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I have exactly same symptoms. I was diagnosed with Chiari Malformation and Psuedotumor Cerebri. The MRI person missed the chiari and it was found by someone else. It can be missed. I am wondering if there is anything  more to this though.

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welcome to the new age

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Get an MRI. I have Chiari Malformation and these were my symptoms before surgery.
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I would try looking into an autonomic dysfunction. When the parts of your body that are supposed to work on their own properly stop working, all sorts of crazy symptoms occur. Anxiety and depression are sometimes caused by as well as linked to this and that is why those meds sometimes help, but not solve, the problem. I have been told I have a form of it called pots, which also causes all of those symptoms. Hope u feel better and wish me luck that I do soon too.
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kerry 25

i have lyme and have all your symptoms.

were you ever diagnosed. what has helped you? so far 8mos of antibiotics for me hasn't helped a ton. and im really frightened of my head pressure and balance issues, and they worsen with light exercise.

i hope u have some answers

kris

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i have been having those symptoms for 4 years now, i just realized 1 week ago i am suffering from something because right now the seizures are its maximum especially after i was exposed to a stressful month trying to find a job.

besides the symptoms mentioned the most annoying is the 6 hour sleep only no matter what, and the ringing in my ear, within 2 weeks i am going to check a doctor.

i would like to ask something a bit weird, did any of the people having the same symptoms go through a spiritual experience?
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I have all the same symptoms; all tests are normal. did u ever find an answer? It has been like a swinging door from
dr. to dr.
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u mean after undergoing all sorts of tests u were not diagnosed with multiple sclerosis?
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please my mom is having similar problems and I need solutions please
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hi all of last year i suffered a lot of anxiety and stress over some problems i had any way about six weeks ago i started getting some physical symptoms that as lasted everyday and night for six weeks here is a list of symptoms i have had my body feels heavy like gravity is pulling me down i get this feeling when sitting down walking and lying down pressure in head, muscle twitchs/jerks, muscle cramps can't concentrate properly, memory loss today the symptoms are feeling a little bit better i have a had all blood work done a brain mdi all normal the doctor said depression/anxeity could that cause all this they put me on sertraline two weeks ago

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I been feeling the same way like a dont no whats the problem i realy dont no i have anxiaty and allso deprecion and im only 19 yeards old and i feel like very unbalance all the time like sometimes i fill like when there is a pile of aint coming out of it i feel that way in my head.i couldint sleep for more than 6 week i couldint eat when i frist into deprecion i dint even no who i was so i whent to the doctor they tould me that nothing was wrong with me so idk ..i just feel like sometimes ima faint .i dont no if it because i feel that way because i need glases or its just deprrecion i hate feeling this way when i go through that situacion i feel like ima die or something ..i hope this answere worked out for you and dont worry find god in your life he will help
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I am having the same symptoms! I can not even bend over. I can feel gravity pulling me in head then back then knees. I am so dizzy I stumble around even my vision is affected. Does it have anything to do with the shift that's going on in the planet? NASA reports of the earth swelling and techtonic plates moving. Are we experiences these changes too? I could always tell right before an earthquake it was coming because I would get dizzy and off balance.
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I have the same symptoms it would be nice if it was a tumor instead of ms.
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Did you ever find out what it is?
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I really hope you've found an answer by now but if you haven't please see a neurologist and tell him pseudotumor cerebri (idiopathic Intercrainial Hypertension) if he doesn't know those terms request to see another neurologist. I've seen 3 and finally was diagnosed. It is "rare" but so many people are misdiagnosed and it's more common than it used to be. Good luck on your journey and Ihope you become pain free soon.
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