I went to my local Fibromyalgia support Group and a lady gave me a label from a Magnesium Oil Spray (Original spray) bottle.
I didn't have a chance to ask her about it, and wondered if anyone has used this and to what effect.
I have had magnesium injections privately some years ago, but when I had to stop those after I lost access to private health treatment I didn't notice any difference to my health.
As I understand it Fibro suffererers cannot absorb magnesium through oral use.
Any comments very welcome. I live in the UK