Anyone tried boosting their Iodine levels?

19 days of using Iodine & the clarity is abundant. Such a simple common substance, that the human body requires & I’m flabbergasted by the results so far. I’ve even moved up a notch & increased to 8 drops of 15% Lugols in a pint of tap water. 3 to 4 times a day. Along with all the other supplements, healthy eating & exercise. The most noticeable change is my veins seem more pronounced & circulation is far better. My skin & nails are looking healthier & I’m far less jittery. My confidence seems to be coming back, to try more & more. Pushing myself much further. My cloudy vision has improved too. All in all it’s good stuff. Off to the MS group now for chips & chats. Stay positive & hopeful folks.

Terry, have you tried Biotin yet?

Admittedly it can take up to nine months to work at full potential and it works better for some than for others, it’s a natural product (B7) and can now be bought in the UK…I can’t recommend it highly enough!

Nina

I haven’t tried Biotin Nina. I’ve developed a fobia against anything for MS.

The folks I know, compare boils to MS. I get hounded by drunks, addicts & the mentally challenged.

If I say I have a health problem, it’s a never ending list of gobbaldy gook.

So & so cured their MS with this & that. Then became a Billionaire & brought a pogo stick to travel the earth. That’s why we never see or hear from them again. They’re busy doing stuff & contributing to society. Believe it or not.

The B vitamins seem good for most problems. I’ll keep tabs on Biotin Nina, thank you.

I’m just going to take my teaspoon for a walk…

Hi Nina. I just started on biotin this week! I’ll give an opinion in the months to come.

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Good luck Poppy!

I found that some of the odd little symptoms disappeared quite quickly, the problem being that if it gets rid of odd symptoms that you don’t have all the time you don’t actually notice they have gone. I found that when I had to stop biotin was when all the little things came back so I really do appreciate what it has done for me but the biggest improvement was in my walking, I still use a stick when I’m out because I’m so weak but otherwise I think my walking looks almost normal. I do know someone that has had massive improvements even with fatigue and whilst she is far from cured she leads an almost normal life now from being housebound, it’s amazing and well worth a try!

Take Care,

Nina x

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The Iodine trial is going great.

Keep taking what your doctors tell you.

I know what I’ll be doing.

Avoiding the so called experts, with years of experience.

It’s not who you know! I’m nobody & know nothing.

6 weeks using Lugols Iodine so far & the stuff seems magic.

It’s been added to my routine, with Selenium, B12, B6, D3 & CBD oil.

Buying them all from Ebay, so 2 days after paying, they’re at my door.

Happy trails folks. Use it or lose it!

Terry

Hi there Jackie. Take it easy & stick to your system. Whatever works for you, is what works.

Some folks are so trusting of others who haven’t got a clue. Knowing someone with MS, makes some thinks they know it all…

No matter what the subject, there’s always clueless know it alls. Judging things by their imagination.

Peace on Earth.

Terry

Just been to the local MS group & advised on taking other medications, yet again!

Not one person, even considers using Iodine. When it’s plain to see, what it’s doing for me.

Seen yet another wheelchair convert, as some give up. Signing forms to even stand up.

It’s not even a joke.

Take it easy out there & keep trying to boost that circulation.

Hi Terry,

Good to see you on here and that you’ve been to your MS group - I’ve still not ventured to one yet :-/

I’m glad that your Iodine ‘experiment’ is no longer an experiment and is now working wonders for you, and that you’ve been doing great so maybe others who see you will one day suddenly realise that, and think to themselves ‘I’ll have a go at that’.

You just keep doing what’s working for you as it obviously is :slight_smile:

Take Care.

Twinkle Toes x

Howdy TT. I’ll always be here. I might be busy making tunes some times, but there’s not many places to go, where folks understand what PPMS is actually like. I see people from all different walks of life, going to the MS events. Be it volunteers or carers. It’s a very mixed bag of fruit cakes.

Secondary Progressive Multiple Sclerosis seem a tough group.

I suppose when you’ve been through their trials, you get a bit tetchy. People seem to cling on to the hope of a cure for this nasty condition. I wont be touching medication again, no matter what miracles they say.

Trying different things, to see how they improve the circumstance, seems to be good.

No matter what we try. Keeping active & the system circulating. Seems the way.

I play scrabble, word, chess & make stuff. With others suffering MS.

It keeps us ticking over & the brains active.

People tend to avoid traffic jams.

I’m still drinking my pints of water with drops of Iodine & it’s had only positive results. I’m even planning to buy another bottle & the other is half full. Been putting drops on my tongue, to clear it up. Food even tastes better now. I even drip it on my nails after a trim & it’s made them super tough.

Why on earth they took Iodine out of bread & milk in the 70’s is beyond reason. A cheaper chemical, that would kill us quicker, is used these days. Create the problems & cash in later.

Iodine is fantastic!

An update. Iodine is awesome! Months of use & magnificent changes.

It isn’t a cure, but it’s darn good.

Get on with life & do stuff. Avoid scroungers & use it or lose it.

Sit still for too long & the vultures gather.

The Iodine addiction, is like wanting to breath in a smoggy environment. A very natural element, that was once the staple in bread & milk. Then withdrawn because a cheaper more hazardous product could be used.

Be careful not to drink to much tea & you should stop anything they tell you.

Been going for a full English breakfast most days & pigging out. Folks have been commenting on how well I’m looking & doing. My neurologist still refuses to see me & the MS nurses are getting as rare as hens teeth.

Keep taking the medications & fare the well out there.

Eating healthy & exercising is the cure. Steering well clear of stress heads & the gossip squad.

Terry is still doing good stuff & soon I’ll be stuffing a turkey.

Glad to hear you’re sounding more ‘upbeat’ again Terry, take care.

Pam x

Hi there Pam. I try to stay upbeat surrounded by drug addicts with money issues.

It’s tough being a quiet noisy person, when everyone is shouting.

I can still hear their whining, when I’m in natures stillness.

Do this, do that. Have you seen this & that. Saying get lost, falls on deaf ears.

Take care of yourself Pam, before the carers move in. They care about one thing.

It’s time for a pint of water with 5 drops of Iodine.

Greetings fellow Primary Progressive Multiple Sclerosis sufferers. How’s everyone doing out there? Supping Iodine, drinking coffee & feeding the flying creatures. Off bargain hunting in the charity shops today. A way to avoid the constant barrage of scam calls. The local drug dealers seem to be leaving me alone, which is awesome. They must be bored or too stoned. I’m loving these sharp, brisk mornings. Very invigorating. Nature is a bit bare & damp. Stay active & keep doing what works for you. Terry is having a ball.

.i hope you have a nice time Terry .we have some fantastic charity shops in Frodsham. Frazer loves picking his toys from the collection of teddies. He was once very naughty and not the arm of a soft toy cat just so I had to buy it. I sewed the arm back on when we got home and he’s never tried to bite it off again , he’s clever . The worst thing he did in a shop was help himself to pick and mix . The box was at nose level and temptation got the better of him . He was allot younger then and only recently partnered with me. The staff in the shop still laugh over it .

michelle and Frazer xx

Glad to hear you are ok Terry, and I agree I love looking around the charity shops for a bargain.

Michelle that did make me laugh about Fraser, perhaps he could get some pic and mix for me when he is next out and about! I bet the staff had a good chuckle about it.

Pam x

I’m a bit like Frazer. I steer clear of pick & mix these days. The folks I know would claim it causes MS. There’s some very odd people about. They even whine about my charity shop addiction, saying that isn’t why we get financial help. Nowt funnier than folk! I’ve even cured MS with Iodine according to their version of reality. Keep doing things to improve your life. The freaks don’t like it. Posting selfies in front of giant posters at the cinema, claiming to be in another world & they’ll get you sectioned as a looney. When in reality, the shoe fits the stalker. MS (micro soft) fleece blankets rock.