Questions about MS to Lynn

February 27, 2008

Lynn, An MRI shows that I have scar tissue in parts of my brain, they wanted me to wait 6 months for another MRI before they make their determination, which between all this, i love insurance and moved to another state. As far as any symptoms, they may not relate to MS, I don't know, i have memory problems, dirrectional problems, i get off balance alot. Lots of times I can't remember the word i need to say in a conversation, when ever i leave a room to get something 9 times out of 10, i don't know why i went to the other room, so i have to go back where i was and look around and find the reason why i left the room, of course, lots of people do this, but i put stuff in the wrong place, fridge vs, cabinet. When I'm in a car and not driving, it seems as though people are going to hit us, when they are not, like i lost depth perception. Anyone with MS relate to any of this, without thinking it could be

alzheimers...argghhhh Anna Kenn Johnsen <kennj wrote: I got no clue why those bees are sick and disappearing, but I am sure they are not disappearing because of the sting therapy. I do not think that you should sting your self with sick bees, but there still most be healthy bees around, and sure they die because of that, but so it is. According to the web there is thousands of people who is helped by this therapy. Kenn Den 27/02/2008 kl. 00.20 skrev Lynn Ward: At 04:58 PM 2/26/2008, you wrote:Although I've never known anyone personally who's tried it, apparently a number of people have found it effective. While I didn't feel as desperate in past years, I'm approaching that point. I wonder, just saw something on bees last night - they're trying to figure out how or where so many have

simply disappeared to. Turns out, after the bees have disappeared, no other bees will go into their hive. Usually, if nothing is wrong, other bees will go into the hive if it's available and take the honey. With the bees that have disappeared, no bee or bug will enter those hives. They're finding the bees' (the ones that are left) immune systems are compromised (big shock with all the pesticides, etc) and that they're undernourished (so sad, but not a shock). Apparently they also have all kind of mites as well. It seems our bees are not so healthy. So, in a round-a-bout way, I guess I'm wondering - if the bees aren't as healthy anymore, do you think bee-sting therapy would still be effective for some? I don't know - perhaps someone here has a clue.Lynn You probably know all about this.......but if I had this muscle decline, I certainly would try out bee venom, If I lived in the states ( here I can not, only if I

bought some bees myself ) Den 26/02/2008 kl. 18.04 skrev Lynn Ward: At 08:38 PM 2/25/2008, you wrote:Anna,What symptoms have you had? What has caused the diagnosis? I've actually had MS for more than 30 years now. Have had many ups and downs over the years. Lucky for me, when I was first diagnosed, I had Relapsing Remiting (RRMS), and while some things got pretty bad at times, I usually got a lot better with treatment. I know steroids are bad for you in so many ways, but they really helped when I had severe onsets of symptoms. Now, it has turned into Secondary Progressive (SPMS). I know sun is good for you, and I think I felt better, overall when we lived in San Diego, where the climate is, for the most part, temperate. (not too hot, not too cold). However, even while the sun is good for you, the heat is not, and can bring an exacerbation of

symptoms on. Heat is frequently a big issue for folks with MS.I don't know how long you have been diagnosed, or if it is a firm diagnosis. Hope you have a good neurologist? There has been much written about certain diets over the years, but little to show they made much difference over eating healthy and well. Here is a link to a site you might find interesting: http://www.msviewsandrelatednews.com/Lynn I myself have been told its possible that I have MS, so I'd like to see material here, as much as anyone has, endless thanks to whomever can do this for me and anyone else in the group who has just started their journey. Anna MariaLynn Ward <lynnward (AT) earthlink (DOT) net> wrote: I've been hesitant to do this, but here goes....I know a couple of people in the group have MS (multiple sclerosis), but don't recall who. Aside from some of the standard symptoms (which are often so down-played by the media), there is one that has been particularly troubling - the terrible muscle spasms that nothing seems to help much or for very long. Has anyone heard of any particular vitamin or mineral or whatever that can alleviate them?

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