Your Feet Burn Every Night.
Gabapentin Didn't Fix It.
Here's Why.
Gabapentin blocks pain signals in your brain. It doesn't repair the dying nerve cells in your feet. Only 30-40% of patients get relief — while up to 60% get only the side effects. Your nerves need energy to heal, not silence.
Try Loomi Amla →
Gabapentin Turns Down the Alarm.
The Fire Keeps Burning.
Every neuropathy treatment you've tried either blocks the pain signal or provides a nutrient. None addresses why your nerve cells are dying — mitochondrial collapse from oxidative stress. The engine inside each nerve cell is dead.
Gabapentin: 60% Get Only Side Effects
Only 30-40% of patients get meaningful pain relief from gabapentin. Up to 60% experience side effects — weight gain, drowsiness, brain fog, memory problems, dependency — with NO reduction in pain. The drug blocks calcium channels in the brain to dampen signals. It doesn't repair a single nerve fiber.
Lyrica: A Controlled Substance
Pregabalin is classified as Schedule V — the government recognizes its addiction potential. Same mechanism as gabapentin (signal blocking), same side effects (weight gain, cognitive impairment, edema), plus severe withdrawal symptoms. $400-600/month for the brand name. For a drug that doesn't heal nerves.
Nerve Cells Are Running on Empty
Your peripheral nerve cells are the most energy-hungry cells in your body. They maintain electrical signals across feet of fiber and constantly repair their myelin sheaths. When oxidative stress kills their mitochondria — the power plants inside each cell — they lose the energy to function, signal, or repair. That's the burning. That's the numbness. That's the tingling.
The 2am Burning That Never Stops
Neuropathy pain is worst at night because daytime movement and distraction mask it. At rest, the damaged nerve signals dominate. You pace the cold bathroom floor at 2am because tile is the only thing that provides temporary relief. Every night. For months. For years. While the nerves deteriorate further underneath the gabapentin haze.
B12. ALA. Magnesium. Benfotiamine.
Here's Why None Could Have Worked.
Every neuropathy supplement provides something the nerve cell needs. None provides the one thing it needs FIRST.
Vitamin B12 (methylcobalamin) — essential nerve nutrient. But your nerve cells' mitochondria are dead. They don't have the ENERGY to process B12. The vitamin sits there unused. Fuel in a car with no engine.
Alpha-lipoic acid (ALA) — powerful antioxidant that protects nerves from further oxidative damage. Protection is important. But protection doesn't generate new energy. If the mitochondria are already destroyed, preventing MORE destruction doesn't restore power.
Benfotiamine — fat-soluble B1 that reduces AGE damage in diabetic nerves. Addresses one pathway of damage. Doesn't restart dead mitochondria. Doesn't generate cellular energy. One piece of a puzzle with the central piece missing.
Acetyl-L-carnitine — supports existing mitochondrial function. The closest to our mechanism. But "supports" existing mitochondria assumes they exist. If they're dead, there's nothing to support. ALCAR helps functioning engines work better. It doesn't build new engines.
Capsaicin cream — depletes substance P at the skin surface. Burns intensely when applied. Temporary. Topical. Doesn't enter the nerve cell. Doesn't address mitochondria. Doesn't repair. Just numbs the surface while the nerve dies underneath.
The Missing Piece: Your Nerve Cells Need an Engine — Not More Fuel
Every supplement you've tried provides fuel, building materials, or protection. But the mitochondria inside your nerve cells — the engines that power repair, signaling, and maintenance — are dead. You've been putting premium fuel in a car with no engine for years. Amla doesn't provide more fuel. It rebuilds the engine. Through AMPK activation, amla generates NEW mitochondria inside nerve cells. New engines. New power. The nerve cell comes back online with the energy to finally USE the B12, the ALA, and everything else that's been sitting there doing nothing.
Stop the Damage. Rebuild the Engine.
Let the Nerve Heal Itself.
Amla doesn't mask pain. It stops the oxidative stress killing your nerve cells, generates new mitochondria to restore their energy, and promotes new nerve fiber growth — all published in peer-reviewed research.
Cascading Antioxidants Stop the Damage at the Nerve
The oxidative stress destroying your nerve cells is constant — generated by high blood sugar (diabetics), chemotherapy toxicity, statin-induced CoQ10 depletion, environmental toxins, or simply aging. Amla's emblicanins are unique cascading antioxidants: Emblicanin-A neutralizes free radicals and transforms into Emblicanin-B during the process — which is ALSO an antioxidant. One molecule cascades through multiple rounds of radical neutralization. Published research specifically confirms amla reduces oxidative stress in sciatic nerves and restores mitochondrial membrane potential in damaged cells.
AMPK Activation Generates New Mitochondria Inside Nerve Cells
This is the mechanism that separates amla from everything else you've tried. Amla activates AMPK — the master switch for mitochondrial biogenesis. That means: new mitochondria. New engines inside nerve cells that have been running on empty for months or years. For the first time, the nerve cell has the ENERGY to repair its myelin sheath (the insulation that allows clean signal transmission), to process the B12 and ALA you've been taking, and to regenerate damaged fibers. The car finally has an engine.
Neurite Outgrowth — Actual Nerve Fiber Regrowth
Published research shows amla promotes neurite outgrowth — the growth of new nerve fiber extensions from existing nerve cells. This is actual regeneration, not symptom management. Simultaneously, amla suppresses neuroinflammation — the chronic inflammatory process that PREVENTS damaged nerves from healing. Dual action: grow new fibers AND remove the inflammatory barrier blocking growth. The inflammation marker hsCRP dropped 53.8% in a 12-week clinical trial.
3,200+ Happy customers
Nerve Cell Energy & Repair Support — Standardized Amla Extract by Loomi
mitochondria
nerve damage
fiber regrowth
Couldn't load pickup availability
Feel the difference in 60 days or your money back
60-Day Guarante
60-Day Guarante
We offer a 60-day money-back guarantee.
If for any reason you're not completely satisfied with your purchase, we'll issue a full refund, no questions asked. Simply reach out to our support team for assistance.
Shipping & Returns
Shipping & Returns
We offer tracked shipping on all orders.
All orders are processed by our careful fulfilment team within 24 business hours.
We are currently experiencing high volume of orders so delivery times, depending on your location, range from 5-13 business days.
We've made returning products super easy. Simply contact us info@loominutrition.com and we'll handle
Is It Safe?
Is It Safe?
Yes — our supplements are 100% natural, non-GMO, vegan, and made without any artificial fillers or preservatives. All ingredients are third-party tested for purity and potency in a GMP-certified facility.
Your Nerves Don't Need More Fuel.
They Need an Engine.
One standardized compound that stops the oxidative damage, rebuilds the mitochondrial engines inside nerve cells, and promotes new nerve fiber growth. The foundation everything else was missing.
Standardized Amla Extract (60% Emblicanins)
The most concentrated cascading antioxidants ever measured in a food. Published research specifically shows amla reduces oxidative stress in sciatic nerves and restores mitochondrial membrane potential — the electrical charge that indicates a functioning mitochondrion. When that charge collapses, the cell dies. Amla restores it.
AMPK Activation → New Mitochondria in Nerve Cells
This is what no other neuropathy supplement does. Amla activates AMPK — the master switch for mitochondrial biogenesis. New mitochondria inside the nerve cells that have been running on empty. Once the engine restarts, the nerve cell can finally repair its myelin sheath, restore signal transmission, and process the B12, ALA, and other nutrients you've been taking. The foundation that was always missing.
Neurite Outgrowth + Anti-Neuroinflammation
Published research shows amla promotes actual nerve fiber regrowth (neurite outgrowth) while suppressing the chronic neuroinflammation that blocks healing. Dual action: new fibers grow AND the inflammatory barrier preventing growth is removed. This is regeneration — not symptom management.
The First 12 Weeks
Nerve cells regenerate at roughly 1mm per day under optimal conditions. This is slow biology. The burning didn't start overnight and it won't resolve overnight. But the direction changes within weeks.
The Oxidative Assault Slows
Emblicanins begin accumulating and neutralizing the free radicals that have been attacking your nerve cells. You probably won't feel a difference yet — the repair is happening at the cellular level. The mitochondrial damage cascade that's been running unchecked is finally meeting resistance.
The Burning Edge Softens
The "hot" quality of the nerve pain often reduces first. Not the aching or numbness — those take longer. But the sharp, burning, electric sensation that wakes you at 2am starts becoming less intense. Many customers report sleeping through the night for the first time in months. Inflammation markers are declining. AMPK-driven mitochondrial biogenesis is generating new cellular power.
Sensation Begins Returning
This is the phase people describe as "pins and needles but DIFFERENT — like the nerve is waking up." Areas that were completely numb may start tingling as nerve fibers reconnect. It can feel strange — sometimes uncomfortable — but it's the nerve rebuilding signal pathways. Customers report being able to feel textures underfoot again, or noticing temperature changes in their toes.
Sustained Improvement + Medication Conversations
By week 12, many customers have meaningfully reduced their gabapentin dose (with doctor guidance). Balance improves as sensation returns. The fear of falling decreases. Some report walking barefoot again — something they hadn't done in years. Continued daily use supports ongoing nerve maintenance and repair. Recovery continues beyond 12 weeks for more advanced cases.
Real People. Real Nerve Recovery.
"Diabetic neuropathy for four years. Both feet — burning, tingling, numbness in my toes. I was on gabapentin 600mg three times a day. I was a zombie. Couldn't drive, couldn't think, gained 30 pounds. My A1C was managed but my nerves kept getting worse. Started amla because someone in my diabetes group mentioned the mitochondrial mechanism. Five months in — I'm down to gabapentin once a day. I can feel my toes again. Not perfectly. But I can feel temperature. I can feel the carpet. That hadn't happened in two years."
"Breast cancer survivor. The chemo saved my life but destroyed the nerves in my hands and feet. My oncologist said it might improve over time. That was three years ago. I tried B12, alpha-lipoic acid, acetyl-L-carnitine — the full protocol my naturopath recommended. Nothing changed. My daughter found amla and told me about the 'engine' metaphor. Four months later: the burning in my hands is 80% gone. My feet are about 50% better. First real improvement in three years. The nerves were just waiting for the energy to heal."
"Idiopathic peripheral neuropathy. No known cause. Every test, every specialist, no answer. Just: 'your nerves are damaged and we don't know why.' Gabapentin made me gain 22 pounds and feel like I was thinking through mud. I spent $2,000+ on supplements over two years — B12, ALA, benfotiamine, magnesium, evening primrose, capsaicin cream. None made a difference. Three months on amla: the burning at night is reduced by about 60%. I'm sleeping through. My doctor is cautiously impressed. He still doesn't know the cause. But the direction finally changed."
"Honest review at 7 weeks. My neuropathy started 8 months after beginning atorvastatin — tingling that progressed to burning in both feet. My doctor denied the connection. I believe the statin depleted my CoQ10 and damaged my nerve cell mitochondria. On amla for 7 weeks now. The tingling is slightly reduced and the burning episodes are shorter — they used to last hours, now they're 30-45 minutes. Not a transformation yet. But this is the first thing that's changed in any direction. Four stars. Giving it the full 12 weeks."
Everything You Need to Know
No — never stop gabapentin or pregabalin suddenly. Abrupt withdrawal can cause seizures, severe anxiety, insomnia, and pain rebound. If your symptoms improve on amla, discuss a GRADUAL tapering plan with your prescribing doctor. Amla works at a completely different level — it addresses nerve cell mitochondria, not brain calcium channels. They're complementary, not interchangeable.
B12 and ALA provide fuel and antioxidant protection. Both are important. But if the mitochondria inside your nerve cells are dead, the cells don't have the ENERGY to use that fuel or benefit from that protection. Amla rebuilds the engine first — through AMPK-driven mitochondrial biogenesis. Once the engine is running, B12 and ALA can actually do their jobs. Think of amla as the foundation. B12 and ALA work better WITH that foundation in place.
Published research specifically tested amla on diabetic nerve damage and confirmed it reduces oxidative stress and inflammatory cytokines in sciatic nerves, improving the nociceptive threshold (pain/sensation normalization). Diabetic neuropathy is driven by oxidative stress from hyperglycemia — exactly the damage mechanism amla's emblicanins address. It does NOT replace blood sugar management — glycemic control remains essential. Amla supports the nerve repair that good glucose control alone can't achieve.
Chemotherapy drugs like taxanes and platinum compounds cause neuropathy by generating massive oxidative stress in nerve cells and destroying their mitochondria. The mechanism is the same as diabetic neuropathy — different cause, same downstream damage. Amla's antioxidant protection and mitochondrial biogenesis address this damage regardless of cause. Always coordinate with your oncologist before adding any supplement to your post-treatment protocol.
Yes. Amla works through a different mechanism than B12, ALA, benfotiamine, or acetyl-L-carnitine. It addresses the ENERGY layer — mitochondrial function inside nerve cells. Your existing supplements provide nutrients and antioxidant protection. Amla restores the cellular power to USE those nutrients. They're complementary. Many customers report that their existing supplements seem to "finally work" after adding amla as the foundation.
Most customers notice reduced burning intensity around weeks 3-5. Improved sleep (fewer 2am wake-ups) is often the first change. Sensation returning to numb areas typically happens around weeks 6-9 and feels like "pins and needles but different — like the nerve is waking up." Full 12-week commitment recommended. Nerves regenerate at 1mm per day — this is biology, not a quick fix. The 90-day guarantee matches this timeline.
In published clinical trials, amla extract showed zero adverse events, zero liver toxicity, and zero significant side effects. It actually has stomach-protective (antiulcerogenic) properties — the opposite of NSAIDs. Compare that to gabapentin: weight gain, drowsiness, brain fog, memory problems, edema, and dependency. Amla has none of these.
90 days. No questions asked. Nerve healing is the slowest biological process in the body. We designed the guarantee around the science — 90 days is what the biology needs. If you don't notice reduced pain, improved sensation, better sleep, or reduced medication dependency within 90 days, email us for a full refund.
Your Nerves Don't Need More Fuel.
They Need an Engine.
Every supplement you've tried provided fuel to a cell with no engine. Amla rebuilds the engine — new mitochondria inside the nerve cells that have been running on empty. The foundation everything else was missing.
Try Loomi Amla →Important: Loomi Amla is a dietary supplement intended to support healthy nerve function. This product does not treat, cure, or prevent peripheral neuropathy, diabetic neuropathy, or any neurological condition. It is not a replacement for gabapentin, pregabalin, or any prescribed medication. Do not stop or reduce any prescribed medication without consulting your doctor. If you are experiencing progressive weakness, loss of balance, or loss of bladder/bowel control, seek immediate medical attention.
*Neuroprotective data cited is from published preclinical and in vivo studies including sciatic nerve oxidative stress models and neurite outgrowth cell studies. Anti-inflammatory data (hsCRP reduction) is from a published randomized, double-blind, placebo-controlled human clinical trial. Individual results vary. Testimonials represent individual experiences and are not guaranteed outcomes.
These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
© 2026 Loomi Nutrition. All rights reserved.