#crps

I’m just a mom of five trying to make something out of this little TikTok space. I won’t ever recommend anything I wouldn’t spend my own money on—because I know how hard money is to come by. I’ve got a bad leg, a big heart, and a dream to get out of debt and do more for my family. So if you’re here

November is CRPS awareness month! Come along with me this month as I teach you all the things about CRPS, and the struggles that. One along with it as a CRPS warrior. #crpswarrior #crps #crpsawarness #lemon8challenge

Spent the majority of the day in the ER. Thank you chronic diseases that are slowly killing me. I haven’t eaten in three days and they say they can’t help but rehydrate me. Life with chronic pain and invisible illnesses. 😕😣 #fblifestyle #crps #gastroparesis

You tell me the answer to that question after you watch how I have to bring in my grocery bags. To many this is an every day thing for people to do and never take a second thought about what it would look like for a person who only had one leg to depend upon. Well, here is what it looks like fo

Me and my favorite guy! #goldenretriever #dogmom #dog #dogsoflemon8 #lemon8challenge #servicedog #puppy #puppylove #crps #complexregionalpainsyndrome

Today… I’m spent. Not just tired — empty. I haven’t really slept in days. Last night, I cried myself to sleep again because the pain in my leg felt like it was going to explode. That deep, burning, pulsing pain that never stops — that’s CRPS. Chronic Regional Pain Syndrome doesn’t care about

#gettoknowme #crps #embracevulnerability #recovery #recoveryjourney Mandy is an authentic soul rooted in the heart of Lewiston, Maine—a place where small-town warmth meets the pulse of modern innovation. With a natural ease for striking up engaging conversations, she brings depth and g

Invisible illnesses for the win am I right? #invisibleillness #chronicillness #crps #pots #spoonie

#crps #crpsawarness #crpsjourney

When even your outfit has to fit your health needs. #pots #crps

Chronic pain isn’t just about damage. It’s about your nervous system. I built Nervous System School to teach the science + the strategy behind regulation, flares, and stability. If you’re tired of surviving and ready to understand your body… Link in bio. #ChronicIllness #NervousSystem #Ch

If stress makes your pain worse, this isn’t random. Your nervous system lowers pain thresholds under threat. I teach the science + tools inside Nervous System School. If you want strategy, not just sympathy… Link in bio. #PainScience #ChronicPainEducation #NervousSystemHealing #CRPS #

Complex Regional Pain Syndrome at it’s finest 😰😭💔🎗️🧡 #crps #crpswarrior #invisiblechronicillness #chronicpain #unfiltered

IT’S TOO LATE……. This is something I hear a lot with all the doctors because CRPS NEEDS TO BE DEALT WITHIN THE FIRST 3-5 MONTH.. That is why a lot of this is so frustrating. I’m going on 2 years and 6 month and I waited over 2 years to see a pain specialist and now I’r seen 3 so far.. one was c

What I hate about CRPS #nervedamage #crps

Being young and being chronically ill is not for the weak. I became chronically ill at 21 and got a diagnosis at 22, no matter what I’m getting done whether it’s a referral or surgery / procedure new doctors they all say she’s way too young to be in this much pain this shouldn’t be here life. Man o

Favorite shoes for nerve damaged feet @FitFlop #crps