This is my first post, but I have been following all the RLS posts with much interest. My daughter suffers from RLS and as her mom I’m just trying to understand and support her struggle. And what a struggle it is. She has been on all the usual RLS meds with nothing working except for the low dose morphine she is now on. The problem with that is staying with the prescribed dose because often it stops working and she takes more with the end result of no meds at all for 1-2 days until her prescription renews. This, of course, puts her into withdrawal. I have also noticed that there is not much discussion of family support. We are from the US and her diagnosis is met with much skepticism from other family members, from disbelief to outright denial that it’s all in her head. This has been very difficult for her to deal with and only adds to the pain of RLS. After reading some of the posts, I am convinced she suffers from the augmentation mentioned by many of you. I will discuss this with her and have her discuss it with her doctor, who is very supportive. I would like to thank all of you for sharing your struggles as it helps to know you’re not alone.