Finishing Mavenclad was a massive milestone for me, but as anyone living with Multiple Sclerosis knows, crossing that finish line doesn’t mean the daily battle magically stops. Today, my journey is focused on symptom management.
When it comes to fighting the daily onslaught of MS pain and spasticity, cannabis has become my absolute go-to. It hasn’t just improved my quality of life—it was the very thing that allowed me to finally break free from high-dose opiates. For a long time, heavy pharmaceuticals felt like the only way to blunt the severe pain but they left me in a heavy fog. Shifting my focus to high-quality cannabis didn’t just mask the symptoms; it gave me my mind back. It gave me the physical relief and muscle relaxation I needed to safely step away from opiates altogether, which is a victory I never take for granted.
Since I’m a bit of a stoner who found what actually works, I wanted to share my daily setup in case it helps anyone else out there navigating this mess.
For that heavy-hitting, long-lasting relief from deep nerve pain and severe spasticity, my foundation is RSO (Rick Simpson Oil). It is a full-extract oil, meaning you get the benefits of the whole plant instead of just isolated THC. It keeps my pain at bay for hours at a time, especially on the rougher days. Then, for those sudden muscle spasms or daytime breakthrough pain, I keep a live resin vape cartridge close by. Live resin uses fresh-frozen flower instead of cheap distillate with fake flavors, so you get a true, clean, strain-specific effect that immediately melts away spasticity. It lives on my person.
The biggest game-changer? I recently tried a transdermal patch, and let me tell you, this is the future.
The slow, steady release directly into the bloodstream is an absolute savior for long-term symptom management. Instead of peaks and valleys, it just provides a smooth, baseline level of relief. The only downside right now is availability. What we really need next is for a certified medical provider to step up and add these patches that meet medical complience standards.
In fact, that is my next big goal. I want to work directly with a certified medical provider to bring real, raw patient experience to the development table. Companies can look at lab data all day, but they need to know what actually works for a body dealing with MS every single day. If you are a medical processor looking to build better, more reliable patches for people who actually need them—hit me up.
(And yeah, I’m looking at you, Falcanna—let’s make this happen!)
Symptom management looks totally different for everyone, and it takes a lot of experimenting to find your sweet spot. For me, combining full-spectrum medicine with fast-acting relief—and hopefully more reliable transdermal options soon—has been a total lifesaver.
Disclaimer: I am not a doctor, just a fellow MS warrior sharing what works for me. Always consult with your healthcare team before changing your medication routine.
wheels & red 