Re: new here and questions

[Guest guest]

I also used the shots in the past and I prefer the spray. We've seen some

amazing stories

about benefits... and some experience the same results... and some don't like

the spray. It

seems some people will do better on the spray and some the shots... some maybe

both.

Time will tell. Until then we need to figure it out for our own families the

best we can.

Trying it is the best way to find out for now.

Yes! Valtrex can help on CMV. I would take it asap if I had CMV. There is a

Valtrex

document in the " files " section of our group. Just go login at

http://health.groups.yahoo.com/group/mb12 valtrex/

and click on the " files " link and look for the Valtrex PDF document and look up

dosages.

I believe the adult dosage is 1000mg three times a day and most of the families

with kids

in this group do 250mg 3 times a day. This was the dose my three year old son

was on.

- Stan

>

> I just joined the group, and have a few questions. I have 2 children

> with ASD - they are both on nasal mB12/folinic (we started the spray

> about 1 month ago, after doing the mB12 shots for 1.5 years). I also

> just switched to the nasal spray from the shots. I haven't seen much

> change in the kids from the change, but I feel better on the spray (I

> have autoimmune problems myself) than on the shots. Have others

> noticed a change in their kiddos from the switch?

>

> We do a lot of other biomed also - gfcf diet, LDN, various supplements

> including liposomal glutathione, chelation for my 6 year old.

>

> I have had extreme fatigue after coming down with cytomegalovirus

> about 1 1/2 years ago. I've seen some improvement from MSM, SAMe,

> glutathione, minerals, amino acids, etc. Is there any reason for me to

> think that a course of valtrex might help? Any info appreciated!

>

> What is an appropriate dose of valtex for both me and my son (49 lbs,

> 6 years old)?

>

> thanks!

>

>