Been on HRT for a month now. But restless legs have got so bad with it.Anyone had same problems.
Hrt and restless legs : Been on HRT for... - Restless Legs Syn...
Hrt and restless legs
The estrogen in HRT makes RLS worse for many.
When I was on combination HRT, my RLS would flare up with the progesterone tablets taken for 9 days in every 28. Many others find it's the oestrogen that worsens their RLS.It may settle.
I take a combined one and it doesn’t affect me.
To be honest, I don’t know whether the deterioration of my RLS has anything to do with the HRT since it could also be occurring due to my age (56). I’ve been a bit concerned that my patch is a bit high but I had terrible reactions to cutting a bit off the patch (which is oestrogen only).
I found the HRT actually somewhat helped my RLS. It certainly hasn't made it worse. I am now taking a combination of estrogen and progesteron continuously.
I was hoping hrt would help RLS but unfortunately it's made it unbearable. So off it for a month and see if RLS gets better
HRT made my RLS a thousand times worse. Definitely a no no for me.
Feel your pain. My RLS is so bad. GP taken me off HarT for a month to see if RLS settles. So far been a week and it's still bad.
I went off bio-identical hrt for one month, and now it has turned into six months, and I still have rls. Try ordering red vein kratom powder to get you through the bad nights-works within minutes.
I started bio identical HRT in 2005 when I was 52. Before HRT I had had occasional, mild RLS all my life. After beginning HRT it became chronic and severe. Not knowing much about RLS at the time and nothing about triggers, instead of stopping HRT I began taking Ropinirole. Worst mistake of my life. I’ve been off HRT for 5 years. I’ve been off Ropinirole for a year and a half. Unfortunately Ropinirole did enough damage to me that I feel I will never recover. So, for me, HRT was the start of a very negative RLS journey. Of course I can’t recommend you stop HRT, just passing along my experience. Good luck.
I understand. I feel as if RLS has affected my quality of life in many ways. Not only in the symptoms themselves but also in the decisions we are forced to make regarding medication, prescription and OTC, and what we eat and drink. ☹️