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| This image in particular: Protozoan infection that causes MALARIA. Protomyxzoa (FL-1953) also can manifest itself in malaria-like symptoms, as you see clearly in my case since day one of onset. |
Lasting healing takes time.
(if you wish to know more about my own story, and the countless things my hubby and I have been able to humbly learn over these 5+ years, please contact me at the e-mail I list below ONCE YOU HAVE WATCHED "OUR STORY" which is on our website: www.justinandchrista.ca
Blessings and ta!
The following is what I wrote several months ago...
ATTENTION:
The correct and most recently confirmed scientific name given the protozoan infection known as FL-1953, is to be known now as PROTOMYXZOA RHEUMATICA.
I will continue to add to this specific post as I learn more information, but Fry Labs is hesitant to disclose anymore as they are waiting on a pending grant from the government...
Since there is not yet much information online, we wanted to direct you here, where we've compiled the main information WE'VE learned either directly from Dr. Fry of Fry Laboratories in Arizona, who thankfully HAS that grant from various sources, to continue further research and testing and treatment options on those who, like myself, have tested positive for it, and also I will update this with info from what we learn as we continue to help others internationally and hear of how their treatments are going!
If you (directly or indirectly) come across any more accurate, proven facts about FL-1953 not listed below, please contact me personally through my confidential health+wellness and counseling+prayer e-mail account:
cmvhealth@live.ca
The lab which first discovered this infection almost a decade ago in Arizona, will soon be releasing their government-funded medical findings to the public. When is soon? I'm not sure that even THEY know the timing of this. However, in the meantime, I hope you will find this post even a little helpful, regardless of any new info or just reminders of what you've already come to grasp.
As I address all the details that I have come to know since I myself was positively diagnosed with this co-infecton to Lyme, I hope you will be encouraged, knowing that now as I update portions of this post, I am now basically 100%. Health wise, I sure am 100%! I'm just dealing with some severe pain-issues from TMJ and neck injuries that I got from rollover MVA's while I was soooo sick. Anyways, enough about me! The protozoan infection was called FL-1953 for many years right? (almost more suitable for a flight out of Miami Florida than a label to be stamped on this horrendous illness if you ask me!! haha!) It's newer name sounds much more medically sound! haha
But it is almost always nice to have a name to pin onto the symptoms that you yourself endure, or that your loved ones endure, is it not? There is some talk that it is all bunk, and that EVERYONE has "the fl bug", but I know of MANY who have sent blood to Fry with a negative test for FL and they see nothing of the sort in many people's blood...
More importantly, what's in a name compared with getting well and living unhindered...
With Protomyxzoa (FL-1953), there is definitely hope of total recovery!
The following points are what I can think of off the top of my head for NOW! That being said, please return to this site, as I will be frequently adding to it and altering it as time unfolds and I continue this investigation on the road to healing with my husband, family, and friends by my side!
.........
~ It is often chronic by nature, as it survives within its own protected environment, known as biofilm.
~ It is a protozoan (parasitic) infection. NOT viral or bacterial.
(More information on the topic of biofilm: http://www.frylabs.com/biofilm.php)
~ Since it is a protozoa just as malaria, symptoms often are similar to one another ie. night sweats, searing and aching body pain, and unrelenting intractable head pain, fevers and chills. It can often affect the respiratory tract, causing air hunger and labored breathing. As far as I know for now, it can also greatly impact someone in countless ways, including, multi-nervous system attacks...
~ Detection is very difficult as it hides itself in its biofilm.
~ Biofilm can be starved and thus eradicated by going on a special fat free diet, many prefer to follow the Dr. McDougall Diet, to go ENTIRELY and AGGRESSIVELY fat free... Watch OUR STORY for more details:
~ It can definitely be carried and transmitted by mosquitos, and as far as I know, as mentioned above, can be vector born (vector born: result from an infection transmitted to humans and other animals by blood-feeding anthropods, such as mosquitoes, ticks, and fleas. I.e. Dengue fever, viral encephalitis and malaria).
~ Like many parasites, when under stress they either hide for protection awaiting opportune time to emerge once more, or under trauma they multiply to ensure their survival during times of trauma and thus can make the carrier (human) drastically worse.! Thus symptoms can worsen, ease up, or can even alter in their manifestation over time since your standard blood test will not detect it. So... try to avoid MVA's, traumatic weather/climate change if you have an auto-immune issue, etc!!
~ Treatment for Protomyxzoa aka FL-1953 (not including the overall supplements, detox, vitamins, and other necessary ways to support the body during the die-off phase of the infection) includes a specific no-fat diet to starve out the biofilm which leaves FL-1953 exposed to an alert immune system and effective malaria-like medications. There are a few routes which an infected patient can take regarding the treatment actually used to kill the "bug", but I would highly encourage you to consult Dr. Stephen Fry on his findings and advise in all matters relating to this infection... I can also say that he has a VERY high cure rate (no relapses) and the average patient's return to health usually takes somewhere between four to eight months, depending upon many other possible factors.
~ Ridding your body of anything harmful, be it toxins of various nature and forms, infections of all "shapes and sizes", etc. can be an overload, and some bodies, roughly 1/4 people cannot expel the toxins on their own the way the other 75% of people can, which is why some, after YEARS of treatment, they remain deathly ill, or just still, "not feeling good" yet...
~CHOLESTYRAMINE (csm), which is commonly used to lower cholesterol levels, is what I took in the movie "Our Story" (now on Youtube) that binds to toxins and helps to rid them from bodies that need assistance during detox: please read Dr. Ritchie Shoemaker's http://www.survivingmold.com/protocol and thoughts and WATCH HIS VIDEOS.... And we'll be happy to answer any questions we are able to!... For me, and for MOST, you must undergo proper testing so you know how to treat (and TRY EVERYTHING IF YOU HAVE TO... There is not a cut and dry way of treating effectively necessarily... Each case/person is unique! As you no doubt well know?)
** I am in NO way, shape, or form, a licensed doctor or health professional. Please do not take any of this advise without first seeking the opinions, consultation, diagnosing via tests in vitro and in vivo (live body ie. symptomatic diagnostics!), and in depth guidance from a medical or naturopathic physician. Be sure to send your blood to FRY LABS: http://www.frylabs.com/ and IGeneX Labs: http://igenex.com/Website/ if you have these symptoms, and only after such things as malaria and west nile etc. have been ruled out. Also, coming from a young 22 year old wife who has seen over 45 doctors and specialists, I urge and plead with you to take your own health into your own hands by investigating as much as you can, asking questions, DOUBLE checking things, and never assuming your doctor knows everything. I have found FRY LABORATORIES to be the most useful source on this emerging infection, and will continue to post information and it surfaces to public awareness. We have contact with those at the "front lines", so I will be sure to tack on more facts and helpful tips as the weeks go on and research etc. continues!
There is HOPE, both this side of Heaven and for all eternity! My prayer is that you, my dear reader, wouldn't just be fully of gladness to know you'll be physically restored someday soon, but also that you may be full of JOY! The joy that can only come from knowing just how loved you are by your Creator, and how much you are loved by Jesus Christ the One who took our place so that we may be free to love others (everyone) with His love, and be full of the same powerful Spirit that raised Jesus from the grave! :)
May you understand that it is about so much more than just simply the "high highs" and the "low lows" and the "in betweens" of this life...



Christa, I have just watched your story on YouTube; and a lot of mixed emotions come out of your story. Justin did a great job of putting the video together, it did bring across your pain, your struggles, your love for God and each other. Yahweh Elohim restore your body completely and give you the JOY of restoration!
ReplyDelete"The enemy has come to kill (relationships), steal (finances) and destroy (health); But I (Yeshua Messiah) have come to give you a rich and satisfying life" John 10:10 May your life be filled with the abundant riches of God.
"So therefore, many people, like myself, can become very sick when bitten because of not just one infection like the bacteriological disease called LYME DISEASE, but also by other things." Hi! I know a lot about Lyme b/c I have it and it's important to understand that LYME disease is a co-infection of several bacterias and not just one. It does seem as though we humans can get hit with bacteria and parasites all from a single bug bite. So very sad for us. My heart goes out to you, Christa, and I pray you are victorious in your fight against FL-1953. God bless.
ReplyDeleteMy heart aches for everybody who is suffering from this protozoa illness and the bacterial infection lymes disease. It is such a struggle to get well. I wish you all Godspeed in your fight to get well. You all are in my prayers tonight....
ReplyDeleteIn your film, you mentioned a toxin binder that helped you rid yourself of the toxins. Would you mind sharing the name of this product? My entire family is currently being treated for Lyme and co-infections (and am strongly considering contacting Fry Laboratory to see if our recover is being hindered by FL1953), and we are in our second year of treatment and think this product you mentioned may be an effective tool in our battle. Many thanks in advance.
ReplyDeleteHi -
ReplyDeleteWe will be bringing info from this site as well as Fry Labs to our lyme dr tomorrow. Our 16 yr old daughter spent 6 hrs in the ER last night convulsing and blacking out due to the pain. Her symptoms are so similar to yours we are hoping these tests will give us some answers. We thank you from the bottom of our hearts for sharing your journey with us. We wish you nothing but love, health and happiness.
Christa, Hi, My husband was diag. with protomxzoa 1953 from Fry Labs also and has had some very serious neurological poblems, would you please contact me, ctovias@frontier.com Thank you
ReplyDeleteTHANK YOU for your movie. I just passed the four year mark and have just tweaked part of the detox plan. There's a new level of hope and your story helped re-assure it really could be real this time. So for that, I can't thank you enough. And, yes, faith was key. Bless you both and your supportive family and friends!!
ReplyDeleteThank you so much for taking time out to write about this. My doctor feels like I have this but I cannot afford the $500 blood test. Do you have any info on if this is covered by any insurance or do you know anyone who could help with the cost? My email is Smiley.Riley44@gmail.com
ReplyDeleteThank you for any help you can give me.
My doctor did the Fry biofilm smear test that gave the info via picture of my blood on a slide that I was positive for Bart and protomyxzoa. In August 2011 it cost 350.00 and my insurance covered some of it
DeleteHi,
ReplyDeleteYour story was very inspiring. I'm so glad you were able to heal yourself after being I'll for so long.
Like you, I am also 22. I have been ill for a little over a year. I live in northern California, bay area, and have been dx with Lyme, bartonella, and babesia.
The only thing my docs can't put their finger on is a severe head pain at the base of my skull, where my head meets my neck. I also have this dull pain at the back of my head that has been present every waking moment for over a year.
I heard from a friend this infection causes head pain. Do my symptoms sound similar?
I'd really appreciate a chance to speak with you. If you could email me @ louispoletti@gmail.com
I'd really appreciate it.
Thanks
Have they ever looked at a Chiari Malformation? It's a very specific brain injury where the tonsils of the cerebellum descend too far down from the skull. Can be ruled out by MRI.
DeleteCongratulations on your return to health. What a blessing! Did your doctor ever discuss Protomyxzoa being sexually transmitted?
ReplyDeleteAll the best to you and your husband and thank you for sharing your story and inspiring others to keep fighting their way back to health.
Thanks for sharing all this so that others may be blessed and healed. One comment/warning for others: One of the doctors mentioned above, Dr. Marty Ross of Healing Arts Partnership (LLMND) here in Seattle, offers shamanism as part of his healing practice. We were informed of this only after our initial visit with him; it was not on his website at the time. We found that fact and his lack of disclosure very disconcerting, to say the least, and left for someone else.
ReplyDeleteYou were very fortunate to be diagnosed with Lyme within four years of infection. I was diagnosed after 28 years of infection. I underwent aggressive, iv antibiotic treatment and herxed near-continously for 18 months. My health was irreparably damaged. My Lyme symptoms are far worse now than they were prior to treatment. To treat someone with 28 years of infection and advanced symptoms aggressively with iv antibiotis and to allow for such prolonged, severe herxing is insane. The huge majority of people who have Lyme/coinfections as long as me, or even half as long, do not benefit from antimicrobial therapy, because they herx too heavily. Herxing is a manifestation of inceased neurotoxicity via the kynurenine pathway. This form of neurotoxicity is caused by the increased inflammatory immune response (herx) when the infection is lysed. Yes, antimicrobials can help someone who has been ill for only four years. But for people ill with Lyme/coinfections for 10-15 years or longer, they should not be used too aggressively.
ReplyDeleteWhy did you remove your video on YouTube?
ReplyDeleteTo the person who wrote the comment above: those herxes are a good thing, and need to be endured to eventually come to better health. While they are going on it may seem like you will die, but you will not die. And they do end...
Friends may see your misery and take you to the emergency room, where all that they can do for you is rehydrate you with IV fluids and try to mitigate your pain. The next herx will not be as bad- maybe by only a millimeter, but not as bad, and the next herx after that will again be not as bad as the one before. It might help to educate yourself about the herxheimer effect, which was first discovered in treating syphilis patients. What the herx confirms is that this is Lyme disease, and you are on the path to healing.
And it was not a herx that went on for 18 months. I don't know what it was, maybe co-infections, but not a herx.
To the Auther;
I came to your site because I am trying to find out how to disrupt the biofilms on the Protomyxzoa in my system. My test from Fry labs showed a widespread infection and hemo-bartonella as well. (I have already had the Rocky Mountain Spotted Fever and the Ehrlichia resolved.) My LLMD says we must first treat the Protomyxzoa before we can treat the Lyme effectively.
I am currently on Vermox to treat the Protomyxzoa, but understand that the biofilm which protects the Protomyxzoa must also be addressed.
Please reply at survive in the wild (all one word) at yahoo dotcom.
Thank You,
Huntnlady
I was diagnosed with FL1953 about a year and a half ago. I was resistant to the diet so I tried to make myself feel better with vitamins that would give energy to a normal person. Big mistake! Within 4 months I wasn't able to stay awake past 9:30 in the morning. I thought I was dying. I stopped taking the minerals and felt significantly better within a matter of days. I just went back to Dr. Fry to tell him what happened and to find out what else I should be taking/avoiding. I have to avoid fat, sugar, minerals, protein powders, and he told me I could take an herb called Artemesia if I don't want to take the antibiotic. My symptoms are widespread pain, fatigue, and brain fog. He also said that they now know that there are 5 strains of this infection so we still need to be protecting ourselves during mosquito season to avoid being infected doubly.
ReplyDelete