Dr. Coimbra Protocol

A forum to discuss the Coimbra Protocol which uses high-dose vitamin D3 to treat multiple sclerosis.

Re: Dr. Coimbra Protocol

Postby Kittie » Wed Apr 25, 2018 4:08 am

I have had a week in Southern Spain and found 52,000iu too much after the first day. I went down to 42,000iu and stayed on that for the whole week. The weather was wonderful changing on the day we got there as the weather had been pretty awful previously. We had nearly the whole week with full sunshine. I was feeling good all week and felt really well at the end of it.

On the first morning back, Sunday, my bad leg lifted under the covers all by itself again. Just the once though. I am constantly able to lift my leg in the knee bent lying down position every morning on waking.

On Monday, 23rd April, I took 46,000iu vitamin D3, Tuesday 50,000iu vitamin D3 and today the same. I am going to start decorating my kitchen today too. I will make sure I do not overdo it, taking my time, some every day. Just painting and emulsion. So you see I am getting back to my normal active self. I would not have even attempted this last year. More energy now.

I have also decided to try the Atlas treatment. My right shoulder is two inches higher than my left. I had a car accident when I was twenty but always thought it was my MS that made me that way. Now not so sure and will have xray to see if it can be sorted. I did have my neck put back in place years ago but it didn't last.

Onward and Upward Love and Light,

Kittie.
Kittie
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Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

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Re: Dr. Coimbra Protocol

Postby Kittie » Sat Apr 28, 2018 3:40 am

Last Tuesday my good leg threatened to drop me to the floor occasionally. Then Wednesday, on 50K vitamin D3, it happened more often but not actually giving way. Thursday I dropped D3 to 48K and yesterday, Friday, no problem. I have had good energy all week and at the moment I feel really good.

I am still decorating but making sure I rest often. My energy levels are very good and I feel I am close to the final figure which is good for me. Funny thing I was on 48K when I had to go down to 34K because I couldn't absorb the magnesium. So twice I have ended up at 48K. Maybe this is it. We shall see. What I can say is last year I wouldn't even have had the energy or the incentive to decorate and that is a fact.

This morning, lying in bed, both my legs lifted to the bent knee position together. Normally I have to do the good one first so the bad one knows what to do! When they say that the longer you have had this MS the worse the chance is that you will get the use back in these limbs, I have just thrown that out of the water. I don't know how much I will get back but I will never stop trying to get those messages out and into my limbs. It might be a longer battle but I will do it!

The feeling that I am getting better is wonderful and I wish I could share it with you all, I am contiuously progressing now. It has been a struggle at times but I would say to anyone that this journey has been worth it. Go for it but with a Protocol Doctor who knows what he is doing. I would like to thank my Protocol Doctor Michael Cawley for all he has done for me and would recommend him to anyone.

I will let you know how my Atlas treatment goes and also will keep updating my blog.

Lots of love and light,
Onward and Upward,

Kittie.
Kittie
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Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

Re: Dr. Coimbra Protocol

Postby Kittie » Mon May 07, 2018 2:40 am

Nothing new to report but enjoying the British sunshine while it lasts.

The only problem I have, at the moment, is my bowels opening all the time. What with the diet and ruffage and Magnesium Citrate (only two each morning) my bowels are quite 'soft' and my muscles are not as good as they used to be. Not sure what I am going to do or change at the moment. Okay while I am at home.

I am now going into my 7th month on the protocol and feeling much better than last year. Again time will tell. I am still taking all the supplements listed, taking 2 1/2 litres of water every day, dairy free and meat free. I am having the occasional gluten. The bread in Spain didn't have the same effect on me so I have been trying a few fresh loaves of bread. I eat gluten free bread mainly.

Onward and Upwrd,

Kittie.
Kittie
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Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

Re: Dr. Coimbra Protocol

Postby Kittie » Wed May 09, 2018 6:45 am

I went down to 46K Monday, yesterday and also today. I am also out in the sunshine every day.

Yesterday while puttting my FES machine on I noticed my toes on my bad leg were moving very well. Better than they have for a long time. All of them were moving. I decided to try lifting my bad leg from a sitting position on my typist chair. It also lifted much better than the last time. I have videos to prove it. Something is slowly happening. I must check my lifting into a bent knee position when I am lying on my back. I do that on a morning before I get up.

So when you think things aren't happening, they actually are. I don't think I am any better walking yet.

Onward and Upward,

Kittie.
Kittie
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Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

Re: Dr. Coimbra Protocol

Postby Kittie » Sat May 12, 2018 3:23 am

Still on 46K and feeling really well. Just after my last post I banged my toes coming down stairs. My right leg throws forward and I am not in proper control of it. Still badly bruised but it is okay walking now.

To be honest if it stays like this I will be satisfied, but I feel there is more healing going on. Only time will tell.

Onward and Upward,

Kittie.
Kittie
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Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

Re: Dr. Coimbra Protocol

Postby Kittie » Tue May 15, 2018 9:58 am

Still feeling fine and I have been trying 48,000iu vitamin D3 for a few days but today I took 40,000iu to see if there is any difference. I also took another Ionic magnesium extra yesterday and will today too. My right hand has stayed loose but not as loose as it has been before so trying a few things.

There has been a bit of a change on Facebook and Michael Cawley has his own page now. MS Recovery With Vitamin D3 & Michael Cawley. It is great to have all the people I have made friends with in this group. I feel we are moving forward. Learning all the time.

Onward and Upward,

Kittie.
Kittie
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Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

Re: Dr. Coimbra Protocol

Postby Kittie » Wed May 16, 2018 3:38 am

Yesterday afternoon I felt I was walking better and today also my hand feels better. I have taken 40,000iu vitamin D3 again today and see how it goes. I know using the Gall Pharma B2 Riboflavin whch is activated means you need less vitamin D3. I have posted my videos of my journey on the 'MS Recovery With Vitamin D3 & Michael Cawley' Facebook page.

I think you must always listen to your body.

Onward and Upward,

Kittie.
Kittie
Family Elder
 
Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

Re: Dr. Coimbra Protocol

Postby Kittie » Thu May 17, 2018 12:27 am

Again yesterday my walking was stronger and my hand more relaxed. I am taking 40K of vitamin D3 today again and might even try it lower later. I will see.

Two weeks today is my Atlas treatment and I am getting excited to see what they say.

Onward and Upward,

Kittie.
Kittie
Family Elder
 
Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

Re: Dr. Coimbra Protocol

Postby Kittie » Wed May 23, 2018 5:53 am

Hi again, I am now on 54,000iu of vitamin D3 for the last three days and feeling really well. Michael Cawley suggested I should be going up as I should be able to absorb more vitamin D3 now after all the removal of heavy metals. I have been in my garden the last two days putting in plants. My husband did them all last year so I am thrilled to do them again. I am having a day off today because my legs feel they need a rest. Last year I had terrible balance problems and found it harder and harder to even go out of the front of my house to look at the flowers.

I have recently started taking Biofilam, which is a Natural Iodine Dietary Supplement, one every night before bed. Biofilam's patented brown seaweed extract process was developed by Russian scientists following the Chernobyl nuclear disaster. It is a Radiation and Heavy Metal Detox Support. Other people are having good results from all these detoxing too. Remember the first time I took PectaClear? I got a fine pain shoot up into my brain the first night I took it? This had a similar effect but with loads more like tadpoles shooting everywhere. It didn't hurt but it was weird. Nothing has happened since apart from the odd, short lasting, thick head occasionally. In 2006, approximately, I had three weeks of radiation after going through a lumpectomy so I think there was a lot to be removed!

My new regime is Monday three PectaSol-C, Wednesday the same and Friday (three PectaClear increasing one weekly till I reach 6.) The Biofilam every night. These are all taken before bed and don't forget I have worked up to this level.

I will continue increasing the D3 until my body tells me not to. Always listen to your body! I don't think I will go far though but who knows. I am feeling really well at the moment and pleased with my progress. My Atlas appointment in just over a week.

Love and Light,

Kittie.
Kittie
Family Elder
 
Posts: 143
Joined: Fri Sep 08, 2017 7:53 am

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