Doctors are stumped. Maybe this community can figure it out. NEW PROTOCOL REGIMEN.

Fall - Thank you, your post is greatly appreciated. I know I will beat whatever this is and it will make me healthier in the long run.

Sky - I am doing CDH at 3000ppm in my regimen. The bumps never really "break", or become blisters, but they do itch at the onset and during the duration of the outbreak. While I don't know for a fact that it is HSV2, I know I have something. One doesn't simply continue to break out in bumps they never had before simply because they think they might have something. It all started, along with the swollen lymph node, after unprotected sex with one particular girl.

I will know I am cured when my lymph node returns to it's normal size. It swelled up at the first outbreak and a year and a half later is still swollen. I start my MMS2 tomorrow and am very optimistic. I will actually follow through with the updates as I have read hundreds of posts where people just stop posting halfway through. Whether it works or not, you will have status updates here.

I am currently running protocol 1000+ at 3ml CDH and 3 drops DMSO 99% every hour for 12 hours a day + protocol 3000 (40 drops MMS1 mixed in 2 ounces of water) and DMSO 70% sprayed over my entire genital area. I was spraying my spine (where the virus apparently lives), but I experienced extreme irritation. I am also alternating spraying my forearms and legs with the mix as I don't get any irritation there.

Will keep you posted after introducing MMS2 and switching over to protocol 2000 tomorrow.

Yesterday I had another OB, which is typical. Every month around the 15th is when it happens. I have one little bump, I popped it, sprayed my 20mms:1 ounce water on it, and this morning it was almost gone.

So far, this is the smallest OB I've had which gives me hope.

Last week, when introducing the MMS2, I took a 3/4 full size 0 capsule and ended up puking. Brutal on an empty stomach.

I'll keep you updated.

Another update. About 3 weeks in. I am getting really itchy and puffy around my typical outbreak area. Nothing has broken out, but it's trying. I have been spraying my protocol 3000 mixture on it w/ the dmso and it is reducing the itching and swelling.

I really think it's working, I feel like it's trying to surface. I figure every time it surfaces, and I kill it, that particular group of parasites/infection will not return. Now it's just a matter of how many groups need to be killed before the virus is gone.

My lymph node is still really swollen, I figure because it is still fighting the infection. I am up to 5ml CDH / hour and I'm doing 8-14 hours a day.

not sure about the MMS
keep this in mind,
the Creator gave man HERBS for healing.
find a good herbalist..ayurvedic type naturopath
bulk up on minerals....everyone is low on them
take regular dosage 3x a day for 90 days

coconut oil is a mild antimicrobial, rubs some on and go from there!
alfalfa is an incredible herb, so is olive leaf and pao d'arco
then check out essential oils.....

best wishes

What are you not sure on MMS about Kenneth?

It works....

Correctly applied - it works.

Another update:

I have changed how I am taking it.

I am now putting 10ml CDH into a graduated cylinder, putting in 10 drops DMSO 99.9%, waiting 3 minutes, then shooting it back with distilled water only. Before I was mixing the doses into a bottle and diluting with water, pouring out 1 diluted dose, then adding the DMSO.

My hope with adding the DMSO directly to the CDH, instead of the diluted dose, is that it will bond to the MMS directly to carry it through the body, instead of struggling to bond with the MMS because of the dilution.

I am doing 10ml/hour for as many hours as I am awake. Whenever I take it orally, I apply protocol 3000+ to the area which breaks out.

Every other hour, half hour after the CDH, I take MMS2. I do not take MMS2 before I have eaten, as it was causing me to throw up. The CDH is fine on an empty stomach (huge difference from MMS mixed the standard way).

I was also chasing it down with a pomegranate/water mixed drink, to kill the taste, but apparently pomegranate juice is filled with antioxidants? I am very confused as to the diet/restrictions when taking MMS. There seems to be a lot of conflicting information when it comes to diet.

Everywhere says that you can't take vitamin C with the protocol, which makes sense, but then I read all over the place that you should be eating fruits and veggies, which are packed with vitamin C....

I read that you can use fruit juices, if they are freshly squeezed, to take MMS. Fresh squeezed juice has a higher concentration of vitamin C than packaged juices...

I read that you can take it with pomegranate juice, which has no vitamin C, but apparently its full of antioxidants...

There are also debates on eating meats, cheeses, pastas, rices, etc.

I also take a shot of coconut oil, 1000mg of lysine and 5000iu of vitamin D with every meal, which is about 3 times a day.

Can someone please clear this up for me?

Have you read 32 Reasons MMS not working ? Reason #32 may apply in your case.

I suggest to take all supplements 1 or 2 hours after the last protocol dose of the day.

The CDH is fine on an empty stomach (huge difference from MMS mixed the standard way).

I was also chasing it down with a pomegranate/water mixed drink, to kill the taste, but apparently pomegranate juice is filled with antioxidants?

I would only use water to dilute CDH. And distilled water is probably the best water to use.

For taste, SweetLeaf Brand liquid stevia works for me and it does not taste like other stevias I have tried. This brand has been checked and it does not kill CLO2. I assume you are using 4% HCL when making CDH. I tried using 50% citric acid and it tastes terrible! HCL has no taste.

Thanks for keeping us updated because we can learn from your protocol tweaking, eating habits, etc.

not sure about the correct dosages....for whatever is ailing him.

so, some info til he can figure it out.....sure won't hurt him.

Are you referring to the Lysine and Vitamin D? I should only take those once, at the end of the day?

I am currently not taking any other supplements.

I actually am using Citric Acid 50%. The taste is awful... It's also burning my throat because I am no longer diluting it. I am looking into switching to HCL, I just have a lot of extra citric acid that I have been trying to use.

Also, any insight into the diet questions? I appreciate your responses and the following of this thread. I will use this tweaking/testing to rid myself of whatever this is and spread the word to help others. I can't do it alone though.

Are you referring to the Lysine and Vitamin D? I should only take those once, at the end of the day?

I would take those at the end of the day, yes.

Diet can be tricky. We do need to eat throughout the day, but try not to eat at the same time as dosing. What to eat may make a difference in restoring health. Jim says to eat meat. That may not apply to everyone. If you are not getting better, then try changing your diet.

From Kerri Rivera's 2014 autism book:

Juice is not permitted on this protocol as it has proven time and time again to annul CD and cost families precious time and money.

CD is the same as MMS1.

I am rereading this thread to refresh my memory.

Spray protocol - I would spray undiluted CDS instead of MMS1 or CDH. MMS1 is 7% activated and CDH is 50%. CDS is 100% activated.

Would also suggest to try CDS, diluted, in an enema. Think you could use dosing from this protocol .

Was chatting with a friend on Skype a few minutes ago and he suggested: CDS + DMSO on lower back & upper spine, Iodine and selenium, B12.