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I was wondering if anyone has switched from transdermal cream to pills?

Do IBD'ers experience issues with the pills if they have adjusted to

transdermal LDN?

Also, when would I know it's time to up my dosage from 3 to 4.5?

The McCandles transdermal RX from Coastal is making a difference- I am

not experiencing such intense bouts of stiffness? Does this make sense?

Thanks for all your help and although late happy T'giving everyone!!

Jodi

Crohn's/Colitis

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