Am I the only one that can feeling my RLS turn off? It is such a weird feeling, lying in bed, like a flushing effect then calm.
I started noticing it when I first took Gabapentin. I now take Dipyridamole and it happened the other night.
Does anyone else experience this? Thanks.
I think the NSAID is reducing your hepcidin, allowing more of the iron to be absorbed which then permits you to feel the RLS melt away. ncbi.nlm.nih.gov/pmc/articl...
Wow, great article! Thanks... it will take me a bit to read through it.
Yes! and it is such a wonderful calmness as you say. I never had it when my RLS was bad, real torture, but now I’m so much better I quite often notice the exact moment that it just melts away…..
I do hope everyone can get to experience it soon if not already 🤗
Physically yes. Mentally no. I've had too much trauma about RLS from such a young age that even in the absence of any sensations I am still hyper aware of what it can be and that breakthrough symptoms can happen at anytime. Kind of my personality type though. Even with decades of therapy to try and work against these thoughts, they are extremely hard wired in. Alas, neuroplasticity of the brain isn't the quick easy remedy many pop psychology articles make it out to be.
Yes, most definitely. I have had this experience on medication and without medication. It's like there's a calm and I know there won't be any more limb movements for the time being. It's as though i have developed an innate sense of when the limb movements have ended.
Yes! I'm not taking any meds at the moment but sometimes I get that same feeling of RLS just switching off...usually after many hours of suffering. I've often wondered what makes this happen so I can try and control it. I once experienced it on a long haul flight after 14hrs of torment when the cabin had been in darkness, within minutes of the lights being switched on I felt the RLS going. Made me wonder how much light/ darkness has to do with the condition?
I also wonder why RLS often comes on in the theatre , planes and other cramped/ restricted spaces? Friends keep telling me it must be psychological/ in my head but I know that this is common in RLS sufferers so there must be some physical cause. Research needs to be done on all these unknowns!
Thank you RLS-UK
Do I have RLS or not? 
Do I have RLS?
Transitioning off Pramipexole for RLS
What helps you when you have a RLS attack?
