Fw: Stem Cell Treatment

[Guest guest]

Having read the articles in MS Matters and the local news sheet. It is time some

one else had a say about the Stem Cell Therapy after the bad press issued by the

Drug Companies, Neuropaths and Doctors. People who themselves cannot supply a

cure, only drugs to hopefully, in about 25% of cases, slow down the progress of

MS, which have in a lot of cases side effects that themselves could require more

drugs.

Soon after I was diagnosed I joined the branch where I met an MS'er who had had

the MonSter for 39 years. I said " There will be a cure in the next few years "

Her reply was " They told me the same thing when I was diagnosed "

Now that was 33 years ago " What has improved. "

Doing some research on the internet the only MS'ers that are showing signs of

improvement are those who are taking the Alternative route. Not slowing down but

actual improvements. All of these therapies are cried down by the professional

medics. Low Dose Naltrexone is showing a 76% improvement rate. Stem Cells are at

about 80%. But it must be said the only people claiming the success are those

who are actually having the treatments.

The LDN not being supplied by the NHS it's one of the " post code " lottery items,

but it can be obtained from a Doctor in Wales, who himself has MS, at a price.

The same can be said about Stem Cells available at a price.

Other stratagies include Glyconutrients, bee stings, goats serum, the Prokarin

patch and Colloidal silver.

Symptoms can also be relieved by doing the Best Bet Diet, food supplements,

exercise, detoxification and a low stress life style. So all is not lost.

I'm now secondary progressive, so what can I do? Too late in MS stakes for the

interferons, just sit back and wait patiently for the drug companies to find a

new stem cell treatment. Talk of about a 10 year time lapse. Just waiting for

the next piece to stop working. There's not many left I must add.

So with my mother's help I took my only option to have the Stem Cell Therapy and

4 weeks later I'm pleased to state there have been some improvements in my

health. My hands are steadier, body temperature control has improved, my spine

has gained back some agility, energy levels are up and I can now enjoy long

days. The effects of the one treatment as the cells multiply goes on for up to a

year, so I'm looking for even more improvements to follow.

What a difference in life, to wake in the morning wondering what extra can I do

today.

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