Showing posts with label lyme disease. Show all posts
Showing posts with label lyme disease. Show all posts

Wednesday, April 18, 2018

Why I disappeared AGAIN the last 6 months

A wise friend of mine suggested I start this back up to document my journey, again, in trying to stay on top of my disease.  For the last few years I have not been fully well.  I just assumed that there is nothing more to do in recovering so I just quit trying to get better.  I didn't stop all at once.  A few things here...  a few things there.  It wasn't until a few days after my birthday this past October 4th, 2017, that I came crashing down again.  Everything started to come back.  Every haunting, agonizing, tortuous symptom of Lyme Disease that I had before was creeping back in.  It started with higher pain levels until eventually the neurological problems started returning.  I had to up my antidepressant and use the heating blanket on its highest setting to get some kind of relief.  I took supplements, did cleanses, and kept distracted so I didn't go mad thinking about it.  I had to give up on a lot of my normal activities just to save energy for things I had to prioritize.  I stopped talking to friends, skipped going places and stopped calling people because I just couldn't and didn't want to explain, again, what was happening to me.

When I tell someone I have Chronic Lyme, or Post Treatment Lyme Disease Symptoms, I usually get a few "try my product" friends who come out of no where.  I know most is all in good intention, but scientifically there is a bigger picture into treatments than cannot be explained in one conversation.  I also hear the "I heard that someone was "cured" from Lyme Disease" quote and it makes me sigh.  It's a Disease.  There is no cure.  The only proof that it has been eradicated is in an autopsy.  At least at this point.

There are SO many conflicting places to turn to for Lyme opinions and support.  Just like treating Cancer, there is no one sure fire way to choose.  Many patients are left getting a second and third opinion after doing hours of personal research just to find a method to attempt.  Mostly just to end up switching paths or tweaking the protocol a bit to help it become more effective or less damaging to the body.

Back to my story...  in January of this year, my nerve damage in my extremities was getting bad.  I knew it was not a good sign.  If I went back into my doctor they would surely put me back on IV medications.  But in March, I started to have heart palpitations again.  It was early signs of Heart Block that suggest that there was a lot of miss firing going on in the wiring of my heart.  I DO NOT want to have a pace maker.  So I just knew I had to see the doctor.

It was March 22, the day of my two beautiful daughters birthdays, (born 7 years apart,) that I was volunteering to work in our church's temple.  It was a happy and calm day!  I was caught off guard when my heart just stopped beating.  Then it spazed out for a bit only beating in partial areas. I became very light headed and felt like I was suffocating.  It started to beat regularly before I could collapse and I just sat there and stared at the computer and waited until I felt better.  I never told anyone there or they would have panicked and called an ambulance.  I knew what was going on and if it was a real problem I would have fainted completely.  I took my health seriously again after that day.

Since then, I've had that happen 3 more times.  This last week has been uneventful as far as my heart.  Thankfully I have time to take care of my surroundings before anything gets too bad, but so far I have been OK.  If I had not started treatments 3 weeks ago...  I would be worse for sure.

As for now, I am doing a round of oral antibiotics until a PICC line can be placed.  Once again I am having trouble with insurance in getting a company to place it.  Hopefully in the next week I can start that...  I will have it for a minimum of 12 weeks.  That's not bad compared to some who are on it for longer than a year so I can handle it!  I have been herxing pretty well and have learned better probiotic and detoxifying methods to help in treatments.  I eat gluten free, dairy free and sugar free...  (well, sugar and dairy is at a very minimal if any.)

The hardest part of this all is not being the sick one.  It is watching all your friends not know what to say or do.  It is watching yourself not get included in things because I can't last the whole time or go anywhere adventurous.  It is trying to not bombard your husband with all your details because there is not much he can do to help me get better.  It only makes him worry more.  It is watching your children have to give up more things and have events canceled like Easter. (Yes, I was physically not able to give them their own Easter baskets or egg hunt in the morning OR color eggs.)  I kept 3 of the 4 kids birthdays low key because I just couldn't do any more than that.  I see my children worry about my illness and they see when I am not well.  It is them not wanting to go to school because they want to stay and be with me.  It is your 15 year old daughter having a panic attack that I could die young from this.  Unfortunately, once I get the PICC line it will be a bigger physical reminder that I am seriously sick...  besides the enormous amount of pills I take daily or the amount of pain or physical limitations I have.

I have seen a bigger change, a change for the better.  We slow down and talk more about what really matters.  We hug, cuddle and spend time together.  We help each other more willingly and serve when another is in need.  We love more unconditionally and forgive more freely.  There grades may not be the best right now, but all there tests show that they are learning a ton!  We may not have the healthiest meals or even anything besides toast or cereal, but we mostly eat together.  Our testimony of the gospel of Jesus Christ is stronger.  We know that Christ can and will heal us.  He will never leave us alone.  He may not take the physical pains away but he can heal our heart and spirit.  We all know He lives and loves us all.  He knows our name.  He has given us everything we need as long as we use it.  I am so thankful to be born at this time when the True Gospel of Christ is here on this earth again.  I am SO thankful to live so close to a temple of God that I may do his works and serve Him weekly.  I am so grateful to be sealed to this amazing family for all time and eternity.  I am truly blessed and am a better person because they are in my lives.  They are my rock and keep me going.  If you are going through a difficult time, I ask you to pray and search the scriptures.  Answers may not come all at once or sometimes not at all.  Do your research and ask for guidance.  He will show you the way.

Tuesday, March 15, 2016

Freedom to be OK with me!

As a kid I always loved the freedom to ride my bike, be outdoors and spend time on a great adventure.  The older I became, the passion grew more inside me.  I chose a path in my late teen years that required me to work a lot and some of this was put on hold.  I savor a few times where I went on adventures with friends.  It was exciting...  exhilarating!   I felt one with nature and absorbed as much as I could.  Hiking, biking, driving, boating, beaching, walking...  I was at peace!

I have a few moments since being married where I continued my passion.  Definitely not as many as I'd like and unfortunately not as many as I had wished to share with my family. 

Now that I have a chronic illness, and possible other health issues that have not allowed for me to fully recover, I have done a lot of spoon saving.  (Google "The Spoon Theory" if I lost you here.)  If I were to go out and let's say hike...  it would take a few days to recover enough to function properly.  Extreme fatigue, body aches and almost a complete body shut down occurs.  I've found ways to help the aftermath and I take less time now to recover, which is a blessing!  But, I still need it.  One day for fun, the next day or two to rebuild.

Lately I feel everything has been worse.  I've been through a period of 3 weeks of sickness.  Started as a sore throat, progressed to a sinus and ear infection. Then came the horrible, chest burning, hacking cough.  Then came the high temps, chills, and migraines. Now, most of my symptoms are gone, but I still have ear aches, chest tightness, and extreme fatigue, (which I expect from 3 weeks of being ill.)  I'm worried about my adrenal glands and how exhausted they are from being sick.  I'm worried about how my cuts on my hand and arm have healed slowly, including getting infected too easily.  (It's a small sign my infection marker is high.)  We still don't know why my WBC is low and why I cannot stay healthy after treatments.  

Sometimes I just feel numb from it all.  I just sit and stare at things and shake my head.  No reason to be angry.  No reason to fear anything.  No reason to complain.   No reason to let it stop me from at least trying to be functional.  When I drive, read, type, cook, stir, lift, fold, dry, wash, hold....  I constantly have to give my arms and legs a good rest and a shake.  I rotate limbs and extremities.  I roll my neck and back around constantly.  I dream of living in my tub just floating away in a very hot bath.  I dream of the house we almost bought that had a spa and a small pool...  I was going to buy one of those neck-flotation-pillows and let my body go.  Water therapy is amazing for my body! 

Everything is in short bursts or in sheer endurance as if I were in a gym pushing my workout to the limits.  I often fold laundry as if it were a competition at the gym...  I probably sound funny counting the pieces of clothing as I near the end of my reps.  I have to make it ridiculously silly or I end up crying at how crappy it is.

I always see the quotes from the support pages I follow about living with an invisible illness and how hard it is for others to understand.   I have never related to it much because I have the most amazing friends and family who believe me and love me no matter what.  But somewhere deep inside I've noticed that just maybe I feel a bit frustrated because I have made myself feel as if I'm supposed to do it all.  First of all...  I'm a stay-home-mom of 4.  What the heck am I thinking!   Haha!  Second, I have a disease that limits me.  What am I doing to myself?  Why would I even give into that crap...  I'm supposed to be super woman, which doesn't exist,  and take on the world??

As I've brought my crazy idea of who I should be back down to reality, I realize I'm pretty awesome.  I don't need to list why...  just know I figured it out.  And I did so while enjoying the outdoors.  I did so while driving my car with the windows open, while laying on my patio chair watching my kids play, (or fight....)  So I thought, why not get out more?!!  I've read my scriptures more and allowed time to contemplate them.  Being sick I was made to let go of even more and to sit back and think about how everything is.

I need to step away more for contemplation. I need to get out for more focus and grounding.  And while I'm at it I can throw in a little adventure to ignite my soul again!  Maybe, if I'm feeling really adventurous, bring the kids...!!  (I love going places with them...  but let's face it...  they are getting older and they fight a lot.  They seem to be grounded or in time out a lot lately.) 

As I write my random thoughts down, I have to remind myself that I'm in good hands.  I have faith in the Lord that I will be healed.  As scared as I may feel at times, it's just a small hiccup in my faith.  I know everything will be ok.   I know I'm in good hands.

Sunday, March 6, 2016

The mask I wear

It's challenging enough being a stay at home mom, a wife, church member, friend, daughter, cousin......  but to have a chronic illness that stops you at a moments notice from functioning....  you end up embarrassed all the time or leaving with a lower self esteem.

This last year I have done my very best to keep my mask of faking "being well" on when living my life day to day.  I cannot explain enough how much daily pain I am in.  I have found ways to help distract me from the torture.  Music, hugging my children, warm baths, taking a drive, watching a movie, doing chores, organizing a drawer, calling a friend, studying my scriptures....  I've learned to  keep moving.  If I sit I will notice the pain more and end up focusing on it which in turn makes it seem maddening.

I have been positive about how "well" my pain level is for that day.  Or how "well" my mind is functioning.   I do tire of feeling like a "woe is me" or "Debbie Downer," or a "let's talk about how crappy it is for me."  I want to be apart of the society I live in but feel so far from.  I give my best smile and spunky energy to anyone I may see.  (I really think Lyme disease can help people to become amazing actors!)  I only let ot all down for my family and maybe one close friend.  Mostly I cave to my husband and thankfully he still loves me and picks up the slack without any complaint.

I have avoided talking about my disease.  No videos, doctor visits, research, or sharing my journey as much on here or on YouTube.  I've been in a constant battle between trying to feel normal and  knowing when to give up... let the day pass by.  Another always comes!   I have this to look forward to at my weakest moments.  Time will pass and I will be in less pain once this moment is over.  It's when I either take a nap, watch a movie until I pass out, or hide away in a dark hole until my senses can function again with all the noise, lights and smells.

Thankfully I've never had a seizure from Lyme.  I've thrown up only a few times because of the pain but not too many since I've learned to meditate through it or distract myself.  (Also I use ginger, or end up taking Zofran!)

I've never been wheel chair bound, although I was pretty close to it before I received my diagnoses.  I was so weak that just getting up from bed to use the restroom would make me crash for hours.

Although my pain has increased since being diagnosed and my fatigue seems the same, I have been made stronger through my perseverance of wanting a normal life.  By wanting more for my kids...  them to not be affected by this disease and to have a functioning mom.  They already give up so much.  Because my life has been slower, I see that they are gaining many opportunities to know how much I love them.  I've spent so much time with them cuddling on the couch and it never would have happened if I had been so busy as I once used to be.  I have had great talks with my kids and get to spend extra time with them.  You just cannot replace that with any activity, sport, trip or club they may be missing because I cannot keep up with a busy lifestyle.

I've become stronger in my identity of who I am and why I have the trials that I do.  I hear all the time many translations of how we are to overcome our trials...  my favorites are two.  One, that adversity can bring us closer to Him.  And two, we are placed here on this earth to be instruments in progressing his kingdom. 

How does this help me overcome trials?

Well, I will tell you. It's one thing to have sympathy for another, but empathy is true understanding. Some things are given to us, for good or bad, so we may understand them better if we but look and listen.  Instead of asking "Why me?"...  ask what good can I do for another in their time of need with what I have been given. 

I may not be helping others with Lyme disease every day, but I know from what others have told me that I have inspired them to hold on.  To keep their chins up in their trials and to seek progression as well.  I've been able to give others opportunities to serve that have helped them to feel more purpose and belonging in this world.  I have learned of the unconditional love that so many of you have by supporting myself and my family in our journey.  I've seen others lives changed because of an illness that I've had to bear...  and even though I wouldn't wish this on my worst enemy, I would do it again knowing I am helping God's kingdom. 

Our time here is short and we have much to learn.  I know my mask is currently hiding what's truly inside....  I bet yours is, too.  As I learn to show myself more and accepting that who I am is OK to be everywhere I am, I hope you can,too.  I hope we can all become instruments in His hands by allowing more to see us with the masks off.  That our trials don't make us weaker or less desireable.  That we will choose to make them glorify our lives and help to bring everyone the peace and joy they so deserve.

Saturday, January 31, 2015

Sinus Surgery and Lyme battles

First four weeks of the new year down and I have done well so far!  I have shredded three kitchen trash bags full of paper, sorted out my whole room, and started donating more of our unused things.  Considering I was down for almost two weeks of that to recover from surgery, I'm pretty much on a good track!

My surgery went well.  The results came back unexpected but noting that would never resemble cancer so for that I'm grateful!  It did show Cholesterol Granulomas and they will more than likely come back.  They are usually in the spaces of the inner ear so for mine to be in the maxillary sinus I was a "rare case study" to look up.  I'm not looking forward to that again and hope it won't be for many years to come if at all.  That was NOT fun.  I was on pain pills for a solid 5 days.  I took myself off of them and only used them if I couldn't deal any more with the pain.  I have refilled my Rx but haven't used any more yet.  I almost did today, but I braved it out because I had places to be.

My calling at church is going well...  I don't feel I do enough and tomorrow plan to reorganize my next 6  months to prepare for the worst and hope for the best.  I need to restart myself...  Reading scripture s every day and studying them.  My prayers need to increase and so does my temple attendance.  I need all the help I can in my calling and I don't mean just spiritual.  If it weren't for my amazing presidency, I would be lost.  They are my rocks.  I can count on each one and they go above and beyond without asking.  I used to be upset at myself for not thinking of the things they do, but I have to remember my brain is not what it was since last October.  Neither are my cognitive skills, my reaction times and my ability to jump back and answer quickly to questions.  

I am anxious for summer and warmer weather.  My body aches consistently and my headaches are nonstop.  My fatigue levels are high and my sanity is low.   It is so difficult to explain the mindset of chronic pain.  It can be so "dark" when you are at a higher pain level but knowing that it will pass is really what gets me through.  I know for sure it's when I do my most praying.

I am going back to see my Infectious Disease doctor on Wednesday and then we will decide where to go with this round of treatments.  My guess is we won't go to a IV at first and will try oral antibiotics with blood work and a bit more testing to make sure I don't have any other secondary infections.  I really am hoping to go against the PICC line....  Having to go in EVERY day by myself for 20 minutes, (yes, it could be worse!,) is really annoying especially when the drive is 20-25 minutes one way.  I will deal with whatever comes and cannot wait until I am back on track.

This time I did not last long in between treatments because my immune system dropped.  We have had employment issues, a death in the family, a pending move based on our landlords status with the home, and my heart and health issues.  All of this plus the stress from the holidays and life in general with 4 children has allowed Lyme to take over again.

This time it's different.  I know what it is and how to work the "Spoon Theory" into my daily life.  I know how to rest and save energy for upcoming days and I know how to plan for recovery days.  I also have learned to delegate and always have a back up plan for everything in case I am "out" for the day unexpectedly.

I have lots to do for my fundraising, since I have not lifted a finger since before the holidays.  I am going to update my GoFundMe page and eliminate Envita.  It will never happen.  I believe they are too expensive anyway.  I just really liked what they had to offer.  So it made me think.  I can offer some of that in my own home with a few minor adjustments.  The plan for now is to purchase a RIFE machine and hopefully an ozone sauna.  Once we buy our own home I can look into an infrared sauna and a few other essentials.

I am excited for February and what I have planned in store.   It may not seem like a lot to you, but to me it is.  Here is to month 2!!!

Saturday, October 25, 2014

One year anniversary

One year ago today, on October 25, 2013, my life changed forever......

In a recent interview for the company Just Perfect, I had to create a script or list for our families first video.  I thought since I don't have much energy to make a one year anniversary post, I thought adding pictures to the interview would be suffice.  (Yes, I added a bit!)
Thanks for being a dedicated follower of my blog.  A bigger thanks to everyone who has helped, donated, called, shared, prayed, checked in, babysat, cleaned, bought groceries, cooked meals, donated food, gave us a night out, said words of encouragement and loved our family during this last year.  

I know I could NOT have made it with out you.  I love you ALL!!!

~~~~~~~~~~

Hi my name is Melissa Severance.
I was born and raised in Las Vegas, NV.
I went to high school as the first freshman class to start at the new Las Vegas High School.

After High School I worked my way up from an entry level position at a large bank to almost becoming manager of an entire operations department at only 23.  I worked with the company doing Six Sigma and Kaizan and I loved every minute of it.  I had found my passion. 

I then met my husband, married and soon after had my daughter and decided that staying home with her was my new passion.  We now have 4 beautiful, amazing, and silly children.


Our family was always busy and we owned our own company having our young ones working by our side.  We now own another company, and hope that it may grow, too someday.  For now daddy works at a family fun center.  We all, that’s right ALL of us, help daddy at work doing random things in trade for some fun time on the trampolines or playing laser tag.   We love to travel, hike, camp, go to the beach and absolutely love going to the lake with our friends on their boat.  

Before Lyme

Trying new things
Hiking in new places (Mammoth Cave)

Getting dirty with the kids

In the fun

Conquering with the kids 

Teaching new traditions

Adventuring to new places

Marshmallow roasting 101

Softball with friends

Midlife crisis convertible (wish!)

Spinning sail boats

Selfies with my kids

Favorite place with my favorite person

Super Summer Theater with my girl

Dress up days

Silly is a must

Animal lover

Playing tag

Photo bombing 

Look-a-like days

Pushing too much

Being blown away

Memories in motion

Dancing in the rain

13 mile walks to the temple

Brick House....  do I need to explain??!!



How did you find out you had Lyme disease? 


By accident!  I had been very sick for months.  I was in a store one day and received a call that my test results came back positive for Lyme.  I had a doctor that finally took interest in my well being and was about to send me to the Mayo Clinic in Scottsdale, AZ until these surprising results came in.


THE DAY IT ALL CHANGED

Ready to camp!

What was I doing???

The beautiful evening

Our family tent

Walking the line

A day with friends
One in a million...  or a hundred or so.


What is Lyme disease?

Lyme disease is a spirochete bacteria, which means it is spiral or cork screw, and goes by the name borrella burgderfori.  It most commonly is transmitted by the black-legged deer tick.  A majority of the victims, including humans, are animals, dogs, rodents, reptiles and birds…  The list goes on.  It is found in all 50 states and on every continent except Antarctica. 

Additionally, studies have revealed that Lyme disease can also be passed through the placenta of a pregnant woman to her unborn fetus, therefore allowing Lyme to be a gestational disease.  DNA of the bacteria has been found in breast milk, as well as suspected in cases of sexual transmission, but research on these two potential means of transmission is still pending.

When someone is bitten by the tick it is usually in its nymph form which is about the size of a poppy seed.  Transmission takes 12 or more hours as once the tick is done feeding it puts back anything it doesn’t need.  In this process is where the bacteria are transferred.  %50 of people will later see the bulls-eye rash that accompanies a bite.

When detected in its early stage, Lyme disease is treatable with an appropriate course of antibiotic therapy. Some develop flu-like symptoms a week or so after becoming infected. If undetected and untreated, the bacteria replicates and the disease progresses into its late stages, becoming chronic.  However, many people have no symptoms but can develop Lyme symptoms months, years or decades later.   

The spirochete bacterium screws itself into the body’s cells meanwhile releasing toxins that the body naturally fights off.  When it cannot reach the bacteria it continues to attack the cells surrounding the toxins causing it to become an autoimmune disease.  The body begins to attack itself.

Treatment for Chronic Lyme disease is prolonged and complex.  Patients often require years of intensive conventional and alternative therapies to fight the infection, recover immune function, and gain strength.

Lyme is not the only thing that can be transferred.  Many other co-infections such as Babesia and Bartonella come along with the tick bite and can be worse than Lyme itself. There are also secondary infections that with a normal immune system could be fought off without the host even knowing of its existence.  Any one of these alone can have debilitating symptoms and a combination can only make matters worse and harder to treat. 

The Lyme spirochete bacteria is hard to detect and hard to kill. Lyme disease is growing at epidemic proportions in the United States.  The medical community is divided over the diagnosis and treatment guidelines. Health insurance often doesn't cover the treatment for Chronic Lyme disease.

It is called the great imitator; looking like many other health problems (Fibromyalgia, Arthritis, Chronic Fatigue Syndrome, Bells Palsy, ALS, ADD, MS and Lupus).  

Common Symptoms include: fatigue, neck stiffness or pain, jaw discomfort, muscle pain, joint aches like arthritis- typically in the knees, swollen glands, memory loss, cognitive confusion, vision problems, digestive issues, headaches and fainting, heart problems and even death….  I’m starting to sound like those medicine commercials!!


What has Lyme disease done to you? 

It has taken me away from my family and friends.  I have multiple symptoms and have been hospitalized from some of them.  At times I am in such severe pain that even the best pain pills aren’t working anymore.  I am nauseous and bed ridden for many days on end.  I miss school award ceremonies, church activities, birthdays and my children have missed out on SO much from mom being sick.  Even the triple birthday party that we throw at the end of March every year for our kids that share birthdays within 3 days apart had to be canceled.   We have tried to travel with the kids but it proves to be too strenuous for me so we just stay home.  Even going to the park is difficult for too long.


 My husband had to quit traveling to care for me and the kids when I couldn’t.  The past year has been financially hard mostly because Bryan could not work as much as was needed to pay the bills.  Everything is behind or in shut off status.  Our car is almost paid for and we are struggling to keep it.  We have support from friends and family and have been very grateful…  It has kept us a float thus far.  Keeping our heads above water…  That is what we have been doing for the past year.



I make voice notes all the time so I can remember things...  This one is about what else in our lives has been effected.



LYME CHANGED ALL THAT

In bed all the time
Otter pops for breakfast, lunch, and dinner
Too tired to swim

LOTS of blood work

Lots of tests run

Visitors made it better

Bunny loves

Too sick to get up

Other diagnosis...  put on the back burner

Sundays were exhausting

Laying in bed...  again

Family still loves me...  even my leg...  that they were hugging

Comforting me when sick

Watching others 
kids miss me being active

starting to become part of the couch

watching others freedom

Still loves me

Family visiting me in bed

Noise cancelling headphones...  that is all.
Started "band-aid" treatments
New adventures?
 
Picking up kids at school

ALL BECAUSE OF WHAT YOU CARRY

What have you had to change in your life? 

All I can think of is: WHO moved our cheese?  Oh, it was Lyme.  I already have Celiac Disease which is another autoimmune disease so starting the forever gluten free diet was easy…  I’m already doing it.  I also have to eliminate diary.  I love cheese so this was hard.  While on antibiotics I have to eliminate sugar as well so as to not feed the bad bacteria.  I have to detox every day and take multiple supplements as well as more prescriptions to aid with the symptoms of the antibiotics. 


I no longer have the energy to do the things I once used to do.  I was a busy body always trying to make our home a better place for my children, playing with them and helping others as much as I could.  Now I am the one who needs the help.  What used to take me 30 minutes now takes hours…  Sometimes days if I have memory or concentration issues.  I cannot do anything strenuous or I will pay for it for days afterward.




THE SPOON THEORY

Click on the link below for a perfect example of what I deal with now because of Lyme.





Why are treatments SO important?

I've had many ask why treatments are so important.  Besides to avoid having all the symptoms of Lyme and to prevent my body from further damage from this auto-immune disease....  Well...  I don't want to die from it.  Plain and simple.  When someone says they have cancer they have a choice to make based on the stage it is on.  The same goes for Lyme.  

I am in the beginning stages of Chronic Lyme... Which is a final and irreversible stage.  Doctors say this because of the Cardiac and CNS damage that has already been done.  Some of it can and will repair itself on its own.  Most of it won't.  Getting treatments will push the bacteria back, help my immune system recover and will stop further damage to my body.  The reason for the high cost is weighed in on costs in different scenarios.

1. Living nearer to a doctor is my first pick.  This means moving out of state.  I will need a doctor that specializes in Lyme and the recovery of the whole body if I want to keep on top of this.  The doctors here are great but they are not able to treat the whole disease.  This is not something we can do right now.  It would be the cheapest and most effective way but not quite feasible.

2. Going to Envita one trip for 8 weeks, (every 5 to 10 years or more) Staying with family and friends, high cost but not every year.

3. Traveling every week to a doctor out of state.  Staying with family and friends.  Cost of travel every time I need to see the doctor.  Annually it may vary but during treatments it could be for months.  Oh, and don't forget out of state doctor costs.

4. Treat it on my own as most have to do in my current situation.  Use Infectious Disease doctors and natural medicines and treatments to try to attack the bacteria during flares.  This includes whatever is not covered by insurance, hospital visits and having the quality of life not return to a full life-style.  Living in between the flares.  For me I seem to not be out of a "flare" yet from treatments.  (Still have to follow up with the doctor in town.)


When Lyme is addressed early a tick bite is $400.  If we wait until early Lyme disease, the cost increases over 4-fold to $1,700.   By the time, we are dealing with late Lyme the cost is through the roof at over $21,000 and has been commonly reported to cost patients in the hundreds of thousands. 
If no treatment is reached then the patient eventually withers away to nothing from the diseases it mimics and eventually passes away.  

MY FUTURE WITH OUT TREATMENTS

Bad days more than good

Get to meet the next cute EMT or Firefighter!

Where everybody knows your name....

Keep me alive

New goals

New stats

New toys

New friends

Certificate of death.....


DUE TO:  Lyme disease

DUE TO:  Lyme disease

DUE TO:  Lyme disease


(Am I subtle or what??!!)



Web site for funds?


I have a web site where you can donate to help us in our journey to better my life style in managing this disease.


MY GoFundMe SITE