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  • Title: VixPix Tits Out for Multiple Sclerosis
    Descriptive info: VixPix.. Tits Out for Multiple Sclerosis.. Well, over a few drinks at the pub, I was approached by two chaps who had made a bet.. One had bet the other £10 that I would flash my boobs.. I queried the bet, saying that if I did.. the 'loser' of the bet got to see my boobs, but the winner got £10 AND got to see them.. They decided that if I did it, they would give me the tenner to give to a charity of my choice.. Deal done!.. I lift my tee shirt.. I pocket the tenner and promise that I'll give it to.. a Multiple Sclerosis charity.. When I am next in my local pub, the  ...   to raise awareness of this illness (maybe even some people may.. donate cash.. ?) and have a little fun in doing so.. What’s all this about, then?.. News.. Click here for Vix’ new blog - Started December 2010.. Click here for the December 2010 update on “Why MS?”.. Click here to hear me on the BBC!.. 23 August 2008: VixPix MS charity event at The Anvil, Mansfield Woodhouse raises £1,020.. 54 for the MSRC!.. VixPix nears £7,000 ($14,000US) in donations on behalf of MS-UK!.. Click here to read about VixPix in The Sun!.. Click here to read the story of my diagnosis.. Wanna help spread the word? Click.. here.. for info on adding a banner link to your site..

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  • Title: VixPix Tits Out for Multiple Sclerosis Why MS?
    Descriptive info: Tits Out for Multiple Sclerosis.. Why MS?.. Easter 1998 and I wake up with 'pins needles' in my feet and erm.. other more personal places.. Nothing odd there, I figure it is just one of those waking-up kinda things.. In an hour the pins needles are still there.. In fact, they seem to be increasing and I am not sure, but my hands seem a little 'fuzzy' feeling, too.. I give it another hour and as it seems to be still worsening, decide to phone the doctor.. I don't want to hassle the doctor by going in to see him.. It's the Easter holidays.. My doc though, has other ideas and tells me I better go see him.. Once there, I am saying how I probably have a trapped nerve or somesuch.. He looks at me and says that is possible, but he just wants to check a few things.. He sticks me with pins.. He hits me with hammers.. He makes me close my eyes and touch my nose.. OK - whatever turns him on, I guess.. He tells me to come back after the Easter hols, which will be 3 days time.. Unless things get worse, in which case, I am to call the surgery and get to see someone.. Well, over the next few days, my legs and arms become increasingly useless.. It is odd.. I cannot really feel them.. It is like there is cotton wool all around my limbs.. Bizarrely, I can still stand.. I am walking like a toddler in a full nappy.. My feet are 2ft apart as I am sure I will fall.. I have not called the doctors.. I 'feel' just fine.. Nothing actually hurts.. I am sure this trapped nerve will shake itsself out and if not, I'll go see the damn doc again, as soon as the Holidays are over.. The Holidays are over.. guess what? I am still walking like I have crapped myself and I seem to have no feeling whatsoever in my hands.. This is becoming a 'party trick' and I am whacking my hands on the table and am amazed that I feel nothing.. Cool! Am a bit annoyed that I have little or no sensation in my 'Jack and Danny' though.. That's something that I can get concerned about.. OK, I'll go see the doc.. Within minutes, my doctor (having stuck me with pins, hit me with hammers, etc, etc) decides I should see a Neurologist.. Now.. Well, there isn't one in my home town, in fact I have to go about.. 60 miles.. It would have been further, but I have medical cover through an employer, so I get myself to see the Consultant Neurologist that afternoon.. He wants me to have an MRI scan.. The closest place to have this done? Back in my home town.. So I get myself back there and go to the NHS hospital.. They stick me in a wheelchair ( Let me walk! ) and then in a bed and then tell me that the MRI scanner is 'switched off' and I have to wait until the morning.. Come the morning, I am still in the bed ( Where can I go for a smoke? Oh, nowhere.. Right ) and I am promised the MRI by 3pm that day.. I'll not hold my breath.. Three MRI scans later and I am wheeled (under protest) back to bed.. Someone comes and says to me Well, your spine is fine.. There are a few things we're not happy about on your brain scans, though.. And with that - they leave me on my own.. What is wrong with my brain scans? They took two because they were unhappy with the first.. Only one spinal scan though.. What have they seen? Have I a tumor? What the f**k is going on?!?.. Finally someone comes and sits on the end of my bed.. Looking at his hands, he asks me if I have heard of a disease called Multiple Sclerosis.. Yeah, course I have.. Old people.. Wheelchairs.. That kinda thing.. He manages to gesture towards me with a slight incline of his head.. The penny drops! He means me.. He hands me two small leaflets and vanishes onto the ward.. (Chicken).. I am filled with steroids via a drip and sent on my merry way within a week or so.. That's it.. No-one told me anything more.. No-one seemed to have anything more to say.. Except there is one drug that may be of use to me in the coming years, however, my local health authority will not let me have it, as it costs too much.. Thank the Lord that I have the internet.. Over the next few weeks I am downloading, printing, reading.. soaking up information about MS.. I find the MS Society and they tell me that my experiences are not unusual.. No-one has anything to tell you, as no-one knows anything.. Super.. I was 28 when I got my diagnosis.. The neurologist at one point said that looking at my brain scans, he thinks I have an 80% chance of serious deterioration within 20 years.. Well, that was 6 years ago.. I guess that changes the odds as I am fit and well right now.. Hopefully will be tomorrow, too.. I'm not going to bore you (any more) with tedious details, but if you want to know more, there are places that you can go, such as the MS Resource Centre and Jooly's Joint web pages.. Visit the.. MS Links.. page for more info.. Why Multiple Sclerosis (MS)?.. Well, it's a couple of months down the line and I am prompted to update things here.. At the end of last year, I was having a bit of a relapse.. I was much weakened and upset by this.. My GP made me a referral to the Neurologist.. However, I did not mention this, on this page, before because I thought it was just December weariness (too much food, too much money spent, far too much drunk, etc.. ) but, in hindsight, I now know it was the start of a relapse.. I was off work for the best part of March this year with increased symptoms.. I was suffering a lot of pain, spasticity and loss of sensation.. My eyesight seemed to be a bit shot, too.. At the end of last month (March '04) My appointment came through and off I went to the Neuro.. I.. did not get to see the head of department consultant, but I was seeing someone at last.. I was told that I was suffering a relapse at the time and I was having one in November / December, too.. Well, as an upshot of this, I am finally being allowed medication! I can have Beta Interferon or Copaxone.. The decision is mine, I believe.. However, as I did not get to see the main man.. I have to wait for another appointment, this time to see the 'Prescribing Neurologist', so as I can get my meds.. As it is, I believe I am climbing out of my current relapse and although I was in hospital yesterday (went to GP with a pain complaint, he thinks I may have a thrombosis, jabs me with Heparin, arranges for me to go the next day and have dye injected into my veins and get x-rayed, get the all clear on blood clots) and have had another 3 days off work.. I'm going back tomorrow and, hopefully, I'll be back for a long stay this time.. My poor boss! I am so not a reliable employee at present.. Update April 2004.. In July, I was finally given Beta Interferon.. Woo hoo! Less relapses here we come!.. The side effects are bloody terrible.. I had heard that this might be the case, but decided to take the Disease Modifying Drugs (DMD's) just the same.. Hey, I'm ill anyway, what more can there be?.. Well.. The injection, self administered, three times a week, isn't too bad.. But it does hurt.. Not the needle, but the bit where the drug is squirted in.. That hurts.. Also I get a skin reaction where it has been done.. You have to vary the injection site because of this, but despite doing that, I get red welts about an inch and a half in diameter that are raised and itchy and very, very rough.. Recently, I have stopped using the auto-injector device they provide you with and have started manual injecting.. Putting the needle directly into my own skin and pushing the plunger.. I can do this at a much slower rate than the auto-injector can, and so far, this seems to be making the injection sites less aggravated.. The other side effects did not start that bad, I am thinking it may be having a cumulative effect as the months go on.. They tell you to expect 'flu-like symptoms.. Damn right! My muscles are aching like I have just been working-out for 10 hours solid.. (OK, I imagine it's how you feel after a work-out -- how would I know?).. From the shoulders down I hurt.. I am not sleeping.. I lie awake (hurting) and I have recently been told, by my MS Nurse, that insomnia is also an expected side effect.. This is the first I'd heard of that one.. The blood tests I have, to see how my body is reacting to the DMDs have shown a dramatic increase in something-or-other to do with my liver.. I looked this up on the 'net and got scared by what I saw.. On contacting my Neurologist, he told me not to worry and carry on with the drug.. Here's an example of what I found on the 'net:.. Health Canada warns of liver complications from beta-interferon use for MS.. I am currently off work because of all this.. My boss and someone from the HR department came to visit me at home today.. The HR dude told me not to feel pressured to return to work.. She said that whatever my doctor  ...   not approved for people like me.. Needless to say, I am furious, but even more embarrassed, now.. How dare you assume that that means sex is not important to me? How dare you say that the able-bodied man, next to me in the street, is more deserving of orgasm than I am?.. I speak to my friend, Dave, (who has MS, too) who is astounded.. His neurologist ASKS him if he has problems like this.. He tells me that he can get Viagra given to him, for free, every month.. He says he has not got this problem, his tackle is all in working order! (Thanks, Dave).. Yet every time he sees his doc, or his neuro, they ask him if he needs this treatment.. They ask him if he has any sexual issues, that could due to his MS.. What is his secret? Is it a different Health Authority? No! The rules are the same in all the UK's National Health Service providers.. His secret is.. He is NOT a woman.. Update September 2005.. Well, last year, I finally did it.. I officially gave up working for the bank in May 2006.. In my time, at the Halifax, they were very accommodating towards me and my illness but, as I have mentioned before, there is only so much that can be done.. After all, I was spending more time off sick than actually at work.. Since then, I have set up my own business and am now self-employed, working from home.. This hasn't really changed any of my symptoms.. I still suffer from pain and fatigue, but I no longer have the stress involved with calling in to report another day off-sick.. I have put on a considerable amount of weight, I guess from not moving about so much, but I have not suffered from lack of orgasm at all.. Not once (yay!).. I think this must be due to losing the stress.. To be honest, I don't really care why.. So, I am sitting in my bed and trying to think what there is to complain about - as generally.. speaking, I only ever write an update when there is something to whinge over.. My legs are wobbly at the moment - but that is because I spent three days in Paris, last week, with my husband, where we walked and walked.. Paris, by the way, is incredibly disabled un-friendly.. All cobbles and steps.. The Metro is a labyrinth of corridors with stairs.. I was very glad to not be in a wheelchair, or it would have been a totally wasted trip.. As I was able to walk, it was incredible.. And totally worth having the wobbly-walking after effects.. My eyesight is no better, but there again, it is no worse - so there's another good thing.. Same goes for the continence issues.. All in all, I have been pretty damn fine for the last year or so.. It is hard to not think that maybe this is the 'calm before the storm', but in the meantime, I am squeezing every second of every day.. Which sometimes includes doing new photographs - so keep an eye out!.. Update June 2007.. Snow is lovely to look at, isn't it?.. Through the window, from the warmth of your house.. It's pretty and clean and something of a novelty.. I believe, however, that snow is a cruel trick from the Universe.. Walking is something you learn to do when you are about one year old.. It is quite the achievement, but once you have mastered it, it's with you forever.. Like reading or riding a bike.. (Neither of which I can do any longer).. When I first got ill, I lost the ability to walk without looking like a toddler that has just shit it's pants.. I had what is called a spastic gait.. You walk with your feet about two feet apart.. Nothing you try and do will let you walk like a normal person.. Your head is telling your limbs to do it right, but they just won't.. After a course of steroids my legs (and arms, for I had lost any sensible use of those, too) got about 80% better and I taught myself to walk again.. It was different.. I had to re-learn the art.. It was frustrating and silly.. It's WALKING, Goddamnit!.. So, the way my feet perceive the ground has changed.. I have to just try and rely on the fact that the Earth is below me and is behaving in the way we all know it to.. It is solid and unforgiving and it sucks you down onto it like you're wearing magnet-boots and it's a big lump of iron.. It's the Earth.. It's got gravity.. If I do the whole left foot, right foot thing, I will get to my desired destination without incident.. Then.. the Universe plays a trick on me.. It changes the surface of the planet (OK, the bit I have to interact with, anyhow).. You step out of the door and find that the reliable old Earth (solid, unforgiving, etc) has amended the rules.. For starters, the surface is a good couple of inches higher than it had previously been.. OK, I can deal with that, surely?.. My mind perceives the surface and calculates the pressure required to make that first step.. (You know, you do all this without thinking, from the age of one).. It's snow.. I am aware that this changes things, and that my step will sink through the surface and hit the ground, a couple of inches below.. I know this.. I am prepared for this.. I am an adult.. An adult with boots on.. Boots with a sturdy sole like the tread on a winter tyre.. (The boots I used to wear when I rode my motorcycle.. Another loss).. OK, here we are.. I have stepped one foot into the snow.. There has to be at least another step.. Something is halting my progress.. I think I want to take another step.. I think I am asking my legs to do just that.. Do walking! Go on.. jus DO IT.. For some reason, my legs are unhappy to follow the orders they are given.. This is something my head is doing without my permission.. It has nothing to do with MS, it has everything to do with experience.. This is snow and ice.. You WILL fall over.. If I manage to actually get out of the door I find my old friend, the spastic gait, has come to visit.. I should be using my walking stick.. That would help.. The problem is the stick is in my car.. My car is out on the street, about 30 yards away.. Through the snow.. It will be gone soon.. Where I live is usually too warm for snow to stay for more than a couple of days.. All things must pass, after all.. Back in the house, I am perched on a.. Bambach Saddle Seat.. and making the most of it while I have it on a 30 day trial.. It's marvellous and really helps when I'm in the kitchen, cooking, ironing, washing-up.. I had recently been suffering with such tasks becoming more of a ball-ache than they are usually (for anyone that does them, not just for the broken people).. My feet were swelling up and my legs becoming excessively tired and wobbly.. I now can do all these things on my Saddle Seat and scoot about the kitchen in a comfortable, supported way.. Very soon they will be contacting me to get the seat back (they delivered it and will collect it, all for free) or to ask for £400.. Right now, I don't know if i can afford that.. I guess Visa can afford it, but they want paying back, don't they? And I'll end up paying interest.. Can I justify this expense? I'm having a problem with that.. It's hard to justify getting something that is just for ones own use, when you have three other people to consider, in your home.. Like a lot of people at the moment, my mantra to the family has been No, we can't afford it.. Can I then spend all that money on something that is purely for my use?.. I have a wheelchair, but I also have a standard kitchen, ie: if you're in a wheelchair, you cannot reach any of the surfaces or the cooker or sink and just forget the cupboards.. This wee stool is gas lift and allows me to access whatever I like.. But.. four hundred quid? FOUR HUNDRED QUID?!?.. Health update, then.. Eyes: Still fcuked.. If anything, getting a little worse, but that could be more to do with ageing than MS.. I turned 40, this year.. Bladder: No change.. Still a little unreliable, but manageable.. Legs: Painful.. Incredibly so.. A recent course of Physiotherapy actually made the pain and stiffness WORSE and I was discharged by the Physio telling me it is a textbook case of a known MS thing, blah, blah, blah.. The sex thing: Not really suffering with any disfunction at the moment, but this is a constantly.. changing thing, and what may be fine one day, is far from fine the next.. It is still not something I am even asked about by my Neurologist (I'm on Neuro number five, I think).. Generally, I am still walking and talking with what I can see as a slow downward slide in ability.. I struggle with finding words when I am speaking and I am finding I am having trouble swallowing ( :lol: ), every now and then.. I cough and splutter over a glass of water.. Swallowing, like walking, is something I thought I had mastered quite early on in life.. Things I want to tell you: Refusal of Sativex; increase of dose of other meeds; Physiotherapy debacle; mindnumbing boredom of not going out to w*rk.. I think I need a blog.. Update December 2010.. And I have started a proper blog.. Any further updates will be found.. HERE..

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  • Title: We are so pleased that so many people are enjoying this site, we thought we would share some of the lovely feedback and comments we have received. Please let us know what you think about these pages by clicking here to send us an e-mail. Thank you - Vix.
    Descriptive info: Comments.. Anyone who reads the very moving comments on VixPix will understand why this has been far more than just a fundraising exercise.. She has not only raised what to us is a very substantial sum of much needed money, but she has also changed the view of many people about those affected by this disease.. - Lawrence Wood, Chief Executive of the.. Multiple Sclerosis Resource Centre.. As a man who has had MS for a few years, Vix Sarah Louise's photos have really perked up my day!!! Thanks ladies xx.. Anthony.. Great pics! Great tits! WELL DONE!.. I already have a monthly payment to the Society and I wish you all the very best.. I'll visit your site regularly and advise my friends to do the same.. Take care.. Love, Christopher xx.. God Bless You! I have MS and any help is appreciated!.. I'd like to thank you for stepping up and raising money in an unselfish manner.. Kudos to you!!.. Your site is fabulous.. I've got MS too and I'm so thrilled to read a site that isn't boring, annoying think positive! crap.. You're doing a great thing.. Just wanted to say THANKS for helping us who suffer with MS! Keep up the great work!!.. Hullo! I am a 45 (plus) yr.. old patient.. I was thrilled to find your site and to see that you haven't let this damned disease take away your obvious sexuality.. There isn't much sexy about m.. s.. and I was pleased to see there are people out there that still maintain that part of their lives.. P.. S.. you've got a great pair there - my husband thinks they're awesome!.. Thank you.. For raising awareness, for being brave enough to show us that nothing can stop you from reaching your goals, and for being honest enough to give yet another shining example of what the human spirit can acheive.. My hat's off to you, a hearty warm *HUG* to you for your efforts, and I shall make a donation as soon as I can.. Your obvious Carpe Diem attitude deserve to be rewarded with as many donations as possible to such a noble cause as finding a cure for MS.. Maybe next time you can do another, similar shoot for a cure for Diabetes as well? I think I shall browbea.. errrr (cough) encourage (chuckles) all my 'mates to make a donation as well - I'll tell them to do so instead of spending money on my Christmas gift, thus making donations to a more worthy endeavour! (HuZZAH! What a great idea!) *HUGS* and best of luck to you! Sincerely, A fan from the Other Side Of The Pond.. ;-}.. As a person who was diagnosed with MS 10 years ago, I pride myself on keeping abreast of all new medical developments and fund-raising efforts, but when I stumbled upon your site, it caught me by most pleasant surprise.. What a great idea! You are quite a beautiful woman, one whose ample talents are perfect for exposing the public to the plight of those with MS.. Keep up the good work.. When I finally overcome the Bush Economy here in the States, and once again find a job, I'll send along a donation.. I hope that you have a man in your life that appreciates your beauty, intelligence and dynamic energy!.. If everyone who visited this site so far had coughed up just $1, that would be over $100,000 for MS research.. I say bravo for being brave enough to bare yer boobs for charity.. First, great idea! There are a lot of worthy causes, and MS research is certainly one of them.. You've managed to make it fun to donate.. Best of luck with the website, and best wishes for continued health.. I have just spent a peaceful 20mins reading your site, understanding more about a condition I have seen close up but never knew anything about.. God bless you and keep having fun and I hope your donations to the MS charity grow and grow.. My Aunt and mothers best friend have MS.. My hat is off to you and your efforts.. And may I add you have a wicked gleam in your eyes that bespeaks a razor sharp mind, I just hope others look beyond your physical attributes and see what lies beneath.. I think your idea and your attitude are wonderful! It's so very refreshing to see someone with humor, intelligence, and guts.. I'm so very sorry that it took MS to cause you to create this site.. Best of luck to you.. I sincerely hope your site raises a lot of money and that you have fun doing it.. I also hope the MS goes somewhere else!!.. Hey, great site.. My dad's had MS since I was born, and the thing that pisses me off the most is the Look at the guy in the wheelchair and feel sorry for him mentality that a lot of people have when it comes to fundraising.. Thanks for an innovative and original idea that'll help get rid of the stigma associated with the disease.. Well done, you! My boyfriend was, like you, diagnosed in 1998 (at 17).. We are both now 22.. After we got together in '99 I've seen the some great fund-raising ideas, but this is the best one yet! I've forwarded him the link and we will both definitely be contributing.. You're an absolute inspiration and a beautiful lady.. You have MS, but MS doesn't have you.. Thank you so much for sharing that with us.. Web site's great, well done! Nice to read about someone who's experienced a lot as I have.. I was diagnosed August 1989 relapsing remitting MS.. Things have been better since injecting Copaxone.. Two weeks ago I had my worst relapse ever and am now unable to drive and need help (i.. e.. wheel chair) when out.. But hey, got my head together - positive head on and things are improving.. Thanks for reading this keep up the good work!.. Wow - I never new being diagnosed with MS was going to be this much fun! Seriously, I've was diagnosed with MS almost 2 years ago and was not feeling too well the past few days so I went on the internet looking for information.. I'm a guy in his 30's and let me just say those photos are hot.. Geez your real nice and I love the jeans with the open shirt.. Sooo nice.. I was having issues with sexual function but I think I found the cure - your photos! Thanks so much!.. Firstly, I've checked out your website and I'd like to say: PHWOAR!!! Secondly, I'm sorry to hear about your MS.. My ex had MS also and used to suffer from relapses like you did before you were put on beta interferon.. Unfortunately her MS progressed to secondary progressive MS before she could get on it.. I know this is going to sound corny but I had to tell you that i think it's amazing that you are doing everything possible to lead as normal a life as possible when in a position where most people would simply give up.. I just wanted to let you know how impressed I am with the site and also with you.. I'm a District Nurse based in Liverpool and 3 of my female patients have been diagnosed with M.. I've printed some stuff from your site to give to them (hope you don't mind) cos I want to try and help them regain some of their confidence and femininity.. Like you, they're young women and this debilitating condition has had devastating consequences on their outlook on life.. My hope is that they`ll realise that life can go on and, like you, they can still enjoy a full, happy and rewarding life.. All credit to you.. your pics are fab, and the cause for which you are doing it even better!!!.. Just wanted to say thank-you for putting together such a great MS site.. I was just diagnosed with MS 12 days ago and sure can relate exactly to the early parts of your story.. Got told just the same way - no sign of stroke but you have MS, doc dissappears for 2 hours.. I was sitting here at my puter wondering things like what is going to happen down the road when I go to put my foot down to hold up my scooter and it decides, to friggin pal, now pick me up! Wasn't a fun thought till I stumbled onto your page.. Oh well, guess I keep a spare set of bars or 2 around.. Once again, TY hon - I needed that.. You can count on donations to follow.. Keep the updates coming!.. I read of your site in our branch magazine (MainStream) and just had to have a look.. Thank you so much for being such an inspiration.. I, too, was 28 when diagnosed, had many of the same symptoms and, to look at me, you would never know.. I am so glad I have found somewhere, and someone, who understands.. I'm lucky to have a loving hubby who always makes me feel sexy no matter what.. BUT you are proof that, with or without MS, you can still be all woman.. Thank you so much.. xx.. What a fantastic site - my husband sent me the url.. if I had your assets then I'd be proud to do the same! You may have found it already, but the thing that has done my MS the most benefit (like regaining all important sensation in my Jack and Danny) is diet - check out.. www.. ms-diet.. org.. if you haven't already.. it's a bit of a grind but the difference it has made to me is unbelievable all good.. More power to your elbow and the very best of British to you - King sized regards!.. I just wanted to know that as an MS patient (found out when I was 29, three years ago), and as a big fan of large, natural breasts, I LOVE what you are doing! =) It's nice to see that someone else besides me can have a sense of humor about this disease in the face of abject terror about the future.. My wife loved what you are doing as well.. Keep a stiff upper lip, all right? A woman as beautiful as yourself has MANY things to be NOT stressed over.. =) Dwell on those things and take care.. I've just read your letter which I found on a MS website.. I found it very amusing if a little sad.. But, being a sufferer myself, I know just where you are coming from.. Your humor really gave me a lift.. Just a short note from one MS'er to another.. Great web site and a worthy cause.. You have certainly got some great assets plugging for a great cause! Keep up the good work! Regards from the USA.. I have gone through your web pages and it has helped me a lot.. I now know I am not on my own, as I have not had much support from the outside world.. Congrats to the creativity in driving donations.. MS is a brutal disease and in dire need of funding.. Hats off to all who give it up for the cause.. If only more people had the guts to do something out of the ordinary for a worthy cause!.. Making the breast of a bad situation - good on yer - I hope you make a fortune for MS research!.. Awesome.. :) My best friend with MS sent me your link.. :) She thought it was the best idea she'd seen in a long time!.. Just saw your website thought it was great.. Very informative and I love how you challenge stereotypes in such a clever way.. Great site! Couldn't resist swelling your coffers a little more! I hope you raise lots of money.. BTW - you're very sexy!.. Just to let you know that I am inspired by your courage and other things obviously!! I have donated £20 to your cause and wish all the best of luck in your venture.. Excellent idea for fund raising! In terms of drawing attention and raising funds for a cause, your website is certainly the most original I've seen in quite some time.. It is a most refreshing change to see a fundraising effort that is not based around the conventional sympathy and haranguing techniques.. And speaking as a red blooded male, you look fabulous! Made donating a pleasure.. blush.. I've had MS for at least 15 years, been diagnosed since November 2003.. I've never seen a fundraiser quite like yours, but I think there should be more of them! I'd join in, but I don't think there'd be much interest in Balls-Out For MS.. Anyway, you are beautiful woman, and a beautiful soul.. I think you are very brave and beautiful.. As a senior citizen my finances are a bit stretched, but I will donate as soon as i get a spare fiver.. I will only look at one boob! ;) They are gorgeous, and so are you..  ...   don't work, work with what you got!.. You're showing a whole other face of that.. But it's an original fund-raiser and I applaud you for having the guts and caring spirit to help the M.. fight in a unique way.. Well I have to say I am very impressed! That takes courage, but I wonder what the MS Society would say!!! LOL! You look great!.. The MSRC.. do want to explore the sexy side of MS, and I have done a 30 second film for them on this subject.. The point being made is that although 'MS isn't sexy' at all you can still be sexy and have MS!!!.. Let me know if you are doing a calendar.. I, too, have had MS for three years.. I need to join in if there is a calendar being done! Could you let me know? Thanx!! By the way, you have shown them how it is done.. Go, girl!!! Your pics are great!!.. My wife has MS and we think this is a great way to raise money to help find a cure for this disease.. Have you thought of doing a calendar yet? I bet it would sell.. You are brave and clever as well as untraditionally innovative, contributing to a good cause with personal comittment! -Michelle, Sweden.. Keep up the good work! I take my hat off to you! Very nice photos! How about a calendar next year?.. Just thought you would like to know that a group of people up in Dundee, INSPIRED BY YOU, have decided to have a ladies night (about 350 women!!!) with Male Strippers!!!!!! They are expecting to raise £3500! Fancy that!.. I didn't expect a personal response, and I think that is a good reflection of your character! This world could do with many more people like you and it would be a better place.. Your pictures certainly brought some sunshine into my life.. You are very pretty and deserve all the success I hope you get.. If you do ever do a Calender, I will certainly have one, either all of you or any other recruits you may enlist.. This is a BRILLIANT idea.. Someone where my partner works stumbled on your website and sent it to him because I also have MS.. My boyfriend was reluctant to share it me because he knew I'd probably do something similar and he doesn't want me flashing my tits.. But you go girl, and I'm going to find something to do similarly!! More power to you and keep it up!.. I was looking in the 'heartwarmers' section of ananova.. com, and happened upon a link to your website.. I wish I knew of something which could help your condition.. I hope you are living with it well, and I hope you are comfortable.. I just wanted to say that I think you are extremely beautiful and if your mind is as beautiful as yor body than your partner is a very lucky human being to have found you.. Just to have seen you warms my heart.. Gutsy thing you're doing here.. Fair play to ya gell! I dated a girl for three and a half years who has MS and she found that diet and exercise (especially the abolition of Gluten from the diet) helped a great deal.. As a body builder I would always advocate the implementation of intense excersise and a healthy diet as a pre-requesitve for getting the best out of life.. So go get 'em Vix dont let this bastard beat ya!.. Well, I would just like to say its a wonderful thing that you are doing.. It's a shame there aren't more people out there doing what you have decided to do for charity.. All the best in raising the money and for the future.. Hey.. just wanted to say I recently found your web site.. I have MS (diagnosed in 1993) and appreciate what you are doing.. And, you look GREAT doing it too!.. I was given a link to your site by a friend, and I commend you heartily for having the guts to get 'em out, as well as to fight MS in the first place!.. Just ran across your 'Tits for MS' site.. I think it's wondeful to have a lil fun while raising money for a good cause!:o).. I think what you are doing is fantastic.. Good luck with your campaign and your condition.. An innovative approach to collect for charity and a worthy cause too.. Good luck to you! :).. Thanks for your making MS awareness interesting! Cheers, and keep up the good work!.. Hey Vix.. Love your attitude to it all.. Upfront- in yer face and feelin' good!.. Go Girlfriend! All the very best of luck with raising some real money.. Honey, your breasts are beautiful! Thanks for your work with MS!.. Good luck, and hope you raise lots of dosh for MS.. Congratulations on coming up with such an innovative way to raise funds.. A friend of mine was diagnosed with MS last year, so it's an issue close to my heart.. My mom has MS and is in a very bad way (lost about 60lbs since being diagnosed a year ago) and I will be ECSTATIC about posting a link to you guys from my website! :).. This is a great idea.. I just donated to your cause.. I am a 34 year old guy from the US, and was diagnosed with MS in 1997.. It's been quite a battle but I am doing pretty good with it.. It's quite wonderful to be doing what you are to fight this disease.. Keep up the great work!.. While I've got two kids with special needs (Type I diabetes and Angelman Syndrome) who need their own research for a cure, what you've done takes *guts* Congratulations on your selflessness and may you benefit enormously from the research your donations make possible.. This is a fantastic idea.. There are so many good causes competing for attention and the fact that you are getting this message shows that your idea is really working.. I saw that other people had suggested a calendar and if that idea interests you, I'd encourage you to get other like minded people involved and go for it.. I've just had a look at your website, looked at the photos, and donated some money to charity.. I wish you all the best with your endeavour, and hope you raise a lot of money for the MSRC.. What a neat idea! I wish you all the best of luck - we walk (well, boyfriend staggers.. he has MS) in the local walk for funraising.. I have RRMS and I appreciate you approach for awareness.. I made your picture into a screensaver for my cellphone.. It is great!.. From one MS sufferer to another, your pix are breathtaking! How many people would be as risky as you in search of a cure? Not many, I'm guessing.. MS or not, you are too damned hot!.. I also have M.. and have to say thanks for raising money for the cure.. Love your breasts and if I had two like that I would be trying to raise money with them also.. LOL.. You put a lot more than just a face of an MS patient.. I support your efforts, but you appear to be rather well supported ;-).. I was just at your site.. I think you have such a cool way to raise money to help fight MS.. I never would have thought of it.. Good luck with everything.. I also have MS, DX'd in '98.. Great idea, hon.. I just posted your.. banner link.. on my MS site, too!.. From your friends in Hell's Mensan's in the US - Well Done!.. Good luck with the site - great idea! :-).. Hi vix, just wanted to say that i visted your site after reading about it in a newspaper, and this is the first time i've ever taken the trouble to write an e-mail of support for anything, and to be honest i only checked it out coz i have a thing for large tits (yours are lovely *drool*) but i was so impressed by the whole idea it moved me to make a donation (another first) and it also made me aware about MS, well done and i hope you raise thousands, good luck xx.. My site is not a traffic hotspot by any means - in fact it's an empty cul-de-sac on the information highway - but it now contains your banner and nothing else, so you can consider yourself and your site headliners both.. :-).. Your site has attracted some attention, maybe you should encourage others to show their kit for charity cash.. Basically guys could surf and pay for porn as they do but have the money go to charity.. Takes all the catholic school guilt out of what we're already doing.. ;-).. I'd much rather see money change hands because of breasts for charity than have the Hefners of the world continue to get filthy rich off them.. I say Yay!!!.. What a fabulous way to raise funds for such a needy cause! It's a pleasure to contribute especially to see such a beautiful girl with such a beautiful pair.. So now I have to admit I've paid to see boobs online.. D'oh! Mind you, you're genuine worth every penny.. Well done, luv - an excellent and worthwhile cause.. As I keep telling my wife, If you've got them, show them.. Great globes of grandeur! You can be proud! Nature has blessed you! Thank you for baring/sharing! It has made my day!.. You have Fantastic Tits! Outstanding effort! Good luck with raising money for MS I think that you will do very well indeed.. I hope that you raise a lot of money.. You've got a lovely pair of coconuts.. Good health and best wishes to you.. I always wanted to visit the UK.. I must say that I really like your attitude!.. Ohhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhh!.. 10 out of 10 for the idea - and 10 out of 10 for a fab pair!.. Good on ya Vix.. u look lovely.. thumbs-up.. Great page.. Great bOObs.. Great cause.. YEEHAAAW!!! Udderly Brilliant!!!.. Hmph.. No one ever paid money to see *my* tits.. sulk Yours are way nicer than mine, though.. and you could be starting a very agreeable trend.. :-) Neato!.. If you dont mind me saying.. great pair of breasts.. so why the hell not get them out for charity? I take my hat off to you for having the guts to do it girl! I dont have MS however I am running the 2004 Flora London Marathon on behalf of the Multiple Sclerosis Resource Centre.. Good Luck to you - Well Done!.. I love the way you are keeping abreast of this crappy disease.. And, when asking for donations to the MS Society you do have a couple of points in your favor.. As Bob Hope would have said, Thanks for the mammaries.. TTTYTTFN, (er, that would be, ta ta to your ta ta's for now) I shall return.. Very well done Vix.. I'm a 45m diagnosed 8 yrs.. Have been on beta interferon for 7 yrs.. DMD's side effects - flu-like symtoms, ROFLMFAO.. I do the once a week shot and it's been like getting run over by a bus for two days a week for the past seven years.. Steroids for optic neuralgia numerous times.. Legs numb - drop foot, arms numb, bladder fubar.. yada, yada, yada,.. On the positive side of my truly wonderful life ( I am not being sarcastic ).. I thankfully have decent mobility, 15 minutes of standing or 100 yds walking.. Sexual function can be a miss at times but thankfully I can accomplish the act to mutual satisfatcion 85 + - %.. I am really enjoying my life with my gorgeous girlfriend, ~(who could be your body double) ~.. We do tropical vacations every winter + travel for at least a month every summer with our 5th wheel (caravan in British speak LOL).. I love your open book philosophy on life and see it as refreshing.. I see factual references and occurances when I read your blog and admire you for not being a victim of MS.. I do not see a person who is throwing a self pity party as you see in so many blogs of immuno proficient persons.. On the day of my diagnosis a person close to me asked, Don't you just ask yourself ; Why me ?.. My instant reply was, Why not me.. ( It was years of symptoms before my diagnosis; maybe that's why the Shit Happens - I'm OK with It Attitude ).. Kabitzing will not help any of us; telling it like it is does.. You Go Grrrrrl.. MS is what we live with, It is NOT who we are.. Hugs and such.. We are so pleased that so many people are enjoying this site, we thought we would share some of the lovely feedback and comments we have received.. Please let us know what you think about these pages by clicking.. to send us an e-mail.. Thank you - Vix..

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  • Title: Links
    Descriptive info: Links.. MS-UK.. - MS-UK (previously called The Multiple Sclerosis Resource Centre or MSRC) offers advice on complementary healthcare as well as support for people with the disease and their families and friends.. The Multiple Sclerosis Society.. - Homepage of the UK MS Society.. Campath-1H for Multiple Sclerosis.. - Campath is a treatment for MS or Multiple Sclerosis.. The site author has MS and has been treated with Campath.. This is his experience of that treatment.. Glucosamine Arthritis Information Center.. - The Glucosamine Arthritis Center contains information on arthritis and glucosamine, the latest glucosamine research, glucosamine product reviews and tips for effectively managing joint pain.. Jooly's Joint.. - An award-winning online community of people who live with Multiple Sclerosis.. Living with Multiple Sclerosis..  ...   a treatment for MS.. Also, please be sure to sign the Research Trials in Low Dose Naltrexone for Multiple Sclerosis on-line petition (.. click here to add your signature.. )!.. MS Friends UK.. A chairty whose aim it to assist those with MS, together with their partner/carer, to take a short break together.. A change of four walls, fresh sea air, something to look forward to and look back on.. Meet the people who care, share and understand.. Multiple Sclerosis - A Personal Account.. - A personal account of the author's experience since being diagnosed with multiple sclerosis, the MS symptoms he has suffered, and what he has done to cope.. Please contact me, if you have a link I should add here..

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  • Title: VixPix Tits Out for Multiple Sclerosis The Photos
    Descriptive info: The Photos.. Please help Vix support the MS-UK by.. making a donation.. (contributions accepted internationally through justgiving.. com).. Click on a picture for the full album.. Please help Vix support MS-UK by..

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  • Title: Banners
    Descriptive info: Banners.. Help us spread the word with a banner link on your website! Just choose the banner you wish to use, then highlight, copy paste the HTML code below it to your web page.. 468x60 Animated Banner.. a href= http://www.. vixpix.. org/ img src= http://www.. org/vpbannera.. gif /a.. 468x60  ...   /a.. 270x35 Animated Mini-Banner.. org/vpbannerasm.. 270x35 Static Mini-Banner.. org/minibanner.. 120x60 Animated 1/4-Banner.. org/anibanner.. 88x31 Animated Button.. org/button.. 120x80 Rose Banner.. org/vixrose.. 120x160 Thumbnail.. org/titsout4ms.. jpg.. and, if you have an MS support site,.. e-mail us.. for inclusion on our.. page!.. Thanks so much for your support of VixPix and MS-UK!..

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  • Title: VixPix - Tits Out for Multiple Sclerosis - MS Links
    Descriptive info: Click here for the December 2010 update on "Why MS?".. MS Links:.. alt.. support.. mult-sclerosis.. - Usenet newsgroup and message forum that focuses on supporting those whose lives are touched by MS.. Dopey's Headquarters of Meaningless Junk.. - A personal MS homepage inspired by VixPix.. Edwina's Home 4 MSers.. - The author's aim for this site is to help others with MS by sharing her own experiences and providing useful information and links relating to MS.. Glucosamine & Arthritis Information Center.. - The Glucosamine & Arthritis Center contains information on arthritis and glucosamine, the latest glucosamine research, glucosamine product reviews and tips for effectively managing joint pain.. Also, please be sure to sign the "Research & Trials in Low Dose Naltrexone for Multiple Sclerosis" on-line petition (.. )!.. *UPDATED*.. - A chairty whose aim it to assist those with MS, together with their partner/carer, to take a short break together.. The Multiple Sclerosis Resource Centre..  ...   person you will find both refreshment and inspiration here!.. We are the people with MS.. - MSN user group and message board for sharing information and personal experiences.. World of Multiple Sclerosis.. - An extensive site providing MS symptoms and treatment guide for patients and caregivers, introductory FAQs, recent research, and more.. World's Top Personal MS Websites.. - Vote for this site and access links to the top personal MS websites worldwide.. Other Links:.. Let the Puppies Out dot Com.. - Another "tits out for charity" effort, this one supporting.. Against Breast Cancer.. SayItWithBoobs.. - A unique e-card site, because nothing says "I love you" or "you're a right tit" quite like boobs!.. Please help Vix support the MSRC by.. (contributions now accepted internationally through justgiving.. com).. Wanna help spread the word? Click here for info on adding a.. to your site.. Comments about the site? E-mail:.. vixpix@psio.. net.. VixPix supports:.. The Multiple Sclerosis.. Resource Centre..

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  • Title: VixPix - Tits Out for Multiple Sclerosis - Why MS?
    Descriptive info: Easter 1998 and I wake up with 'pins & needles' in my feet and erm.. In an hour the pins & needles are still there.. Well, there isn't one in my home town, in fact I have to go about 60 miles.. They stick me in a wheelchair ("Let me walk!") and then in a bed and then tell me that the MRI scanner is 'switched off' and I have to wait until the morning.. Come the morning, I am still in the bed ("Where can I go for a smoke?" "Oh, nowhere.. Right") and I am promised the MRI by 3pm that day.. Someone comes and says to me "Well, your spine is fine.. " And with that - they leave me on my own.. What have they seen? Have I a tumor? What the f**k is going on?!?.. Click here for the story of my original diagnosis.. *UPDATE APRIL 2004*.. I did not get to see the head of department consultant, but I was seeing.. someone.. at last.. As it is, I believe I am climbing out of my current relapse and although I was in hospital yesterday.. (went to GP with a pain complaint, he thinks I may have a thrombosis, jabs me with Heparin, arranges for me to go the next day and have dye injected into my veins and get x-rayed, get the all clear on blood clots).. and have had another 3 days off work.. My poor boss! I am.. so.. not a reliable employee at present.. *UPDATE SEPTEMBER 2004*.. Woo hoo! Less relapses here we come!.. Hey, I'm ill anyway, what more can there be?.. They tell you to expect 'flu-like symptoms".. (OK, I.. imagine.. it's how you feel after a work-out -- how would I know?).. From the shoulders down I.. hurt.. This is the first I'd heard of.. that.. one.. She said that whatever my doctor says on Thursday, when I see her next,.. not.. to come back to work yet.. I wanna drive my new car!!.. I am so tired!.. Vix.. *UPDATE JANUARY 2005*.. I can't drive! I can't  ...   has far more luck with women, than I do - Is what I am thinking) I have to tell him that I have not had an orgasm for weeks.. No, months! I have to tell him that no matter how aroused I feel, my "equipment" does not function as it should.. "How dare you assume that that means sex is not important to me? How dare you say that the able-bodied man, next to me in the street, is more deserving of orgasm than I am?".. He says he has not got this problem, his tackle is all in working order! (thanks, Dave).. *UPDATE JUNE 2007*.. After all, I was spending more time "off sick" than actually at work.. So, I am sitting in my bed and trying to think what there is to complain about - as generally speaking, I only ever write an update when there is something to whinge over.. Which sometimes includes doing new photographs - so keep an eye out!.. *UPDATE DECEMBER 2010*.. Snow is lovely to look at, isn't it?.. I had what is called a "spastic gait".. It's WALKING, Goddamnit!.. If I do the whole "left foot, right foot" thing, I will get to my desired destination without incident.. OK, I can deal with that, surely?.. Another loss).. Very soon they will be contacting me to get the seat back (they delivered it and will collect it, all for free) or to ask for 400.. Like a lot of people at the moment, my mantra to the family has been "No, we can't afford it".. Can I then spend all that money on something that is purely for my use?.. four hundred quid? FOUR HUNDRED QUID?!?.. A recent course of Physiotherapy actually made the pain and stiffness WORSE and I was discharged by the Physio telling me it is a "textbook case" of a known MS thing, blah, blah, blah.. The sex thing: Not really suffering with any disfunction at the moment, but this is a constantly changing thing, and what may be fine one day, is far from fine the next..

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  • Title: VixPix - Tits Out for Multiple Sclerosis - The Photos
    Descriptive info: Send a VixPix e-card.. & help spread the word!.. And now, on to.. (click thumbnails to enlarge).. New Behind the Scenes Videos Added - Click Here.. Vix on Wheels!.. (.. click here to see the entire series.. ):.. Photos courtesy of Jonathan Wilson from.. Something Erotic.. :.. Behind  ...   from various photo shoots:.. Purple hair & a pierced nipple - some of my most recent pics:.. My purple corset:.. Photos courtesy of.. Gary Roberts Photography.. My bike pix:.. HAPPY VIXMAS 2005!.. New pix from Vix for 2008:.. Just for Fun - Big Tits Kill Bill.. Just Tits.. 2257..

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  • Title: VixPix - Tits Out for Multiple Sclerosis - Comments
    Descriptive info: Comments:.. Additional comments appear on the.. donation page.. "Anyone who reads the very moving comments on VixPix will understand why this has been far more than just a fundraising exercise.. ".. Love, Christopher xx.. God Bless You! I have MS and any help is appreciated!.. Kudos to you!!.. I've got MS too and I'm so thrilled to read a site that isn't boring, annoying "think positive!" crap.. Just wanted to say "THANKS" for helping us who suffer with MS! Keep up the great work!!.. you've got a great pair there - my husband thinks they're awesome!.. errrr (cough) "encourage" (chuckles) all my 'mates to make a donation as well - I'll tell them to do so instead of spending money on my Christmas gift, thus making donations to a more worthy endeavour! (HuZZAH! What a great idea!) *HUGS* and best of luck to you! Sincerely, A fan from the Other Side Of The Pond.. ;-}.. I hope that you have a man in your life that appreciates your beauty, intelligence and dynamic energy!.. I also hope the MS goes somewhere else!!.. My dad's had MS since I was born, and the thing that pisses me off the most is the "Look at the guy in the wheelchair and feel sorry for him" mentality that a lot of people have when it comes to fundraising.. Thanks for reading this keep up the good work!.. I was having issues with sexual function but I think I found the cure - your photos! Thanks so much!.. your pics are fab, and the cause for which you are doing it even better!!!.. Keep the updates coming!.. xx.. it's a bit of a grind but the difference it has made to me is unbelievable & all good.. More power to your elbow and the very best of British to you - King sized regards!.. If only more people had the guts to do something out of the ordinary for a worthy cause!.. Making the breast of a bad situation - good on yer - I hope you make a fortune for MS research!.. :) She thought it was the best idea she'd seen in a long time!.. BTW - you're very sexy!.. I've never seen a fundraiser quite like yours, but I think there should be more of them! I'd join in, but I don't think there'd be much interest in "Balls-Out For MS".. Good luck with the site!.. they'll be looking at the pictures! Yum Yum! :o).. [.. VixPixWallpaper#1.. ] [.. VixPixWallpaper#2.. ].. The fits can be real bad and all these tablets & doctors get me down.. You are brill 4 doing this site!.. Well done!.. :).. I also thought it was well written, and of course the pictures were great!.. S Badger The Sun to get on Page 3!.. Keep up the good work!.. I read about your cause in "The Sun" and thought good  ...   photos! How about a calendar next year?.. Just thought you would like to know that a group of people up in Dundee, INSPIRED BY YOU, have decided to have a ladies night (about 350 women!!!) with Male Strippers!!!!!! They are expecting to raise £3500! Fancy that!.. But you go girl, and I'm going to find something to do similarly!! More power to you and keep it up!.. So go get 'em Vix & dont let this bastard beat ya!.. And, you look GREAT doing it too!.. I was given a link to your site by a friend, and I commend you heartily for having the guts to get 'em out, as well as to fight MS in the first place!.. I think it's wondeful to have a lil fun while raising money for a good cause!:o).. Good luck to you! :).. Thanks for your making MS awareness interesting! Cheers, and keep up the good work!.. "Upfront- in yer face and feelin' good!".. Honey, your breasts are beautiful! Thanks for your work with MS!.. My mom has MS and is in a very bad way (lost about 60lbs since being diagnosed a year ago) and I will be ECSTATIC about posting a link to you guys from my website! :).. Keep up the great work!.. It is great!.. From one MS sufferer to another, your pix are breathtaking! How many people would be as "risky" as you in search of a cure? Not many, I'm guessing.. MS or not, you are too damned hot!.. I support your efforts, but you appear to be rather well supported ;-).. on my MS site, too!.. From your friends in Hell's Mensan's in the US - Well Done!.. Good luck with the site - great idea! :-).. Hi vix, just wanted to say that i visted your site after reading about it in a newspaper, and this is the first time i've ever taken the trouble to write an e-mail of support for anything, and to be honest i only checked it out coz i have a thing for large tits (yours are lovely *drool*) but i was so impressed by the whole idea it moved me to make a donation (another first) and it also made me aware about MS, well done and i hope you raise thousands, good luck xx.. :-).. ;-).. I say Yay!!!.. D'oh! Mind you, you're genuine & worth every penny.. As I keep telling my wife, "If you've got them, show them.. Great globes of grandeur! You can be proud! Nature has blessed you! Thank you for baring/sharing! It has made my day!.. I must say that I really like your attitude!.. Ohhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhh!.. 10 out of 10 for the idea - and 10 out of 10 for a fab pair!.. YEEHAAAW!!! Udderly Brilliant!!!.. :-) Neato!.. Good Luck to you - Well Done!.. As Bob Hope would have said, "Thanks for the mammaries"..

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