Long Essay Ahead: Beware!

Hi Yulia!Thanks for answer!Yes i live in Poland and system here is wow slowly. Thats why i was shocked they call me so quickly to come to hospital espaccialy that i been told wait 1 year.I visit today again neurologist just to tell him i go to hospital but he also again make some checking (he is great man really care about people)and in some test this this time it was not good with my muscles, also i react to much by this checking with small hammer ( i dont know english name) so still its no said 100% that its not ALS.I know now i will go to hospital for 7-10 days. Will let know results. Thanks for all.Hugs!

Bumping this old thread of mine because I think it would be helpful to a lot of newbies. There are a lot of good responses to my post as well, just read through the entire thread and you will learn a lot.

I'm glad you bumped this. Lately the forums have been mostly full of everything BUT good direction and advice from veterans. This was one of your great posts and it will help direct new twitchers for years to come.

And they never did sticky it either. It was a d@mn shame.

I just wanted to bump this thread and sticky it, since I wrote it a few years ago and it sums up pretty much everything I have to say about BFS. This is the type of thread that will help a lot of newbies who are trying to figure out exactly what BFS is.Also, I should really change the title of the original post. I am not just a 3+ year veteran, now I am nearly a 6+ year veteran.

Mario, I have been posting and reading posts on this for two years now and somehow never read this. I am battling a relapse right now and this was like a slap in the face. What really is getting to me is reading how all these wonderful vets suffered at one point but are in such a good place now which is once again giving me hope. It seems most people snap out of it fairly quickly which means I need to really reevaluate to see if this is how I want to continue to live my life which clearly the answer is NO. I keep thinking that it is out of my control but reading this thread, it seems like my attitude is pathetic and I need to take the control back. Thanking you for making this post come alive. I am a believer that things are meant to be and I really needed to read every word of this thread.

Thank you! Glad I could help. ) The one thing you (and really every newbie) needs to keep in mind is that all of us old timers, we went though the exact same thing you are going through right now. We have all been there. No one knows the way your brain and body are working right now better than we do. So just remember that when you read a post like this. This will be a thread that -you- write about four years from now. You will write the exact same thing. You just have to always keep in mind that battling BFS is a 2 steps forward, 1 step back progression. You are going to have relapses. We have all had relapses, there is no shame in that. But over time things will always get better. Always remind yourself of that.

I wish this was a sticky I wish I read this before I find myself on here only so I can read oldtimers senior members posts I've dealt with a lot of health issues some real and some I totally destroyed my nerves on Even just today I tore my mcl and while knee was raised I was starring at my legs and they were twitching about 200 times a minute and snapped and started hitting legs yelling "for *beep* sakes give me a break already" That lasted a few minutes and then I calmed down and kept thinking on all your good advice I travel to Moreno Valley a few times a year and would love to buy you a gluten rich meal if your free one day Someone please sticky this

It is a sticky now, I just stickied it. I had no idea we had that kind of godlike power until about an hour ago.

I can't tell you how thankful I am to have found this site, and that BFS exists. Because, I have gone through ALL of these things. I'm actually laughing at how crazy it is I can relate to it. I'm such a hypochondriac and always have been, so when I was 16 and started to feel twitches, I remember freaking out and diagnosing myself with ALS and MS. I was scared for so many months, and told my mom about my twitches. My mom graduated from nursing school, and she of course has always had good medical insights. She didn't think I had anything to worry about, but I still would always imagine myself to have something much worse. Fast forward 4 years and I still have the same twitching thing going on from time to time. I have some days when it is bad, and some days when it isn't even noticeable. When I dwell on it and think about it and fixate on it, it always gets worse, and then I think so much about it I start to image phantom headaches, then diagnose myself with another disease and so on and so forth. Back in December I was super hypochondriac about it and it ruined a lot of that month for me. Every so often I get in a depressed state about my twitching. I need to just go to a doctor and get it verified as BFS, because I have a textbook case of it. And I show no other symptoms to anything serious, and I have been fine for the past 4, coming up on 5 years. Again, I'm still just so grateful that after all this time of worrying, that I actually feel better and not so crazy and such an oddball anymore. *WHEW* It's a huge sigh of relief.

Welcome. You are one of us.Did I mention that I beat brain cancer nine different times last year? We BFSers are g*d *beep* medical miracles. )

So glad to have read this post. I have been a lurker for 5+ years, always too nervous to post. This post had me in tears. I am a 35 y/o female (also a computer programmer) and also have a serious history of health anxiety (hypochondria...). It started when I was 19 and my sister was diagnosed with ovarian cancer. This was 16 years ago and she is still alive and kicking with two beautiful girls of her own! After our scare with her, I was convinced I was next, and that whatever I got, since she was cured, whatever I'd get would be the end-all, be-all. Totally irrational, I know..but that is how my hypochondria took root. I diagnosed myself with skin cancer and had moles removed that doctors tested and told me were perfectly normal. I thought I had bone cancer when I had an ache in my arm that didn't go away. Anytime I heard of someone who had some form of cancer, I'd do the "checking" to make sure I didn't have it. I had a kidney stone once and was sure that was the end. I had a swollen node in my neck that was biopsied and is negative and has never grown in size, but I still constantly check it to make sure it's the same. I could go on... I've had two children and both pregnancies were not easy and were 9 months (x2) of serious anxiety. The twitching started in my baby toe sometime between my first and second child. I remember asking my OB if maybe it was pregnancy related (at the time I couldn't really have told you if it started before or after I got pregnant) and she said, "probably...pregnancy does weird things". When it didn't go away after giving birth I figured it was still the pregnancy hormones. When it was still there a year later, I googled it. You know the rest of the story....went down the complete and utter panic path and was absolutely convinced I was on death's door. Went to the doc who seemed totally unconcerned but ordered the EMG and referred me to a neuro because she could tell how upset I was. I've since been to 2 neuros 3 times, and each time they have assured me I'm fine. Just twitchy. At this time, it was still just my little toe, sometimes my big toe, and my lips/chin. I'd get the little finger bumps here and there too. I was given a prescription for Klonopin and saw a counselor for a while. All last year I was "better". Still twitching but generally ignoring it and not letting it get to me. Then in January, I had a friend who's husband was diagnosed with terminal brain cancer and I had a major downward spiral. The anxiety it caused me, worrying for her and her family re-ignited my twitches, and this time they came back with a vengeance. I twitch now in places I never did before - calfs, neck, elbows, knees, eyelids, etc. This of course just fed the flames and once again I was convinced that I had some horrible disease (at this time confident it was not ALS or anything along those lines), but what could it be?? Surely, I would tell myself, I'm just some freak with some unknown medical disease that is progressing...and what's next? The fear and worry is like a chicken/egg (which came first?)...the twitching gets worse because of the anxiety and the anxiety causes more twitching. I was on the verge of a panic attack (and have already made another appt with my neuro, who of course can't get me in until July, which is also stress inducing b/c I want answers NOW!) when I finally came back here. I think it was more than coincidence that I found this post. It is EXACTLY my experience. I actually had a handle on the twitching, but just last Tuesday woke up from a horrible nightmare that caused a major surge of adrenaline - the kind that warms your whole body and sends your heart pouding, and sure enough here I am a few days later with re-ignited twitching and re-ignited worry. I realize that I'm letting this control me and I need to break free of it. I have a long road ahead, but this post gives me so much more hope!! Is there a place that has more veteran stories like this? IT's so helpful, especially when you feel alone and that no one can relate to your experience. My family all think I'm nuts and that this is just another one of my self-diagnosed problems. I'm ranting now...but thank you SO much.

There are lots of veteran stories like this on the board, you just have to look around for them. In fact I would say my story is pretty representative of just about -every- veteran story. The only problem is that the happy veteran common sense stories tend to get drowned out by the louder newbie scared panic posts, so you tend to think the two of them are equals. They really aren't. But I am glad my post could help you out today and I hope you are feeling better.Remember, 95% of BFS is determined by how you react to it. Always keep that in mind. It is always under your control how you respond to it.

I try to bump this thread and remind people of it every couple of months, so here you go. If you are new to dealing with BFS there is a lot of wisdom here. )

Thanks Mario. . .this will never get old

A good list of anxiety symptoms from the anxietycentre:

Ok I found this! It makes so much sense. My twitching still makes me nervous by the way it's so invisible most places, and I'm going to finish the neuro testing. But if I'm blessed and that turns out ok, I will work on my anxiety. I'm quite sure my nerves are fried - between becoming a young widow 8 yrs ago (yup, he passed of ***), to raising teen boys, caring for an elderly mom, and remarrying 4 yrs ago adding some undesired family. Thanks.