Monday, May 11, 2015

Post Surgery Update

It's been about two weeks since my surgery and I'm happy to say that I'm healing well and melanoma free!!

I didn't think the surgery was going to happen because the weekend before I was knocked off my feet by a stomach bug so violent I had to go to the ER. I've never been so sick and after passing out and hitting my head on the bathroom floor, Tim put me in the car and found the closest emergency room.

I can honestly say that the bug was waaaayyyy worse than the surgery!

I sucked it up and went in that Monday for the first procedure. The worst part was the numbing shots. Other than that, I had no pain, just a weird tugging sensation. He put a couple of stitches in to hold me over the next 24 hours while the sample was biopsied. 





I received a call the following day stating that he got everything out in the first procedure so the followup would be some more smaller incisions for cosmetic reasons and the rest of the stitches .

The numbing shots were even worse than the last ones because they were in the open wound! I almost came up off of the table! 


I really wasn't in much pain at all. It was definitely swollen and if I accidentally bumped it I felt a jolt of pain but it was so much easier than I was anticipating. The following week I went back twice to have stitches removed in stages and the doctor seemed to be pleased with how its healing.



He glued me up, gave me another bandage and I have to wear it for a couple more weeks.

I really miss washing my face and wearing makeup but I'm just soooo happy it's over with! 


I just need to brag about my husband a little bit...

Throughout all of this medical drama he has been so very helpful. He has taken care of the household, run errands, and done pretty much everything for me, including washing my hair. I couldn't have done it without him! 

Monday, April 20, 2015

Prayer Request

Last week I received the news that I was dreading...

Melanoma.

Just in time for Melanoma Awareness Month.

(I really struggle with sharing this stuff publicly but not only does it help me get my feelings out, it can also serve as help for people going through the same situation. )

Let me back track here. In 2009 when Tim and I were newly dating we took TONS of pictures and he always got close up shots of my face. This was the first time I noticed this mark and I just figured it was a freckle that I hadn't noticed.


I wasn't worried and never gave it a second thought.

Years later it seemed to hit me all of a sudden. I looked in the mirror and it jumped out at me. When did this thing get so big and dark!? Make- up wasn't covering it anymore and it seemed to be spreading.  Eventually it just became part of me and once again, I forgot about it.


Last year Tim and I discussed getting it looked at but I knew it was nothing. Guys, I'm so careful when going in the sun. I always wear sunblock, especially on my face and the times where I did go in a tanning bed I would cover my face with a towel. This had to be a beauty mark.

I was perfectly happy ignoring it until a couple months ago when a cashier complimented me on my beauty mark. That's when I realized it was noticeable and I should probably have it looked at to put my mind at ease. 

I had a biopsy and the results showed that it was a severely atypical mole that could possibly become cancerous at some point in my life. It would need to be removed but we decided it would be a good idea to get a second opinion. It was sent to the best of the best in San Francisco and a week later we found out that it was in fact cancer and my doctor was very clear and very apologetic when he told me this would be a "gnarly scar". 

I went through so many feelings so quickly. First came anger, "What the heck!? Can't I catch a break!?" Health issues have been insanely overwhelming the last 4 years and I didn't need this little add-on. Then came vanity...I have self-esteem issues already and now I'm going to have this ugly scar right across my face. This passed quickly because I'd take a hundred scars if that's what it meant to get this out of my body. 

I'm oddly optimistic. This just seems so cut and dry to me.
It is here, it is melanoma and I only have one option to get rid of it. If it's worse then we think, I'll deal. 

I'm doing all I can not to worry about that what if's and praying that they don't find something worse once they're in there.

I would really appreciate your prayers too. I'll take em all!

My first surgery is April 27th. They will get as much out as they think they need and send it for biopsy. April 29th I'll go back and if they need more they'll do that, if not, they'll stitch me up.

Please pray for Tim also. He is my rock and after so many years of being my rock this one kind of threw him for a loop.  

Thursday, March 5, 2015

Community.

Community.


For the last 3 years I've been blessed to be part of the most amazing group of people that have changed my life.



Our church, like many others, would always pound "community" into our brains and I never felt it was necessary. We went to church each weekend and sat in the nosebleeds in hopes of not having to shake a hand or speak to strangers.




In 2012 I felt called to join a group study at our church called Rooted. This group of people was put together and led to reveal our deepest, darkest struggles and face life challenges along side complete strangers. What happened in those next weeks changed our lives forever.


Here we are 3 years later and we are some of the best friends you could find. These people know so much about me and I know so much about them and we are nothing but open and honest with each other and it's the most refreshing thing ever. 


We really are going through life together. Through the ups and downs we are never alone. When I get knocked down I have a group of people to build me up and chances are, someones already been in my shoes and can offer me the support I need. I thank God everyday for his awesome group picking ability because these people are perfect for me.

Wednesday, February 11, 2015

Catching Up

It's been awhile since I've posted here so I thought I'd do a little update to summarize the beginning of 2015.



I finally got the diagnosis I'd been searching for since 2011. I had suspected something was wrong with my thyroid all this time because I was left to do all of my own research after way too many doctors and specialists couldn't help me. 

It took a visit to an Infertility Specialist to tell me even though on paper my hormone levels were "normal", they were far from normal for me. He put me on medication for Hypothyroidism until I could see another Endocrinologist who confirmed my levels were very off and that I had Hashimotos Disease. Hashimotos is an autoimmune disease that causes your immune system to attack your thyroid like it would a virus. 

I cannot even tell you the relief I felt. Finally! Someone took the time to listen to me and take what I was saying seriously. I've spent all these years thinking I was crazy. So many symptoms with no answers leading me to believe it was all in my head. I felt crazy and I felt selfish. Why couldn't I control this and why was I letting it take over my life? I felt so bad for Tim. He didn't sign up for this. I didn't want to be a depressed, anxious, hypochondriac wife. 

Although the medicine will take time to start working and  it may take awhile to find the right dosage I'm feeling hopeful. I've had a couple of bad days where I've felt worse than I ever did but after doing some research I found that can be normal. Today was one of those days and I've just been feeling so down. 

It's nice to know that I'm not alone and to read stories of hope and healing. I found this blog post and it just sums up everything.

Hi.  My name is Hashimoto's.  I'm an invisible autoimmune disease that attacks your thyroid gland causing you to become hypothyroid.
I am now velcroed to you for life.  If you have hypothyroidism, you probably have me. I am the number one cause of it in the U.S. and many other places around the world.
I'm so sneaky--I don't always show up in your blood work.
Others around you can't see me or hear me, but YOUR body feels me.
I can attack you anywhere and any way I please.
I can cause severe pain or, if I'm in a good mood, I can just cause you to ache all over.
Remember when you and energy ran around together and had fun?
I took energy from you, and gave you exhaustion. Try to have fun now.
I can take good sleep from you and in its place, give you brain fog and lack of concentration.
I can make you want to sleep 24/7, and I can also cause insomnia.
I can make you tremble internally or make you feel cold or hot when everyone else feels normal.
I can also give you swollen hands and feet, swollen face and eyelids, swollen everything.
I can make you feel very anxious with panic attacks or very depressed.  I can also cause other mental health problems. You know crazy mood swings? That's me. Crying for no reason? Angry for no reason? That's probably me too.
I can make your hair fall out, become dry and brittle, cause acne, cause dry skin, the sky is the limit with me.
I can make you gain weight and no matter what you eat or how much you exercise, I can keep that weight on you. I can also make you lose weight. I don't discriminate.
Some of my other autoimmune disease friends often join me, giving you even more to deal with.
If you have something planned, or are looking forward to a great day, I can take that away from you. You didn't ask for me. I chose you for various reasons:
That virus or viruses you had that you never really recovered from, or that car accident, or maybe it was the years of abuse and trauma (I thrive on stress.) You may have a family history of me. Whatever the cause, I'm here to stay.
I hear you're going to see a doctor to try and get rid of me. That makes me laugh.  Just try. You will have to go to many, many doctors until you find one who can help you effectively.
You will be put on the wrong medication for you, pain pills, sleeping pills, energy pills, told you are suffering from anxiety or depression, given anti-anxiety pills and antidepressants.
There are so many other ways I can make you sick and miserable, the list is endless - that high cholesterol, gall bladder issue, blood pressure issue, blood sugar issue, heart issue among others? That's probably me.
Can't get pregnant, or have had a miscarriage?
That's probably me too.
Shortness of breath or "air hunger?" Yep, probably me.
Liver enzymes elevated? Yep, probably me.
Teeth and gum problems? TMJ?
Hives? Yep, probably me.
I told you the list was endless. 
You may be given a TENs unit, get massaged, told if you just sleep and exercise properly I will go away.
You'll be told to think positively, you'll be poked, prodded, and MOST OF ALL, not taken seriously when you try to explain to the endless number of doctors you've seen, just how debilitating I am and how ill and exhausted you really feel.  In all probability you will get a referral from these 'understanding'  (clueless) doctors, to see a psychiatrist.
Your family, friends and co-workers will all listen to you until they just get tired of hearing about how I make you feel, and just how debilitating I can be.
Some of them will say things like "Oh, you are just having a bad day" or "Well, remember, you can't do the things you use to do 20 YEARS ago", not hearing that you said 20 DAYS ago.
They'll  also say things like,  "if you just get up and move, get outside and do things, you'll feel better." They won't understand that I take away the 'gas' that powers your body and mind to ENABLE you to do those things.
Some will start talking behind your back, they'll call you a hypochondriac, while you slowly feel that you are losing your dignity trying to make them understand, especially if you are in the middle of a conversation with a "normal" person, and can't remember what you were going to say next. You'll be told things like, "Oh, my grandmother had that, and she's fine on her medication" when you desperately want to explain that I don't impose myself upon everyone in the exact same way, and just because that grandmother is fine on the medication SHE'S taking, doesn't mean it will work for you.
They will not understand that having this disease impacts your body from the top of your head to the tip of your toes, and that every cell and every body system and organ requires the proper amount and the right kind of of thyroid hormone medication for YOU.
Not what works for someone else.
The only place you will get the kind of support and understanding in dealing with me is with other people that have me. They are really the only ones who can truly understand.
I am Hashimoto's Disease.

Wednesday, December 31, 2014

2014- A Year In Review

2014 FLEW by! People aren't lying when they say the older you get the faster time passes.
It was full of fun activities with friends and family and I can't wait to see what 2015 has in store for us!

January:

We became godparents with a wonderful group of people to sweet Knightly and were honored to be a part of his dedication.



We celebrated Linus' 2nd Birthday with a cake and his first hike.




February:

We actually got really into the Super Bowl this year and went all out for the Broncos and they lost horribly.



Tim went to India 

March:

-March was a rough month for us but these guys helped me through it


April:

-Sam and Michelle came to visit


-I accompanied Tim on a business trip to the Bay Area



- We had a late Easter dinner with my family.



May:

-We had the trip of a lifetime and explored Ireland and London






June:

-We got a private tour of the OC Zoo with our favorite zookeeper, Lauren




-We went beach camping at San Onofre


- We had a Birthday Pool Party



-Went to Glen Ivy on my Birthday



- My sister threw us a Birthday BBQ



July:

-Mom, Devon, and I took a painting class



-We went to Washington for David and Janell's wedding and explored Seattle for a couple of days.




-Tim went back to Ireland for work

August:

-We had a Beach Bonfire and Girls Night





-I threw a Bridal Shower for my sister-in-law



-Tim ran the Disneyland Half Marathon






September:

- We went to Big Bear for Jeff and Leahs wedding



-We moved to Irvine






- We went on a little getaway to La Quinta with Friends



October:

-We celebrated our 3 year anniversary

-A quick trip to Las Vegas for Tim to speak at a conference





-Mom had a booth at the Claremont Village Venture



-We had our first Halloween party in our new place


November:

-We went to LA for our friend Carmen's birthday and had drinks at SUR



- We had 3 Thanksgivings this year! Friendsgiving, Hemet, and Porterville.



December:

-Went Ice Skating with Heather


-Had a Gingerbread House decorating party

-Celebrated Christmas Eve in Porterville and Christmas Day in Huntington Beach





Thank you to all my friends and family for being such a big part of our 2014!