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Wednesday, December 22, 2010

Its been way too long since I've blogged. I've felt overwhelmed at all that I wanted to say / needed to say so I just didnt say anything - not realizing that I didnt have to say it ALL at once. So here I am today.... Mandy.... just to say I feel peace. Not just rested but PEACE. Full to the tip top of my head filled with a sense that I am not the one in control and that its still okay. Dont remember the last time I could say this - if I could ever really say it. Here's to wishing you PEACE this holiday season!!

Monday, November 23, 2009

Faith, Hope and Love


Just returned from another visit to my doctor in LA. This was not a "routine" check up as planned since we thought my meds had spotted fighting the Lyme. I have been unable to drive long distances (meaning out of La Porte) due to extreme dizzy spells, my face had returned to becoming numb, the shooting pain throughout my body came back - is has not fun at all to deal with and the fatigue and other "Lyme" type issues that you've heard me talk about - you get the picture.
With the stress of Shane's pending EGD results - which were clear THANK GOD!!! - PTO things, Ladies Night Out duties, Mary Kay nightmare and other family "issues" I have not been taking the best care of ME. Trying my best to be the best wife, mom, friend, and servant but sometimes the planner doesnt say "MANDY" on it LOL.
So we were driving up today with FAITH - that God would take care of us and guide the doctor. HOPE - that the Lyme was just mad at me and we could continue on the path we had been on cause I had been doing so well - this just hit me last weekend like a train. And LOVE.... for Shane the most amazing husband - I know we all say we have wonderful husband and I know we do -BUT I can not tell you how blessed - words escape me! Love for Sheri and Chris who took care of my kiddos and had to put up with me leaving in tears and checking up (only once) but still - thank you!! Love for Steph for sharing her HOPE before and after the visit :) I was blessed with 2 sisters by birth and then more again in marriage :)
So the findings .....
1. My body was more than mad - it was ticked off and TIRED!!! HOWEVER the meds were still working so I dont have to start all over : ) PTL! He added some kept some the same and wants to try a few different try things.
2. The doctor was 1 1/2 hours late seeing us.... not great right esp when you get up at 3:30 AM to drive to another state - here's the GOOD part of the message - he spent almost 2 hours with us!! He answered EVERY question and even came up with new ones. Do I have more questions now - yes I always do after leaving and driving ( ok riding for 4 1/2) home but the point is HOW many doctor would do that??? HOW BLESSED am I?? That's awesome!! And all I have to do is text him tom and he'll call back to help :) Oh and I got a copy of my labs so that was really COOL to see in black and white my Lyme results! Crazy stuff! 26 years of not knowing what was wrong or being told it was something else and now God's timing for some reason is falling together??? Road maps from heaven would be a wonderful thing ; )
3. There's tons more but it's too much "medical-ish" stuff - if you really care to know - Id love to tell you cause he really thinks outside the box and he's more concerned with getting me well than writing me a RX and sending me home - so it was a great trip.
4. Do you know how wonderful it was it sit in the car with my honey for that long and talk?? and sing and laugh and worship and just enjoy time together!!!


God knows what He is doing!!! In every way!! Do I wish to get sick and drive almost 9 hours in a day to go see a doctor NO! And I was talking to Shane today on the way - I still had not found the silver lining in all this. Dont get me WRONG!!!! I HAVE FAITH! and HOPE! I know this is GOING to work out for the glory of GOD. Dont know how??? But I know it will! I know it's God who is healing me trough prayer and His word and through His guidance of the doctor and the meds he's using - all this I know. I was just looking for a silver lining for now ;) And I think I found it.
Without this trip Shane and I would not have been able to spend the ENTIRE day together - yes we spend time together - but we get busy doing. Its normal - we have 2 kids and a dog and lives. Even on his days off when we are all home together we dont find ourselves in the same room nonstop for 4 hours straight with no distractions. Without this trip I would not realize the extend of the bond I have created with Sheri and hope to created with all my sister in laws. Over the past year she and I have become very close and I thank GOD for her being in my life!! She is truly a sister God placed in my life!! Without this trip I would not have seen the Hope in Stephanie's eyes and voice as she encouraged me as I was leaving for me trip. We all have crosses to carry in our lives - they are ALL different but if we are lucky enough, we are all walking together to the same CROSS and Im happy to have a new member on our journey!
For that - tonight Im grateful for this winding journey that we're on. It's not easy but He never said it would be - Just that HE would never leave us!!!
Today had been about faith, hope and love - and the greatest of these IS LOVE :)

Wednesday, June 10, 2009

Little side blog

Woman's Day Magazine writes about UNDER OUR SKIN. They are interested in writing something in their magazine, if they get enough interest from the blog.
http://dailywd.womansday.com/blog/daily-dose/
Go on and tell them what you believe about Lyme.
Thanks for the support

Friday, May 29, 2009

Learning limits

This week I went back to 2 antibiotics again - just to refresh - I started with 1 then 2 then 3 - once I hit 3 I was having trouble breathing and horrible vertigo - room spinning/couldnt drive/dizzy doesnt even come close to explaining it. So my doc took me off it for a few days then back on again but just 1 for 2 weeks and then back to 2. So I am back to 2 - which I started Monday night - breathing is fine for the most part and no major vertigo - all good news. This means my body is handing the die off of the bacteria better. I spoke with the doctor last night and he told me some other things I need to try to add in - vitamins, supplements, diet restrictions (gulten/sugar/proceeded free food) yum yum! And he added back another B12 shot that he had taken away a few weeks ago. The plan is to go back at the end of June for another visit and see where we are at that point.
Adding more pills and shots I'm good with - whatever will help. Even the diet is ok - not great but couldnt hurt right? The tough part for me right now is realizing my limits - physical limits and stopping before Ive done too much. I start to feel better and I think well I can get so much done right now I need to push and get it done. It's hard to go from doing everything I needed to do - to THIS. And I dont even have the words to express what this is.
Before - I could chase after the kids in the house or outside and just play
Now - We sit for lots of the day - or more I sit - and watch them
Before - I could carry Alex through the entire store while pushing a shopping cart
Now - I'm doing good if I can carry Alex from the kitchen to his bedroom
Before - I could paint an entire room
Now - I was breathing hard painting for 45 minutes
Last night I went up to Grace's school to help with kinder graduation. I needed to cut cakes, plate them, and serve up tons of limeade. Granted I thought I was only needed to 30 minutes so I didnt think I was going to "over do it" - to which my husband of course knew better - he told me that I was not capable of saying no when asked to do something - yes I know he's right lol
So I go in at 6:10 - no one else was there. So I cut, plate, fork and place an entire sheet cake by myself in like 10 minuets - it was more work than it sounds and I was done - hit a wall - DONE. But I could nt stop because the other helpers didnt come. So I keep working and then more mom's came and we work and work - I'm sweating as if I'm doing Tae Bo, my legs are shaking so bad I'm having a hard time walking, I'm breathing as if I'm having my 3rd child and all I'm doing it putting cakes on a tables, setting up cups and adding forks to the plates. - Mind you all the while with a SMILE :) By 7:15 I tell the other ladies I have to go. I get in the car and just want to cry. Before this I would have been not only the first one there but the last one to leave. I would have helped serve and clean up.
The thing is I dont look sick - I feel as if when people see me this way they think I'm lazy or just dont want to do something. And I hate it! I like being able to do things for others. I like running around with my kids.
Shane told me I just didnt know my limits - or didnt listen to them. I think I get so wrapped up in helping or pleasing that I just keep trying to push through - the problem is if I keep pushing my body is going to push back even harder. So the plan is to break it all down. Grace is out of school for the summer and dance is almost coming to an end so that means less running around is needed. I will pick a chore a day and try my best to pull my weight around here - cause let me tell you it's not easy watching Shane run circles around me getting things done that I was trying to get done. We will play when we can play and we will rest when we can rest and we will love and laugh as much as possible!

Monday, May 25, 2009

"Happy face"

I am having a hard time putting on the "happy face." I'm not out for pity or attention or even help really - I am having a hard time when someone asks "How are you?" Do I tell them how I feel? Or just smile and say good or do I just say hanging in there?? Cause yes I do believe when people ask they care to know - but time and time again when they ask it's going to get old if all they hear is .... - the truth. And i guess the thing is I'm torn with this battle Im fighting because I have such a passion inside me to tell my story. No one know the facts about Lyme - I didnt and to be honest I'm still learning them. But I just want to shout it out so everyone will hear about it. SO many battles people are fighting have to do with LYME. They are linking Lyme to several big illnesses (ALS, Alzheimer's, autism, ADD, IBS, the list goes on and on) and maybe just maybe that's how I'm trying to make sense of it all. Maybe I have this to help others. Do I want to scare people or worry them - maybe a little yeah - cause then maybe they will pay attention the next time they dont feel right but the doctors dont have the answers. There is tons more research that needs to be done - they are saying this is not only carried by ticks - they are saying the blood supply that we all use is not checked for Lyme - they are saying that this disease is bigger than the ones getting all the money for research.
Some close friends and family are worried I am becoming consumed by this - and I think to a point I am. This disease does not attack me the same way from hour to hour or day to day. The doctors are learning as they go and I feel the more I know the more I can help - them, others and myself. SO yes it has turned into more than a hobby - but it's not cause Im doom and gloom - its cause it's not cut and dry. It's not : your arm is broken so we need to do an xray and put on a cast. It's not: you have a bad gallbladder - so we remove the gallbladder. It's not: you have diabetes so we monitor and then regulate your sugars. It's you have Lyme disease: AND The meds we give you right now will make you feel worse and then we will have to change them cause the Lyme will not be affected by them and then they will go into a cyst form and no meds will help for a while and then you will think you are better and we will stop meds and then they will come back into your system with vengeance with a new type of pain and area affected to fight. And no we dont know how you will do on the meds or with the protocol cause everyone is different and the lyme likes to hide and change and we just dont know. SO yes I am consumed - but it's only so I can fight the fight.
That all being said, I know I am strong and I am going to beat this - not with my might but because I am loved by the Lord. Yes I do feel as if Im in a valley in my life but that does not for one second mean I do not have faith or belief in HIS power. Without Him I am nothing and can do nothing. Maybe all this journey is a way to share my light. I hope that is what people see inside as Im fighting - His light and the strength He gives me daily to fight. Do I get wary? You bet! I am flesh and Lyme is not friendly. But this will finish well - for His glory. So ask me how I am - give me a hug - say a prayer for me - and encourage me along the journey.

Tuesday, May 19, 2009

10 Commandments for interacting with the chronically ill

-taken with permission from www.truthaboutlymedisease.com

Something you may want to print for family and friends...

"But You Don't LOOK Sick..."

10 Commandments for interacting with the chronically ill

In the realm of chronic illness, one of our more challenging tasks can be gaining support from others. As if finding a knowledgeable and caring doctor wasn’t difficult enough, finding caring and supportive friends to surround ourselves with can be even more difficult. Most people are simply not capable of understanding, unless they have the misfortune of a chronic illness of their own.

How many of us have heard something along the lines of “But you don’t LOOK sick...?” It makes one wonder how a sick person is “supposed” to look. If one were to hobble around on crutches, would their illness suddenly become more believable? Our society understands the visible, physical manifestations of illness, such as a broken bone in a cast or hair loss from chemotherapy. What many fail to grasp is the subtle, invisible manifestations of chronic illness. Symptoms such as pain, severe fatigue, and cognitive impairments are not easily visible to the average observer, which means that sufferers of chronic illness often look “just fine”.

Our society is all about instant results - the mindset that we can just pop a magic pill and all our troubles will go away. When sufferers of a chronic illness do not quickly “get better”, we are often treated as if it were somehow our own fault. We may even be told that we are “hypochondriacs” or that “it’s all in our head”.

Remember when you had the flu? You were exhausted, achy all over, and could hardly get out of bed. But, fortunately, the illness passed and you were back to your old self and usual activities.

Now, imagine if you had never recovered from that flu. Every day, you wake up achingly sore and as tired as if you had not slept at all. Imagine trying to go through your usual activities while feeling this way. Not only do work, school, and regular tasks of daily living become near-impossible, but so do the smaller day-to-day things that so many take for granted, such as simply washing your hair or paying the bills.

It is stressful, it is exhausting, it is depressing... and yet the chronically-ill person continues on in the face of it all.

For those of you who may have, at some point, been the perpetrator of an otherwise well-intentioned comment, please understand that our illness is just as real as that of an amputee or other “visible” illness. To help aid those of you who wonder how to interact with a chronically ill person, allow me to present the Ten Commandments.

1. Thou Shalt Not Imply That We Are Not Truly Ill.

You will not convince us otherwise with remarks such as, “You LOOK good,” or “But you don’t LOOK sick.” Even if you meant them as compliments, we perceive those kind of statements as insults because they imply that you do not believe us.

2. Thou Shalt Not Imply That The Illness Can Be Easily Fixed.

People with chronic illnesses are persistent, if nothing else. We hang on, day after day. We see countless doctors, take numerous medications, do endless research, and continue hoping that the answer is just around the next corner. So please do not insult us by delivering diagnoses, remedies, or comments such as, “Why don’t you just...” or “Have you tried...” or “You should....” If it truly were that simple, I assure you that we would have done it already. We are sick, not stupid.

3. Thou Shalt Not Imply That We Brought This On Ourselves.

We did not choose to become ill, just as we do not choose to stay ill. Simply having a positive attitude is not going to solve our problem. One would never imply that a quadriplegic chose such a trial for themselves, or could get better “if they really wanted to”. Please afford chronically ill patients the same respect.

4. Thou Shalt Not Insult or Argue With Our Limitations or Behaviors.

If people with chronic illnesses push ourselves too hard, we can suffer serious consequences. Most of us have developed coping mechanisms to help us survive, and it is cruel to expect us to do more than we are able. One chronically-ill woman I know was actually told, “I wish I could have the luxury of sleeping all day.” Believe me, we would much rather be out working, playing, spending time with loved ones, participating in normal activities.

“Sleeping all day” is not a luxury for us – it is a critical necessity, one that we must take in order to protect whatever remaining health we have. Perhaps it may help to think of it in terms of being one of the medications we need to take. If you wouldn’t think of denying a diabetic their insulin, then don’t think of denying the sufferer of a chronic illness their critical need, whether it is a mid-day nap, avoidance of certain foods or environmental factors, or something else.

5. Thou Shalt Not Imply That You Can Relate To What We Are Going Through.

Unless you have a chronic illness of your own, you cannot possibly understand just how much suffering is happening. Of course you want to be compassionate and want to relate to people. But when you try to do this by telling a chronically-ill person that you are always tired too, it tends to make the person feel that you are minimizing their suffering. Try saying something more along the lines of, “This must be so hard for you,” or “I can’t imagine what you’re going through.” It really does make a difference to us.

6. Thou Shalt Be Mindful Of Other Family Members.

Chronic illness doesn’t just affect the person who has it, but the whole family as well. The trauma of the illness can evoke feelings of fear, depression, anger, and helplessness in all family members. The balance of family dynamics will most likely change, especially if it is a parent who is ill. The healthy spouse may end up taking on an overwhelming amount of responsibility, and even children will likely be involved in helping care for the ailing family member. Please keep these others in your thoughts as well, and make an effort to direct some special attention to them, without any mention of illness or disability.

Individual family members adjust in different ways and at different paces. All members might benefit from counseling to help handle the stress involved, and each family member also needs to have time to pursue their own individual interests. External support from friends, neighbors, extended family, religious institutions, and support groups may help ease some of the burden.

7. Thou Shalt Acknowledge Our Efforts and Celebrate Even Our Small Successes With Us.

For the chronically ill, any day that we can accomplish a task, no matter how small, is a “good” day! Our lives are often measured in terms of doctor’s visits and lab work, and our “success” measured by a rise in Natural Killer cell counts in our blood, or actually completing an entire load of laundry in just one day. Please do not look at us as if we are joking when we share these celebratory moments with you. Celebrate with us, be happy with us, and do not kill the moment by announcing that you just completed the Ironman Triathlon in record time.

8. Thou Shalt Offer Thy Specific Help.

There are so many ways to help -- the most difficult part is usually getting a chronically-ill person to accept that help. They do not want to feel like a “burden”. If you offer a vague, “Call me if I can help,” the call will probably never come. But if you are sincere, consider extending offers of specific help, such as a ride to a doctor’s appointment, or picking up a few groceries or the dry cleaning. These activities can be done in a way that does not add any extra burden to your own schedule. If you have to go to the grocery store for your own family, it really isn’t much extra work to grab an additional loaf of bread and jug of milk. If you have to swing by the post office, getting an extra roll of stamps or mailing an additional package isn’t much extra effort for you – but it can save a chronically-ill individual a lot of time, energy, and exacerbation of symptoms.

9. Thou Shalt Remember Important Events.

I’m not just talking about birthdays and Christmas. A major doctor’s appointment, lab test, or new medication are all important events to the chronically-ill person. Try to sincerely ask, “How was your appointment? How did the lab test go? How’s your new medication?” The chronically-ill person will appreciate that you remembered, and that you cared enough to ask about it.

10. Thou Shalt Get To Know The Person Behind The Illness.

The illness may be a part of us, but it’s not a part of who we ARE. We want to be known as more than “that sick person”. You may discover that we have a wickedly funny sense of humor, a creative imagination, musical talents, or any number of things that better describe who we are, and what we would rather be remembered for. (It makes for better gift ideas too -- rather than presenting us with yet another self-help book on the power of positive thinking, now you can give us a CD from our favorite singer or movie of our favorite actor instead.)

Most of all, please remember that the chronically-ill person is more than worthy of love, friendship, and support. Most chronically-ill people I know are the toughest nuts I have ever met. Indeed, I have come to believe that a chronic illness is not for wimps – rather, only the toughest of the tough can continually face the struggles of life while battling a debilitating disease. That kind of grit deserves nothing less than pure respect and admiration, even from our toughest critic -- ourselves.

Thursday, May 14, 2009

CDC classic case

It's official - Lyme Panel came back positive - Lyme Disease it is. The good news is it's a CDC classic case - meaning all the "markers" were in the right place. This is good because a lot of the times Lyme is only a clinical diagnoisis because the tests dont always "work". With having this positive test, it will make it easier for us if our insurance tries to fight us. The doctor threw out some numbers about which markers were where but I was very lost - so he said he'd go over them with us in person the next time we saw him - works for me. He said based on a scale of 1 -4 I was a 3 as far as how strong the lyme is in my body. We kinda knew it was a severe case with the CD57 but this just echoed it for us. It's good to finally put a name to what I've been feeling for so many years.
That being said, this has been a pretty rough week if Im being honest. On Monday the dizziness was so bad I felt like I was spinning just sitting down. By Tuesday it felt like I had someone sitting on my chest. By Wednesday I felt like I was breathing in ice every time I took a breathe and just walking and holding Alex at the same time became almost impossible. Lucky for me the doctor called on Wednesday with the test result and also to tell me to back off the meds. He said I was doing too much too fast and my body was reacting. So I took a two day break from the meds and will go back on them very slowly.
Its also been hard because I feel like the Lyme is winning a little bit each day. Every time I have to turn down a play date or school event or put the kids down 30 min early or having to stop taking care of my family I feel as if I've given in to this disease a little bit more. I do not like having to have help - it's nice to have but I hate feeling like I cant do it myself. I do not like feeling like I am whining. So it's easier to put on the smile and say Im fine - even though with one look you can tell Im not.
Thank you to my family (Shane, Mom & Dad and Mom & Dad in law) for being the wonderful people you are and helping make this week run as smooth as it did! Thank you to all the friends and family who have sent email and texts checking on us and offering help, love and prayers.
I know this is going to get better. I know this is a fight we will win.