Hi Everyone
Has anyone else tried PEA (Palmitoylethanolamide)? A friend has suggested I try it to see if it can help withEM. I have only been taking it for a couple of weeks so I cannot report any definite results but I am interested to know if anyone else has tried this. I will certainly report any positive results that I experience.
Also I saw an interesting article about engineers developing a wearable cooling patch.
I cannot seem to find any further information butI thought more internet savvy members of the group might be able to research this further.
Hope this info might be of help.
Good wishes to all
Dimar
I take PEA and the benefit is that it makes my ears be dramatically less sensitive to touch. PEA does not affect flares for me. Best.
Good to know someone else has used this. I thought at first it was beneficial, however, I now think it might be making my evening flares a little worse so I am stopping it for a couple of weeks to see. There seem to be so many things that are helpful to some EM sufferers but can have the opposite effect in others.