GoFund me (or my wife) for Lyme's

An invisible epidemic, lyme. A friend if mine had untreated lyme leading to cardiac issues before it was finally caught. I'm sorry to hear about your family's struggles, hope things get better for your wife
Lyme is the fastest growing vector born bacterial infection on the planet, and one that if allowed to become chronic can produce a quality of life that is worse than almost any other major disease. I was first infected in the 1980's in the Santa Cruz Mountains, but wasn't diagnosed until 2007 when I got extremely sick after a shoulder operation back in 2005. 2 yrs and $30,000 later I finally got a proper diagnosis. Trust me when I tell you that you DO NOT want what I have, so I urge everyone in this industry to take the time to educated themselves concerning this truly life altering disease.

I would encourage anyone who can afford to support this go fund me account to do so. Sumer, Jesse, and their beautiful kids are embarking on a voyage that most here simply cannot comprehend. The emotional, physical, and finacial toll can be brutal, but I have no doubt that with the love and support of her family Sumer will get well.

My lyme riddled brain is sending Sumer sunshine and positivity.
 
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@evo so sorry to hear about your wife’s battle. I went through something similar with my wife a few years ago and can totally relate to trying to work, care for her, and care for kids. One of the darkest times of my life. Money is crazy tight right now but you and yours will be in our thoughts and prayers. Sounds trite but there is light at the end of the tunnel. Hang in there brother.
 

I recommend this guy who says that IV drips are the only way to eradicate it for sure.

I'm sorry to hear your wife is suffering the Lyme disease and hope she gets better.
 

I recommend this guy who says that IV drips are the only way to eradicate it for sure.

I'm sorry to hear your wife is suffering the Lyme disease and hope she gets better.
I can tell you from experience that IV antibiotics are a powerful tool for killing the lyme bacteria, but if you have had a long standing infection the has gotten into your nervous system there is no eradicating it. At that point your a trying to lower your load as much as possible and live as symptom free as possible. There is also the fact that lyme almost never travels alone. Along with lyme (bacteria), there are multiple co-infection to deal with. Babesia (a malaria like parasite), Bartonella (bacteria related to cat scratch fever and the spawn of the fucking devil), Ehrlichia, Rickettsia, Mycoplasma, Viruses (HH6, EBV, ect,) Chlamydia pneumonia, and many other yet unknown bugs. Needless to say many of these will not be killed with antibiotics.

Even if you catch a lyme infection early it is highly recommended that you take a very long round of antibiotics. The standard 10 days of doxycycline will not work, and one needs to do 5-6 weeks. The lyme bacteria is extremely smart and when under attack from antibiotics or other modes of killing some of the spirochetes will go into what is know as a cyst, where they are basically impervious to most antibiotics. You can take Flagell or Tindamax to bust the cyst's but these antibiotic can have long lasting negative effects on ones health. When the coast is clear from antibiotics the spirochetes simply return to going about their business of fucking up your life.
 
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I recommend this guy who says that IV drips are the only way to eradicate it for sure.

That's silly... without debating the merit of the statement...
it's the logic that's flawed.
IV maybe the only way HE KNOWS, but there may be other things that he doesn't know about.
 
One of my friends saw Raxlan for many years and speaks highly of his work, but nobody knows everything. Evo did you see my first post on this thread. Wondering if you may have missed it because you were typing at the same time.
 
They probably called it some kind of weird auto-immune disease and gave her steroids, which is about the worst thing anyone can do for Lyme.

I had my first case of Lyme in 1998. I was 38 at the time and thought I was just getting old and couldn't climb the trees like I used to. When the rash finally showed up, I went to the doctors, pretty sure I had Lyme. Asked him if I needed a blood test, he excused himself and brought every member of the staff into the examination room to look at me and said: "THIS IS LYME". It took me 5 years to fully recover.

I could write for hours about Lyme. the evil biological warfare on Plum island that was the genesis of this and other diseases like West Nile. the millions of misdiagnoses. the spirochetes as a cause of Alzheimer's, Parkinson's, and such.


(Exceeded character count so reduced your post)
We/she can check off most of that list.. Only rife machine that is tangible is for rent (hence the gofundme).. She is working with other "issues" which affects her bodies ability to detox, and take b vit's.
With due respect I didn't post this seeking advise, even though, from my crash course, much of what you have listed is on par.

Truth is I need to be home to care for the kids, and care for my wife. I need to run my business, and need to work to fund our house, business, kids needs, and medical costs.

We are easily 15-20K + in the hole from hard medical expenses pre-diagnosis trying to find out what the hell is wrong with her from the first 14 months of symptoms. The past 3-4 months have been huge (post diagnosis). This is well before any incidental costs, too many to list.

Now there is the cost of treatment! Much of which isn't covered by insurance.

All of my 'free' time is spent caring for the family. Then if I get an hour or so during business hours I'm on the phone with bill collectors and Liberty Health Share. We 'fell' for LHS which was great for just needing (major) medical here and there, but is impossible for anything serious. I'm spending an average of a 2 hours on the phone with them to see what the hell is going on, what the status of each and every bill is, what their ETA for payment is, blah blah... I got blown off the job today, and was on the phone for 3 1/2 hours regarding 3 bills which are about to be sent collections. (been working on her files, calls etc since 2pm) This is only 3 out of a binder full, so $2,400 for a Rife machine (which I hear works wonders for some) is out of the question for the moment.

Then comes needing to test our daughter, she has had patchy dry blotches on her skin which come and go since birth. Moodier than most her age (in my experience), unconsolable moments daily (not the normal terrible two's, but we have moments of that too). Digestive issues with same patterns as her mom. She was exposed to Lyme in utero, which it's very recent that it has been proven to pass as such in 2018. Then there is the possibility of it being a STD.

She has improved from her worst, but is far from 100%. She is getting the best care we can afford (our of pocket, then submit for reimbursement, then hours of phone calls/faxes/scanned documents/medical codes/getting providers to give us the right info/lost submitted bills/ REPEAT).

Her new doc, only takes insurance which isn't available in our county unless the employer offers it. I'm obviously self-employed so I can start offering bennies (not opposed to) however that means brining her on payroll and offering bennies to all. 3 employees (myself, wife and other) > $1500 per month plus other costs (workmans come, GL payroll going up, taxes blah blah).

I'm completely blown away about the amount the gofundme has generated in the past few days, quite a bit from people here on the Buzz whom I've never met. It truly touches me! The hard truth though is, the amount raised will only cover one bill with a little left over for different one.

We have the medical pathways down. That is why I didn't post asking for advise of what treatment is better or worse than any other. It's also why I didn't respond to this post before now.
 
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We/she can check off most of that list.. Only rife machine that is tangible is for rent (hence the gofundme).. She is working with other "issues" which affects her bodies ability to detox, and take b vit's.
With due respect I didn't post this seeking advise, even though, from my crash course, much of what you have listed is on par.

Truth is I need to be home to care for the kids, and care for my wife. I need to run my business, and need to work to fund our house, business, kids needs, and medical costs.

We are easily 15-20K + in the hole from hard medical expenses pre-diagnosis trying to find out what the hell is wrong with her from the first 14 months of symptoms. The past 3-4 months have been huge (post diagnosis). This is well before any incidental costs, too many to list.

Now there is the cost of treatment! Much of which isn't covered by insurance.

All of my 'free' time is spent caring for the family. Then if I get an hour or so during business hours I'm on the phone with bill collectors and Liberty Health Share. We 'fell' for LHS which was great for just needing (major) medical here and there, but is impossible for anything serious. I'm spending an average of a 2 hours on the phone with them to see what the hell is going on, what the status of each and every bill is, what their ETA for payment is, blah blah... I got blown off the job today, and was on the phone for 3 1/2 hours regarding 3 bills which are about to be sent collections. (been working on her files, calls etc since 2pm) This is only 3 out of a binder full, so $2,400 for a Rife machine (which I hear works wonders for some) is out of the question for the moment.

Then comes needing to test our daughter, she has had patchy dry blotches on her skin which come and go since birth. Moodier than most her age (in my experience), unconsolable moments daily (not the normal terrible two's, but we have moments of that too). Digestive issues with same patterns as her mom. She was exposed to Lyme in utero, which it's very recent that it has been proven to pass as such in 2018. Then there is the possibility of it being a STD.

She has improved from her worst, but is far from 100%. She is getting the best care we can afford (our of pocket, then submit for reimbursement, then hours of phone calls/faxes/scanned documents/medical codes/getting providers to give us the right info/lost submitted bills/ REPEAT).

Her new doc, only takes insurance which isn't available in our county unless the employer offers it. I'm obviously self-employed so I can start offering bennies (not opposed to) however that means brining her on payroll and offering bennies to all. 3 employees (myself, wife and other) > $1500 per month plus other costs (workmans come, GL payroll going up, taxes blah blah).

I'm completely blown away about the amount the gofundme has generated in the past few days, quite a bit from people here on the Buzz whom I've never met. It truly touches me! The hard truth though is, the amount raised will only cover one bill with a little left over for different one.

We have the medical pathways down. That is why I didn't post asking for advise of what treatment is better or worse than any other. It's also why I didn't respond to this post before now.

Sounds tough going. Been there but not quite to the same scale. Prayers and best wishes on full recovery for your wife and daughter...
 
What a beautiful family you have!
I can only imagine the stress for all of you and the actual pain for her. I’m sorry to see this happening and I hope for tons of happier and easier years coming for all of you.
You’re a good dude, doing everything you can for those who matter most.
All the best to you and yours man :)
 
Not an easy position to be in. Just running a tree biz is a herculean task for many. I'd put out a local request for a rife machine and see if you can find someone locally to lend you theirs. If not I'll send mine out on loan.
Thanks we will see how it goes. The plan currently is to rent one for a month and then reach out for loaners. If the go fund me cover out ass and then some we will invest in one for ourselves
 
I hope you get all the help you need. Personally I gave most of what I had to charitable causes, etc. so have little if anything to give away.

I've never had Lyme to my knowledge. When I was typing the Raxlin link a friend from Old Lyme, Ct was stopping in ironically. Lots of ticks in Sam's fields in Old Lyme, for some reason they don't bite me. I've invested a lot in my health but am financially low income. I saw Raxlin in the early 80s for a food allergy when he was in Ridgefield. I'm sure he is expensive. Natural alternatives I guess are not strong enough, echinacea in the highest doses and other immune boosters like organic garlic.
 
I’m an avid hunter. I’ve scales way back due to the constant fear of tick bites. I hardly bow hunt due to the insane amount of ticks in VA. I’ve struggled with my own health issues and so far no test has revealed anything. It’s scary
 
I’m an avid hunter. I’ve scales way back due to the constant fear of tick bites. I hardly bow hunt due to the insane amount of ticks in VA. I’ve struggled with my own health issues and so far no test has revealed anything. It’s scary
It is scary, both on the micro picture and the macro. Lyme can seriously mess a person up, and we know so little about it.
I try not to get wrapped up in conspiracy theories, but the reason why most are so believable is they have some ground in truth. I don’t know (nor does it matter right now) if this is some crazy government engineered biological warfare weapon run amok. But it is fact that we did testing on insect vectored pathogens.
It’s crazy at how it’s estimated that over 300-400,000 new cases there are per year! We don’t even have proper tests with effective rates over 60% at best! Then there is the nuts and bolts of how this bug works. It’s been proven as recently as 2018 to cross the placenta. It’s been found in semen and vaginal fluid, proven to sexually transmit in mice but it’s a hard fast belief it can’t do the same in humans?!
Right now it’s bigger than the AIDS epidemic and I really don’t see ANYthing close to the same public awareness campaigns. Most folks who I speak to here aren’t even aware we have ticks let alone Lyme in the PNW.
The island I live on has basically banned hunting, everyone loves to tame the deer down and feed them. No predator other than vehicles. I know of at least 4 motorcyclist who have died from hitting them in about as many years.
I can’t believe how well my wife is keeping it together emotionally. At her worst she would have panic attacks which wouldn’t allow us to go out in a crowd (dinner included). She has some affect which messes with her balance, vertigo and she chronically feels like she is rocking back and forth as if on a boat. This has been the primary symptom for the past 12-14 months.
What we need is to kick this lymes ass on the macro picture. There is so little knowledge, the researchers need to research, the gov needs to fast track funding! We NEED universal healthcare. Many folks don’t even know they we’re bitten, the bullseye rash happens something like 20% of the time, and my wife is proof that sometimes the only first symptoms are kinda like the flu. Out of the four bites she knows of ALL of them were super tiny bugs, we are talking that we used a magnifying glass to ID them as ticks. I’ve seen bigger grains of ‘play ground’ sand.
I’m not the praying type either, I respect those who are.
It’s amazing to be a part of this community. Even if we argue with each other and sometimes fight we still will put a hand out to pick each other up when down.
Love ya all!
 
I’m an avid hunter. I’ve scales way back due to the constant fear of tick bites. I hardly bow hunt due to the insane amount of ticks in VA. I’ve struggled with my own health issues and so far no test has revealed anything. It’s scary
You need to get a good reliable test done Steve. The average doctor is gonna do a cheap western blot test which is notorious for giving false negatives. The last thing you want from a lyme test. Igenex Lab in Palo Alto Ca. is the best test I know of, but it aint cheap. You should also be tested for the main co-infections that are usually present with a lyme infection.

If you ever feel like chanting about your symptomology, PM me and I can tell you if you sound like a candidate for better testing.
 

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