Hi everybody,
I'm going to briefly explain how my consultation on last thursday with Dr. De Meirleir went, in case it might be worthwhile to some of you.
After 11 months on ABX for Lyme, he told me to stop them and put me on antibiotic herbs (samento, cumanda and banderol), on last december. Samento put me in bed the very first day, so I decided to stop them, in order to be able to take my exams in January. Just after finishing them I started the herbal protocol, and the Herx was so hard that I spent the last two month bedridden.
I explained this to my doctor, and he told me to stop the herbal protocol, and go back to oral antibiotics. I asked about the Intravenous ABX and he told me it would be a good idea to take them, so if I am able to get the money, I'll stay in Brussels for 3 months, since august, in order to have the I.V. ABX done, 3-5 days weekly.
I asked him about the poster Lombardi presented on the IACFS/ME conference, on HERVs as a marker for CFS, and on the inhibition of specific Toll Like Receptors of the macrophages of patients with CFS as a possible way by which some pathogens or toxins could trigger the expression of these HERVs--Note that there's evidence on how EBV, HHV-6 or Borrelia, wreck the immune system by attaching to these receptors. He told me there was research underway on this subject that possibly could be used for CFS in a couple of years.
I asked him for some drugs that have come up recently as possible treatments, such as IFN, peptide T and others. We didn't have much time to discuss this in deep, but it seemed he was familiar with them and thought they were not the "answer". I also asked him for Ibudilast and told me he would look in to it.
So this is more or less it. Now that I have switched to ABX, I hope to recover enough to take some exams in summer, and if possible, maybe do IVs in Brussels afterwards...
Hope it helps,
Best!
Sergio
I'm going to briefly explain how my consultation on last thursday with Dr. De Meirleir went, in case it might be worthwhile to some of you.
After 11 months on ABX for Lyme, he told me to stop them and put me on antibiotic herbs (samento, cumanda and banderol), on last december. Samento put me in bed the very first day, so I decided to stop them, in order to be able to take my exams in January. Just after finishing them I started the herbal protocol, and the Herx was so hard that I spent the last two month bedridden.
I explained this to my doctor, and he told me to stop the herbal protocol, and go back to oral antibiotics. I asked about the Intravenous ABX and he told me it would be a good idea to take them, so if I am able to get the money, I'll stay in Brussels for 3 months, since august, in order to have the I.V. ABX done, 3-5 days weekly.
I asked him about the poster Lombardi presented on the IACFS/ME conference, on HERVs as a marker for CFS, and on the inhibition of specific Toll Like Receptors of the macrophages of patients with CFS as a possible way by which some pathogens or toxins could trigger the expression of these HERVs--Note that there's evidence on how EBV, HHV-6 or Borrelia, wreck the immune system by attaching to these receptors. He told me there was research underway on this subject that possibly could be used for CFS in a couple of years.
I asked him for some drugs that have come up recently as possible treatments, such as IFN, peptide T and others. We didn't have much time to discuss this in deep, but it seemed he was familiar with them and thought they were not the "answer". I also asked him for Ibudilast and told me he would look in to it.
So this is more or less it. Now that I have switched to ABX, I hope to recover enough to take some exams in summer, and if possible, maybe do IVs in Brussels afterwards...
Hope it helps,
Best!
Sergio