Cancer Cured in Canada? Big Pharma Says NO WAY!

By george she's got it!!!

Yes had the scan last Friday and I have CCSVI, so now it's onwards with the fund raising. I can't explain to you all just how emotional that day was, i walked more that day than i have done in months, i think i was on my feet for as total of 19 hrs, yes i kept stopping to rest and drink yet another cup of tea/coffee, but my legs are still aching something rotten still now. I think it was pure adrenalin that kept me going, but it was so worth it, now i have something to fix, let's hope that the procedure does as much for me as it has for so may others, we just want our lives back, and I am not waiting for the NHS. Oh don't get me wrong I will be pushing the scan results for treatment on the NHS, but not holding my breath, but you never know, if you don't ask you don't get. So it was the result that i was looking for, i will keep you updated as i go.

Luv to you all.xxx

Heat..good or bad?

Well, over the weekend it has been as high as 29 degrees celsius... Have i suffered? NO thank god, so I think I have escaped the dreaded MS heat intolerance for now, so if things go ok for the next cple of mths, then maybe, just maybe, me and my boys will go away for some sunshine and R&R

AND ENGLAND YOU SUCK AT THE BIG GAME............GGGGRRRRRRRRR!!!

2 weeks from today....Is it?

On Friday the 9th July, which is 2 wks away, I will know whether or not I have CCSVI? I have been feeling incredibly anxious and still am, this has meant that my MS has been rearing it's head. Some numbness in my face and the legs have been a little wobbly when I overdo it. So, now trying to keep calm and await my trip to Scotland for the scan and results. I am wondering whether I have become heat intolerant, this weekend will be a tester, the forecast reckons it's going to hit 30 degrees celsius, so sunbathing or hiding indoors? let's see.

God my life seems to be full of unanswered questions.....??????

So if I'm not back on before the 9th July, then I will let you all know after that date.

Low Dose Naltrexone - How It Works

Each Tear SUCH INSPIRATION!!!!!!!!!

Afternoon people, long time no see? LOL XX

Hello all, popping on to let you all know what's happening with me.

As of two days ago, I have reduced my LDN dose to 3ml, the reason for this is that I seem to not be doing as well with the health and mental state, as when I was on a lower dose. I think that i went all the way to 4.5ml because i know that I could, however it did not seem to be for me. My legs and tiredness and various other, all be them small symptoms were rearing their heads. So, two days on and I can see positive changes, I feel a little calmer, my legs should be better, but unfortunately I had a fall, not due to MS, but due to a piece of a drain cover missing, I am dealing with the company that maintains that car park where this accident occurred. So, i will now keep a close eye on the other symptoms, fingers crossed, i'll keep you all updated.

So the moral with LDN, just because we know we can take 4.5ml does not mean that it's the right dose for all of us. I know several people who are on 3 or 3.5ml.

As for everything else, still very busy with work and life.

A constructive day!!!

Having been on LDN since Feb 18th, life is pretty good, not everyday is symptom free, but it would be so much worse if not for LDN. I get some tightening and fuzziness in my left leg, I can identify these symptoms with the life around me, more stress and upset brings out the worst in the MS. However, it is all tolerable and fades away as soon as i get other factors in hand. The bottom line is that LDN is continuing to hold me head above water and I hope it continues and gets even better. In the world of LDN it is still very early days.

Today I spoke with the Essential Health Clinic, I wanted to know if after my scan on July 9th, if i have stenosed veins, will i be able to have the procedure in the London Clinic, they said yes, although still have not finished setting up the London clinic, so will hope to have a better idea of a treatment date when I go to Glasgow for the scan in July.

Still doing bits and pieces with the LDN Research Trust and we are now bringing more things together for the Birmingham conference in October, it's going to be great, if you want come to the event of the year for LDN, join us.

With tomorrow being the World MS Day, there are lots of things going on, including ms-ccsvi-uk you can find them on face book, or here, they are having an open meeting with the MS Society in London about CCSVI, it's going to be very interesting, let's see what they say, the world of CCSVI Is moving on, will the MS Society be part of it or will they shun it AGAIN!!

Ooops, I did it again!!!

Once again life as taken over and I keep forgetting to come and blog for you all. SORRY!

Well, not a lot has changed in the last few weeks, still busy and now taking 4.5ml LDN. It does seem to being it's job. I still have to remember that I have MS, also have some nerve damage in me legs, so even though the energy levels are still up there, I will hurt myself if I do too much. Who knows, maybe one day It will have gone away.

I am going to Glasgow tot the Essential Health Clinic on 9th July for the doppler scan for CCSVI, so fingers crossed there is something that can be done and will improve life even more.

Off to walk the doggie now, so will try to remember to get back to you sooner rather than later with updates

So sorry to have left you all for so long!!

Hi people,

My world has been so busy and crazy, but GOOD!!!!

Health is still good, however dealing with some dizziness at the moment, gets a bit annoying, so tonight I have increased to 4ml, so fingers crossed and it will kick any negatives in to touch. The energy level is huge, working hard and doing lot's for the LDN Research Trust, also running training courses, so busy busy busy.......

So people, life is good, yes? NO LIFE IS AMAZING!!!!!!!!

So now I've been on LDN for just over 2mths, nearly up to 4.5ml and still seeing improvements all the time.

Don't forget that you can join us on the LDN FB page, have a look at the LDN Research Trust website, get the information you need and hopefully help yourself or someone else who has a health issue. All links are on the right.

Love to you all xxxxxx

7.5 weeks in on LDN!!

Well I went to see my GP this week, that is one positive GP, he is now getting more enquiries about LDN, might have something to do with me...LOL and he is willing to prescribe to his many patients if he feels it will not be a negative to them, Go, go, go DOCTOR!!!! He can see my improvement and is very pleased for me.

I did try to move my dosage to the morning's, but no, had some symptoms rear their heads and i felt incredibly tired, so moved straight back to night time dose. Am currently on 3ml and moving up to to 3.5 next Thursday.

Been very busy with my Salon and the LDN Research Trust, constantly seem to be in contact with people with all sorts of ailments and am passing on the information on LDN to them. I also did an interview which is now on the podcast/ldn research trust site, link on the right, there are also a few others on there for other conditions and q&a's, so go have a listen people.

I have another busy week ahead, as I'm sure all weeks will be from now on, but it's all good and positive.

Health wise, thing's are good, and the sun is shining, bring on the spring.

Hope you are all well, take care4 for now. xxxxx

Seeing my GP tomorrow!!

Well, tomorrow I am going to my GP, he needs an update on my condition since starting the LDN, nearly 7 weeks now. I can't wait, I hope the sun is shining, then It can match my mood, when I go bouncing in to his room and throw my arms around him to express my gratitude for prescribing it for me. Well, ok, maybe I'll just sit and smile a HUGE BIG SMILE!! He then needs to give me my next script and then we are off again.

Life has been such a ride lately, now I'm involved with assisting the LDN Research Trust, it's a great thing that we are doing, spreading the word and getting so many people the information on LDN and where and how they can obtain it. It feels very good indeed.

So, me, I'm now almost 7weeks into the journey with LDN and I can't tell you how much of my life it has given me back, I know I still have a way to go, but I can watch and wait while it slowly but surely returns. I'm currently taking 3ml each night. I have had some minor yet repetitive problems with sleep, so after being informed that it can and probably will still work if i take it in the morning, I have decided to start morning dosing prob Friday or Saturday, so I'll let you know how that works.

I have put a link on the right for the BIG ON LDN 2010 in Glasgow in two weeks time, take a look and see if you can come, it's going to an incredible day, so many people and doctors there, that are working with LDN and I am looking forward to hearing from the doctors about the history of their use with LDN.

Also, I have now booked for the Doppler scan for CCSVI in Glasgow at the Essential Health Clinic, I'm going for that appointment on the 9th July, so fingers crossed that it goes well.

I'm gonna pop off now, need to rest and get up for a busy day with work tomorrow. I truly hope that you are all doing well, don't forget, if you need any answers about LDN, I can and will get them for you, just shout.

Luv n gentle hugs
xxxx

Quickie, before i forget...LOL x

To let you all know that, THANK GOD FOR LDN!!

The amount of things i have been doing over the last few days, well, not possible without LDN. I have been very busy helping the LDN research trust in raising awareness and assisting people obtaining information on LDN, from all over the world. It feels so good to help others! I will be back to update with more info in the next couple of days, just for now though, I'm doing great and hope you are all well too.

Love and gentle hugs to you all. xx

FREE to download LDN Research Trust April Newsletter (Low Dose Naltrexone)
PLEASE TAKE A LOOK

Thank You XXX

Long time no see......Happy Easter........

Morning peeps,

Not posted for a while, so here's an update.

Let's get rid of the rubbish stuff first then. My sister finally got in touch this week, it's been 7 weeks since she was just bloody horrible, anyway, nothing has changed and she still believes that she did nothing wrong, so no apology and I finally snapped, I knew that when I said what I said to her, it meant our relationship was over, but enough is enough, I expressed what I thought and then I put the phone down, I did get a lovely call from her husband only minutes later, chastising me for not making it up with her (as he had requested, no ordered me to do) so I also told him where to go. So, I feel sad that this has happened, but at lest I now have closure. So let's move on.

More important things, last night I increased my dose of LDN to 3ml, this mean I am potentially
half way through the dosing amounts now, so if I can tolerate it up at 4.5ml then I have six weeks to go. Still LDN is continuing to improve my condition, however I have had over the past week some cold patches and tingling bits in my legs, it has not stopped me doing anything at all, I'm just aware that this is there. I do really think that with the sister issues and some other stress that has been happening that if i was not on LDN, I would be feeling pretty bad by now, maybe even in relapse? who knows, whatever LDN is doing to my body IT'S WORKING. I've had many late night's and still been pretty fine working and doing bit's the next day, that was not like that before LDN!

Sally and I have been working on the LDN awareness film this week, it's gonna be fab, hope to have up for you all to see soon. It would happen faster if more people would give us a picture of themselves to appear as a snapshot in the film. Come on people, be part of this awareness film, we need real people using LDN for all different conditions, jump on board guys and girls, it's good to help others....

On a lighter note, thought I would let you know that yesterday, out lovely dog Buster, got hold of my sons Vit D3, we think he ate about 300 thousand iu, he is completely fine and showed no signs of anything bad, so just goes to show the VitD3 is very safe.....PHEW!!!!!!!

I will be seeing my GP next friday, need to fill him in on my progress and get my nect script for LDN, I can't wait to go walking, not sjuffling in there with a HUGE smile on my face, and thank him from the bottom of my heart, for giving me a chance to fight this with LDN!

Now then people, don't eat too much chocolate this weekend and take care.....xxxxxxxxxxxxx

LDN awareness video!!

LDN AWARENESS VIDEO

WE NEED YOUR HELP

Hi, we are putting together a video to raise awareness of LDN and its use with the many wide and varied illnesses that it has been associated with. Right, you ask, why do we need your help? Well, we have decided that we would like to include one photo of a person with up to ten of the listed conditions.

Ideally, we would like people from all areas and with all conditions i.e.:
Multiple Sclerosis
Fibromyalgia
Cancer
Crohn's
M.E (CFS)
Graves
ASD
and so on!!

What do we need from you?

Simple really, if you would like to be a part of the video, which we are hoping will be not only
uploaded to Facebook, Twitter and Youtube, but will also be highlighted and shown around the
world on many of the LDN websites, then we need two photographs of you. Both taken on a plain
white or cream background.
Both photos need to be head and shoulders only, one of you looking down at the ground with a neutral facial expression. The second photo needs to be looking directly at the camera, but this time smiling, maybe head tilted or whatever you like.

The purpose of this video is to highlight the positives of LDN and its use, hence the reason we have decided to portray it like this.

There are only two requirements for you to take part:
1: You are willing to have your name and photo included on the video, along with your diagnosis
2: You are using LDN and have had a good response!

We will need nothing further and if we get a large response, then we will notify those selected as soon as we are ready to put it all together.

So, if you are amazed by what LDN has done for your condition, whatever that may be, and if
you, like us, want to spread the word and raise awareness, then please get in
touch.

We need just 2 basic photos as stated above, in colour, (they can be edited, cropped etc this
end) along with your name , contact email (to let you know if you have been chosen) your condition and date of diagnosis, and when you started using LDN. Please forward all entries to
butterfly-ldn@live.co.uk

And that’s it...

Come on, help us spread the word and let’s make this world a better and safer place

Love & Light

Suzanne Harvey & Sally Darin-Brame
xxx

I've missed you all,,,,,,,

Have been so busy this week, not blogged for quite a fewd ays, anyway am back with you today.

LDN Is still doing well, but have had so much to do this week, work, seeing people and catching up with a friend for 2.5hrs on the phone the other night, have not had contact with her for over 7yrs, so alot to talk about, then general stuff to be done for my boys birthday tomorrow. SO BUSY BUSY BUSY!!!!

I am feeling quite tired and can't wait to finish work today. Then I have my son's friends coming over straight from school, pizza and general craziness and then OMG they are staying the night. God help me, roll on Sunday when I can sleep.......AAAAhhhhhhhhhhhhh!!

I have decided to stop taking the high level of VitD3. I started taking it about three wks ago, I think there may be a possibility that it is increasing my body temperature at night, that is causing a major disruption in my sleep. I did not have sleep problems when I started LDN, in fact quite the opposite! So I am going to leave LDN in my system and let it do what it needs to on it's own! Thing's are so much better for me, I can't have and don't want any negatives in my health.

DAY 31 LDN!

Well people, my life is getting better everyday.

My symptoms have exaccerbated again after I increased the dose last Thursday night, however, not as much as 2 wks ago and I have not been that bothered as I was prepared this time. The only symptoms to show up again, are the fuzzy feeling in my arms, maybe a little on my legs, but no biggy, me bothered? Nah!!! At lease now being on 2.5ml, there is actually something to swallow....LOL
I have booked an appointment with my GP for 2 wks time, next script due then. I can't wait to go in there with a big smile on my face, walking with energy and looking, according to dozens of people who know me, "so much healthier and brighter"! :o)
LDN Is working and I can see improvements everyday. I have to keep tagging thing's, it's typical really, when everything is bad it gets noted, but as thing's have improved so much, i keep forgetting to keep a record of them, what seems like little things. Like, when I climb in and out of the bath, I'm not holding anything for my balance, when I stand on one leg to towel dry the other, no wobbling, when I get out of bed, our bed is quite low down, I just get up, no more "brace yourself, lean back, hold on to the bed, then the wall, coz you'll feel weak and dizzy!" The dizziness is pretty much gone, will show it's head when I'm tired or rushing around, "must remember that I should slow down" Yeah right, I've been given a little bit more of a chance again, I'm grabbing it with both hands, Isn't that what life is all about? I'm even thinking about going out on the bike again with my mate Helen, we used to do an average of 30 miles a week! No, won't be doing that much, but a little here and there would be lovely.

Life is good, the sun is out, well a little bit..LOL Spring is here/coming, don't now the official date...LOL and LDN Is wonderful, EVERYONE SHOULD HAVE ACCESS TO IT!!!

Now what else has been happening, well, on Friday night I put up a video, top of my page. It went on You tube and Face book. OMG!!!! The responses I have had,, people have been messaging me, tagging themselves in it, passing it on. MSRC have put it on there pages too, thank you to them! It has been a brilliantly busy and emotional couple of days, it's not over yet either. Messages are still coming in and the video has been around the globe and back again at least a dozen times, it's FAB!!! Helping others, helps us to heal ourselves too!! Feels good, try it!

Sorry not been on to update.

Been a very strange week, Lot's of emotional stuff, some good, some bad, but it's been keeping me wrapped up and away from here. Anyway, am back now.

Firstly you will see a new video at the top right hand of the blog, please watch and leave me your comment's. It's a very personal expression of how MS makes me feel, but not all bad, there are some inspirational and important messages within it, so watch, comment and share it on to as many people as possible. I truly hope it helps many people in expressing to people who don't understand just how MS and many other conditions rip our lives apart, then it's up to us and only us, to rebuild it all again.

So LDN, well I have now passed the four week marker, now on 2.5ml and still seeing improvement's, stamina still going the up, working and generally doing more, shopping, cooking and being part of my little family again. I have seen further improvement in my balance and eyesight too. Sleep is generally disrupted every night, i am still getting overheated at night, but seem to go back to sleep fairly quickly, so not losing too much sleep. So, onwards and upwards I go. Am looking forward to the next increase in 12 days time, wonder what changes that will bring.

Off to la la land now.

Take are my darling friends.

Luv n hugs xoxoxo

Day 25 LDN

Well the sun is shining again, YAY! Most of my symptoms have returned to normal, gonna be careful not to do too much, but all I want to do is go out in the sun. LDN Is working, I can't stress enough how everybody should have access to it, it's so beneficial and is only going to keep on making me stronger. I am definitely going to increase the dose again this Thursday, will be going up to 2.5ml, if I have exacerbation's again, then I will ride through it again.

Saw my mate Sally yesterday, she has just got back from a week or R and R in Italy, she's just over two weeks in on LDN for Fibromyalgia, she's doing so well, look's brighter, more energy and virtually pain free and only taking paracetamol if she needs anything, how cool is that, I mean she had stocks and shares in the drug industry, the amount she used to take was incredible. Luv u Sall, soooo happy for you babes..xxx

Right gonna put the roof down and pop to the shops.

Happy Tuesday to you all

Luv luv luv u xxxx

LDN Doing it's job!

Well just time for a quick update.

I would say, that when I stand back and evaluate, the increased symptoms over the past week are subsiding, so i think that I might go up to 2.5ml next Thursday, however, if I see anything on the negative I will wait a few more days until it looks like a clear run ahead.

I have been out driving around in the sunshine today, with the roof down. 4 weeks ago I thought that, that part of my life was gone, it made stop and take a breath, no, not because I was getting chilly, but because I was reminded that I have, all be it small, but another chance to carry on living. I am well aware that I have MS, but, for now I will continue to heal and hope that the LDN and whatever future treatment's that come my way, are going to mend my body and take away the black cloud that continues to follow me around. It's like walking down the road and being convinced that someone or something is following you. I would so much like not to have that negative lurking behind me. It will go away, it has to. I am not meant to held back in life, there is too much out there.

So off for dinner now, then a full day's work tomorrow.

Wow, a full day? well I never.

Love to all of you xx

Ladu luck is shinging on me today!!!

I am so happy, I've just booked to see Micheal Buble In October at Wembley Arena!!!!! Can't stop smiling....:))))))

Genuinely Caring People!

Wanted to tell you all about the people in my life.

Over this past week, clients have been in and asking me how I am am, you can see how genuinely concerned they are. They also have been asking where David Is (hubby) to which I tell them he had returned to work on Monday. There faces have lit up and you can see how happy they are for us, it touches my heart! I also cleared down my answer machine yesterday, so many repeat messages, checking up on me, my darling husband, my mother in law, my friends and other genuine kind people in my life. It hit me that I am surrounded by so much love, from such lovely people, made me stop and think! I am so lucky, not everyone has this kind of circle to protect them, that's such a shame. We need these people in our lives, we depend on them to hold our hands in the tough times and share our laughter in the good times!

Talking of good times, my darling boy comes home today, after 5 days on an outward bound school trip, we have received text updates from the school on a daily basis, it sounds like they are all having a lot of fun. Picking him up at 5pm, I am so looking forward to seeing him. Of course I will be back on here over the weekend moaning about my stroppy 10yr old that refuses to have a bath and eat his dinner and go to bed when he's told...LOL x

OMG Not posted for 3 days!!

Sorry guy's.

I've had a lot on my mind this week.

Won't bore you with that though.

Day 20 today on LDN. This week I have experienced a recurrence of some symptoms, not awful, but did get me down as it just reminds me that I have MS and it ca n attack at a moments notice. Anyway, glad to tell you that they do seem to be on the way out, so fingers crossed that they continue to bugger off and let me get on with life.

A big thank you to Silvia, I phoned her to get some advice/support, and she was a star, she gave me her time and knowledge of experience on LDN, it set my mind at rest and on we go. Thanks Silvia, you are a star!! xx

Am working this morning, then off to town to get my god-daughter's birthday present, she's 8 tomorrow, I can remember her being born, so tiny and innocent, Not so tiny anymore, innocent? well maybe, although she probably think she knows everything that there is to know, bless her.

So, carrying on with LDN and it's still continuing to keep me out of bed and back to work, it can only get better.

Luv to you all
xxxxxx

Sorry not been on to update, but...

I have been pre-occupied. I have been busy getting my son ready for his first big school trip, he is now away until Friday, no I did not cry when the coach drove away, nearly though! LOL. Also my darling husband went back to work today, they clearly realised that they had made a mistake and asked him to return after laying him off at Xmas. Well it has been a learning curve about the way we live, so lesson learn't, now let's move on.

So LDN?

Well last Thursday night I increased my dose to 2ml, seemed Ok, but late on Friday I noticed how tired I was, then when I went to bed I also noticed a return, all be it small, of some of the fuzzy and cold patches in my lower arms and legs, my eyesight started playing up on Saturday too. Now I don't know if it was the increase in the dose, or the anxiety of my boy going away, or even the fact that although happy for my hubby to return to work, I knew that after two months of him being at home with me, I was going to miss him like crazy. When I look at these factors, who knows what has caused some symptoms to resurface. Well today it looks like they are on there way out again, so we'll never know. What I do know is, after waving off the coach this morning, I went to the bank, then came home and took my dog out for a nice long walk, yes i needed a little rest when I got back, the nerve damage in my left leg was felt on my way home, but then I had been on my feet for a few hours. Have rested and had some lunch, now chilling on-line until my client comes in at 3pm. By the way I also seem to be having a bit of an upset tummy, not blaming the LDN, there are a lot of nasty bugs going round, or maybe it's stress/anxiety?

So two and a half weeks in on the LDN and I would, YES it is working, I have some way to go and need to take care of myself, but with time I am very hopeful that i will continue to improve and keep getting stronger.

Later peeps. xx

THE BEST NEWS!!!!

Today my darling husband has confirmed his new job, he will be starting next Monday! This has put the biggest smile on my face. The last two weeks have been so very positive. What with my health taking a major turn for the better, now his job. Also we had parent's evening yesterday. My boy is either on parr or above and Is doing really well in school. Life is getting better and better. Bring on the CCSVI!

Here I come world, are you ready for the new and improved ME!?

xx

Tonight I'm increasing to 2.ml.. WOOHOOOO!!

Evening all, no I'm not a copper...LOL

Tonight I'm increasing my LDN dose to 2ml, well it's yet another step and am excited as to how it will effect this positivity? We'll see and I'll keep you all updated.

Have had another productive day. Busy with work, popped out in the car, did a little shopping, took our lovely dog out for a walk in the glorious sunshine and worked a few hours. Still increasing energy and getting some seriously deep sleep, god it feels good.
There looks to be some good interest in the information about LDN that I've been passing on, I hope that people manage to get it.

Have a look at the new link I've put up, Invisible Illnesses!. It was made by me dear friend Sally, it is about many condition's, very true and touching, get the tissues out and share it on.

So, another day goes by and I'm getting further and further back to the old me, I only pray that the good times continue, for me and for all of you. Keep safe my friends.

XXXXXXX

OMG!

Forgot to mention that one of my client's came in today, she produced an article that was in her village magazine about the use of LDN for MS, she thought it might be something that I would be interested in. You can imagine my delight at telling her that I have been taking it for nearly two weeks. When I explained to her that it could be used for many other thing's, including Arthritis, she was astonished and is now looking into it for herself. See how one good turn deserves another.....FAB!!!

Day 13....Busy day!

Another productive day!!

LDN is still pushing me back into normal life. My eyesight has definitely improved more, soon be back to complete clarity I hope. The legs are getting stronger, the fuzzy sensations are decreasing too. Still getting a little bit of warm and cold patches randomly throughout the day in arms and legs, but it's getting to the point of being barely noticeable, so it's all good!

Worked a longer day again today and popped out to pick up Sally's little boy from school, he needed to come home because he's hurt his neck, bless, he's having some well deserved bed rest.

Have been passing on the information of LDN to a few more people today. It's shocking just how many people that I see on a daily basis that could benefit from taking LDN! If that's a regular occurrence for most, than it's even more evident that the NHS should look at making it a front line drug option. Will it ever happen? Let's hope so!

Hopeful that my lovely husband has a new job, although back with his previous company. Yes, he was laid off at Christmas. It's been a strain, but we've got through it! Should know for sure over the next couple of days.

Can't think if there's anything else to update you all on, just that life is looking a lot rosier!
Hope the same can be said for some if not all of you.

Take care and see you tomorrow.
xx

Day 12 and rocking n rolling!!!!

Afternoon all,

Today has been a really good day!
I have been very busy and worked for the longest since I came back to work. I am buzzing with energy and could probably have worked for another couple of hours. Am glad I have finished now though, I can sit down on here for a bit then have some grub with my boy's. I have yet again passed on more information to a few more people who will benefit from the use of LDN. It's all I can do to stop talking about LDN, it has made such a huge difference to me in only 12 days, I still can't believe it. I was so close to starting the disease modifying drugs, with such harsh side effects, I feel as if I have had lucky escape, that I have been included in this great secret of LDN! I feel blessed, it has given me so much of my life back that I am so excited as to what will happen when I up the dose this Thursday night, well we'll see. I'll keep you all posted.

Also, my mate Sally is having more good result's, she is on her way to a better life, Soooooo happy for her too!

Have a scrumptious evening all. xxxxxxxxxxxx