Who's tried LDN, and what are your results? PART II

Hi ! I'm new to the forum. Longtime UC sufferer like everyone else I have tried just about everything under the sun to treat my symptoms during a flare.  I am going next Thursday (2/16) to see my Gastro Dr and I will be bringing up LDN! He seems open to it when we last spoke briefly about it I didn't have all the information that I have now.

I'm thinking of printing out the Penn State Trials and other articles to bring with me. Anything else I should bring or bring up other than the success stories ?

I searched online for a compounding Pharmacy near me and found one so hopefully he will write me an RX for the medication and I can start on my way! This forum is great for support and no one can understand the disease like US and what a toll it puts on one's life.

Wish me Luck

HockeyGuy1175,

Welcome to the forum.

So great that your doc is open to LDN.

Be careful with fillers, if he's prescribing the oral pills - ask him to write it with sucrose filler which is the hypo-allergenic filler.Unless he's trying you on transdermal LDN first?

Yes, print out and bring with you the Pennstate studies for sure.

Come back and let us know how it goes with the doctor, ok?

Good luck.

 

Please start using Part III. This thread is locked due to length.

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