Ok Howie, I’ll tell you that I got a very late diagnosis about 20 years ago. Another clue is I should have gotten it at least 25 years before then, maybe 35 years before.
You said it yourself--MS affects "mostly women." There are many men with MS too. Do you remember Eldon Deakins, Richard Long, Stevesjpr (not sure I have that user name right), and countless others on here years ago? Steve in Alaska ( Steve L?)? Even now on here there are several other males. They're not here often but they drop in now and then. You're not alone.
There seems to be no reason anyone has come up with about why MS affects women more than men though some think hormones have something to do with it.
This is from the MS Society Webpage:
Gender: MS is at least two to three times more common in women than in men, suggesting that hormones may also play a significant role in determining susceptibility to MS. Studies have suggested that the female to male ratio may be as high as three or four to one.
:) I finally got a diagnosis in 1987. However when taking my medical history the neuro said he thinks I have had MS since I was 18 and I am now 78.
I had a thyroid storm, mono, cancer 3 times, silicone poisoning, etc. I have three lesions, central optic nerve, central auditory nerve and left medial nerve. Jeanie :)
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