Has Twitching Decreased with Xyzal?

Has anyone had experience with reductions in muscle twitches and taking anti histamines for allergies?I have been twitching for several years and recently my allergies have been flaring up and I have been taking an anti histamine Xyzal.My foot arches and calves twitch constantly. When taking the anti-histamine I have definenly noticed a decrease in twitching activity when the muscle is at rest.
 
First of all allergies are an immune response to the environment, so it would certainly cause flares with any type of condition such as this because it does have very strong autoimmune components. Taking an antihistamine which reduces the body's immune/inflammatory response will have some affect on this condition not so much directly but rather in calming down the body's overall response. So yes, it will have an effect but I would not recommend hi doses of benadryl as a prophylactic "cure" for BFS:)))Smooches,Kit
 
My symptoms started after taking benadryl for a long period. I have also seen twitching as a side effect of this medicine. The problem is the twitching did not stop after I stopped using it.Krackersones
 
I started twitching after 2 rounds of poison ivy last summer...treated with Prednisone which I had a horrible reaction to. I'm definitely on board with the autoimmune theory. I have not taken an antihistamine so I dont know if it reduces my twitching. I'm over the anxiety thank goodness. For the most part I ignore the twitches...they dont bother me so much and I have no anxiety over them...so I really just...dont care if I twitch anymore.
 
Now that I think about it I did take some benadryl last summer while we were on our honeymoon in Costa Rica (vicious mosquitoes there!). I do recall the twitching letting up a bit then, although it might have been because we were having a nice relaxing vacation, it may have had nothing to do with the benadryl! Anyway, about a month after that was when the twitching started to get bad enough that I got concerned.I too really think this is autoimmune related. I really hope the rhemy I see at the end of the month with shed some light. I am starting to believe maybe mine has to do with a vitamin deficiency related autoimmune thing (like I am not properly absorbing B12 or something). Did anyone ever find this to be the cause, or at least a significant contributor to symptoms?
 
My un-scientific theory is as follows. For some reason our nervous system is compromised. This could be hereditary, could be from a medication an illness, or a number of other reasons. Then major stress sets in for one reason or another and our nervous systems reaction is to have our neurotransmitters start firing off for no reason. The neurotransmitters are constantly activating as a response to stress. When the stress is reduced the nervous system settles down and starts firing off less. Along with major stress is broken sleep patterns and that can cause these neurotransmitters to fire off as well. So stress, anxiety and broken sleep is our enemy. If we can control these things then we can control bfs. I don't think that it will take it away completely because we can never fix that original vulnerability of our nervous system. But we can control it to a level that will not effect our daily lives. I mean if all of us could get it down to a few twitches a day and lose the anxiety along with it then I think we can live happy, healthy normal lives. The path is up to you. Some people need an holistic approach, I personally like modern day pharmacology another thing to try would be therapy for anxiety. Whatever works for you to calm the system. p.s. I use meditation, warm baths, 300mg of neurontin 3 times daily, 0.5mg of klonopin to sleep and jiu-jitsu for a hobby and exercise. I also use a journal to track my success and try to use positive affirmations everyday. When all this isn't enough I just try to challenge my thought patterns. If I have negative thoughts I try to replace with positive ones immediately. Then get active. My appraoch won't work for everyone and is far from a cure for me. But I am on the right track and will get there as will all of you.
 
^ I think you hit the nail on the head with all of it. Broken sleep is the enemy of the nervous system. Get the sleep and nerves back under control, and you will be on the path to recovery. The only problem is that recovery will likely take months or even years to get your body back to a normal resting state. You just have to be patient and learn to relax for a while.
 
Hell somtimes I think I have had it for a while. I always remember twitching, tingling and vibrations. Some sleep starts and bad sleep. I think I just didn't notice until it got real bad. Anyone else here think the same?
 
Benadryl really puts me out so I only take it if I can go lay down :whistle: ....... but I do have something to add. I tried a histamine restricted diet and felt bit better - less symptomatic that is. An allergist told me she thought it would work because a lot of histamines in anybody's system is asking the body to deal with toxins (albeit often natural), people with sensitive nervous systems (like us) may respond more to the natural histamine foods and histamine releasing foods than others.
 

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