Bio Melatonin.....anyone else tried this for cfs/me???
Posted , 3 users are following.
my 16 year old daughter has been taking this for 3 months now afer suffering for the last 2 years with diagnosed cfs/me congenitive brain disorder.shes not better but getting to sleep earlier and waking earlier.shes awake usually before mid day now instead of 3-4 pm she still had chronic sore throats and aches and pains but this is a good start to recovery.we have also just brought her an energy light (blue light as she gets migranes) she uses this in the morning for a 30 min blast of light and again at midday for another,time will tell if this helps at all.
has anyone else tried bio melatonin or an enery light? if so what results did you get?
thanks x
0 likes, 10 replies
jackie00198 michila
Posted
michila jackie00198
Posted
GeorgiaS michila
Posted
I'm using St John's Wort at the moment so not the light box, though I'm going to try it again soon with the herb because the rash may have not been because of the combination.
Anyway either St John's Wort or the light box are excellent for my moods and energy levels.
michila GeorgiaS
Posted
guy72767 michila
Posted
michila guy72767
Posted
guy72767 michila
Posted
michila guy72767
Posted
melatonin as far as im lead to believe will not help muscle ache it will only aid sleep and move sleep times back to a normal pattern eventually.i find the more my daughter gets out of bed and moves about the less pain she gets now that her pattern has changed so it must be a knock on affect of streching the muscles that weaken as we sleep??
guy72767 michila
Posted
GeorgiaS michila
Posted
Emis Moderator comment: I have removed the link as it was to a site unsuitable for inclusion in the forums. If users want this information please use the Private Message service to request the details.
http://patient.uservoice.com/knowledgebase/articles/398316-adding-links-to-posts
http://patient.uservoice.com/knowledgebase/articles/398331-private-messages