Returning After 3 Year Hiatus- Terrified of MS?

GuitarStrummerBGM

Well-known member
Hello all,Some of you may remember me, some of you may not. I frequented these forums from mid-2007 to early 2008, at which point I received my no-ALS diagnosis. I started twitching in January 2007. Now, nearly 3 years after the onset of my twitching I have new worries and I will say they are not about ALS, but rather the other sclerosis that terrifies people; multiple sclerosis.First off, I'd like to say that I am in no way, shape, or form weak. Until recently, due to time commitments and being a senior in college, I've gone to the gym every day and have seen marked improvement in both muscle mass and strength. I still twitch, without exception, every day and the frequency hasn't decreased. However, I've developed some new sensory symptoms that concern me. The first were some paresthesia's... pins and needles feelings in my feet and hands. We've all had this. It went away and came back, and I haven't had it in a few days. What I have now is some more odd sensations - mostly warm or cold - in my hands and feet. Burning, hotness, etc. wouldn't be an accurate description, as it's not painful... just warm. I also have a slight headache right now, but no sign of blurry vision or dull color perception, which is normally the first real sign in MS. I also, on occasion, feel brief pains that feel like insect stings on my body, but when I look, no insect is to be found. These don't happen that often and I've had these a long time... I can remember these even well before I started twitching. I also have some pretty bad upper back pain, which I've had for a while. Do any of you experience anything like this?
 
I believe I've experienced all of that at one time or another. When this all started, my hads and feet were the worst as far as strange sensations. I get that insect sting feeling still, especially in my toes, but can be anywhere. I think these symptoms are "normal" for BFS-overactive nerves. I know that when I am anxious or stressed, I get that hot feeling a lot as well.Being that you are a senior in college, I'm assuming you are very young to be concered about most degenerative diseases. More likely the ongoing effects of BFS.
 
Brian, it really sucks that as a senior in college you have to worry about some horrible disease, while instead you should be swinging the world by its tail. (Some of you thought I might say boinking ;) )Seniors in college should be doing the following:Studyingdrinkingsmoking pot (optional)boinking (I said it) :p going to bed too latesleeping in lateeating junk foodcarousinglaughingand meeting tons of new peopleYou don't have MS!! You have a body that is alive and lets you know it through a few sensory symptoms. Lots of us share your plight, if you want to call it that, and so you have a peer group here of perfectly healthy people. We are the test group that shows you that you are well, indeed. Forget about all those things you've read on the Internet. You got checked out and you're doing fine. The back pain is just back pain. You probably pulled an intercostal at the gym, or you may have strained it by using too much weight or doing the exercise incorrectly. Take an anti-inflammatory, be consistent with your stretching, and it will go away. Stay away from these kinds of websites that are full of mentally unhealthy people. You may get some good advice, but there will also be those who will start asking you questions about what you are feeling and trying to allay their own concerns through sharing with you. It's all bullshyt. I wish I was in college again; I envy your youth. Don't squander it here with a bunch of obsessive-compulsives, or GAD sufferers. Don't become one of them. True, there are lots of lovely people here, but they are in the minority, and when one is anxious it tends to be the unhappy people that really get under ones skin.Move on, you are WELL.Basso
 
Brian,I agree with Basso (and we rarely agree). College is one of the greatest times in life and a true privilege to experience. Nothing you described is at all worrisome. You have some nerve hyperexciteability (that is what twitching is). At most, you could say that whatever is causing your twitching is impacting your sensory nerves and causing the harmless sensations you describe. I have been on this board more than anyone should and know that most (if not close to all) have experienced the sensory symptoms you describe. It is all part of the same thing that is maybe not something everyone experiences but is nothing to worrying or do anything about unless it interferes with your life APART FROM THE WORRY ABOUT IT. If you are gaining strength and these symptoms do not interfere with concentration or sleep then it is only your worry that is the problem. Everyone has worries about something. This is one worry that is a waste of time unless weakness or real disability develops. You are no more likely to develop weakness or disability than anyone else on campus so find other topics to occupy your mind. Hopefully, more enjoyable ones.Krackersones
 
Of course we do have those sxs. At one point I was sure I had MS. No, just BCFS. I underwent a 3-Tesla MRI to debunk that theory. Do you have an MRI of the brain within a year or two that would indicate even slight demylenation? Try diabetes, being overweight, pinched nerves...just a host of other things. You have been around a while. What would make you think you might have MS? I mean solid tests not just suspicions? Have you gone blind in one eye in the recent past?
 
Hey Basso I see you are still setting people straight. Well, not sexually...but emotionally. I have not been around a while myself but I thought I drop in and see what's going on with all my worry wart friends!. Good to see an old shyt like yourself still kicking it. By the way I don't have OCD or GAD. Why do you say there are so few of us happy people around? Did the place burn down while I was gone? Mostly the same kinds of questions!GuitarStrummerBGMyou have been around to long....you know the drill! Get it checked and verified before you start worrying.
 
Don't you mean "GOOD old shyt?" :LOL: Yup, same ol' questions, same ol' worries. Good to see you are likewise doing well and dealing handily with your OCD. :mad: Basso
 
Yes, all of the ones you described but that was mostly at the beginning of my symptoms - nearly 5 years ago. I also once had the feeling that my foot was wet - that was the scariest thing that happened on a sensory basis. Again, all of that subsided over time though occasionally I still get some pins and needles, etc.This is typical for bfs if that's a logical statement :)
 

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