Severe COPD-Heart-Thyroid and a few more...

Nothing really went wrong except I don't think my son diluted it enough. now today the batch was perfect. I had told him to put some more water in the jar with the shot glass. it was alot better today.

Megg,

Ok, thanks for clearing that up.

Could you tell me what ppm you try for and what do you start out with, like

how many drops of each into shot glass and how many oz or ml of distilled water do you start out with,

what does it test out at on the test strips and how much water do you add to get your ppm!?

---

THIS question is for anyone,

referencing the shot glass method ;

have you found the right mix of drops to water to get it right most times?!

kw

KW,

I am using 24 drops of each in the little bottle. And in the large quart jar I fill halfway, 2 cups of distilled water.
Close it real tight with a plastic lid and I place it in a cupboard for 14 hours.

The solution in the little bottle has very little color. I remove the little jar and then I pour half of the concentrated CDS
from the large jar into another empty quart jar.

Then I filled both jars to the top with distilled water, now each bottle has 32 ounces of ready to drink CDS.

Refrigerate both jars and drink one jar per day by drinking 4 oz every hour for 8 hours.

I used the test strips and the color was on number 50. I asked Pam and she said it is good. It has to be between
30 and 50. But if you do exactly like this you don't need the strips to test.

Charlotte will have specific information for all of us how to make it stronger for those that need to take more.
We are all waiting, hopefully she will have it soon. But the strength I am taking is working really well. My symptoms have
improved so much. I posted my latest report on the Asthma thread and also in the My Progress so Far.

Best wishes to you!
Evanir

Evanir,

Thank you for the details!

And I'm happy for your successes!

kw

Megg,

I read somewhere else that you feel a little better when you take MMS2. I am glad you noticed already, maybe
when you are able to take more you will se a bigger difference.

I am sorry I don't know anything about DMSO. Michael should answer you on that.

Always praying for everyone here in this forum, we need special blessings and healing.

~Evanir

I am working closely with Pam. She guides me and if I have a question she helps but if she doesn't know then she doesnt 't know. So far she has kept me from getting g=sick from the MMS so MMS2 and MMS so are are doing me good. HOw long should one be doing this? I have been on this stuff since July. very small does mind you. My CDS is equivelant to 6 drops and hr and I ma doing great I missed a few days there due to it being so harsh no matter what I did and now my shoulder hurts again. ugg back to square one ...

Maybe not square one Maybe just a day's setback? I hope that's all! The same thing happens to me -- if I slack for any reason the symptoms are worse the next day. The wake up call gets me right back in the saddle and then my symptoms ease off again. It's hard work, but we'll get there!

Mark,
I saw your quote a couple of days ago, but was not a member, so it took a bit to get on again.
I have COPD, Celiac Sprue and also oustio-arthritis. I started using the MM a couple of weeks ago, but had not checked out the site as to a chat type room.
I am a year younger than you, and I want to continue to be busy and help others too. Thank you for your posts on her to Meg. I am going to check out some of the stuff that you did.
Have a blessed one.
Betty

Hye Betty ..welcome to the forum. YEs feel free to search the forum for other tips and sits that they list here also. read read read lol How bad is your COPD betty? My arthritis or wahs getting better until i messed around a few days and didnt take full MMS for a few days and now my leg and arm hurt again.It will get bettter as soon as i get back on course. if you just miss one day its seems like it messes u up for sure.There are a few people on here that can help you if you need specific help on something. Michael...Pam.. are the 2 that I speak to on a regular basis for advice. Good luck in your journey to wellness post any changes or what you are taking and what for so we all know how its going ...again WELCOME

I am on oxygen, and have been for 19 years and a few days.

A friend of mine mixes the stuff for me, and brings it down, as I help him with other things. I told him yesterday that I joined this site, as he is the one that told me about MM. I ordered a bottle, but ended up giving it to him, and thus now I am really getting into using the stuff. I take the tub baths, plus the oral. I am seeing a difference slowly.

I have been searching the other areas of MM site. That is where I decided since their is a chat room of sorts to get to know other people with problems like mine.

My COPD is not the worst that is for sure, and I want to do what I can to get healthier. My siblings are all gone, cancer and heart disease got them. I do belong to COPD International.com.

I am a bit of a health nut in a way, but not always good at following through with my advice, thus I run into problems. Thankful that I can do all that I do, do.

Betty