Crystal's MS,TM & LDN Website
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1208 Comments
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DeAnna
05:45 PM on February 09, 2009
I just like to compliment you on your site. I am 32 years old and have been diagnosed with MS, it was a long road and was diagnosed w/ so many things in between.
Bless,
DeAnna (RI)
Bless,
DeAnna (RI)
reply
DeAnna
05:45 PM on February 09, 2009
I just like to compliment you on your site. I am 32 years old and have been diagnosed with MS, it was a long road and was diagnosed w/ so many things in between.
Bless,
DeAnna (RI)
Bless,
DeAnna (RI)
reply
Jim
04:24 PM on February 09, 2009
Crystal,
If you have a list of LDN please send it to me as soon as possible. My area is: Athens, GA, but can go anywhere in the Atlanta area. Thanks so much.
Jim
If you have a list of LDN please send it to me as soon as possible. My area is: Athens, GA, but can go anywhere in the Atlanta area. Thanks so much.
Jim
reply
Jim
04:24 PM on February 09, 2009
Crystal,
If you have a list of LDN please send it to me as soon as possible. My area is: Athens, GA, but can go anywhere in the Atlanta area. Thanks so much.
Jim
If you have a list of LDN please send it to me as soon as possible. My area is: Athens, GA, but can go anywhere in the Atlanta area. Thanks so much.
Jim
reply
steve mcmanus
02:17 PM on February 08, 2009
Hello Crystal.
Lovely to read your story and long may the ldn work for you.
Ive been on ldn for some months now and it hasnt worked as well for me but then i dont know how bad i may have been wothout it! I have more feeling in my hands late of a night, after taking the ldn, but this doesnt last through till the following day. Suggests it is doing something for me; but i am also experiencing new symptoms at a constant rate of progression?Best wishes
Steve
Lovely to read your story and long may the ldn work for you.
Ive been on ldn for some months now and it hasnt worked as well for me but then i dont know how bad i may have been wothout it! I have more feeling in my hands late of a night, after taking the ldn, but this doesnt last through till the following day. Suggests it is doing something for me; but i am also experiencing new symptoms at a constant rate of progression?Best wishes
Steve
reply
steve mcmanus
02:17 PM on February 08, 2009
Hello Crystal.
Lovely to read your story and long may the ldn work for you.
Ive been on ldn for some months now and it hasnt worked as well for me but then i dont know how bad i may have been wothout it! I have more feeling in my hands late of a night, after taking the ldn, but this doesnt last through till the following day. Suggests it is doing something for me; but i am also experiencing new symptoms at a constant rate of progression?Best wishes
Steve
Lovely to read your story and long may the ldn work for you.
Ive been on ldn for some months now and it hasnt worked as well for me but then i dont know how bad i may have been wothout it! I have more feeling in my hands late of a night, after taking the ldn, but this doesnt last through till the following day. Suggests it is doing something for me; but i am also experiencing new symptoms at a constant rate of progression?Best wishes
Steve
reply
Joe Lomonico
06:15 PM on February 05, 2009
Hello Ccrystal, Recently i have been diagnosed with an auto immune disease called ITP. I was wondering if the LDN has ever been used for this disease, have you erer heard of it's use for ITP? My doctor has had me on the steriod Prednisone for about three months and has started to lower the dosage to see where my platlett count goes. Last week they gave me two injections of a human plasma antibody drug called WIN-RHO,I have responded very well for now and my platlett count came up to arround 200.000.Your web site is awesome and I wish you the best.
reply
Joe Lomonico
06:15 PM on February 05, 2009
Hello Ccrystal, Recently i have been diagnosed with an auto immune disease called ITP. I was wondering if the LDN has ever been used for this disease, have you erer heard of it's use for ITP? My doctor has had me on the steriod Prednisone for about three months and has started to lower the dosage to see where my platlett count goes. Last week they gave me two injections of a human plasma antibody drug called WIN-RHO,I have responded very well for now and my platlett count came up to arround 200.000.Your web site is awesome and I wish you the best.
reply
Eric Fong
12:42 PM on February 04, 2009
Hi Crystal.
I have started LDN since 1/1/09, not much changed on my MS condition, so I guess I may not be part of 70% of people who have improved. I also tried Prokarin before also and the only change was I was able to move my left toes after 1 month. But my GP is only willing to prescribe only one of the two (Prokarin or LDN), still need to use walker in order to walk at home.
I have started LDN since 1/1/09, not much changed on my MS condition, so I guess I may not be part of 70% of people who have improved. I also tried Prokarin before also and the only change was I was able to move my left toes after 1 month. But my GP is only willing to prescribe only one of the two (Prokarin or LDN), still need to use walker in order to walk at home.
reply
Eric Fong
12:42 PM on February 04, 2009
Hi Crystal.
I have started LDN since 1/1/09, not much changed on my MS condition, so I guess I may not be part of 70% of people who have improved. I also tried Prokarin before also and the only change was I was able to move my left toes after 1 month. But my GP is only willing to prescribe only one of the two (Prokarin or LDN), still need to use walker in order to walk at home.
I have started LDN since 1/1/09, not much changed on my MS condition, so I guess I may not be part of 70% of people who have improved. I also tried Prokarin before also and the only change was I was able to move my left toes after 1 month. But my GP is only willing to prescribe only one of the two (Prokarin or LDN), still need to use walker in order to walk at home.
reply
Wanda Lilly
05:39 PM on February 02, 2009
Just started LDN about 3 weeks ago for my MS. I want to keep up with what is going on with LDN. I seem to have more energy and my Legs seem some stronger. I hope some day soon it will be FDA approved. My doctor want take me off my Copaxone, since it is not FDA approved.
reply
Wanda Lilly
05:39 PM on February 02, 2009
Just started LDN about 3 weeks ago for my MS. I want to keep up with what is going on with LDN. I seem to have more energy and my Legs seem some stronger. I hope some day soon it will be FDA approved. My doctor want take me off my Copaxone, since it is not FDA approved.
reply
Eric Fong
04:18 PM on January 26, 2009
It's great to see your website after I was laid off July of 2008 and have Ms since Nov 2002 after taking my first flu shot which contain Thimerosal. I have just started LDN since 1/1 of 2009 and hopefully I will regain some of my ability and help other to notice the usefulness of LDN.
reply
Eric Fong
04:18 PM on January 26, 2009
It's great to see your website after I was laid off July of 2008 and have Ms since Nov 2002 after taking my first flu shot which contain Thimerosal. I have just started LDN since 1/1 of 2009 and hopefully I will regain some of my ability and help other to notice the usefulness of LDN.
reply
dave lyons
06:51 AM on January 09, 2009
very good job with all this helpful info on ms!!
this is one of a kind!
this is one of a kind!
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dave lyons
06:51 AM on January 09, 2009
very good job with all this helpful info on ms!!
this is one of a kind!
this is one of a kind!
reply
leighdu
03:52 PM on December 31, 2008
Love the site, and will be coming back again. I have it bookmarked as well !
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