posted
My white blood cell count has been very low for a few years now. It isn't getting any better!
I have been told I am a prime candidate for cancer.I am looking for a way to boost my count.
Does anyone know if Transfer Factor really works?? It is SOOO expensive that I don't feel like pitching my money into a useless supplement if it doesn't work.
Has anyone ever used IP-6 and Inositol too and boosted their count?
I am still struggling with Babesia, so I am hoping treatment will bring it up too? Thanks!!
Posts: 477 | From Pennsylvania | Registered: Nov 2015
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posted
I have tried transfer factors. I really couldn't tell much of a difference, but I did not do a before and after look at white blood cell.
I think the idea of transfer factors is great. I just don't know if they really do as the theory suggests.
Sorry, I'm not more helpful.
Posts: 798 | From Cincinnati, OH | Registered: Jul 2016
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Jordana
Frequent Contributor (1K+ posts)
Member # 45305
posted
If you have an infection that lowers your wbc (like Ehrlichia or Bart) I really don't think it does much. I've tried all the stuff for my immune system and it had no effect at all.
It's worth trying I guess based on studies but I'm convinced a lot of these things are just well-meaning junk.
Posts: 2057 | From Florida | Registered: Feb 2015
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posted
Make sure you are taking meds that will clear ehrlichia .. that is the number one cause of a low wbc in the lyme world. Second would be RMSF.
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96222 | From Texas | Registered: Feb 2001
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TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
When I was treating lyme, babs, and bart, my white cell count eventually went low. My lyme doc said that the body senses the antibiotics and eventually decides that, due to them, it does not have to make so many white blood cells.
When my count went low, he put me on Transfer Factor. In 2 weeks, my count was up to normal and I stopped the TF. Next time it went low, did the same thing. Third time it went low, he told me to just stay on the Transfer Factor until I was finished with treatment. I did.
TF enabled me to continue my antibiotic treatment uninterrupted. And, I was cured of all my diseases as a result. So, it worked for me. This was over 11 years ago.
I took TF with bovine colostrum in it. So, that is the active ingredient that you want to look for. Colostrum is the mother's first milk; bovine refers to cows. So, it is the cow's first milk that is transferring good things to the newborn calf.
I believe the brand was called 4Life.
If you have a low white count without even being on antibiotics, that would be a different case from mine. I can't speak to that case.
I agree that it is expensive.
Posts: 9931 | From Maryland | Registered: Dec 2007
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I think mine dropped after being on treatment too!
Thanks a lot for telling me a good brand. I had bought researched nutritionals, but they are twice as expensive as 4life. (bummer)
I will know what to get next time! It doesn't seem to help peoples symptoms, but I don't want to get cancer! Right now a good lab report would be great!
Posts: 477 | From Pennsylvania | Registered: Nov 2015
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posted
my llmd prescrbes me leucovorin. works great everytime.
Posts: 832 | From Somewhere | Registered: Nov 2010
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TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
Right, the Transfer Factor doesn't help your symptoms at all. The only way you know that it is doing its job is by getting your white blood cell count tested.
Posts: 9931 | From Maryland | Registered: Dec 2007
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posted
thanks terv! I will google this. I have no idea what leucovorin is?? But that it works sounds great!
Posts: 477 | From Pennsylvania | Registered: Nov 2015
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posted
hmm so I just looked it up. Interesting med... I wonder if since it protects cells against cancer if it would protect your red blood cells against Babesia??
I know, I know... a WILD card... but hey?
Posts: 477 | From Pennsylvania | Registered: Nov 2015
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posted
I never thought to ask how or why it works. Dr usually gives it to me when my wbc mid to upper "2s". I will take it for a month and I will get the count to about 3.5.
I am not on it all the time only when I need it.
Posts: 832 | From Somewhere | Registered: Nov 2010
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bluelyme
Frequent Contributor (1K+ posts)
Member # 47170
posted
Folic acid will help anemic effects ...collostrum has hgh and may help if you can do dairy. .
-------------------- Blue Posts: 1539 | From southwest | Registered: Dec 2015
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posted
thanks bluelyme for the tip about folic acid.
Right now I can't breathe.... uuugh...
I don't know if is a mepron/zith babesia die off reaction or if my meds aren't working...Seems like I just can't get air, which I assume is from low red blood cells.
So I don't have red cells and I don't have white ones!! Maybe the purple ones are still there?(jk) Posts: 477 | From Pennsylvania | Registered: Nov 2015
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- TF, how handy that your initials are the same as for Transfer Factor. I often have trouble finding detail that I know I saved.
I saved your post and when I go to find in future, whether thinking of your name or the product, the TF should work for memory prompt with file name:
TF post, Transfer Factor, 2016 -
Posts: 48021 | From Tree House | Registered: Jul 2007
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Medical mushrooms might also have some positive effects.
Medical Mushrooms - Links -
Posts: 48021 | From Tree House | Registered: Jul 2007
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TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
I just want to throw in here to the discussion that Dr B. found that Transfer Factor works based on his experience. I think he treated more lyme patients than anybody here on LymeNet.
Here is his writeup from page 30 of the Guidelines:
"TRANSFER FACTORS are the body’s natural signals meant to activate the pathogen-killing effects of the cellular immune system. Therapy with these agents consists of taking both a general stimulator, plus specific transfer factors for the infection you have.
Personal experience made me a believer in transfer factor therapy. For Lyme patients, use Transfer Factor Multi-Immune as the general stimulant, and Transfer Factor Lyme- Plus as the specific agent.
Both are exclusives from Researched Nutritionals, and I have found them to be surprisingly effective in making the very ill respond better to treatment. Take as directed on the label."
Hey, Keeb. I saw your post!
(breaking up a paragraph for easier reading for many here)
posted
My doc believes in good mushroom products for boosting immunity, like Host Defense with 17 mushrooms in it. I am a sensitive person, and I can take this product fine. I get it at the health food store.
Even cooking with reishi, maitake, shiitake mushrooms etc is fine to do.
Posts: 13116 | From San Francisco | Registered: May 2006
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posted
good to know TF! thanks... so do you think I should only stay with researched nutritionals? You took 4life right?
Posts: 477 | From Pennsylvania | Registered: Nov 2015
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TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
In my particular circumstances, my lyme doc had me take 4life. It worked for my low white cell count.
Burrascano may be saying to take the other brand for something else. I am not sure.
" to activate the pathogen-killing effects of the cellular immune system." and "surprisingly effective in making the very ill respond better to treatment."
I was NOT very ill when I had the low white cell count. I had beaten lyme and bart and was down to just treating babs. I was responding very well to treatment--extremely well in fact.
So, maybe all you need in your situation is the 4life.
Posts: 9931 | From Maryland | Registered: Dec 2007
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Right now a good lab report would be great!
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