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Hallo all,

just want to say " everything is going well " till now.

Starting tomorrow with round 10 DMSA (25 mg.); taking lots of supplements.

I have m.s. for about 27 years ( " just the symptoms " = diagnosis),

am mobile in the house, can drive the car, but cannot walk outside/longer

distances

anymore, this year. I manage(d) to walk from the car to the dentist (thanks

god).

So use a wheelchair for outside.

Lots of little things are happening, but 2 " big " changes are:

numbness under my feet is less (sometimes totally away, especially in the night)

..

And the feeling of my fingers(tips) is almost normal again.

Also my mood often is better/great. Sometimes my energy is great too.

But 50% of the time it is as bad as it was before. Stiff legs, poor balance are

almost always

there. During, after rounds: no real difference; everyday (or part of a day) is

different.

But I am about (3) years pretty bad, have just started and am 2 months

amalgam-free.

In about 2 weeks I am going to add ALA (25 mg.) with the DMSA. Off course I hope

my

balance and stiff legs are more brain/spinal cord issues and I'll " notice "

something, but I

understand that everything will take/needs time, every person is different, etc.

Could you

comment something about these last lines, about the brain/spinal cord ?

By the way: great site; you can learn a lot !!

Thank you in advance.

Greetings, Simon

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