Discussions By Condition: I cannot get a diagnosis.

lumps on head and headaches

Posted In: I cannot get a diagnosis. 9 Replies
  • Posted By: eympyresk8er
  • February 12, 2009
  • 04:06 AM

For the past year i have been having off and on headaches after having viral Meningitis, they are dull and achy headaches and seem to be triggered to get worse by strong scents, cold, being physical. I have had an MRI and a Ct scan done but nothing was found. About a month ago i found a lump about 2 cm in diameter behind my left ear, than found one on the back right side of my neck and two on the back of my head. They are all hard and feel like a bone when you push on them, and there is not pain when touched or pressed. My neck seems sore all the time and i space out a ton no matter where i am or what i am doing. Anyone think of what might be wrong???

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9 Replies:

  • Yeah I do use a cell phone and cordless phones but I really do not use my cell phone to talk I usually text and don't use the home cordless phone all that much. Could that still be the problem?? I am 17 years old.
    eympyresk8er 3 Replies
    • February 13, 2009
    • 06:29 AM
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  • I tought that i needed to add that there are 25 towers within 4 miles. The closest one is about .32 miles and that is a regular size tower by gte. And the closest tall tower is about 2 miles from my house. Could that still be the problem? And how can I get tested for that??
    eympyresk8er 3 Replies
    • February 13, 2009
    • 07:32 AM
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  • I'm not sure what you have,but I can assure you that it has nothing to do with cell phone towers.If you'll check a few posts,you'll see that our resident ''psycho''Blaze blames everything on electromagnetic sensitivity,and I do mean EVERYTHING!
    richard wayne2b 1232 Replies
    • February 13, 2009
    • 02:03 PM
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  • Plus,she has a severe case of OCD.You be the judge.
    richard wayne2b 1232 Replies
    • February 13, 2009
    • 02:04 PM
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  • I just had a thought.If the areas feel as hard as bone,they need to be checked out.
    richard wayne2b 1232 Replies
    • February 13, 2009
    • 02:07 PM
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  • The ''forum for support and info'' that Blaze gave you is nothing more than an article that could have been written by anyone.She's our ''chicken little,'' the poor thing.
    richard wayne2b 1232 Replies
    • February 13, 2009
    • 03:10 PM
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  • Okay, so you need some names of doctors who agree that these exposures are not safe? Here you go - so you don't miss them this time... http://www.laleva.cc/environment/freiburger_appeal.html Pay special attention to "The So-far Undersigned". And by the way, EMF Refugee IS a support forum. You were evidently too lazy to scroll past the header paragraph. If you did, you'd find support and informational threads for those who suffer. Why dont you stay on that forum then Blaze ? give every one peace ! I see your location on your profile is Sweden, UK...........lol :D what planet are you on ??? eympyrisk8er "Blaze" spams everyone with this stuff, & adopts everyones symptoms, 2,763 posts & counting.........information does not equal wisdom !
    Tootsie 628 Replies
    • February 13, 2009
    • 03:57 PM
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  • Okay I think I'll go to see my doctor than...thanks for the help!
    eympyresk8er 3 Replies
    • February 13, 2009
    • 04:20 PM
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  • Blaze,isn't it getting lonely out there?(Did you read what someone else said about you?) Even if you're a tenth right,you come on way too strong.Plus, not every goddamned thing out here is caused by ''electomagnetic sensitivity.''I know it must be hard for you to do with your OCD,but try to chill a little!Oh,yeah,I read that ''undersigned list.''There are nothing but Scandinavians or Germans on it,which prooves what?
    richard wayne2b 1232 Replies
    • February 13, 2009
    • 05:10 PM
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