ajSuzieQUEEN9
New member
I have BFS for about a year now. At first like everyone else, I was so afraid. I read that fasciculation is a symptom of *** (the three letters words that everybody knows about). I had a EMG done, nothing, not even a fasciculation came out. The neurologist who’s did mine also suffer from BFS, so even if they doesn’t show up, he believed me. At that point I wasn’t sure what it was. The neurologist didn’t feel it was important to make the correct diagnostic because it wasn’t something life threatening. I my case the fasciculations started in my feet. I thought at first that it may be restless leg syndrome. It has the same symptom. I was always trying to move my feet because of weird sensation, like electricity in my feet and it prevent me from sleeping. My toes would curl up. I was referred to a neurologist specialised in sleep disorder. He was very nice to me. He prescribes me Lyrica (pregabalin). At this point, I stated to get my life back. I was able to listen to the tv at night and sleep properly. It was life changing for me. In parallel, I was also doing CBT to lower my anxiety level. I’m still doing it. It helps very much. I always suffer from anxiety as long as I can remember. My parents were anxious themselves. My dad in particular was always telling me to be careful. I grew up being afraid of everything. My anxiety wasn’t a problem until I started to develop BFS. Before, I had sleeping problem but that it. I never thought about going in therapy. But with BFS, you start to realise how much you are anxious. If there is one thing I can be grateful for it 's this, the twitches help you realise it’s time to stop. Other time, I’m getting very frustrated not being able to push myself as much as I want (working long hour, etc.). So, for the short time I have this condition I want to share my strategies to cope with it. First, the thing that work for me the most it’s a relaxation technique called: cardiac coherence. It’s very simple. You just inhale for 5 sec and exhale for 5 sec. You do this 5 min each time, 3 time a day and that it. It helps adjust for sympathetic system. I also find that light exercise and bath help. Getting appropriate amount of sleep is of course crucial. I also would like to share my symptom with you. At the beginning it’s started in the arch of my foot. It was like an electric shock that would curl up my toes, very freaky. I had also pin and needle sensation. Sometime it’s would just hit me like I been stab with a needle. The pain would stay just for one second and go. Really weird. I have also some time a spot where it stated to vibrate. I had those in my foot and finger. Recently I had a big twitch next to my knee that could move my whole leg. This week, it’s started in my eye lid. Not enough to close it. It’s just tickle constantly (I'am exagereting, let just say several hour a day). I started to get very annoyed you this one. You started to get use to a twitch and it changed and you have to start again. I don’t know if I’m the only one, but I started to focus on it and I can concentrate on anything else. Sometime, it’s on my mind whatever I do. It’s very hard for me to ignore it. I hope I could one day. When I talk to my father about that he said he had the same thing as me. He never told me about it before because it doesn’t bother him. My grandmother also has the same thing on her feet. They both have this for so much time, it just part of their life, like breathing and blinking. I hope it can work like that for me one day. In the meantime, it’s very difficult to live with this condition someday. I feel like people around me don’t understand what I go throw. They get one twitch on the eyelid one night and think that it. Yeah me to, if this happen to me once in a while, It's would be great! But no, it’s every day. Someday better that other, but there always something for reminding you you have this condition. I wish I never had this… I need some support from people who gone through what I did. I need to know that will get better at some point.