CCSVI

[Guest guest]

Janet,

I'm sorry-I didn't mean to worry you with that article.

I think made an excellent point that article is just one " expert

opinion " and this procedure is very new and there are many expert and non-expert

opinions out there that difffer..... As an analogy, look at something like all

the different " expert opinions " on the " right " way to chelate heavy metals. For

every expert who will say chlorella is great, there is another " expert " who will

say it is harmful. Same thing goes for DMSA or DMPS or Zeolites or MMS, etc,

etc. The experts completely disagree. Some people follow Cutler, or Mercola, or

Klinghardt's chelation suggestions with great conviction--yet all of these

protocols are completely different from each other, while others feel strongly

that a particular diet will provide or has provided chelation,etc.....So hence,

again, what said, I agree, this is just one person's opinion regarding

CCSVI, and really doesn't mean much. Besides you do so much research in blood

thinning supplements that I don't think you have anything to worry about in that

regard.

I think because for myself personally I am fearful of CCSVI and scheduled to

have it next month that I am looking for reasons not to proceed, so I find them.

Hence, I will likely cancel my appt as it seems in my head and heart I am not

ready for it. Ss we all know all MS cases are different. In my case, my mobility

is not affected at all but I have many other difficult symptoms which do

interfere very much with my life, but I am always afraid of doing something that

could take away my mobility. Whereas I think for someone who already has

mobility issues, such as being in a wheelchair or walking is getting

progressively worse then I think moving forward with the CCSVI would be more of

a no-brainer.

I hope that takes away any potential worry I might have planted with the article

I posted. That wasn't my intention. It is just I am not ready in my head/heart

for CCSVI. I was hoping someone could contradict the article, which did.

As it is I am worrying about this Prokarin thing I am trying at the moment, but

we will see. When I feel the slightest exta symptom I am ready to stop using the

patch. That is just the way I am wired--a worrier, perhaps

contributes/contributed to my getting MS in the first place.