There is also the notion of load dosing in the beginning (2 t for an adult) if you are low and then moving to a maintenance dose ( 1 t for an adult)once the body has “refueled” with Parkinson’s and other conditions. I think I saw that with us. I was testing GSH quite a bit and at first I remember increasing GSH and having the results not showing in the blood test – but then at a point the tests seemed to respond to the dosing…Now we have been at our dose for the last 7-10 lbs.; now about 39 lbs. and about ¾ t. + 2 nebs a day of GSH Plus. I did an annual blood test and GSH was in range, and health seems good so I am just staying at 3/4t. as maintenance. At first I just went by the scale – if weight was climbing I felt like I was OK. Interestingly once we had a nagging cough and I panicked and I knew that another CF parent had used 3 t per day (for a few days) to get over an illness so I tried increasing the dose for a couple of weeks. The cough didn’t go away – in hind sight it was prob. allergies – but the weight went way over the trend line. (I was keeping notes and graphing weight then in an attempt to get a grip on things) Isn’t that interesting? I would love to know if anyone else has thoughts on dosage of lipo vs. caps.... We are giving so many supplements that I try to mix things up – chewables, hiding supps in food. Taking pills, taking liquid – it’s so hard with a child. But it is getting easier. (Wow what a day it was when pills could be swallowed! Changed my life It might be nice to have the option in the house– caps and liquid so life can be as stress less as possible? (Dr. G feels that Lipo can be taken once per day ) I would think as long as you are getting GSH the form wouldn’t matter – but I ‘m not an expert…And - if you are doing well now , maybe not change anything…
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