Guest guest Posted October 12, 2004 Report Share Posted October 12, 2004 In a message dated 10/12/2004 9:16:59 PM Central Daylight Time, yashagrawal@... writes: Cilantro, chlorella, waste of money, IMHO Y. My opinion: They probably are very good in a natural sort of way to help rid the body of some toxins, but if one is in a crisis, chelation would be much more powerful and faster. Also, I did some expensive cilantro drops and powdered chlorella at one time, but the taste was just awful! I actually got sick on the chlorella and could never make myself go there again! It wasn't fun! And I'm not usually one to have a problem with bad tasting supplements if I think they may be helping. These, in my opinion, weren't helping enough. Marcie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2004 Report Share Posted October 13, 2004 Hi, My MD who is helping me with ms and LDN is also recommending a millions expensive tests. I think the idea is to root out all possible toxins that could be contributing to your MS. I cannot afford all these tests right now but I am going to prioritize and then get them done as I can. I am in the dumps about this disease too. I am tired of all the symptoms and having to deal with each one and wondering which ones will go away after LDN and which ones am I stuck with - it sucks. Don't feel pressured to get the tests - just know about them and get them donw as you can afford it. The tests may or may not make any difference. No one knows for sure. Alice --- In low dose naltrexone , " kcapozza " <kcapozza@h...> wrote: > > I had my initial consultation for ldn today. Dr. scott also > recommended quite a few expensive blood tests to see if I have lyme > disease. Since I had my amalgams removed 5 months ago, he also > recommended cilantro and chlorella. > > He started me on 1.5mg dose. Has anyone done all these other > tests? > > I am soo sick of spending money on this disease. > > karen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2004 Report Share Posted October 13, 2004 Cilantro, chlorella, waste of money, IMHO Y. --- In low dose naltrexone , " kcapozza " <kcapozza@h...> wrote: > > I had my initial consultation for ldn today. Dr. scott also > recommended quite a few expensive blood tests to see if I have lyme > disease. Since I had my amalgams removed 5 months ago, he also > recommended cilantro and chlorella. > > He started me on 1.5mg dose. Has anyone done all these other > tests? > > I am soo sick of spending money on this disease. > > karen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2004 Report Share Posted October 13, 2004 --- In low dose naltrexone , " kcapozza " <kcapozza@h...> wrote: > > I had my initial consultation for ldn today. Dr. scott also > recommended quite a few expensive blood tests to see if I have lyme > disease. Hi, . Dr. also pushed for us to have the Lyme testing done on my son, so I asked him to send me the info on it, which he did. (By the way, he has done the same with several other people who are using him to get LDN for MS.) I have the info in hand, but haven't done anything about it yet. You are right, it is very expensive, and it is also still in research stages, so my question is how would I feel about the results if I had them??? Would I trust that diagnosis anymore than I trust the one we have? I have always felt my son could have Lyme, since the testings wasn't done until much later in his illness, and the window of opportunity for accurate test results was long past. When I got the packet that Dr. sent me, I went into " full Mom research mode " again, and I learned that 99% of the people who have used this particular form of testing come back positive for Lyme, and the testing is based on the theory that Lyme is contracted in many more ways than just a tic bite. I believe this to be true, have always believed this to be true, but my son's diagnosis has been changed so many times that I don't know if I want to utilize research testing or not. (We've run the gamut from inoperable brain tumors to encephalitis to MS...He was covered with mosquito bites at the onset.) I'm really on the fence on this one. I am hesitant to have the expensive testing done (no insurance will cover testing in the research stages) when I don't know how I will feel about the results when we get them. With all the recent talk about antibiotic treatment being beneficial to MS, we have to wonder, since antibiotics and detoxification are used to treat Lyme. Please keep us posted on your decision. Take care! Kim Quote Link to comment Share on other sites More sharing options...
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