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FW: update, saw , following Dr. Shoemaker protocol

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Posted

Starting week 4 of CSM therapy and he said I will probably be on that for

awhile since it is making some dramatic progress in eliminating many MS

symptoms, fatigue, muscle pain and essentially put me in my first MS and

otherwise remission in more than 4 years. He cautioned that my MSH blood

level was low (12), magnesium was very low, herpes zoster is highly positive

(not sure why), he is doing some more cultures of my throat looking for

staph which keeps coming back and is labeled MSRA, and anticardiolipin are

elevated but leptin was normal. ( am very thin but used to weigh 125 lbs

more than I do now <120 lbs> about 10 years ago)

See him again in 6 weeks. He said I might consider seeing Dr. S myself due

to the MSH level etc.

In NC

Posted

Glad you are making progress . What does Dr. S treat the low

MSH with? I haven't had time to read anymore of his book. I do recall

that low MSH means low endorphins also. I think that is where the

low dose naltrexone had helped me and still is to a point. Those air

scrubbers really did a number on me as well as the heat. I wonder if

me taking the LDN will not show my true MSH levels. I wouldn't want

to stop my LDN if I get the chance to take CSM. I hope to hear from

my Dr. this week or I may call him. I really want the CSM now.

Anyone else have State Blue Cross Blue Shield insurance that have

seen Dr. S? I emailed with some questions about my insurance and

waiting for a reply. I may call but low on my cell minutes right now

and do not need a long distance telephone bill for the call.

I woke up with that horrible feeling gone thank goodness. Just have

some pricking/shocking right now but I think the barometer def. goes

along with this crazy symptom and I hope the CSM will make this go

away. Never felt such a thing and it will drive me insane if it

keeps doing this. I wish I'd not stayed in my house when the

remediation was taking place.

Rhonda

--- In , " L " <knightshotter@...>

wrote:

>

>

>

> Starting week 4 of CSM therapy and he said I will probably be on

that for

> awhile since it is making some dramatic progress in eliminating

many MS

> symptoms, fatigue, muscle pain and essentially put me in my first

MS and

> otherwise remission in more than 4 years. He cautioned that my MSH

blood

> level was low (12), magnesium was very low, herpes zoster is highly

positive

> (not sure why), he is doing some more cultures of my throat looking

for

> staph which keeps coming back and is labeled MSRA, and

anticardiolipin are

> elevated but leptin was normal. ( am very thin but used to weigh

125 lbs

> more than I do now <120 lbs> about 10 years ago)

>

>

>

> See him again in 6 weeks. He said I might consider seeing Dr. S

myself due

> to the MSH level etc.

>

>

>

> In NC

>

>

>

>

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