Liver Fluke Fasciola Hepatica and the lives it wrecks
I have come to learn that if you have a parasite infection that you unknowingly give people free rein to discriminate and dehumanize. It started in fall 2020, like I'd had my chest filet open. The most god awful pain ever, lump in throat that continued to swell to where I couldn't swallow solids, spine would swell, neck and into ears and jaw so swollen like it was wired shut, my ear canal eventually swelled shut and the taste of amphibian came to mind as I developed a unusually disgusting constant slime feeling in mouth. Then the lump in throat seemingly ruptured one day in March 2021 as if I was stabbed from inside out, knocked the wind out of me.then proceeded to salivate for several days so much so I had to walk around with a cup and it continued to get thicker and then gritty and I noticed I was spitting up these little white things that looked like sesame seeds and they were moving so went to local ER and they diagnosed me as delusional right out the gate. I went to the emergency room and urgent Care combined a total of 14 times in a two week period as I knew that something much more sinister was coming down the pipeline from my symptoms I was having far worse than the one I already had and I proceeded to choke up things that look like that's what I said I even told them that it looks like flukes nobody would listen to me nobody would do anything and in fact I treated myself with albendazole and praziquantel and all it did was slow it down. Oh did I forget to mention that it's subcutaneous as well yeah it's not just in my gastrointestinal tract and I'm sure you guys will learn to who I am if it kills me because it's imagining it's in my central nervous system because one came out of my eye on January 3rd and it's only a matter of time literally I can feel quicker in my brain sometimes and like my whole head almost stutters on my head thinking problems timing scheduling I can't do anymore I've lost my job because I can't work it's all I can do to get through the day every 12 weeks it goes through a peak. And what I mean by that is goes crazy under my skin and the ones under my skin and in my eye and for my bell I'll look completely different cuz they're all in different stages of morphology and I don't think I'm a doctor but education is education and I've been forced to educate myself on this and I've been doing nothing but trying to save my own ass since March 21 and it's my story and if I don't tell it nobody else will and this disease right here I should not have to be beating down doors to get a blood test that should I have been to me in a country where we were made to think that we don't have this issue here but let me tell you I've done my homework and it's a known thing and we'll see the vets are well aware of the liver flick issue and virtually no farm is free of liver fluke in California and it is waterborne that's a fact and it was also a fact is that the doctors are so poorly educated on parasite infections that they would rather dismiss you and send you home sick as hell even though I've had plenty of signs that point to supporting what I'm saying I have but they don't care it's seriously like I'm living in la la land I mean I don't know how to explain it it's like the Twilight zone it's almost like it's being done on purpose because all they're doing is setting me up to die I'm going to die and if the last thing I can do before I die or in my desk is get the law changed so that people don't have to go to the CDC to get this blood test or the medication then that's what needs to happen because I shouldn't have to be fighting with what little energy I have in my body to just get simple freaking help the CDC said it's diagnosed by either eggs in your stool or by seeing adult flukes well here's my adult flukes take a look
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I just now found this thread. Is there a way to easily see what they recommended as a fix? It sounds like the original poster is out of time. Like the typical BS we get from Western medicine, denying them for months while they slowly die. I'm going through that phase right now. I'm starting to lose my ability to think and sleep. To me it seems like they take three or four different forms. Or they cohabitate with some other parasite. But getting someone in Western medicine to believe you? I have literally had doctors cancel appointments the day before and then try to schedule me for 6 months out. That's b*******
I'm glad somebody is making progress. Basically I am positive I got flukes from fresh Alaskan salmon flown directly into Dayton ohio. This was last year where they caught the fish at the worst possible time for spreading liver flukes. The fish market that sold them denies it. The CDC denies it. Every doctor I've talked to is denying it. One doctor even left the state to go to another state because he once found liver flukes in a woman. Just watch the special monsters inside me about liver flukes.
Why is it so hard to get a simple blood test? Why is the CDC the only one that can order triclabendazole? There is a systemic Nationwide problem with parasites and the CDC is culpable in the cover-up. Why not help us fix them while they're in the early stage? Or are they afraid they've become immune to everything
I'm new to this form but it seems like I'm signed in properly. So if there's a way to private message me please do. I've been struggling with these since late fall a year ago and I haven't really made much progress except they are getting bigger. How did you convince anyone in the medical field to help you?
As soon as I read the first post and then the rest with all the photos and I started to cry as I sit here going through the same things for so many years. I feel like I’m dying. And I keep trying to do all the right things. I had an episode so bad I wa sure I would die that night. It’s a long story scary as hell. I met one other person via posts over at curezone. This man was experiencing the same thing that happened to me and he too almost died. I’m dealing with other chronic illnesses but this is the thing that seems to be beating me. I’ve fought for years. I’m so sad to see you all going through the same thing, yet I feel a little less alone. I’m an older woman and my family acts like I’m crazy. And I’m not. I’m just very ill and need help. Thank you for sharing your stories. I’ll share photos in my next post here. So happy to find your posts. Hang in there and keep fighting. We can’t give up. 💗😢