Hi, and welcome. You'll find this forum a wonderful place to bounce off ideas, vent, rant and otherwise learn heaps of info. Check out the health pages (icon on upper R side of this page).
I'd get a second opinion. You may go through numerous neurologists before you get some almost concrete answers. I don't know what Ireland's health care system is like - hopefully closer to the French model than UK's. MRIs with and without contrast are essential, unless your neurological exam is super positive, and your history is carefully accounted for. Again, look at the Health Pages.
Cheers,
Guitar_grrrl
http://www.takingcontrolofmultiplesclerosis.org/index.php?mode=Immunoglobulins
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC495893/?page=1
Hi there,
Thanks for input. Here just some of the links re:the cholesterol, Also did you ever take antihistamines before you where diagnosed as there is an old study done in that area too.The natural amino acid derivative is histamine, a very small and simple molecule made by every human (and animal) body from the naturally occurring (and conditionally essential) amino acid histidine. Yes, that's the same histamine that most of us are told is the "bad guy" of the allergy world, against which we're all urged to swallow the latest patent (and prescription-only, until the patent expires) "antihistamine" medication. Apparently, individuals with MS either don't make enough histamine in their own bodies, or just need more. Perhaps both. No one knows for certain.
Also the cholesterol is thought to be the body's protective system kicking in, protecting the spine through some process or another. There is number of study's present into this and other ways of protecting nerves through the active phase. Then other frame thought state exactly the opposite .
http://www.lifeclinic.com/fullpage.aspx?prid=512492&type=1
Hello,
Welcome to the forum. I'm guessing this is your first visit ...? At any rate, I think you should get a second opinion if you are having all these troubles. But be prepared, limboland can be so frustrating. Every doc will see things differently and diagnose differently unless you show super classic signs.
I'm not a doctor, but I've been through this process being recently diagnosed, and I had issues with my VEP too but was told it was nothing either. Also, you should have a contrast MRI b/c in my novice knowledge it shows lesions better ... Quix, if you read this, can you fill in my inept blanks here. ;-)
A second opinion is important no matter what, I think. My first doc sent me away with a diagnosis of an essential tremor despite my numbness, parathesia, vertigo, clumsiness and the list goes on.
My second doc gave me a clinical diagnosis based on my tests, his review of my MRIs and my symptom diary. Even so, I didn't find out about his diagnosis until I was having a medical screening over a year later.
I guess what I'm saying is, no matter how frustrated you can get don't give up until you know exactly what is going on with you. If you are feeling you need a second opinion, trust your instinct.
By the way, I'd be interested in hearing more about the cholesterol research you found ... I have the same issues and eat pretty darn healthy. If you can remember where you found it or come across it again, please let me know. Thanks!
Hang in there, and please stay with us. There is terrific support and friendship here.
Blessings,
ArmyGirl73