My deepest condolences Dee. My battle to try to save my fur-daughter Ginger from what turned out to be Hemangiosarcoma was what lead me to discover MMS. Unfortunately, all I knew up until the day I lost her was that she had a tumor in her spleen.
With a combination of CS and MMS1, she almost doubled the average diagnosis to death time for this killer; but, my not knowing that it also attacks the liver and kidneys made it all but impossible for me to get her "ahead of it" without Herxing; since, her liver and kidneys were too compromised to handle the detoxing needed to get ahead of such an aggressive form of cancer. I understand that it doesn't help the feelings of loss; but, it does help to remember that dogs are spiritual beings with souls, too; and, that those we are very close to are part of our soul groups. We WILL be reunited with them - if not on this side, on the other.
I'm, personally, pouring my grief and anger into fighting back against those who are responsible for our not having access to effective treatments (for both 2 and 4 legged loved ones.) In "a perfect world," MDs and DVMs would have learned about all the effective (alternative) treatments in their years of study and would have things such as dialysis and Rife machines in their offices. Instead of GARBAGE like prednizone (which I refused to give her because of the damage it does to the immune system), they'd be using things like MMS, CS, H2O2, etc. Because of greed, we're left scrambling for solutions while running on almost no sleep when an emergency occurs. I'm learning things now which could potentially have saved her (had I known what I was really fighting); but, the time just wasn't there to cram that much info. into my sleep deprived, fibro-fogged brain.
All I can do at this point is learn every thing I can to be better prepared in the future; and, share what I've learned as I go along, to help others AND to divert every cent possible away from the greedy scumbags who've prevented effective treatments for so many things from being commonplace within mainstream medicine.
I don't know the answer to your original question; but, as for treating Lyme with MMS, yes it does work; but, it takes longer to treat Lyme than it does almost anything else. The spirroquettes (I know I butchered the spelling; but, I'm too tired right now to google the correct spelling) are quite effective at hiding themselves from the immune system. I've been looking into this as I have time, due to the possible links between undiagnosed Lyme and fibromyalgia.