Stuart
Senior Member
- Messages
- 154
I find this fascinating and one of those things you're not likely to talk to your doctor about. While intolerance to alcohol and caffeine is common, I have both in bouts, the benefits is also apparent to many of us.
I survived on coffee when I could work, but only just manage work, and nothing else. Coffee sometimes can have several positive effects, and I'd expect just a caffeine tablet would not do the same.
Some of us note specifically red wine's benefits, but simply supplementing with resveratrol does not work the same way, so something is also involved with the alcohol. I like dark beer as well, I am sure there maybe some beneficial compounds there as well.
These have benefits that a shot of pure alcohol would not, but the alcohol is also doing something. I have some awareness that not all alcohols are the same either, that there are forms or esters of alcohol, the ingredients, fermentation, distillation processes might all contribute, so peeling this onion might be rather involved.
The red wine vs resveratrol vs pure alcohol distinctions reminds me that many with FM or ME find Vicodin or Norco or Co-comadol to be one of the few medications that works well for them. Not only as effective pain relief, but we notice some alleviation of other symptoms. Something about an opiate whether it is hydrocodone or codeine plus acetaminophen (ACET) aka 'Tylenol' or 'Paracetemol,' works in ways taking just one alone does not.
The side effects and potential damage @Mary has noted about these is true as well, I always tried to take minimum doses needed for acute conditions, not to take as a daily regime. We often have liver and kidney issues as downstream or comorbid issues, many medications take a cumulative toll on both. It is hard to find something that works, but then having to decide when it is worth using it when it may lead to further medical complications.
I have yet to make my way through this thread on opiate medications relieving symptoms, but I am certain I will find some common experiences. It is unfortunate that how these things work are not well known, and that these common patient experiences are not likely to be discussed with our clinical nor research people.
http://forums.phoenixrising.me/inde...ome-of-my-neurological-me-cfs-symptoms.22751/
I survived on coffee when I could work, but only just manage work, and nothing else. Coffee sometimes can have several positive effects, and I'd expect just a caffeine tablet would not do the same.
Some of us note specifically red wine's benefits, but simply supplementing with resveratrol does not work the same way, so something is also involved with the alcohol. I like dark beer as well, I am sure there maybe some beneficial compounds there as well.
These have benefits that a shot of pure alcohol would not, but the alcohol is also doing something. I have some awareness that not all alcohols are the same either, that there are forms or esters of alcohol, the ingredients, fermentation, distillation processes might all contribute, so peeling this onion might be rather involved.
The red wine vs resveratrol vs pure alcohol distinctions reminds me that many with FM or ME find Vicodin or Norco or Co-comadol to be one of the few medications that works well for them. Not only as effective pain relief, but we notice some alleviation of other symptoms. Something about an opiate whether it is hydrocodone or codeine plus acetaminophen (ACET) aka 'Tylenol' or 'Paracetemol,' works in ways taking just one alone does not.
The side effects and potential damage @Mary has noted about these is true as well, I always tried to take minimum doses needed for acute conditions, not to take as a daily regime. We often have liver and kidney issues as downstream or comorbid issues, many medications take a cumulative toll on both. It is hard to find something that works, but then having to decide when it is worth using it when it may lead to further medical complications.
I have yet to make my way through this thread on opiate medications relieving symptoms, but I am certain I will find some common experiences. It is unfortunate that how these things work are not well known, and that these common patient experiences are not likely to be discussed with our clinical nor research people.
http://forums.phoenixrising.me/inde...ome-of-my-neurological-me-cfs-symptoms.22751/