Mikaila's Lyme Disease Germany Cure
Donation protected
From Tyler Moon, Mikaila's fiance and Elsa's Daddy:
Hello family and friends,
The first thing I want to ask you to please do is to share this via all of your social media and ask them to do the same! Today I wanted to talk to everyone about Mikaila and how she has recently been diagnosed with having Lyme disease. There are many, many strains of Lyme Disease and associated co-infections and she actually has two of them, one of which is the nastiest form of Lyme there is.
Growing up, I never knew much about Lyme disease and how especially terrible it is. The most recently discovered strains, if left untreated, can even eventually be fatal. Iknow there are a lot of people who don't know about Lyme disease either so I hope this will help someone from one day contracting this terrible disease.
After Mika was bitten by three ticks in Gainesville, FL in April of this year, she developed the infamous “Bullseye” mark and started experiencing the classic symptoms of Lyme disease, extreme joint pain, headaches, nausea, trouble with her memory, brain fog, fevers, muscle spasms, eye pain, blurred vision and discomfort all over.
Many people who have contracted Lyme disease go to their doctors exhibiting these symptoms and sadly, their doctor is not familiar enough with Lyme and do not test for it. These organisms microscopically, are shaped like corkscrews and literally screw themselves into your tissues, muscles, bones & brain. Often when they do test for it, the tests come back with a false negative so the patients are told they don't have Lyme disease and are left suffering and without help. Sometimes it takes many tests to finally yield a positive result but there are no false positives so when you do get a positive result you are confirmed to have Lyme disease. After close to $1,000.00 in testing, Mika was confirmed to positively have Lyme disease.
From what we have gleaned having studied and researched about Lyme disease exhaustively these last few months, it seems as though it is not taken seriously by most doctors in this country even though cases of Lyme disease are skyrocketing. Even the CDC and the FDA do not yet recognize Lyme disease as a chronic illness. Mika's Dad Eric will explain more about that below if you are able to take the time to read what he's written.
Over the course of the last four years, cases seem to be doubling each year and studies show that there are 10 times more Lyme patients than HIV patients. If Lyme disease is not treated with the correct antibiotics within the first four weeks of being infected, you are now labeled as having CHRONIC Lyme disease for the rest of your life, never to be cured, but only treated with taking antibiotics for the rest of your life, which leaves you having a terrible immune system and feeling weak and destroying your liver which leads to leaky gut syndrome. Sadly, without our realizing it, Mika was given the WRONG ANTIBIOTICS for her early treatment, they did not work and now she is a chronic Lyme patient. The antibiotics she was given can only suppress the Lyme bacteria and can only get it to maybe go dormant. The actual bacteria is a cousin of syphilis and a lot of people do not know that Lyme disease can be sexually transmitted.
Through our research, we discovered that there is only one Clinic in the entire world which actually offers a CURE for Lyme disease and is only practiced in Germany where they will raise her body temperature to 106.9° multiple times to kill off the bacteria completely. This is a three-week treatment. We plan on going as soon as possible to better her chances of destroying this terrible disease before it destroys her. We will have to be there for twenty-one days. Here is a link to a video of Dr. Douwes at Klinik St. Georg in Germany explaining this treatment he discovered.
https://youtu.be/3bId9ycVuds
Also, we were Initially told by several medical professionals, that Lyme could not be transferred through breastfeeding but we just found out the other day that it indeed can be so Mika had to stop breastfeeding our one-year-old daughter Elsa cold turkey overnight! We are now praying fervently that Elsa will not contract Lyme because this treatment cannot be administered to infants. Lyme can easily kill a baby.
I love Mikaila so much and I know you all do as well. She is my best friend and soon to be wife. We have set up this GoFundMe page to help with the costs of ridding her body of this terrible disease.
The overall cost for the treatment, medications, travel expenses, aftercare and other miscellaneous expenses are expected to exceed $75,000.00. This treatment is not covered by insurance and you can read why that is by reading what Mika's Dad Eric also wrote below.
Elsa and I need her in our lives, just as the rest of her family does too. We want to have a normal life so that Mikaila can be happy and healthy because that is what good people deserve. We want to have more children, Elsa needs some siblings haha. Left uncured, there is an increase of as much as 70% of the possibility of a miscarriage, and if the baby survived they would contract the disease and have an increased chance of autism and other health problems throughout their lives.
We appreciate everyone's kindness regarding the situation and would very much appreciate any help that you are willing to give to help this wonderful person have a wonderful life. Thank you to everyone who took the time to read this. I really hope we are able to meet our goal and to get Mikaila the treatment she so desperately needs.
Please take the time to know the precautions of how to prevent getting Lyme disease and always check yourself for ticks so that you or a loved one never has to go through this. If you would like to know more you can ask us or there is a good documentary on Lyme disease and its long term effects called “Under Our Skin”.
https://topdocumentaryfilms.com/under-our-skin
Our names are Eric and Ruth Bright. We are Mikaila's Mom and Dad.
From Eric (Mikaila's Father):
I just wanted to add a couple of things to our story which will help you to understand what Lyme disease actually is and how it came about in it's current & deadly form.
Amazingly enough, what I am about to tell you, prior to Wednesday, July 17th 2019 just this last week, when it finally came to light in the national news, was being brushed off as a conspiracy theory by the US government, military and CDC. Had I not had this video to link to, you might assume that I too was just being another wacko conspiracy theorist.
http://www.fox5atlanta.com/news/house-orders-pentagon-to-reveal-whether-it-turned-ticks-into-biological-weapons
That said, the reason that neither the CDC nor the FDA will acknowledge Lyme disease as a chronic disease is because Lyme disease as we know it today is a result of the US government conducting biological warfare testing on Plum Island in the 1950s, 60s and 70s and if conclusive and beyond reproach evidence can be forced to be acknowledged by the government then they will likely be on the hook for billions of dollars in lawsuits. Despite the fact that in most cases you generally cannot sue the US government, TORT law in this case, seems to suggest you can. This is the main reason Insurance companies won't cover this "experimental" treatment. The strange thing is, is that this exact treatment is approved by the FDA for some forms of cancer.
There's also a book that was just recently published on May 14th 2019 by Stanford University researcher Kris Newby called
"Bitten, The Secret History of Lyme Disease and Biological Weapons".
Kris's book has broken this thing wide open.
http://www.harperwave.com/book/9780062896278/Bitten-Kris-Newby/
Please Donate if you can. My daughter and granddaughter, as well as all of our other nine grandchildren, mean everything to us.
Even if it’s only $1.00. Please help us save Mikaila!
Even if you can't donate, please share this link on all of your social media!
Thanks and God Bless,
Eric & Ruth Bright
Help spread the word!
Hello family and friends,
The first thing I want to ask you to please do is to share this via all of your social media and ask them to do the same! Today I wanted to talk to everyone about Mikaila and how she has recently been diagnosed with having Lyme disease. There are many, many strains of Lyme Disease and associated co-infections and she actually has two of them, one of which is the nastiest form of Lyme there is.
Growing up, I never knew much about Lyme disease and how especially terrible it is. The most recently discovered strains, if left untreated, can even eventually be fatal. Iknow there are a lot of people who don't know about Lyme disease either so I hope this will help someone from one day contracting this terrible disease.
After Mika was bitten by three ticks in Gainesville, FL in April of this year, she developed the infamous “Bullseye” mark and started experiencing the classic symptoms of Lyme disease, extreme joint pain, headaches, nausea, trouble with her memory, brain fog, fevers, muscle spasms, eye pain, blurred vision and discomfort all over.
Many people who have contracted Lyme disease go to their doctors exhibiting these symptoms and sadly, their doctor is not familiar enough with Lyme and do not test for it. These organisms microscopically, are shaped like corkscrews and literally screw themselves into your tissues, muscles, bones & brain. Often when they do test for it, the tests come back with a false negative so the patients are told they don't have Lyme disease and are left suffering and without help. Sometimes it takes many tests to finally yield a positive result but there are no false positives so when you do get a positive result you are confirmed to have Lyme disease. After close to $1,000.00 in testing, Mika was confirmed to positively have Lyme disease.
From what we have gleaned having studied and researched about Lyme disease exhaustively these last few months, it seems as though it is not taken seriously by most doctors in this country even though cases of Lyme disease are skyrocketing. Even the CDC and the FDA do not yet recognize Lyme disease as a chronic illness. Mika's Dad Eric will explain more about that below if you are able to take the time to read what he's written.
Over the course of the last four years, cases seem to be doubling each year and studies show that there are 10 times more Lyme patients than HIV patients. If Lyme disease is not treated with the correct antibiotics within the first four weeks of being infected, you are now labeled as having CHRONIC Lyme disease for the rest of your life, never to be cured, but only treated with taking antibiotics for the rest of your life, which leaves you having a terrible immune system and feeling weak and destroying your liver which leads to leaky gut syndrome. Sadly, without our realizing it, Mika was given the WRONG ANTIBIOTICS for her early treatment, they did not work and now she is a chronic Lyme patient. The antibiotics she was given can only suppress the Lyme bacteria and can only get it to maybe go dormant. The actual bacteria is a cousin of syphilis and a lot of people do not know that Lyme disease can be sexually transmitted.
Through our research, we discovered that there is only one Clinic in the entire world which actually offers a CURE for Lyme disease and is only practiced in Germany where they will raise her body temperature to 106.9° multiple times to kill off the bacteria completely. This is a three-week treatment. We plan on going as soon as possible to better her chances of destroying this terrible disease before it destroys her. We will have to be there for twenty-one days. Here is a link to a video of Dr. Douwes at Klinik St. Georg in Germany explaining this treatment he discovered.
https://youtu.be/3bId9ycVuds
Also, we were Initially told by several medical professionals, that Lyme could not be transferred through breastfeeding but we just found out the other day that it indeed can be so Mika had to stop breastfeeding our one-year-old daughter Elsa cold turkey overnight! We are now praying fervently that Elsa will not contract Lyme because this treatment cannot be administered to infants. Lyme can easily kill a baby.
I love Mikaila so much and I know you all do as well. She is my best friend and soon to be wife. We have set up this GoFundMe page to help with the costs of ridding her body of this terrible disease.
The overall cost for the treatment, medications, travel expenses, aftercare and other miscellaneous expenses are expected to exceed $75,000.00. This treatment is not covered by insurance and you can read why that is by reading what Mika's Dad Eric also wrote below.
Elsa and I need her in our lives, just as the rest of her family does too. We want to have a normal life so that Mikaila can be happy and healthy because that is what good people deserve. We want to have more children, Elsa needs some siblings haha. Left uncured, there is an increase of as much as 70% of the possibility of a miscarriage, and if the baby survived they would contract the disease and have an increased chance of autism and other health problems throughout their lives.
We appreciate everyone's kindness regarding the situation and would very much appreciate any help that you are willing to give to help this wonderful person have a wonderful life. Thank you to everyone who took the time to read this. I really hope we are able to meet our goal and to get Mikaila the treatment she so desperately needs.
Please take the time to know the precautions of how to prevent getting Lyme disease and always check yourself for ticks so that you or a loved one never has to go through this. If you would like to know more you can ask us or there is a good documentary on Lyme disease and its long term effects called “Under Our Skin”.
https://topdocumentaryfilms.com/under-our-skin
Our names are Eric and Ruth Bright. We are Mikaila's Mom and Dad.
From Eric (Mikaila's Father):
I just wanted to add a couple of things to our story which will help you to understand what Lyme disease actually is and how it came about in it's current & deadly form.
Amazingly enough, what I am about to tell you, prior to Wednesday, July 17th 2019 just this last week, when it finally came to light in the national news, was being brushed off as a conspiracy theory by the US government, military and CDC. Had I not had this video to link to, you might assume that I too was just being another wacko conspiracy theorist.
http://www.fox5atlanta.com/news/house-orders-pentagon-to-reveal-whether-it-turned-ticks-into-biological-weapons
That said, the reason that neither the CDC nor the FDA will acknowledge Lyme disease as a chronic disease is because Lyme disease as we know it today is a result of the US government conducting biological warfare testing on Plum Island in the 1950s, 60s and 70s and if conclusive and beyond reproach evidence can be forced to be acknowledged by the government then they will likely be on the hook for billions of dollars in lawsuits. Despite the fact that in most cases you generally cannot sue the US government, TORT law in this case, seems to suggest you can. This is the main reason Insurance companies won't cover this "experimental" treatment. The strange thing is, is that this exact treatment is approved by the FDA for some forms of cancer.
There's also a book that was just recently published on May 14th 2019 by Stanford University researcher Kris Newby called
"Bitten, The Secret History of Lyme Disease and Biological Weapons".
Kris's book has broken this thing wide open.
http://www.harperwave.com/book/9780062896278/Bitten-Kris-Newby/
Please Donate if you can. My daughter and granddaughter, as well as all of our other nine grandchildren, mean everything to us.
Even if it’s only $1.00. Please help us save Mikaila!
Even if you can't donate, please share this link on all of your social media!
Thanks and God Bless,
Eric & Ruth Bright
Help spread the word!
Organizer
Tyler Kenneth Moon
Organizer
Hollywood, FL