Twitching Getting Worse After BFS?

I was diagnosed with BFS about 2 months ago by a Neurologist after a clean EMG and blood work. About 3-4 weeks prior to that, I noticed non-stop twitchin in my calves and feet. The twitching was (and still is) strong enough to move my toes back and forth. The anxiety went away for awhile after the diagnosis, but it seems like the twitching is getting worse. Also, I've been feeling a lot more aching in my calves, the arches of my feet and the tops of my feet. Further, recently, my feet have been cramping a lot more and it's making me have panic attacks again.I went to another Neuro last week. He did the typical strength tests and reflex tests and said he was 99% certain the first neuro was correct and that there would be muscle and reflex symptoms with the twitches.But I constantly feel like I have creepy crawlies in my calves and feet and it just gets depressing.On the up side, I ran twice last week (4 miles each time) with no problems. I've been working out and my legs have not gotten any weaker that I can notice. However, I stupidly went on the ALS forum and read about all these people who said their first sign was twitches and that the weakness and atrophy came on months later. That really doesn't help. I also feel occasional twitches all through out the day in random places on my body. And a few weeks ago, I got a constant twitch on my face (near my mouth) that lasted for almost a week and then went away. A day or two after I run or work out, my feet usually ache on the top (in the front where it joins the ankle) and on the bottom in the arches. The ache is a "weird nerve feeling" as opposed to the muscles being sore after a workout. It's hard to describe. The cramping in my feet really gets my uptight. As I can tell, my cavles do not cramp when they ache and hurt. And the calf pain comes and goes and moves around to different parts of the calf. Other symptoms I noticed recently have been tremors in the arms and hands (only essential tremors - when I hold up my hand against gravity or work out), and my neck often feels heavy, depending on the day. I know anxiety may be playing a part. But honestly, I went almost 2 months with hardly any anxiety and the symptoms didn't change. Now I am feeling anxiety again. When I go to sleep, I'll wake up and it will feel like my heart is beating 200 times a minute. But then I'll check my pulse and it is normal. It also feels like my body is shaking and tremoring, but it's not. Last night, my wife told me I woke up in the middle of the night and told her that everything shaking (though she said it was not). I never remember even waking up. I'm 34 yr old and I know my odds of ALS are .08 in 100,000 (or 8 in 10,000,000), but my rational thought is being beaten by this anxiety of having ALS. It drives me crazy b/c even if it is "benign", it is still being caused by something! I was tested for Lymes (negative). I eat healthy (5-7 servings fruit/veg every day, plenty of meat, multivitamins, etc), I exercise 3-4 times per week, drink lots of water. I only drink 1-2 cups of coffee a day (I tried quitting, but after 2 weeks, still no difference in symptoms). I even started doing yoga and stretching. NOTHING WORKS! I know it's stupid to live my life in fear and I know stress is incredibly bad for the body. I just keep thinking that there is more going on than what the docs are seeing. The constant creepy crawling and twitching is driving me nuts. My feet often literally twitch over 100 times per minute. Is anyone else experiencing this? I figured after 3 months of no atrophy or weakness, I'd calm down. Any help or suggestions are greatly appreciated.
 
Your symptoms sound very BFS like and you've had 2 neuro exams. I also tried EVERYTHING non-medicinal and still felt awful. I finally had to take the medicines offered to me by the neuros. Whether or not you go this route, know you are among friends here and we have been where you're at. Right down to the moving toes for many of us.
 
The title of your post says it all.....relapsing into anxiety. Get a handle on your anxiety (easier said than done I know) and the rest will slowly fade to background noise. Your symptoms are so very clearly not ALS in my non-medical opinion, and more importantly your neuros agree. When I fully accepted the truth that I didn't have ALS, then my anxiety improved. It just takes time.
 
I appreciate the replies. It's such an emotional rollercoaster not knowing what's causing these symptoms. I agree I have to address the anxiety and stress issues. I've got an amazing wife and 4 young children who are such a blessing in my life. Those evil thoughts of thinking they may have to watch me go through something like ALS causes those panic attacks to hit hard. I've just got to have faith. I just have to be thankful for today. So easy to say, but such a different story to put into practice. Good to know I'm not alone. Thanks again!
 
Dang I feel like I just read a post about me, just add some eye symptoms in there somewhere...I'm 34 also :unsure: Just try to beleive the neauro and move on best you can, these people on here have proved thousands of times that this is a benign and never once has it turned into anything else. My Doc put me on a beta blocker and it helped tremedously with the pulse feelings. God BlessRandy :D)
 
You sounds exactly like me, pain and twitches in my calves are my main problems, but as well I´ve got twitches in eyleid, pain in arms etc. Right know I am happy if the twitches occurs in every spot of my body, then I´m even more convinced its not als, just bfs. After all my tests EMG, MR etc my neuro says I don´t have to worry and my anxioes has decreased a lot and I´ve got a feeling that my symtoms is relaeted to my mind, but of course the symtoms hasn´t disapeard totaly, but I think they are connected. I excersice a lot and when I am moving, training my twitches are increasing, but I´m learnig to ignore them. I also visiting a psychiatrist in a regular basis, he says I´ve got to handle my mind in two ways:First, you dont have als, you are not diagnoes by your neuro - you are healty, you are not deadly sick, you have bfs -ENJOY YOUR LIFE. Second, accept your fear, IF you against all odds really got als you must face this fact. I have really been into this state when and I was convindes that I was dying and had to leave my 4 kids and wife, but I started to accept this and tried to ENJOY MY LIFE and live for the day. The reason my psychiatrist told me to accept this was to go furhter and if I dont accept my fear it would be a great risk that I´m in the future will find a new deadly diseases in my body that will grow in my mind. The brain is programmed to this, you have to find the rootproblem incl accept the truth that you can die tommorow, no one is immortal.Dont know if this is a good theori, but I think it helps me...I live with theese thoughts every day..just working me the way out of this "mind illnes", but it´s hard very hard
 
First off, STAY OFF ALS SITES. You can drive yourself crazy going there. Also, don't believe everything you read over there. I remember someone once saying that sometimes people post there who don't even have ALS (I can think of one who used to post here). You also don't know the true stories behind those people. Second, your doctors told you it's BFS so believe them. If they thought it was ALS they wouldn't let you just walk out the door. Third, the symptoms you describe are everything I have had in the last 2 years. My feet have twitched non-stop for 2 years now. Go back and read my old posts. You will see. What I'm trying to say is that everyone here has experienced what you are feeling. Are you on any anxiety medication? I took Lexapro and it helped me greatly. The anxiety is the worst part of all this.
 

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