MediTest
5 Apr 2019
Author
Kiki
Title

NEWBIE- advice and experiences please! Protocol starting JAN 2019

Body

Hi all incl Sarah and David! I'm new to here. Just recently weeks ago I was diagnosed with intermittant relapsing MS. Seemingly it all started in 2006 with optic neuritis then 2011 with lower limbs tingly,/ numbness. I have been started on daily Copaxen injectitions. But with a severely disabled child Im struggling both physically and mentally. Please help with advice as to how where, who, how much etc to get started on Wheldon Way of treatment. I believe in going in for the underlying cause rather than just band aid stuff. Thank you! Kiki Bojanic

Comments

Lizzie excellent news. Keep us informed as you have been doing. So good to know double hammy improvement in walking and your head. Wonderful!

neena

I am 76 years old. My daughter-in-law was diagnosed with MS and we are all very keen for her to start this new antibiotic treatment. We hope to be able to do this in the next couple of weeks by finding a doctor willing to deal with any issues like reactions that may crop up. My daughter-in-law is 43 years old.

I have been an active poilitical journalist most of my life and have felt for a long time that there must be a cure out there for MS which the medical community has largely ignored. I am very excited by the Wheldon protocol.

Hi everyone,

What I've noticed since Sunday:

at the start and end of the day I'm limping like before, but in between I'm walking totally normally, no limp, and my balance is good. I noticed that I am not swerving to the left. Nor do I have to watch my feet.  

Notice how calm and measured I'm being about this? Impressed? Tee hee! I know I have a loooong way to go, but by god, it's wonderful! 

Byeeeee!

 

Elizabeth Anne

Kiki

dont despair. Just carry on . As Sarah says keep to the five day pulse or three day pulse every 3 weeks. Give your body time to flush out toxins and see how it goes. You will turn a corner so don't lose hope.

best best wishes

neena

I am 76 years old. My daughter-in-law was diagnosed with MS and we are all very keen for her to start this new antibiotic treatment. We hope to be able to do this in the next couple of weeks by finding a doctor willing to deal with any issues like reactions that may crop up. My daughter-in-law is 43 years old.

I have been an active poilitical journalist most of my life and have felt for a long time that there must be a cure out there for MS which the medical community has largely ignored. I am very excited by the Wheldon protocol.

Sarah--

Have a look:

https://europepmc.org/abstract/MED/30148869

 

Also, I think it is very important for anyone trialling Vitamin K to state the type of Vitamin K they are using, so that readers will know what to buy.   The above article is about Vitamin K1, not K2 ... but interestingly is discussing it's use for MS.

 

56 y.o. with possible dual diagnoses that I am working to confirm this year: Ankylosing Spondylitis and Scleroderma, and minor Psoriasis.

Wondering..

So about to start next pulse this coming Monday and theory growing in my mind so thought I'd ask yous all whether you've had/ have samish thought.

Do you feel/felt that when actually doing the pulse you feel physically better ie bad symptoms improving for that brief moment? Im now half year past on doing pulses so the general extra tiredness and sleepyness don't quite affect me as much. Probably as I'm used to this now so don't think about it too much.

I still feel the emotional changes due to taking the Tini and also feel it somewhat til 2/3 days post pulse. But it's been almost as if during ( and only during pulse to be fair) pulse my physicality improves tiny bit making me think I wish I ate the Tini all time. But due to the emotional effects I'm not even going there. Was just wondering whether I'm imagining the feeling better physically bit whilst on Tini.

I shall observe more come next week but if you think thoughts re this please jot down and share. However much of thoughts really.

Kiki💖

So this day has gone all topsy turvy and I just managed my own dinner and last of supplements for the day at 18.45 pm. Question is WHEN  can I  take my Tini pulse dose now? Plus when can I now take the activated charcoal before bedtime?

Normally I take Tini after dinner as all else been taken before. Tho not today..😳

I should leave it for today, maybe taking the charcoal later, then things might be better tomorrow!

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

Hey Kiki!

Your two-hour window around taking Activated Charcoal (AC) is right according to Mayo Clinic.

In general:

AFTER taking any meds and supplements:  I wait at least 1.5 hours BEFORE taking a dose of AC, .... otherwise the AC will just absorb the stuff I've taken.

AFTER taking a dose of AC, I wait at least 1.5 hours BEFORE taking more meds and supps..... otherwise they are just absorbed by the charcoal and I've wasted my meds/supps/money.

I am pushing the window by taking AC at the 1.5 hour mark... I TRY to wait for the full 2 hours on either side, but like you, I am often crunched for time to get all meds and supplements in during the day.   

Sometimes, I just wait until after I've gone to bed.... get up at midnight and take my dose of AC.

 

Wishing you well on this Pulse.... I also started today.

Cheers.

 

56 y.o. with possible dual diagnoses that I am working to confirm this year: Ankylosing Spondylitis and Scleroderma, and minor Psoriasis.

Thanks a million Jan for answer! Popped the Tini 2 hrs past supplement. Just gone to go to bed without the AC as didnt want to risk loosing the Tini purpose but will go back downstairs now to get some AC in me as been 2.5 hrs by now. Feeling loads better armed with your info!

All best Jan with pulse too💖

Kiki

Hi all!

Yep- Im still here albeit sooo busy with kiddies off school!

Just a question if any of yous have found a supplements or such that boost your energylevels up somewhat? All ears and happy to hear all suggestions.

I know protocol might render ones energy somewhat " missing in action" but still..is there anything out there ?

Kiki💖

Caffeine!!

You can get caffeine tablets from Amazon, either plain or with additions.

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

You and bananas..me and coffee haha Sarah!

I did the coffee route loads in my student days. Im thinking more how to get umph back in this weery slow coach of body. Or am I to just have to accept this is the journey now until better days ahead? Has anyone tried ginseng, guarana etc? Or are they poss too weak to have any effect when in combo with abx?

Kiki

Dear Kiki

The Koreans swear by Ginseng but I do not not like it much. Green tea tastes nicer and makes me feel good. Have you tried those green tea jasmine chinese pearls that unfurl when hot water poured over. Simple to make too. No sugar, no milk. just hot water and loads of antioxidants, I am told. xx

Neena .

I am 76 years old. My daughter-in-law was diagnosed with MS and we are all very keen for her to start this new antibiotic treatment. We hope to be able to do this in the next couple of weeks by finding a doctor willing to deal with any issues like reactions that may crop up. My daughter-in-law is 43 years old.

I have been an active poilitical journalist most of my life and have felt for a long time that there must be a cure out there for MS which the medical community has largely ignored. I am very excited by the Wheldon protocol.

How about glucose: I suffer from hypoglycaemia sometimes but a couple of tablespoons dis#olved in water rights that in about 15 mins.

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.