i just wanted to pick peoples brains on here if they have come across it
my girlfriends daughter has it, she's 2 and a half and one of the nicest kids you would ever meet. i have pretty much taken her on as my own
it's unbelievable what she as to go through daily ! medicines (a plenty) physio, hospital trips lasting 2 weeks when she gets something as simple as a cold or a cough. all this impacts massively on life, and working life. she seems to take it all in her stride
i was just wondering if there were anything out there to help ? (alternative wise) i have mentioned mms to her to keep the bugs away, but she is wary doing it with someone so young, which i can understand
any help or advice would be gratefully received
thanks
Location: On Earth right now, Tomorrow ~ who knows?
Posts: 168
Cystic fybrosis is a tough one. It's claimed that there is no cure.. though there has been some advancements in treating the symptoms.
Alternatively I believe it's easier to break down it's parts for better understanding.
Cystic or "Cysts": are fluid-filled, round or oval shaped sacs, and be found in different parts of the body, thus leading to the different associated names of disease resulting from them.
Fybrosis or "Fibrosis": normally refers to a large amount of fibrous tissue, the same material that ligaments and scar tissues are made of, whereas the areas of fibrosis feel rubbery, firm, or hard to the touch.
Cystic Fybrosis, is a tough case, since it deals with the scaring of tissue within the lungs mainly. So with reasoning, MMS could possibly help with the symptoms, but since both CDS and MMS primarily deals with pathogens, this might not be the best approach towards getting to the lungs with enough actions to do much good.
Ozone therapy, being the highest on the scale of voltage interactions, is extremely effective in stopping lung congestion, and opening the very small sacs within the lungs for free breathing, and oxygen exchanges with the cells within the blood.
I do tend to question the modern medical concepts that Cystic Fybrosis is caused from the absence of the DNA Chromosome 7, thus thought to be a inherited disease. [According to our modern scientific medical research!]
The deficiencies of proteins as a result from loss of the DNA Chromosome 7 is where the cause lies.. I could be wrong of course, but I think not.
~To try to explain what I'm thinking, is that various proteins, though they are mainly produces in bone marrow, are controlled and regulated by the thymus gland, which also controls the body's hormones & metabolism.
~Another piece of this puzzle with protein deficiencies, [such as found in the loss of functioning of proteins of Chromosome 7] that is associated with growth factors, such as cysts, breast tumors, and goiters.
~Thus I believe that the root of the problem doesn't stop at a defiency of the Chromosome 7, but the "deficiency" of two primary "proteins" that makes it as a part of our DNA.
~ I further believe that a deficiency of Iodine within the thymus gland, could very well be the key to a deeper understanding, and could very well provide positive outcomes, especially since past research of Iodine deficiencies has been established in connection with the formation of goiters, cysts, and deformation such as seen with cretinism.
~Perhaps someday, through more medical research, new discoveries will come ~ to help those suffering from this terrible disease.
Cystic fybrosis is a tough one. It's claimed that there is no cure.. though there has been some advancements in treating the symptoms.
Alternatively I believe it's easier to break down it's parts for better understanding.
Cystic or "Cysts": are fluid-filled, round or oval shaped sacs, and be found in different parts of the body, thus leading to the different associated names of disease resulting from them.
Fybrosis or "Fibrosis": normally refers to a large amount of fibrous tissue, the same material that ligaments and scar tissues are made of, whereas the areas of fibrosis feel rubbery, firm, or hard to the touch.
Cystic Fybrosis, is a tough case, since it deals with the scaring of tissue within the lungs mainly. So with reasoning, MMS could possibly help with the symptoms, but since both CDS and MMS primarily deals with pathogens, this might not be the best approach towards getting to the lungs with enough actions to do much good.
Ozone therapy, being the highest on the scale of voltage interactions, is extremely effective in stopping lung congestion, and opening the very small sacs within the lungs for free breathing, and oxygen exchanges with the cells within the blood.
I do tend to question the modern medical concepts that Cystic Fybrosis is caused from the absence of the DNA Chromosome 7, thus thought to be a inherited disease. [According to our modern scientific medical research!]
The deficiencies of proteins as a result from loss of the DNA Chromosome 7 is where the cause lies.. I could be wrong of course, but I think not.
~To try to explain what I'm thinking, is that various proteins, though they are mainly produces in bone marrow, are controlled and regulated by the thymus gland, which also controls the body's hormones & metabolism.
~Another piece of this puzzle with protein deficiencies, [such as found in the loss of functioning of proteins of Chromosome 7] that is associated with growth factors, such as cysts, breast tumors, and goiters.
~Thus I believe that the root of the problem doesn't stop at a defiency of the Chromosome 7, but the "deficiency" of two primary "proteins" that makes it as a part of our DNA.
~ I further believe that a deficiency of Iodine within the thymus gland, could very well be the key to a deeper understanding, and could very well provide positive outcomes, especially since past research of Iodine deficiencies has been established in connection with the formation of goiters, cysts, and deformation such as seen with cretinism.
~Perhaps someday, through more medical research, new discoveries will come ~ to help those suffering from this terrible disease.
thanks a lot hobo (AGAIN)
would the mms not rid the body of the colds and couughs that would damage her lungs though
that was the theory in my madness so to speak
Location: On Earth right now, Tomorrow ~ who knows?
Posts: 168
Hello nickmatt,
Concerning MMS, it works well on cold and flu, however, there is another method to consider, that would require a little time to study, but well worth the reads. okay.
~ if you research into my above post, you'll find it enlightening . Here are some studies: https://www.drugs.com/ppa/iodine.html
Hello nickmatt,
Concerning MMS, it works well on cold and flu, however, there is another method to consider, that would require a little time to study, but well worth the reads. okay.
~ if you research into my above post, you'll find it enlightening . Here are some studies: https://www.drugs.com/ppa/iodine.html
cystic fibrosis
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