Linda Thompson Facebook ad: “If you have chemo neuropathy, read this”

About this ad

Meta Ad Library ID

2807692892937574

Platforms

Facebook, Instagram, Audience Network, Messenger, WhatsApp and Threads

Relaunches

0

How we count

Ad text

I spent 11 years with chemo neuropathy until Dr. Vance told me this… Turns out chemo never actually causes neuropathy directly. It damages nerve vessels. It started as cold sensitivity during the first cycles. Which usually subsided within 2-4 days. But with each cycle, things got worse. After 6 cycles we reduced the oxyplatin and dropped it after 10 as the neuropathy worsened. I thought I'd start to feel better after finishing chemo. But instead: It peaked and got to the worst point two month after I completed my last cycle. If you’ve experienced chemo neuropathy, then you know exactly what I’m talking about: You can’t walk or stand for longer than 30-60 minutes because of the discomfort, pain and tingling. You have to walk very slowly and carefully because at any moment you may just randomly stumble and potentially injure yourself. Your fine motor functions like tying laces, opening bottles/jars, buttoning shirts, cutting food are seriously compromised. You can’t sleep at night because of pain and burning. You constantly drop things because you're losing grip strength. This is what the last 11 years of my life looked like before I met Dr. Vance. But here’s the thing: The chemo neuropathy wasn’t even the worst part. Nope. The worst part was this: Our lives may be saved but quality of life is not included. I wondered if I'll ever feel "normal" again. It felt like I was losing part of myself. It still makes me emotional just thinking about it. And it wasn’t like I wasn’t trying to address it either. My oncologist prescribed me Gabapentin. It did nothing but made me foggy and dizzy. I tried vitamin B complex, alpha lipoic acid, magnesium, acupuncture, exercising, creams. Everything other women in the neuropathy Facebook group recomended. But nothing changed in any meaningful way. At some point, I just accepted it. That this is part of my life now. That there's nothing that can be done for it. That I'm gonna be suffering from it for the rest of my life… So I stopped expecting things to change. Until my friend called one night and said: "You HAVE to hear what this neurologist says about chemo neuropathy. It's nothing like what we've been told." Dr. Donna Vance is a board-certified neurologist who went through breast cancer and severe chemo neuropathy herself. "Ladies," she explains in her research, "Forget everything you've been told about chemo neuropathy being just nerve damage." "Because that's not what's happening to your vasa nervorum." My heart started pounding. "There are tiny vessels whose only job is to feed the nerves in your hands and feet. Scientists call them vasa nervorum." "Chemo doesn't damage nerves directly. It damages vasa nervorum specifically, cutting off circulation to the nerves. So when that happens, your nerves begin to starve." “That’s why it starts in your fingertips and toes and then gets to the worst point after a few months." She showed microscopic images. Healthy nerves had dense, open vessels feeding them… And the damaged ones showed vessels that were collapsed and starved. "This is why Gabapentin alone never works," she explained. "You're trying to feed a plant while the roots are being compressed." "This damage is blocking anything you take from ever reaching your nerves and slowing your body's own ability to repair the damage, all at once." Suddenly, EVERYTHING made sense. The timing, why it got worse even after finishing chemo. The pattern, why it hit my fingers and toes first. The failures, why nothing I tried ever worked. I wasn't just dealing with dying nerves. I was dealing with vessels that had been destroyed, leaving my nerves to starve. And my doctor either didn't know… Or didn't think to explain it. After learning this, I was desperate for answers. Tears in my eyes. "Please," I said to myself. "There has to be something that actually works." That's when I discovered the research behind restoring blood flow to these vessels directly. "You see, this damage happens right at your hands and feet. So that's where you need to provide support: with three therapies directly to the nerve vessels there. Not pills that can’t reach them." I started seeing photos. Women my age. Women who'd lived exactly what I was living. Numb feet that could feel the floor again. Burning that had quieted enough to let them sleep through the night. I couldn't believe what I was reading. The transformation was remarkable. "How?" I wondered. The key is heat, vibration and compression calibrated to the exact depth, frequency, and duration required to actually reach those nerve vessels. But here's the thing: All the massagers are applied in the wrong places because none of them were designed to specifically target chemo neuropathy. RESense is the first device that was engineered based on PubMed research that identified damaged nerve vessels as a key factor of chemo neuropathy. So it applies heat, vibration, and compression, directly where the highest concentration of damaged nerve vessels is located. My hands were literally shaking. "Does this actually work for women like me? Women who've tried everything?" The research was clear: 86% of women who used this targeted approach reported reduced numbness, tingling and burning in just 14 days. I haven't cried for months. I was close. Because for the first time, I felt something I hadn't felt in YEARS. Hope. Real hope. I ordered RESense that evening and started using it for 15 minutes every morning and evening. Day 3. I got into bed and noticed something. The burning was different. Not gone. But quieter. Like someone had turned the volume down just slightly. I'd fooled myself before. I didn't let myself think about it. By the end of week one, I slept through the night. The burning that had been waking me at 2 AM didn't wake me. I woke up at 6:30 in the same position I'd fallen asleep in. I was laying there, looking at the sunrise. I hadn't slept through the night in over 3 years. Then came week two. I stepped into the shower and felt the temperature change when the hot water hit my feet. Felt it. I turned the water hot and cold, back and forth, standing there in my shower, just feeling my feet register the difference. I started crying. Such a tiny thing. But God, it meant so much. Week three, my husband noticed something. "You're moving differently," he said one morning over coffee. He wasn't trying to be kind. He looked almost confused. "Your face looks different when you walk." Over the weeks that followed, I didn't lie awake at night thinking about my feet. I wake up and use RESense for fifteen minutes with my morning coffee and then I get on with my day. Last weekend my daughter and I walked a 5 mile hiking trail. Real uneven ground with roots and rocks. I didn't look down once. Didn't slow down for anything. Didn't spend the whole time calculating my next step. I just walked. Last month my granddaughter asked me to chase her. She grabbed my hand the way she always does and said “come on Nana” and I just went. Across the grass, over the uneven ground near the garden, laughing the whole time. I didn't stumble once. My daughter was watching from the porch. When we came back she had tears on her face. "When's the last time you did that?" she asked. I had to think about it. I genuinely couldn't remember. It sounds like a small thing. It isn't. Six months ago I’d have held my granddaughter's hand and said: “Nana can't run right now, sweetheart.” I’d have smiled and made it sound fine. But inside, I was grieving who I used to be… Standing there, in my yard, I thought about everyone who is still where I was. Still dropping things all the time. Still asking for help with the buttons. Still walking very slowly and carefully while trying not to fall. Still lying awake at night waiting for something to quiet that never does. I know that feeling. I lived inside it. So If you're reading this and wondering if your chemo neuropathy will ever go away. If gabapentin did nothing but made you foggy and dizzy, and nothing else helped either. Please know this: it doesn't have to be this way. You can take action. You can target the actual problem. Without spending $100+ monthly on pills that don't reach your nerves. Without $200 Amazon massager that touches the surface. But with something that actually targets the chemo neuropathy. With something that proven to work by 2,000+ chemo neuropathy-free Americans. RESense gave me back my hands and feet. It gave me back ME. If you want to get your RESense, they have a huge sale going on right now. And they’re so confident it’ll work for you too… They offer a complete 100% money-back guarantee. No questions asked. Try it for 30 days. If you don’t see the same kind of transformation I did… Get every penny back. You have absolutely nothing to lose. You didn’t sit through every infusion, every side effect, every hard day of treatment, just to survive cancer and spend the rest of your life like this. Don’t let chemo neuropathy win another day. Click below and give your nerves the support it deserves. https://tryresense.com/products/pdp5 Your future self will thank you.

Where the ad sends people

tryresense.com

If you have chemo neuropathy, read this 👆

Cancer left me with permanent chemo neuropathy. But everything changed after Dr. Vance told me this…