Re: Re: LDN in London/okay U Europeans..Update.

[Guest guest]

Hi ,

Thanks for helping me. I spoke to on the telephone and she emailed me all the info I need to bring to my GP for a prescription. I will be seeing my GP this week so fingers crossed.

Ta

scott_627 <kuriouskat@...> wrote:

Hi :I see just posted a message here on this board, #28909 "LDN Research Trust Update". You could reply to that message and get to her directly.Good luck!> > > > > I've just heard about LDN from my sister in Ireland and I'm > > hopeful as > > > > > I have Primary

Progressive MS and have been offered > absolutely > > nothing > > > > > (steroids beta interferon etc). Tell a lie I've been given > a > > > > > wheelchair and crutches!> > > > > > > > > > I'm going to try my MS Consultant in Leeds as I have just > > moved to > > > > > London and have no Consultant down here. If I have no joy > > with her > > > > > any other suggestions for obtaining scripts? Are there any > > dispensing > > > > > Pharmacists in England?> > > > =============> > > > > > > > Help this person get LDN in London.> > > > > > > >

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