Showing posts with label aches. Show all posts
Showing posts with label aches. 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.

Friday, October 24, 2014

Pole Position Raceway Las Vegas Helping Family In Need!

We had another amazing company help our family out.  This time it was by giving us a much needed family night!  Pole Position Raceway invited us to come and drive a few laps around their course.  The kiddos were able to do it twice!  It was so much fun!  I was able to race once, too.  It was so awesome!  It made me happy to be doing something exciting again!

I absolutely love adventures, traveling, the great outdoors, new experiences....  Most of all I love to share it with my kids.  To see their faces light up with excitement is absolute joy to my soul.  Tuesday night was just that.  As shy as my kiddos were they were very excited to get in and try it out!  Gracie is a bit too short still but thankfully she was able to play arcade games with Ashley, James's girlfriend.  She is such a sweetheart and Gracie really likes her.

The next day I was down in bed for most of the day.  It was no surprise.  Having a day with too much excitement will put me out for a while.  Having a day with excitement AND go cart driving....  Well, Let's just say I am thankful I only raced once.  I wasn't prepared for the pain I was going to be in.  I haven't taken a pain pill in a long time....  I had to.  I have gained a new level of pain tolerance....  But not that much!  Two days later it was worse.  Last night I was completely down in bed because of my neck pain.  It still hurts but at least I can sit up now.  I have been on pain pills since and can tell that it is wearing off now.  Yea me!

Well, Yesterday was tough emotionally for me.  I barely could get up to do anything and I was asked to do two things...  ALL DAY.  So as I tried to so the first thing my neck froze.  I still had to pick up the kids from school.  I called my hubby and thankfully he took over.  I can tell you I was a mess.  I don't usually have moments of weakness like that.  I am great at keeping it together and pushing through.  All the advice was great and I knew it all too well.  I just overflowed my bucket and it all came out.  My phone was completely dead...  It wouldn't charge anymore.  So I couldn't call anyone.  Grace finally found the emergency phone so I could call Bryan....  but after that I just decided to let it all go.  I wasn't depressed or sad...  I was SO MAD!!!  I was so tired of being helpless. Sometimes a girl just needs a good cry.  After I exhausted all my strength from the drama I knew I had to pick myself back up and keep going.  Well, I couldn't get up until the next day!!!  So I worked on family history until I passed out.  (I have this new app from Ancestry.com and it's great!!!)

Oh, and my good friend Ammie came over and dropped off some very yummy treats for us.  I now have a great gluten free stash for just me.  OK, I might share....  if there is any left over!!  HA HA!  It was good to talk to her again.  Besides Church and my presidency meetings I really don't socialize much.  It was SERIOUSLY great to talk to her again.  I miss my friends.

Anyhow, they shot a video of our evening...  Check it out!

Pole Position Raceway Las Vegas Helping Family In Need!

Wednesday, September 3, 2014

6 weeks in...

Today makes it 6 weeks.  I should be happy.  But I feel horrible...  again.  The last two weeks were so much better!  Then BAM!  Back to how I felt before treatments...  NO, it's even worse.  I'm not even on the Tindamax right now.  This is ridiculous.

Monday I met with the Doctor's PA, Stephanie.  She is great.  I really love her.  We went over test results.  Only one thing changed from the previous week...  My white blood cells are dropping.  I can only be on the Rocephin another week and will have to give my body a break.  I will infuse next Monday and will just maintain my PICC line at home for a week.  Then we can see if I have any flare ups and can decide what path to take next.

I have been trying to put together something for my fundraiser but my brain is not cooperating.  I cannot function and the pain is unreal.  I am trying to focus on breathing while listening to soothing music.  I am not sleeping well again.  My appetite is shot.  I really want to give up or crawl in a hole and give in.  I know I won't...  Just having a moment of weakness.

My kids have been home from school sick.  All of them.  We are having problems in this house and for some reason our family has never been sicker than the 2 years we have lived here.  I think it is either in the air ducts or we have another rodent issue.  It's embarrassing to me to think maybe some of this could have been prevented if I was just well enough to do something about it... or maybe not.  My house is a disaster, the children run wild, (when they're not sick,) and nothing is in order.  It's too much for me right now.

Anyhow, It's taking me too long to type this.  I need to go lay down if I'm going to keep this broth down.  I feel like I'm about to pass a kidney stone again...  Lovely.

Saturday, August 23, 2014

Spoons

For the longest time I had a problem explaining how this disease affects my daily life.  It's easy to explain symptoms and the science of the disease.   It's right there on the surface to see or can be researched online.  But how I live with it is another story.

I found this video and it helped me to understand my own disease.  It explains the spoon theory.



Here is a link to the written story straight from Christine Miserandino's blog @ www.butyoudontlooksick.com





Yesterday I borrowed spoons from today and possibly tomorrow.  If I don't rest and do VERY light duty tasks every day then I am completely spent by late afternoon.  Yesterday I was not on my Tindamax so I thought I would take advantage of a day of less herxing.  Boy, was that a mistake.

Although I do not regret the time spent with my husband and children...  I am regretting that I didn't take it easy yesterday.  My Dr warned me about this.  Just because I have a "good" day I still have to take it easy.  Recovery will take me a year or more to be close to where I once used to be.

Words cannot express how HORRIBLE I feel right now.  I don't know what it feels like to be hit by a bus, but I imagine this would be it.  (Now, I didn't say crushed or mangled...  Just hit.)  EVERYWHERE HURTS. Everywhere...

I am going to take a detox bath and try to take a nap.  I also have to get going on my fundraiser....  My insurance is only covering 10 days a month of Tindamax.  I just purchased 5 days, (10 pills,) for $82.27.  Not too bad, but I hope I am not on these pills for long.  I have not been doing much for fundraising lately.  

OH, here is another link to Christine's site about some of the things I deal with every day.  She has Lupus but Lupus, Fibromyalgia, Rheumatoid Arthritis....  It's all about the same as Lyme all wrapped up into one. 


Have a great day everyone and keep on keeping on!!!  LYME WARRIOR!  (Although I feel more physically defeated today...  The show must go on!!!)

Tuesday, August 19, 2014

Herxing

I hurt.  I hurt, hurt, hurt.  My body is finally herxing to the max and I am taking it one breath at a time.

Sounds are hard to bare.  Lights are too bright.  Air conditioner hurts my ears but I'm overheated and need the cool air.

I ache...  Everywhere.  My knees, ankles elbows, shoulders, hips....  Hurt SO much.

My fingers ache.  My back and neck are stiff and my muscles are knotted everywhere. 

My head is pounding and I cannot type this fast enough to document so I can sleep. 

I will do a video but wanted to journal my experience.

Thursday, July 10, 2014

Entry on 07/10/14 from GoFundMe - Mommy is in need of treatments

Please help our family get mommy better. Any donation helps and sharing this page does, too. We are still waiting for test results that will inform us of the proper treatment plan. 

Last night we all went swimming and it was so much fun but today is a true testament of how bad things really are. As time passes the disease continues to wreck havoc and puts mom out of commission. Having even a few hours of fun with the family makes for days of recovery. Not to mention all the daily tasks of taking care of the kids and home. Just vacuuming or doing the laundry can put mommy down for at least a day. Going to church on Sundays always make for tough Mondays. It is a challenge that is making us all stronger as a family but still no way for mommy to live.

Every day there is intense pain. Some days its hard to walk. Others mom walks around in a fog, unable to function or talk correctly. Her heart is continually feeling the effects of this disease and we have now added a cardiologist to the long list of doctors on the list. 

We are hoping for a miracle but we know that miracles do not come with out the instruments of God, (which is all of you!!) He is on our side and we know we can get this disease under control. 

We are so very thankful for all the friendships we have. It is a testament of how truly blessed we are. We know someday we will pay it forward... It has always been mom's love language to serve others. It always brings her great joy! 

Thanks again and may God bless.

Love,
the perSeverance Clan

Entry on 06/30/14 from GoFundMe - Lyme's sad news...

Its 2am. I'm all cleared to go in a few hours. Yesterday, (Sunday,) I learned something very important. I think this will be my last post for a while until I know more of what's wrong with me. I'm tired of scaring my kids, of being in need, of being weak. I learned something very sad and I need to process it for a bit. I have a follow up appt later this week and will decide, by myself, what to do then. I just need a break from all this. It sucks... Sorry for everything. Thank you for all your love. It has meant a lot.

Entry on 06/28/14 from GoFundMe - Hospital visit for chest pains

I am here still in the hospital, waiting for more tests. I have had chest pains since the 13th and two days ago my back, between my shoulder blades, started to hurt tremendously. Yesterday, both were excruciating. It would fade off then come on strong. Then my shoulders and arms became numb and tingling. I couldn't take the pain anymore even with my pain meds. I called my husband home and called 911. I was taken to Centennial Hills Hospital in Las Vegas. They confirmed with my blood test and EKG that I did not have a heart attack. But my EKG did not look good. Something about a line that should be going up is going down. It suggests my Aortic Artery, the one that goes behind the heart. Or it could be something else... First they are eliminating heart issues. Lots of blood work, Echo on my heart and still waiting to do a stress test. The Doctor said I'm too young for this, even though he has seen 34 and even 26 year olds in here before with issues. So, one step at a time to figure things out. Keep the prayers coming and thanks to everyone for their support! I feel so loved!

GoFundMe account established 06/12/14 - the LYME LIFE

It's amazing how fast things can come tumbling down when you hear "You have Lyme Disease."

Some of the first comments I heard from others were, "I knew someone who died because of Lyme Disease." Can you imagine my reactions?

I have heard of it before but never quite understood how horrible this disease can be if left untreated. The symptoms mimic other diseases. So if by chance you test for Lyme, you are one of the lucky few who will get a diagnosis.

Rheumatoid Arthritis, Multiple Sclerosis, Fibromyalgia, Lupus, ALS or Lou Gehrig's Disease, Chronic Fatigue maybe even Alzheimer's and Autism... Just to pull out the more common misdiagnosis's.

I am one of the lucky few with a diagnosis. But not lucky as much as you'd think. You see, I discovered it after my 4 week-ish window of oral, no-biggie antibiotics CURE. 

Testing and treatment for Chronic Lyme Disease, (and oh, don't forget about it's co-infections,) can be over time added up in the  tens of thousands, (for some around half a million). Not to mention the expenses of travel, lodge, food.... And don't forget to include care of my 4 young children while I am away. A good baby sitter isn't cheap these days!

We have a wonderful family who has done so much for us and many friends near and far who have gone above and beyond to help. We are so thankful and are deeply grateful for all you have done.

As far as my care, our family has hope to go to Envita to help us in our journey to get my health back up to as close to normal as it can be. They are located in Scottsdale, AZ.  Check out their site if you like.  You can learn more about Lyme Disease as well as Chronic Lyme Disease and maybe even help someone who you may think is suffering with an unknown diagnosis.

http://www.envita.com/conditions-we-treat/lymedisease

Although I have a lot of support it will be difficult and the costs will add up. 

Everything from our GoFundMe site will go towards labs, treatment, travel and any other expenses occurring from the care that will be needed to help our family.  This is a life long battle we will have to face until they find a cure.  You can go to my site and donate here:

http://www.gofundme.com/a8w6xg

I want to send a heartfelt thanks to everyone in advance. Our journey has just begun and you play a huge role in my speedy recovery... No matter how you can help it will be appreciated!

We love you and may God bless us all!