Anyone have experience with Low Dose Naltrexone instead of prednisone?
I have been diagnosed with PMR and can’t take Prednisone.
LDN has been suggested - it has been used off label for autoimmune disorders. Has anyone heard of this?
Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.
My Mom has PMR, GCA, Raynauds and she is on a low dose of that drug and it's been fantastic for her. Not a single flare up and she's had some very stressful times with my Dad passing suddenly, she's selling her home & building another one and so much stress with all of that which can trigger a flare up and she's been good 🙏
Best of luck to you!
Sounds like you're in good hands with that naturopath...The one I chose had listed autoimmune as one of her specialties. I take LOTS of supplements under her care, but I am feeling so much better. Best wishes for your recovery!
So sorry about your Dad passing. Your mom's response to the LDN is so encouraging. Thank you for sharing!
I'm more than happy to get some more info from her, I don't know all the details.
Wishing you all the best on your health journey ❤️