Guest guest Posted March 2, 2005 Report Share Posted March 2, 2005 I have a general and perhaps dumb question. Is muscle cramping a common experience with mito? I sometimes get very severe cramps - in foot or leg mostly. They are totally debilitating at the moment but they don't last long. I never connected them with mito, or was too concerned about them, because they always release rather quickly. Ann Maire It is interesting, I never saw anyone describe my head pain like you did. It feels like someone has shoved a poker into my head from the top down, right past the inside of my left eye down into my jaw. When it hits, I feel my face get contorted with pain, I get out of breath and I can't - don't want to- talk Have gotten it for years. But, blessedly mine only lasts for a very short time. Most of the time it comes at the end of a yawn, although it does also come spontaneously. I always feel it is a muscle in my head cramping, and it always goes away like a cramp would. Years ago I was diagnosed with TMJ - Tempo Mandibular Joint problems. I really don't know how much the TMJ ever contributed to my general neck pain, which is different than this head thing, but I do feel TMJ is related to the one sided " cramps " I get sometimes. When I get an attack I find someplace private immediately, and try very hard to relax my face/head neck, let my jaw drop a little bit, and sometimes massaging my neck near and around my on that side. It usually does release quickly, and I can't remember one episode that has lasted longer than 30 seconds. I say that with gratitude, because it is an awful pain. Regards Sunny Sorry to hear that you have some kind of stroke like events. > > I also get what I call " Brain Pain " . It is absolutely horrible pain > that is sharp, stabbing and burning pain that travels from my left > side of my head from the top to my eyes, down my whole side of my > face, ear, and into my jaw. When I get this it comes and goes, it can > last from a half hour to hours at a time. My last round of this lasted > a total of 5 months. The docs said it was Neurological. > > Was it Athena Labs that ruled out the 2 more common forms of glycogen > storage diseases? And do you know what tests Athena is doing on your > biospy? Did you have the blood test to check to see if you have the 2 > gene mutations associated with MELAS? Alot of people don't like > Athena Labs and won't send their muscle biopsy or blood work there to > test for Mito disorders. They have messed up quite alot of results. > Some people here have had bad luck with Athena Labs and I am sure if > you asked they would tell their stories. > > Good Luck. I hope you get your results back sooner than another > month. waiting is just so hard. > > Hugs, > Ann-Marie > > > > > > > klaga5 wrote: > > > That's why I wonder if I may have mito (or MELAS). They always > assumed I had a stroke in college, some 20 years ago. Again 2 1/2 > years ago they had to rule out stroke. With the new technology, > they could tell I've never actually had a stroke. I've had > absolutely terrible sharp pains in my head on and off as long as I > can remember. I've even had my right hand, arm, and side of my face > go numb for weeks. I have a couple calcifications on my MRI also. > > > > > ---------- > > No virus found in this outgoing message. > Checked by AVG Anti-Virus. > Version: 7.0.300 / Virus Database: 266.5.7 - Release Date: 3/1/2005 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2005 Report Share Posted March 2, 2005 > I always feel it is a muscle in my head cramping, and it always > goes away like a cramp would. > Sunny Sunny, Mine isn't anything like a cramp. It sharp stabbing and I just have to wait it out. Kim Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2005 Report Share Posted March 2, 2005 I describe my sinus pains as a " railroad spike " in the head. The sharp pain I get in my temple is more like a really long needle. TMI probably! The temple pain is often associated with me collapsing, at least briefly, luckily it is intermittent. Sinus pain tends to bunch up, although before I had surgery I had it continually - the dentist even said they thought it was causing my chronic tooth pain. Take care, RH > > >> > > >> > > >> That's why I wonder if I may have mito (or MELAS). They always > > >> assumed I had a stroke in college, some 20 years ago. Again 2 1/2 > > >> years ago they had to rule out stroke. With the new technology, > > >> they could tell I've never actually had a stroke. I've had > > >> absolutely terrible sharp pains in my head on and off as long as I > > >> can remember. I've even had my right hand, arm, and side of my > > face > > >> go numb for weeks. I have a couple calcifications on my MRI also. > > >> > > >> > > >> > > >> > > >> ---------- > > >> > > >> No virus found in this outgoing message. > > >> Checked by AVG Anti-Virus. > > >> Version: 7.0.300 / Virus Database: 266.5.7 - Release Date: 3/1/2005 > > >> > > >> > > >> Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.