.

Especially for the treatment of AD, supplements must be free from wheat and gluten, soy, dairy, eggs, tree nuts, peanuts and sesame, artificial colours, flavours and sweetners, coatings and shellacs, GMOs, unnecessary binders fillers and preservatives, magnesium stearate, trans fat and hydrogenated oils.

Simultaneously with sufficient immune modulation the following needs to occur:

Environmental trigger removal - not as a general suggestion, but as a clinical priority. Your immune system is hyperreactive. Every DAMP and PAMP signal it receives keeps the alarm running. This is individual to each case.

Biofilm-aware infection management - understanding that recurring skin infections in this context require longer treatment windows and strategies that address bacterial colonisation at the source, including nasal carriage of Staphylococcus aureus.

Addressing the Cell Danger Response - supporting the body's ability to complete its healing sequence and move out of permanent defence mode.

This is not about abandoning medicine. It's about using a more complete picture of what's actually happening and working through it with a sequenced strategy.

The skin is where you see it. But the driver is systemic. And when you treat it that way, things can genuinely change.

Save this. Share it freely. This education if for everyone.

Lee.

24/02/2026

Your skin used to do this without being asked.

Renew itself overnight. Rebuild collagen after stress. Hold moisture without trying. Repair what broke down. It just worked.

Then at some point - quietly, gradually - the output slowed. Not dramatically. Just enough that one day you looked in the mirror and something had shifted. The tone. The texture. The way your skin sat on your face.

Here's what that actually is: your cells are tiny factories. And like any factory running for decades, production slows. The quality of what gets made changes. Collagen doesn't get replaced as fast as it's lost. Pigment becomes uneven. Oils oxidise and create that yellowish cast. Hydration leaks out because the molecules that hold water in aren't being made in the same numbers anymore.

This isn't aging as a surface event. It's your metabolism. Your hormones. Your cell biology decelerating in ways that show up on your skin before anywhere else.

Most people think IPL is for removing blemishes and damage. And it does that. But that's not the most important thing it does.
What it actually does is give your cells the right signals to start producing again.

IPL removes the blemishes and damage you can see — and reprograms the cellular factories you can't.

It's a controlled biological event. It targets red vessels, pigment, and water in the skin — fragmenting damage, sealing vessels, activating the heat shock proteins that switch your cellular repair systems back on.

Within days, damaged cells are being replaced with new healthy ones.

Within weeks, collagen production surges, your dermis thickens, pigment regulation normalises, and your barrier begins to fully restore.

Within months, gene expression shifts — the genes responsible for collagen production upregulate, the enzymes that break it down go quiet. Some of those changes become permanent.

Your skin doesn't just look better. It actually is better.

And the single most important thing you can do daily to hold and build on those changes? Vitamin A. In the morning it blocks the proteins that break collagen down. At night it switches on the genes that build new collagen up.

IPL establishes the reprogramming. Vitamin A maintains it.

Together they don't just slow what's happening - they reverse it.

But here's what most people don't realise.

When I stimulate your skin, I'm accelerating cell turnover dramatically. Construction speeds up. And that process burns through nutrients fast. If those nutrients aren't being replenished daily - through your diet, your supplements, your home care - the stimulus is there but the raw materials aren't. Your skin stalls. Or quietly goes backwards while you wonder why things aren't changing the way they should.

What you do at home every day will either support your results, counteract them, or undo them. There is no neutral.

This is why I don't just treat you and send you home. Part of every appointment is sitting down and working out what's actually going to support your skin between sessions - your skincare, your nutrition, the gaps that might be slowing things down. I want you to leave not just treated, but informed. Because the treatment does its job in here. The other 60 to 70% happens out there, every single day.

And that part matters more than most people realise. Your skin can only build with what you give it. Fail to supply what your metabolism needs and your skin loses its ability to heal and rejuvenate itself — not eventually, but progressively. Structure declines. Function declines. And no amount of treatment can outrun a foundation that isn't being fed.

Your home care has to match the result you want to get - and keep.

Thats why it's not damage to hide. It's function to restore.

For the rest of February and all of March I am offering a Full Transformation Starter.

It's a one hours appointment that includes:

Anthelia Full Face IPL + Osmosis Vitamin A Infusion + Dermalux LED Phototherapy + Take-home Dermaviduals 30ml Lotion N

One session that covers the full picture, all for $349.

The IPL reprograms your cellular factories. The Osmosis Vitamin A Infusion drives gene regulation deep into the skin. The Dermalux LED supports your recovery and amplifies the healing response. And the Dermaviduals Lotion N goes home with you - a lipid-rich barrier-restoring formula that helps your skin recover properly and hold its results in the days after treatment.

Because what happens after matters just as much as the treatment itself.

I'm also offering 20% off Osmosis Vitamin A to take home with your treatment - because keeping that daily signal going is the difference between results that last and results that fade.

If you've been wondering what's actually going on with your skin and what would genuinely help, feel free to book a consultation or click the link below to book the Full Transformation Starter session - limited spots available.

https://bookings.gettimely.com/medacare/bb/book

24/02/2026

There is something really profound about the moment a client stops feeling like they need to hide.

I see it more than people might realise. The quiet withdrawal. The foundation applied before anyone else is awake. The way pigmentation, sun damage or uneven skin tone can make someone feel like they are not quite themselves anymore - comparing, covering, avoiding.

It is not vanity. It is identity. And when your skin doesn't reflect how you feel inside, it affects everything.

That's what drives everything I do here.

Watching someone get that back is something I genuinely never take for granted.

When it comes to treatment, every tool I use is chosen because it allows me to do my best work. I'll be honest - I'm fussy. My standards are high and I won't work with anything that doesn't meet them. The Anthélia is no exception. Physician-grade and manufactured in Paris specifically for the medical industry, it works at a level most IPL devices simply cannot reach - targeting pigmentation, sun damage, uneven tone and redness with a precision and safety that produces results I am genuinely proud of. Visible from the first session, building with every treatment that follows.

But the technology is only part of it. Every person I treat has a different story, different skin, different drivers behind what they're experiencing. That's why I don't offer a standard package. I build a plan around you - your skin, your health, your life - because that is what creates real, lasting change.

If you have been covering up for long enough and you are ready to feel like yourself again - naturally beautiful, without the armour of foundation - I would love to help you get there.

If you're ready, I'm ready.

Pigmentation removal is not just a science, - it's an art, so a consultation is the best first step, or you can book a free Anthelia IPL test patch.

24/02/2026

First post of the year - and after five weeks back I'm already reminded of exactly why I do this work.

Every year I see people who have tried everything and still feel stuck - and every year I get to be part of changing that. If that's you, keep reading.

If you are still experiencing the same skin flares, breakouts, inflammation, or energy crashes year after year, the issue is not effort - it is strategy.

This isn't about more information. We're already drowning in that. This is about correcting the direction entirely.

Skin is a regulatory organ. It reflects immune activity, hormonal signalling, nervous system load, and inflammatory burden. When treatment is reactive rather than structured, cycles persist.

What seems "random" is frequently anticipatory biology - stress load, immune shifts, environmental pressure building before you consciously feel it.

Guesswork and surface fixes keep the pattern alive. What changes everything is working deeper - with clarity on what to target, when, and why. When your biology is supported in the right order, everything accelerates.

The Next Step Is Clinical, Not Cosmetic.

If you are ready to stop managing symptoms and start addressing source drivers, the first step is a structured consultation to build a sequenced treatment strategy specific for you.

This is not a generic skin review. It is a clinical reset.

If you are prepared to work with your biology rather than against it, you can book your consultation online.

Break the pattern. Correct the direction. Create measurable change.

01/12/2025

December Only Christmas Promotion

An elite skin treatment designed to maximise results and minimise expense.

PLASMA PEEL $129 (Usually $199)
December Exclusive: With complimentary Exosomes to boost recovery and results as a gift from Medacare for your valued support.

Exosomes are tiny messengers that tell your skin cells to repair, regenerate, and function better - helping treatments like Plasma Peel give faster, longer-lasting, and more noticeable results.

Book online at www.medacare.co.nz
Limited spaces left

Can be performed as a single session, between other treatments to amplify results, or as a course of 6 sessions for progressive, cumulative optimal results.

This isn’t just resurfacing — it’s repair focused renewal

Why This Peel Is Different

Traditional peels rely on acids to break down the surface of the skin, forcing rapid shedding. While effective short term, they don’t address why the skin isn’t functioning optimally in the first place.

What “repair-focused” actually means:

Plasma energy delivers controlled energy to the skin that activates cellular repair pathways instead of wounding pathways, stimulates fibroblasts and keratinocytes without breaking down the barrier, enhances mitochondrial activity (ATP), improving the skin’s ability to repair itself, and modulates inflammation rather than triggering it

So the skin is encouraged to function better first, then renew.

How Plasma energy works:

Plasma is an ionised form of gas that delivers controlled energy to the skin, stimulating biological processes rather than chemically damaging tissue. When applied to the skin, plasma energy:

- Activates fibroblasts to support collagen and elastin production.
- Enhances mitochondrial energy (ATP), improving cellular repair and turnover.
- Modulates inflammation instead of triggering it.
- Strengthens the skin barrier while accelerating renewal.
- Improves cellular communication for more even pigmentation and texture

Rather than stripping the skin, plasma signals the skin to regenerate itself—making it ideal for sensitive, inflamed, ageing or relapse-prone skin.

The Result

- Smoother texture
- Brighter, more even tone
- Stronger barrier function
- Improved healing and long-term correction

This is a peel that goes beyond exfoliation. It resurfaces and regenerates — using your skin’s own biology.

What Exosomes are:

- Tiny extracellular vesicles released by cells (often stem cells or fibroblasts).
- Contain signalling molecules, including growth factors, cytokines, and microRNA.
- Act as cell-to-cell messengers, instructing recipient skin cells to repair, regenerate, and function better

How They Boost Treatment Results:

- Stimulate Skin Repair.
- Activate fibroblasts → more collagen and elastin production.
- Promote keratinocyte activity → faster epidermal renewal.
- Improve wound-healing pathways, reducing downtime
- Reduce chronic low-grade inflammation in the skin.
- Encourage regenerative rather than injury-driven healing
- Enhances cellular communication by telling skin cells how to behave: repair, regulate pigment, strengthen barrier.
- Coordinates multiple repair processes simultaneously
Improves longevity of results.
- Supports structural proteins and extracellular matrix → longer-lasting firmness, tone, and texture improvements

Synergistic with treatments like microneedling, plasma peels, or laser resurfacing

Why They Work Better Than Traditional Add-Ons:

Traditional serums or growth factors often remain on the surface; exosomes enter cells and trigger internal signalling

They don’t just mask damage—they directly activate repair pathways.

Medacare Skin Clinic

20/04/2026

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Tuesday	10am - 6pm
Wednesday	10am - 6pm
Thursday	10am - 6pm
Friday	10am - 3pm