Message: 2

[Guest guest]

No, Louise I did not know that about homeopathy. What is your experience with it? Up until recently, mine has been very good. I've been using the same homeopath for over ten years and I think she's terrific. Nut when I began having symptoms last Fall, and then even after I was diagnosed in December, I didn't call her. I began taking LDN the same week of my diagnosis, because my boyfriend knows Dr. Bihari. I waited three months before going to see Sylvia, because I wanted to see how my body was responding to LDN--you know, one weird thing in my body at a time!

The remedy she gave me three weeks ago is called Conium. It was a high-potency dosage--1M. Truly, it has made me miserable. I haven't had leg spasms since November and this remedy has even brought a couple of those back. The first week I felt like I had the flu. Now it's causing my legs to burn and feel twisted, symptoms I haven't felt in months. I'm supposed to go back to Sylvia mid-May, but I don't think I'm going to take the remedy again. I've only been on LDN for four months and I started physical therapy about a month ago. I thought I could also handle a homeopathic remedy, but I was wrong. I think I was too proactive and I'm paying for it. When I saw Dr. Bihari in February I asked him about it, and he it was perfectly fine. I've since called his office and told Bill that it was a bad choice on my part. I know they collect information that they can share with other patients, so... Perhaps I did not wait long enough to see how I'd be affected by LDN, and, of course, everyone's different.

It's ironic, because I was also feeling better before beginning physical therapy. I had much more energy. But that I can accept more easily, because I do have to do something about the leg muscles that have atrophied.

At the risk of sounding ignorant, what does "patibulary" mean?