Lyme and protocol 1000 plus, rash, exhaustion.

Thank you so much for your reply. Unfortunately I had a sudden death in my family and had to travel to the other side of the globe stopping completely my MMS after just one month. Interesting the itch is almost gone, barely there, my legs healed. Your description though matched almost perfectly my symptoms. Scratch till you bleed, no matter what...yes. I do plan to restart MMS soon and see what happens. I am also going to see a new dr in June who specializes in Lyme and see what he says. Sharing every little bit of info helps, so thank you again.

My sons found out they have had Lyme for years and other co-infections along with everything else that goes along with late stage Lyme. They take things to help keep the liver flushing and they had to go Very slowly with MMS. They have probably been taking it for about 8 months. One of them is up to 8 drops a day and the other about 13. They will have days of bad herxing and will have to back down a drop or two, but they never stop and then they work back up again. They can only get to feeling so bad because they have to work. They mix their drops in 24 ounces of water and drink it throughout the day. In our experience we don't feel enough is said about if someone is really bad they may have to go really slow. When my son received is results from the Lyme his Lyme doctor said he had not seen levels that high in years, so it could be because he had so much going on in his body. He would herx so bad we had to call the squad different times.
Has anyone else had to move this slow?

Hi yes l have been chronically ill with Lyme for 40yrs. I was bed and housebound for 10yrs and still have to pace and rest l have spent thousands of pounds on every treatment under the sun.  My worst symptoms are neurological tremors, joint pain, eye sight, and fatigue. I started mms 4 months ago and  an only manage 1 drop hourly for 8 hours and e even that is giving me herx. My moods though have really improved and l feel a lot more optimistic. At the moment the mms is causing a lot of pain in my hips and back which have always had problems. This l can see is going to be a long journey but it helps to read other people's stories and recoveries. 
 

Hello Zizi50, I understand your concern as I too have Lyme disease I’m new to this as well I went from taking two doses two days ago that first day to taking three yesterday, I too got a little nauseous and lots of diarrhea. Yes you should slow down I’m going back to two drops later today. As far as your exhaustion I believe it is a detoxing reaction from the Lyme though probably from the mold. You always want to the starting procedure first then the mold fungus procedure the the standard protocol 1000. I was very exhausted when doing the clay protocol though it was easy and I did a quicker version of the starting procedure. I recommend just being consistent on the two drops and I believe it’ll improve with time. Something I’m learning is dealing with the taste which is terrible I’ve had a lot of bad tastes from supplements and drugs, etc, over the years nothing compares to MMS. I recommend if the taste is troublesome to take the dose while not breathing through your nose then right after drink a little bit of water with stevia in it. This will help get rid of the taste almost instantly. Also there have been studies done showing stevia can be promising in killing Lyme disease by destroying the Lyme biofilm over time. Two Lyme destroyers at once. Can’t be too bad, Good luck and be safe.

Hi - for those who were taking MMS already at the beginning of the year, would you mind sharing your update on progress? I seriously suspect that I have given Lyme disease, EBV and coxsackie to my daughter during pregnancy. She's 15 now, and it proves difficult to 'keep the faith' for her to keep going. We need some promising stories, please anybody out there who was successful with this for lyme, can you comment please?

Greetings!
You said you’re new with protocol for Lyme Disease. A friend in Texas has Lyme D. With Morgellons. Lots of biofilament coming out from all parts of the body including urine. She went through antibiotics supposedly from a Morgellons “expert”. It hasn’t done anything to reduce Morgellons. 

Just wondered if you would kindly keep us abreast with this mms endeavour?And if not intruding, do you also have Morgellons? 

Regards,
Cupped. 

Hi Marino, I'm also interested in comments you might receive from your post today. My daughter turns 20 tomorrow and has been progresively sick and disabled with Lyme/co-infections since she was 15. She tried really hard for almost three years with herbals, diets, etc. and finally lost faith to the point where now she won't even discuss doing any treatment... I recently starting taking MMS for some skin cancer on my face and even though I have Jim Humble's book and have read it several times, I decided to watch The Universal Antidote and learned more. You might be interested and encouraged to watch a testimonial of a young woman using MMS to heal from Lyme around the 57 minute mark. Blessings to you and your daughter and I hope you get comments here.

rumble.com/vdey7t-the-universal-antidote.html

Hi Marina!

im a 31 year old recovery of chronic Lyme and ebv… I also almost died after contracting Coxsackie from cleaning a composting toilet… so I feel I can offer some hope…

it does work but you have to think of it in two stages… first is killing and removing the pathogens… second is rebuilding all the tissues and organs they’ve destroyed…

Killing everything won’t take longer than a month or two if you follow the protocols correctly… however it could be a long haul to heal all the damage that’s been done. First you put out the fire and then you repair the building.

I think I’ve flushed the Lyme out of my system but now I’m rebuilding all the damage and I feel a lot of fatigue in this process.

how long has your daughter been on mms?