Guest guest Posted December 15, 2006 Report Share Posted December 15, 2006 --- In , " moldcankill " <moldcankill@...> wrote: > > Can anyone tell me (in a way that my broken moldy brain will > understand) what low levels of VEGF and ADH and High levels of C4A and > Leptin mean? I tried reading about it and I think I am more confused > than when I began. Thank you for all of your help. > This is my layman's understanding of what these things mean: If you have low VEGF, then your tissues don't get enough oxygen, so if you exercise or do more physical activity than normal, you'll often have extreme fatigue for up to several days afterwards because you burn glycogen for energy (since your muscles don't have enough oxygen, they get the necessary energy from stored supplies) and it takes several days for your body to replenish that. When you have low ADH (Anti-diuretic Hormone), your kidneys are getting rid of water about as fast as you can add it, so you are often very thirsty and often have to pee alot. If your osmolality is also out of wack (above the normal range), then a doctor can prescribe a synthetic hormone that will help with that. High levels of leptin means that your body is very efficient at storing rather than burning fat for energy, thus the side effect of high leptin can be low energy along with being overweight. My understanding of C4A is that it is a modulator for inflammation - i.e. high levels mean you have high levels of inflammation. And, that just makes you overall feel bad and I believe contributes to the overall flu-like achiness. B --who has experienced all these things except for the high leptin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 15, 2006 Report Share Posted December 15, 2006 Yes I have them. What can be done if anything? mhbarnes_99 <mary.barnes@...> wrote: --- In , " moldcankill " <moldcankill@...> wrote: > > Can anyone tell me (in a way that my broken moldy brain will > understand) what low levels of VEGF and ADH and High levels of C4A and > Leptin mean? I tried reading about it and I think I am more confused > than when I began. Thank you for all of your help. > This is my layman's understanding of what these things mean: If you have low VEGF, then your tissues don't get enough oxygen, so if you exercise or do more physical activity than normal, you'll often have extreme fatigue for up to several days afterwards because you burn glycogen for energy (since your muscles don't have enough oxygen, they get the necessary energy from stored supplies) and it takes several days for your body to replenish that. When you have low ADH (Anti-diuretic Hormone), your kidneys are getting rid of water about as fast as you can add it, so you are often very thirsty and often have to pee alot. If your osmolality is also out of wack (above the normal range), then a doctor can prescribe a synthetic hormone that will help with that. High levels of leptin means that your body is very efficient at storing rather than burning fat for energy, thus the side effect of high leptin can be low energy along with being overweight. My understanding of C4A is that it is a modulator for inflammation - i.e. high levels mean you have high levels of inflammation. And, that just makes you overall feel bad and I believe contributes to the overall flu-like achiness. B --who has experienced all these things except for the high leptin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 15, 2006 Report Share Posted December 15, 2006 --- In , Edy Rayfield <edyrayfield@...> wrote: > > Yes I have them. What can be done if anything? > This is where Shoemaker's protocol comes in. Taking the CSM over a period of time and thus removing the toxins should help reduce the inflammation. My osmolality did get back into the normal range after a couple months on the CSM, so I didn't need to take the desmopression, which can be prescribed to increase your ADH. As well, my C4A has also come into the normal range after 7 months on the CSM - I think that was a combination of taking the CSM and taking lots of fish oil on a regular basis. As well, I use grapefruit seed extract daily which may have anti-inflammatory properties (I was taking it as it's supposedly a good natural antibiotic and anti- fungal). Another thing that may reduce C4A and increase VEGF is the Procrit, which Shoemaker is currently trialing that's been discussed on this list previously. As far as the leptin, I think that's where Actos is supposed to help, but I don't have any personal experience with that one. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 16, 2006 Report Share Posted December 16, 2006 Does Dr Shoe say why our bodies get less oxygen? Is it a function of toxic effects on lung tissue? I don't have lung inflamation but I have the symptom of needing days to regain my strength after relatively normal amounts of exercise. INTERESTINGLY to this subject I went to take a hyperbaric oxygen treatment after alot of exercise to see if that would help...........I MOVED, and you know what kind of strength that takes, even though I moved no furniture and just a bare minimum of things, I was exhausted but could not sleep AT ALL. I get like this when I 'overdo' things. You would think the exact opposite. However it like I am going on pure adrenal since I didn't have real energy and it takes forever to 'come down' from it. Affect centers around heart which seems like it just can't relax even though I am not breathing hard. It is hard to describe. So I went for hyperbaric oxygen treatment and afterwards my heart felt normal, my eyes which were hurting from lack of sleep felt better and I went home and fell asleep..then took it easy next day, so it must have something to do with not being able to make up that oxygen. I have noticed this and read up on oxygen alot and also in regards to numerous migraines I got. I think I posted here that I discussed with my doctor and he suggested that I just take deep breaths and then *demonstrated* what he meant by that, by inhaling deeply, like I was a moron or something. I had read about successful studies of oxygen used to treat migraines. I mentioned that also but he implied that deep breathing would = oxygen treatment. > >> If you have low VEGF, then your tissues don't get enough oxygen, so if > you exercise or do more physical activity than normal, you'll often > have extreme Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 16, 2006 Report Share Posted December 16, 2006 > > Does Dr Shoe say why our bodies get less oxygen? Is it a function > of toxic effects on lung tissue? I don't have lung inflamation but > I have the symptom of needing days to regain my strength after > relatively normal amounts of exercise. INTERESTINGLY to this > subject I went to take a hyperbaric oxygen treatment after alot of > exercise to see if that would help...........I MOVED, and you know > what kind of strength that takes, even though I moved no furniture > and just a bare minimum of things, I was exhausted but could not > sleep AT ALL. I get like this when I 'overdo' things. You would > think the exact opposite. However it like I am going on pure > adrenal since I didn't have real energy and it takes forever > to 'come down' from it. Affect centers around heart which seems > like it just can't relax even though I am not breathing hard. It is > hard to describe. So I went for hyperbaric oxygen treatment and > afterwards my heart felt normal, my eyes which were hurting from > lack of sleep felt better and I went home and fell asleep..then took > it easy next day, so it must have something to do with not being > able to make up that oxygen. I have noticed this and read up on > oxygen alot and also in regards to numerous migraines I got. I > think I posted here that I discussed with my doctor and he suggested > that I just take deep breaths and then *demonstrated* what he meant > by that, by inhaling deeply, like I was a moron or something. I had > read about successful studies of oxygen used to treat migraines. I > mentioned that also but he implied that deep breathing would = > oxygen treatment. > Barb, I think that the low levels of oxygen are due to the inflammation. My understanding is that the turning off of the inflammation is what's broken for certain genotypes. It's these high levels of inflammation that cause the lung problems (and not the other way around from my understanding). I don't know that they know why oxygen levels fall when inflammation increase, but it is known that happens, per the following: http://www.aarda.org/infocus_article.php?ID=12 " This much is known: when tissue damage mounts due to prolonged inflammation, oxygen levels in the damaged area fall. This in turn leads to increased amounts of adenosine outside cells. Dr. Sitkovsky theorized that the excess adenosine binds to the adenosine receptors, which then initiate a chain reaction that slows and eventually stops inflammation. " And, if you follow this through, this adenosine that they attribute to being the thing that controls inflammation has a relationship with MSH. I found this article, although I can only read the abstract: http://www.blackwell-synergy.com/doi/abs/10.1111/j.1365- 2826.2003.01116.x?journalCode=jne But here's results that seem interesting: " Together, these results suggest that adenosine, acting through A2A receptors, may modulate the release of á-MSH in the cerebral cortex and amygdala. " Now, I'm hypothesizing that since we have chronic inflammation, then we likely don't have this adenosine doing what it's supposed to do to release the MSH which may be an additional reason why we usually have low MSH or this is yet another example of the damage to the Hypothalamus by the toxins. It may also be a chicken/egg thing whereby the inflammation increases the amount of oxygen used, thus decreasing the overall availability of oxygen for other functions and since our bodies are shutting off the inflammation, we seem to need more oxygen than normal which would explain why folks get good results with hyperbaric. I find it interesting that this adenosine is something that is part of ATP, which is a key building block for energy in our bodies. This might also explain why we just don't have normal energy at all. I do find that I can feel almost normal if I take NADH supplements, which is something that's produced from the ATP. The only downside for when taking the NADH supplement is I don't sleep well when I take it, so I have to be very selective in how often I use it. Barb, I don't know that this explains your over reactions other than as you suggest, your adrenals were over-stressed and adding the oxygen reduces the stress on the adrenals because your body is able to produce the energy without going into fight mode. B. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2009 Report Share Posted October 5, 2009 Dara, If I remember correctly, the initial tests that Dr. J did for my son a few years back were Igenex for Lyme, but Medlab for all the coinfections. I'm not sure why he did all the coinfections there and we were new to all the Lyme stuff so I didn't question. I do remember that the medlab tests were very expensive (I think about $1000) but my insurance didn't cover them, but did reimburse their portion after the fact. We did have an issue though that my son tested negative for Mycoplasma Fermentans initially and then after a couple of years and him not completely recovering, they said they wanted to retest him for that, and they said the lab they used initially had changed their practices for analyzing for M. Fermentans about the time that he had been tested, and they were using robotics instead of people, and since they did that our doctor NEVER got positive results for this infection from them. I'm thinking that the lab they used initially for the M. Fermantans was Medlab but I'm not sure so if they are testing for this, you may want to research it further. My son did test positive for it the second time around with the different lab they began using and we adjusted his treatment accordingly and he's doing much better. I hope this helps. Patty [ ] lab questions Anyone have any experience with Medical Diagnositc Laboratory in New Jersey? My LLMD ordered some co-infection tests there, and they take my insurance. All of my other testing was done at Igenex, but he thought they did a good job with these specific tests. I took my daughter to a different LLMD who says to only use Igenex. If there are any tests that are ok to do at another lab that takes my insurance I would rather do that. Any thoughts? Thanks, Dara ------------------------------------------------------------------------------ No virus found in this incoming message. Checked by AVG - www.avg.com Version: 8.5.420 / Virus Database: 270.14.3/2415 - Release Date: 10/05/09 06:19:00 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2009 Report Share Posted October 5, 2009 I liked MDL b/c my daughter got a (+) Lyme PCR, Dr. J told me they triple test their results on that. From: darabeth2003 <dara.alewine@...> Subject: [ ] lab questions Date: Monday, October 5, 2009, 12:13 PM  Anyone have any experience with Medical Diagnositc Laboratory in New Jersey? My LLMD ordered some co-infection tests there, and they take my insurance.. All of my other testing was done at Igenex, but he thought they did a good job with these specific tests. I took my daughter to a different LLMD who says to only use Igenex. If there are any tests that are ok to do at another lab that takes my insurance I would rather do that. Any thoughts? Thanks, Dara Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2009 Report Share Posted October 5, 2009 Hi Dara MDL is very reputable--I am familiar with their lab director-they were the ones involved at the very beginnings of Bartonella testing and worked with the prominent Drs about that bacteria--making it known that it does come along with tick bites. (one of the pioneering Drs is my LLMD and so I am knowledgable of and was one of the first few patients studied at MDL, re: Bartonella) Igenex is a bit hyped and a bit controversial--so far theyre reliable but they have " connections " in and out of Lyme community that make some uncomfortable.Theyre expensive and as youve pointed out other labs take insurance, may be cheaper,and yet they do as good a job!! Finette Re: [ ] lab questions I liked MDL b/c my daughter got a (+) Lyme PCR, Dr. J told me they triple test their results on that.? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2009 Report Share Posted October 6, 2009 Patty are you talking about Medical Diagnostics Lab,calling it " Medlab " since the one Dara mentioned is abbreviated MDL, not " medlabs " ?? I just dont want all of us to be confused about which lab is which. FWIW our son went to too and he did NOT use MDL even though we live in NJ and that wouldve been easy to do. Since Dara asked about MDL aka Medical Diagnostic Labs its a bit confusing to see info about " medlabs " . Patty, did the test stationery have a logo of a big black tick with " legs " forming letters M,D,L ?? thats MDL's logo. Finette Re: [ ] lab questions Dara, If I remember correctly, the initial tests that Dr. J did for my son a few years back were Igenex for Lyme, but Medlab for all the coinfections. I'm not sure why he did all the coinfections there and we were new to all the Lyme stuff so I didn't question. I do remember that the medlab tests were very expensive (I think about $1000) but my insurance didn't cover them, but did reimburse their portion after the fact. We did have an issue though that my son tested negative for Mycoplasma Fermentans initially and then after a couple of years and him not completely recovering, they said they wanted to retest him for that, and they said the lab they used initially had changed their practices for analyzing for M. Fermentans about the time that he had been tested, and they were using robotics instead of people, and since they did that our doctor NEVER got positive results for this infection from them. I'm thinking that the lab they used initially for the M. Fermantans was Medlab but I'm not sure so if they are testing for this, you may want to research it further. My son did test positive for it the second time around with the different lab they began using and we adjusted his treatment accordingly and he's doing much better. I hope this helps. Patty Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2009 Report Share Posted October 6, 2009 Hi Finette, It was MDL in NJ that our testing was done at. I think Dara had listed it as Medical Diagnostic Labs and I quickly typed medlab in my response but then saw someone refer to it as MDL and remembered that abbreviation as being correct. Sorry for any confusion, but yes, I was referring to the same lab. I also actually just looked up the old paperwork to confirm that my memory was serving me correctly, and it was definitely MDL in NJ that did the testing for all the coinfections -- that was in March, 2005. Thanks, Patty Re: [ ] lab questions Dara, If I remember correctly, the initial tests that Dr. J did for my son a few years back were Igenex for Lyme, but Medlab for all the coinfections. I'm not sure why he did all the coinfections there and we were new to all the Lyme stuff so I didn't question. I do remember that the medlab tests were very expensive (I think about $1000) but my insurance didn't cover them, but did reimburse their portion after the fact. We did have an issue though that my son tested negative for Mycoplasma Fermentans initially and then after a couple of years and him not completely recovering, they said they wanted to retest him for that, and they said the lab they used initially had changed their practices for analyzing for M. Fermentans about the time that he had been tested, and they were using robotics instead of people, and since they did that our doctor NEVER got positive results for this infection from them. I'm thinking that the lab they used initially for the M. Fermantans was Medlab but I'm not sure so if they are testing for this, you may want to research it further. My son did test positive for it the second time around with the different lab they began using and we adjusted his treatment accordingly and he's doing much better. I hope this helps. Patty ------------------------------------------------------------------------------ No virus found in this incoming message. Checked by AVG - www.avg.com Version: 8.5.420 / Virus Database: 270.14.4/2416 - Release Date: 10/05/09 18:23:00 Quote Link to comment Share on other sites More sharing options...
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