Hello All
I have been off dopamine agonists for more than two years now, thanks to methadone and buprenorphine. Both were - and are - a blessing (insofar as any drugs could be called such), as many of you will know.
But I would like to know how many of us feel, even long after quitting dopamine agonists, that things have never been the same and that we have suffered some degree of damage to the delicate dopamine system, resulting in a lowered quality of life. It can be hard to recall just how good life was before dopamine agonists because many of us were taking them for so long.
But I do know that my before-drugs life, even with RLS and sleep loss every night, was superior to the life I experience now.
When my blood levels of the opioids dip, many of DAWS symptoms arrive. I thought I had escaped it, but I am no longer sure.
I had thought that the opioids caused the symptoms I was suffering. Now I believe that the opioids are acting as a cover-up.
Typical DAWS symptoms include anxiety, panic attacks, agoraphobia, depression, dysphoria, fatigue and pain. Full-blown DAWS always occurs amongst those who suffered Impulse Control Disorders while on the drug.
It seems to me that there must be a long scale between full recovery from these monstrous drugs and long-lasting DAWS. (Or everlasting DAWS).
How many of us feel that we are somewhere on this scale? I think that there are many of us, judging by comments made over the years.
I attach a link to a site that allows patients on psychoactive drugs - which dopamine agonists most certainly are - to tell their stories and to comment.
It is a litany of sadness that makes one weep. And wonder, yet again, how on earth is this drug still being prescribed for RLS without doctors asking searching questions.
rxisk.org/sos-dopamine-agon...
May I have your input, please?
All best and thank you, Parminter