Added: 2 years ago
From: 67Raggen
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  • The good point is that you have nice muscular calves ^^

  • nice leg!

  • looks like there is an alien in there

  • I and most other bicycle racers I know get these after long/hard days...I like watching them sometimes they last for days..and if it is a hot/dehydrating day they turn into EVIL cramps...but I don't normally get them sitting around. Best of luck

  • This is also a symptom of MERCURY OR HEAVY METAL POISONING!

  • fracking HUGE calf muscles. i didnt know arnold swarzanegger had a youtube account!!#@)* TTTcv a35ethdjlby53qharfb

  • reminds me of when Goku is super saiyan, when his muscles are just pulsing

  • Lyme. lol NO I think not .. Try Candida.. I showed positive for every Lyme bug there is.. Bartonella, west nile, rocky mt spotted fever. borellia.. all that bull shit.. Do a good candida cleanse. Get your atlas adjusted and laugh at lyme..

  • U must be a bodybuilder cuz those calves are big as hell!!

  • I have this a lot too...im not going to die lol

  • Alien!!!!!

  • Wait this can be a problem? I've started getting these and thought nothing of it...

  • Lyme Disease truly sucks.

  • your calves are huge

  • how did you get lyme desease ? Has your twitching slowed down .. I think I have the same thing

  • @anthonycentoni . Please see my answer to sixdeep357

  • This could be BFS(Benign Fasciculation Syndrome)

  • @metalheadoooo . Yes, but caused by lyme desease, proved from blood test.

  • Hey how are the lyme disease treatments coming? I've had the same thing since August 09, mostly in my calves but everywhere else at times too. I had the EMG and they said BFS. I'm curious about the possibility of lyme disease.

  • @sixdeep357 I have had two antibiotics cures; 7 weeks (Doxylin and Flagyl) and 6 weeks (Chlaritromycin and Quncyl in addition to B12 and vitamins). Unfortunately no effect! If any experience with this and have proposals, let me know:)

  • @67Raggen perhaps mitochondrial disorder?

  • WOW man that is HUGEEEEEEEEEEEEEEEEEE, hot big is that??? i have a MAJOR fetish for calves...i thk im in love with you man...i want to see more PLEASE!!!

  • Any history of pesticide exposures, esp, organophosphates or pyrethroids like permethrin? Even or esp. years ago.

  • Thanks for your comment. Finally on the 3rd and 4th test I tested positive on Lyme desease. Now I am on the antibiotic Doxylin 100mg * 2 tablets for one months since last Friday and I cross my fingers. I have had it since minimum 1,5 years, maybe much longer.

  • Dear Raggen:

    I am glad that you tested positive for Lyme Disease. Many people never test positive who have the disease.

    Which test did you Dr. order? Elisa or Western Blot? How many bands do you have positive on the Western Blot.

    There are a few better tests you can do.

    Unfortunately, your treatment is following the IDSA (Infectious Disease Society of America) 2006 Guidelines which are under review by the CT Attorney General because they are "seriously flawed."

  • I do not know, but the nevrolog writes positive test on Borrelia IgG and positive immunblot IgG serum from blood test. I took a spinal test last Friday and are awaiting for the answer. Anyway, the most effektive treatment is the most imprtant for me now. After one week treatment, it seems even worse, but it is maybe positive due to that soemthing happens?

  • Hello 67Raggen

    I have this since 5 years now..

    You can see "about BFS" forum.

  • This is common in Lyme disease. Often it is caused by a low magnesium level. Additonally, it can be caused by low oxygen level to the muscles.

  • Thanks. I have had a standard Lyme test, since my fascicualtions are so extreme. Blood test from Mg was ok, but I have taken Mg for the last 2 months, without effect. Oxygen could be true, maybe indirectly from acid blood or a traume I have had (mental)

  • Thanks for your comment. Finally on the 3rd and 4th test I tested positive on Lyme desease. Now I am on the antibiotic Doxylin 100mg * 2 tablets for one months since last Friday and I cross my fingers. I have had it since minimum 1,5 years, maybe much longer. If you have any comments on other and maybe more powerfull treatments, please let me know.

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