Hi Crystal, you have a wonderful site here and you are truly an amazing lady. I watched your youtube video. Not only are you smart, you're very pretty too. I don't know when you'll get this but please write back when you can.
I have been diagnosed 2 weeks ago with MS had my first scare at 19 am 47 now awaiting to see a neurologist about mt results have always worked hard for 24 years mind not as now am in UK anyone who wants to contact myself may do so anytime.
Lynne
What are everyones thoughts on the Swine virus vacination?? Also I have reached the golden age of 50+ and have been recomended for a colonoscopy....does the LDn interfere with the test...any special instructions...thanks
Hi,
Just starting out finding all there is to know about LDN for MS. I know several people with MS who went the way of the "usual" treatment. I've see it do them no favors. So when I started to lose the use of my legs, I decided to look for something else. Does anyone know of a dr. local to Hartford Ct that prescribes LDN?
I don't know what I would do without you here, Crystal, to help me along with information and starting LDN. You're making it possible and I thank you so much!
I live in Lapeer, Michigan and would like to find a doctor in my area who would prescribe LDN. I see that there is a compounding pharmacy in Ann Arbor, MI. Could there be a doctor possibly somewhere near? I'm looking in the bounderies of about Detroit to Port Huron to Lansing to Saginaw area (the thumb). I would really appreciate any help you can give me. Thank you very much. Life will be better for it! Carolynn
Hi Crystal, I have no idea whether or not LDN will work for me or not, I just found out about it. But, thank you for your web site. For the first time in 20 years I feel hopeful and I can't wait to see a doctor who will prescribe the LDN for me.
Carolyn Sunday
Hello, I was doing some research and found your website. Wow...I want to share that I too am getting over (hopefully) cellulitis. I came down with it Jan 28th, 2008 and was hospitalized for 10days. Now home doing oral antibiotics (6th week now). Still feels a little warm and some swelling. Dr's say it is healing good but just read tonight it can come back!!! God will it will never for me or you or any others that have it. I'm paranoid now about any kind of cuts on my feet or ankle or anywhere else! Anyway, I just wanted you to know my story too. I'm doing physical therapy now and still going into the Dr. to have his check it every 2 weeks. Wish me luck. Thanks Scott
Hello Crystal...I was forwarded your website by Skip's. I have Crohn's and I am looking for a Dr. in my area to write a prescription and they said you would be able to help. Thank you so much for the time and effort you put into all this. Great website!
My wife is bipolar. I have a close friend who is dying with cancer, hospice already there. Other friends with Lupus and MS. I can't get a doctor to write a prescription for LDN. I understand you can help. My address is lbrman@bellsouth.net
Do you know what people take for cramping that seems to be intensified by LDN? I have been experiencing toe cramping in early morning hours after taking LDN. I was having calf cramping at one time but that has subsided with taking calcium/magnesium. I have lowered the LDN dose but find, symptom wise, I do better at 3.0 but experience the cramping. I take Baclofen 20 mg at about 1 am, but it causes leg weakness for me if I take it during the day. Leg weakness is my biggest problem with MS. Any suggestions would be appreciated. tree55@comcast.net (e-mail address)