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Multiple sclerosis -UK based homeopath or smo treating MS

Hello, I am searching for trusted homeopath who is in UK, esp. London based and who has experience with people suffering from Multiple sclerosis. If the person is from another country we can follow advices only online.
My partner has been diagnosed for more than 1 year. He started with conventional medicine - Copaxone injection with no possitive result. Then he started with alternative mdicine like - Chinise accupuncture, massage, hypebaric oxygen teraphy, herbs and teas. He aven tried homeopatic remedies and got worse. There is no enhancement and he is getting worse.
Please, help me find out someone who can really help.

Thank you very much in advance.
  Mishelina on 2012-10-28
This is just a forum. Assume posts are not from medical professionals.
Many people are finding relief with Low dose Naltrexone.
Google this and ldnrs.org-Naltrexone is FDA approved in
large doses for drug addicts. Small doses at night shut down
opiate receptors and then when it wears off the nerves are flooded
with endorphins. You have to get the low dose either by
ordering the high dose and making low dose yourself or finding
right compounding pharmacies. Tons of groups of these
people helping each other and sharing info. I spent an entire
day reading some blogs of people taking it for other reasons-
(autoimmune) and found that now some are using it in Ultra
low dose and moving up in potency as a more effective way-But to
do ultra low dose - you have to get 'pipettes'to draw out
the micro dose.

On homeopaths-MS is hard to treat. You can go to Minimum books
dot com and google Andre Saine ( head of homeopaths in Canada)
you may want to purchase his 'MS' papers- he has healed MS.
But he is someone who is probably as easy to see as the Queen.
You have to keep googling countries and asking who has
done this well etc.

Another option is go to You tube and click on MS patients who
got treatment at Panama City in Panama ( stem cell therapy)
Not costa Rica but the Panama city hospital. Very impressive.
They are using cells from your own body and from donated
umbiical cord cells so this is ethical and they are having
very good results-see the patients speaking from USA.
simone717 9 years ago
Dear Simone717,
Thank you very much for your prompt response. I forgot to mention that he has taken LDN from the very beggining since he was diagnosed. He makes the liquid by himself, once he had it made by pharmacists. He takes now 4 ml. every night. However the symtopms are getting worse and he still has an active zone in the brain and spine. His body is rejecting steroids and Copaxone. The neurologist recommended taking Rebif, but he rejects taking any Interferons (expensive crap made by pharmasuitical companies.
We are googling for more info every single day, hoping that we will find something that can help him.
I have also done a research about the stem cell therapy, but I've always thought that MS cannot be treated with stem cells.
We were also considering ozone theraphy, but after the failure with HBO, we decided to wait.
If you think of anything else you want to share, please let me know.
Thanks again,
[message edited by Mishelina on Mon, 29 Oct 2012 08:27:50 GMT]
Mishelina 9 years ago
I hope you looked at the youtube MS patients that
were from USA and talking at the clinic in Panama City.
It makes sense to me that it can work and it has
worked- as some other autoimmune diseases where
nerves are being destroyed are being helped by
stem cell hospital stay in China where they have combined
the stem cells with acupuncture treatment at same time
to restimulate and regrow the nerves. An Aussie woman
is coming out with a book on her treatment there.
and another woman in USA a health worker was
asking for donations on the street corner in Santa Barbara
one weekend and it so happened that some Tech
billionaire got lost and was on that street corner. He funded
her entire treatment and is now trying to make efforts
that this system is available in USA.

I think the China cost is$30,000 and the Panama cost
is less but still up there. If I find things I will let you know.
[message edited by simone717 on Mon, 29 Oct 2012 20:05:04 GMT]
simone717 9 years ago
Dear Simone,
Thanks again for the comprehensive answer and understanding.
Well, the stem cell therapy is quite expensive and at this stage we cannot afford it.
However, we will try other alternatives and I will let you know.

Take care,
Mishelina 9 years ago

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