Guest guest Posted March 27, 2008 Report Share Posted March 27, 2008 I have Dr. Gluck's permission to post the following letter. Warm wishes to all, Jan ******************************************************* Dear LDN Supporters, WE NEED YOUR HELP! Once Dr Tom Gilhooly's first trial of LDN on the bladder is complete, it will lead the way for the next trial. Dr Tom suggested THAT an all-singing all-dancing trial of LDN for Multiple Sclerosis will cost in the region of £2 million, which isn't a great deal of money in research terms, although for a small charity like ours it is a vast fortune. With this in mind, we need to set the wheels in motion and get fund raising underway as soon as possible. We have a great way in which you can help us to raise funds, thanks to Alan Howland, who is undertaking a 300K cycle ride from London to Paris . Alan is paying ALL his own expenses so that 100% monies donated will go towards a FULL TRIAL. Alan's employers are supporting him all the way, and will MATCH DONATIONS up to £500. We thank them for their help and support. Are you up for the challenge to help us raise £2 million? What I would like to ask each and every one of you is for all your help and support. We can't do this alone; we really need your help! Every penny helps- together we can achieve SO MUCH. · Could you sponsor Alan for just £1? (Or more if you can afford it.) This would become £2 with the help of his employers. Plus, if you are a UK taxpayer we can claim 22p tax back, which would turn your £1 into £2.22. · Please check out Alan's sponsored page…. www.mycharitypage.com/alan · We want to start an LDN campaign · Could you pass the above link to everyone in your address book? · Could you post the link on as many MS & LDN websites as possible? · Would you be interested in taking part in press coverage in your area? (If so, please email me). .. You can send your sponsor money either: v Online, using Alan's page v Posting to: LDN Research Trust, PO Box 1083 , Buxton, Norwich NR10 5WY v Paying Directly into our bank account: Barclay's Bank Sort Code 2-03-26 Account No 60515213 I'm sending this email to over 3,000 people and that is just the starting point. If each of you then send it to just 2 people that makes 6,000. If they each send it to 2 people that is 12,000. I think you can see where this is going… If each person made a donation of just £1, the £2 million would soon be reached. This will only work if YOU help and not think " I will leave it to the others to take part " We really do need YOU. We could all make excuses why we can't or don't want to get involved, but by doing nothing, nothing will ever get done. We have just over 4 months. Can we count on you to help please? I know there are a lot of if's, but isn't it about time people with MS had a drug like LDN, which isn't toxic, has been fully trialled and tested and is readily available to all? It would mean so much to people NOT to hear from their Neurologist. " I'm sorry you are Secondary/Primary Progressive MS, and there is nothing more I can do for you. " Hopefully with YOUR help we can make statements like that a thing of the PAST!!! It is important to remember that the LDN Research Trust doesn't pay any salaries, and only running costs are covered by the charity. I hope you are as passionate about LDN as I am, and I hope to hear from you if you have ideas to share or your LDN story. Be part of the BIGGER picture today, by forwarding this email. I sincerely thank you all for listening to me. contact@... www.ldnresearchtrust.org Tel. No: 871 989 96 66 A note from Alan…… The reason I'm sponsoring the LDN Research Trust is because of my good friend Graham Robson- who has MS. I've known Graham for about 16 years, first as the " bloke " at the pet shop, then as my boss and recently as a close friend. I'm sure you can appreciate its always difficult to see a very active person start to lose their mobility and dexterity and suffer in the way they do. Please support me all you can to get a full LDN trial underway. Many Thanks Alan Howland Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2008 Report Share Posted March 27, 2008 Hmmm, this looks familiar. Message number 62447. Art -- > > I have Dr. Gluck's permission to post the following letter. > > Warm wishes to all, > > Jan > ******************************************************* > > Dear LDN Supporters, > WE NEED YOUR HELP! Once Dr Tom Gilhooly's first trial of LDN on the > bladder is complete, it will lead the way for the next > trial. > Dr Tom suggested THAT an all-singing all-dancing trial of LDN for > Multiple Sclerosis will cost in the region of £2 million, which isn't > a great deal of money in research terms, although for a small charity > like ours it is a vast fortune. > With this in mind, we need to set the wheels in motion and get fund Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2008 Report Share Posted March 27, 2008 What do you mean Art (for us who are new)? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2008 Report Share Posted March 27, 2008 I posted this today at 12:53PM message number 62447. -Art Diagnosed with MS April 1988 Using LDN since March 2005 -- > > What do you mean Art (for us who are new)? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2008 Report Share Posted March 27, 2008 I will donate $100 US. Aletha [low dose naltrexone] "We Need Your Help!" I have Dr. Gluck's permission to post the following letter.Warm wishes to all,Jan*******************************************************Dear LDN Supporters,WE NEED YOUR HELP! Once Dr Tom Gilhooly's first trial of LDN on the bladder is complete, it will lead the way for the next trial.Dr Tom suggested THAT an all-singing all-dancing trial of LDN for Multiple Sclerosis will cost in the region of £2 million, which isn't a great deal of money in research terms, although for a small charity like ours it is a vast fortune. With this in mind, we need to set the wheels in motion and get fund raising underway as soon as possible.We have a great way in which you can help us to raise funds, thanks to Alan Howland, who is undertaking a 300K cycle ride from London to Paris . Alan is paying ALL his own expenses so that 100% monies donated will go towards a FULL TRIAL.Alan's employers are supporting him all the way, and will MATCH DONATIONS up to £500. We thank them for their help and support.Are you up for the challenge to help us raise £2 million?What I would like to ask each and every one of you is for all your help and support. We can't do this alone; we really need your help! Every penny helps- together we can achieve SO MUCH.· Could you sponsor Alan for just £1? (Or more if you can afford it.)This would become £2 with the help of his employers.Plus, if you are a UK taxpayer we can claim 22p tax back, which would turn your £1 into £2.22.· Please check out Alan's sponsored page…. www.mycharitypage.com/alan· We want to start an LDN campaign· Could you pass the above link to everyone in your address book?· Could you post the link on as many MS & LDN websites as possible?· Would you be interested in taking part in press coverage in your area? (If so, please email me)..You can send your sponsor money either:v Online, using Alan's pagev Posting to: LDN Research Trust, PO Box 1083 , Buxton, Norwich NR10 5WYv Paying Directly into our bank account: Barclay's Bank Sort Code 2-03-26Account No 60515213I'm sending this email to over 3,000 people and that is just the starting point. If each of you then send it to just 2 people that makes 6,000. If they each send it to 2 people that is 12,000. I think you can see where this is going…If each person made a donation of just £1, the £2 million would soon be reached. This will only work if YOU help and not think "I will leave it to the others to take part" We really do need YOU. We could all make excuses why we can't or don't want to get involved, but by doing nothing, nothing will ever get done.We have just over 4 months. Can we count on you to help please?I know there are a lot of if's, but isn't it about time people with MS had a drug like LDN, which isn't toxic, has been fully trialled and tested and is readily available to all?It would mean so much to people NOT to hear from their Neurologist. "I'm sorry you are Secondary/Primary Progressive MS, and there is nothing more I can do for you." Hopefully with YOUR help we can make statements like that a thing of the PAST!!!It is important to remember that the LDN Research Trust doesn't pay any salaries, and only running costs are covered by the charity.I hope you are as passionate about LDN as I am, and I hope to hear from you if you have ideas to share or your LDN story.Be part of the BIGGER picture today, by forwarding this email.I sincerely thank you all for listening to me.contactldnresearchtrust (DOT) orgwww.ldnresearchtrust.orgTel. No: 871 989 96 66A note from Alan……The reason I'm sponsoring the LDN Research Trust is because of my good friend Graham Robson- who has MS. I've known Graham for about 16 years, first as the "bloke" at the pet shop, then as my boss and recently as a close friend. I'm sure you can appreciate its always difficult to see a very active person start to lose their mobility and dexterity and suffer in the way they do.Please support me all you can to get a full LDN trial underway.Many ThanksAlan Howland Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2008 Report Share Posted March 27, 2008 That would be nice and helpful!Aletha Wittmann <Aletha@...> wrote: I will donate $100 US. Aletha [low dose naltrexone] "We Need Your Help!" I have Dr. Gluck's permission to post the following letter.Warm wishes to all,Jan*******************************************************Dear LDN Supporters,WE NEED YOUR HELP! Once Dr Tom Gilhooly's first trial of LDN on the bladder is complete, it will lead the way for the next trial.Dr Tom suggested THAT an all-singing all-dancing trial of LDN for Multiple Sclerosis will cost in the region of £2 million, which isn't a great deal of money in research terms, although for a small charity like ours it is a vast fortune. With this in mind, we need to set the wheels in motion and get fund raising underway as soon as possible.We have a great way in which you can help us to raise funds, thanks to Alan Howland, who is undertaking a 300K cycle ride from London to Paris . Alan is paying ALL his own expenses so that 100% monies donated will go towards a FULL TRIAL.Alan's employers are supporting him all the way, and will MATCH DONATIONS up to £500. We thank them for their help and support.Are you up for the challenge to help us raise £2 million?What I would like to ask each and every one of you is for all your help and support. We can't do this alone; we really need your help! Every penny helps- together we can achieve SO MUCH.· Could you sponsor Alan for just £1? (Or more if you can afford it.)This would become £2 with the help of his employers.Plus, if you are a UK taxpayer we can claim 22p tax back, which would turn your £1 into £2.22.· Please check out Alan's sponsored page…. www.mycharitypage.com/alan· We want to start an LDN campaign· Could you pass the above link to everyone in your address book?· Could you post the link on as many MS & LDN websites as possible?· Would you be interested in taking part in press coverage in your area? (If so, please email me)..You can send your sponsor money either:v Online, using Alan's pagev Posting to: LDN Research Trust, PO Box 1083 , Buxton, Norwich NR10 5WYv Paying Directly into our bank account: Barclay's Bank Sort Code 2-03-26Account No 60515213I'm sending this email to over 3,000 people and that is just the starting point. If each of you then send it to just 2 people that makes 6,000. If they each send it to 2 people that is 12,000. I think you can see where this is going…If each person made a donation of just £1, the £2 million would soon be reached. This will only work if YOU help and not think "I will leave it to the others to take part" We really do need YOU. We could all make excuses why we can't or don't want to get involved, but by doing nothing, nothing will ever get done.We have just over 4 months. Can we count on you to help please?I know there are a lot of if's, but isn't it about time people with MS had a drug like LDN, which isn't toxic, has been fully trialled and tested and is readily available to all?It would mean so much to people NOT to hear from their Neurologist. "I'm sorry you are Secondary/Primary Progressive MS, and there is nothing more I can do for you." Hopefully with YOUR help we can make statements like that a thing of the PAST!!!It is important to remember that the LDN Research Trust doesn't pay any salaries, and only running costs are covered by the charity.I hope you are as passionate about LDN as I am, and I hope to hear from you if you have ideas to share or your LDN story.Be part of the BIGGER picture today, by forwarding this email.I sincerely thank you all for listening to me.contactldnresearchtrust (DOT) orgwww.ldnresearchtrust.orgTel. No: 871 989 96 66A note from Alan……The reason I'm sponsoring the LDN Research Trust is because of my good friend Graham Robson- who has MS. I've known Graham for about 16 years, first as the "bloke" at the pet shop, then as my boss and recently as a close friend. I'm sure you can appreciate its always difficult to see a very active person start to lose their mobility and dexterity and suffer in the way they do.Please support me all you can to get a full LDN trial underway.Many ThanksAlan Howland Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.