I have been hunted ....

Or should say contacted, by 2 women, both elder to me by 3 / 4 years :) From India itself, local :)

Is that a smile I see in your pic? ;)

sure do, i forgot good people are best met in person, not over the internet. :)

big thumbs up

Ahhhh, junglelion, the hunter becomes the hunted.

;) :p :D

Yay, good for you! Let us know how it all goes..

Ahhhh, junglelion, the hunter becomes the hunted.


hehe. Was the thought I had!

Now let me find one of those lines you like jungle that is fitting to these women persuing you!

Here we go:

Distant water won't quench your immediate thirst. :D

hehe. Was the thought I had!

Now let me find one of those lines you like jungle that is fitting to these women persuing you!

Here we go:

Distant water won't quench your immediate thirst. :D

Very true, I don't believe in a relationship unless and until the person is in my paws.

One is 4-0 widowed from canada and the other is 36 divorced from delhi, and i am yet to meet them in person. If it hadn't been for my wheelchair like situation I would have gone to them instead of waiting for them to come over.

I hope it goes well!

I thought you said they were both local though?

yep, both are on the same planet :D

Oh well both stopped out after i said I have Optic Neuritis and MS, strange !!

Typical Indian Women, never bother to find out what the problem is, just quit.

Sorry to hear that, jungle. I usually have the same problem (I'm a wheelchair user myself).

I got selected into a research candidate for the 4th largest phamaceutical company in India for multiple sclerosis research.

Till Jan 16th I was in a wheelchair with near 20% vision, currently my vision has returned, and now I walk with support from walls.

I hired an Army physiotherapist, who said my walking problem is from not using my legs, and not MS. MS only acts like a short circuited wire at rare intervals when you fall, not always.

Even you can be out of the wheelchair if you really wish to, wheelchair is not an option but a lazyiness.


MS only affects the nerves and control, not the muscles, build your muscles and you will feel the difference in your lifestyle, even might cure MS.

I don't think it made it clear, I don't have MS.

I got selected into a research candidate for the 4th largest phamaceutical company in India for multiple sclerosis research.

Till Jan 16th I was in a wheelchair with near 20% vision, currently my vision has returned, and now I walk with support from walls.

I hired an Army physiotherapist, who said my walking problem is from not using my legs, and not MS. MS only acts like a short circuited wire at rare intervals when you fall, not always.

Even you can be out of the wheelchair if you really wish to, wheelchair is not an option but a lazyiness.


MS only affects the nerves and control, not the muscles, build your muscles and you will feel the difference in your lifestyle, even might cure MS.

Interesting information. I have fibromyalgia, which is often misdiagnosed as MS, or visa versa. There is no cure for fibromyalgia, and some neurologists believe it's a hereditary condition that involves a person producing too much of the pain transmitter ("substance P") in the spinal cord, so that we feel pain 4 times or more intensely (or 4 times at least sooner) than the average person. Then the brain reacts to what it thinks is all this trauma to the body. Usually, fibromyalgia is also usually accompanied by what they call "chronic fatigue syndrome" (although this name has been deemed inaccurate and hurtful to patients, so a committee is in the process of changing it to something like myalgic encaphalomylitis - or "ME" which is used in Europe).

What I discovered is that exercise makes the pain and swelling worse (this is probably because the brain is getting signals that I'm "traumatising" the body instead of just "exericising" it and the brain sends out signals in response to that), but I figured... if the brain is being tricked.... and I just keep exercising anyway... it should be better for me in the long run. It seems to be so. I worked through an extreme and sudden weight GAIN from the exericsing, and eventually it reversed. Also, I went about eating foods that got rid of cortisol (the stress hormone) in the body, and that seemed to result in an improved condition, too.

Anyway, junglelion... I hope the study you're a part of comes up with some really helpful information and your condition improves, too. Sorry to hear about the women turning on you. I've always told my "suitors" my medical condition from the start. I never wanted to waste time building up a relationship, just to have them cut and run when they found out I'm not "perfect". So far, it's not been much of a deterent. I'm not sure if that's because there are no obvious outward signs of disability, or what, but most have still been interested in me anyway. Well.. come to think of it... I attract men who appreciate my openness and honesty.

It all depends on who conquers whom, either you win over your disease or your disease wins over you.

since its your body you know best what changes are happening, doctors are there to guide only, its you who has to take the initiative, your will power.