Friday, September 6, 2013

Dear Deni circa 2001



Day 6 assignment asks us what we know now that we wish we knew when we were first diagnosed.

Again it's different for me because I was so young, 14, when I was diagnosed. So there are a lot of things I know now that I wish I knew then! 

Such as, there IS such a thing as too much lip smackers cupcake lip gloss, Dr. Martens are not the height of fashion, and having 648 butterfly clipies in your hair isn't as ravishing as you think. 



But I assume the question is in reference to our Ic. In which case there's even more I wish I knew back then. So if I could go back and pass a perfectly folded note to 14 year old Deni, I'd write to her these 10 things. 

1. You are not weird because you're sick. Well... You are weird. But not cuz your sick.

2. You didn't do anything to cause all of this, it's not your fault.

3. The friends that are true will stay by your side, forget about the ones who leave you behind.

4. Cling to your family more than anyone, they'll be with you every step of the way.

5. One day you will get a myspace (you have no idea what that is but don't invest too much in it when the time comes, it's short lived) message from a boy that you know now. I won't spoil the surprise but he is one of the kindest boys you know and he will try to support you through this diagnoses but you'll push him away. Don't worry. He won't hold that against you in 5 years. You will marry him and he will be your best friend. 

6. As much as you feel like your body is turning against you and torturing you during your period. It's going to be the means to a beautiful, blessed child one day! 

7. Don't try to wear clothes that flare up your pain just because you think you have to be trendy! Also, believe it or not leggings will come back into fashion! 

8. Ask Dr. Brown for zofran! It's a miracle drug that helps the nausea. You'll eventually become allergic to it but enjoy it while you can.

9. I'm so proud of you for working so hard to keep up with other kids in school even though you're doing it mostly from home! Keep it up and you will graduate with your class, I know that seems impossible now.

10. Last but definitely not least- you are not IC. You have IC. You are beautiful. You are smart. You are faithful. You are kind. You are hilarious. You are loved by your family and God. 

Thursday, September 5, 2013

Day 3, 4 and 5 of IC Awareness Month!

Day 3's assignment for IC Awareness Month was to pick a theme song for your IC... Which is funny because a few months ago I wrote this little ditty to the tune of the chorus of Last Kiss by Pearl Jam...

"Oh flare oh flare would ya leeeave me be? Lord please take this away from me. My Pain's eleven and I know it's not good... when I just want to saaaay bad words!"

Haha I crack myself up!

Day 4's assignment was to write what IC has taught you about yourself... We have to submit our answers by midnight of the day and I posted it at 12:03 this morning so it's short and sweet but so true about myself!

I’ve heard a few times how lucky I am that I was diagnosed with IC so young because I don’t know what life is like without IC so I don’t miss it as much… Interesting theory…

The truth of the matter is I have no idea who I would be today without IC… it has molded me into the person I am… in good ways and bad! The bad seem obvious and hardly worth mentioning but the many positive attributes I have gained by serving my sentence of life with IC have been surprisingly beneficial.
I would say the biggest gift IC has given me is my ability to laugh and smile through whatever life throws at me. It’s funny because I feel like people underestimate my pain because I’m a cheerful girl usually with a smile and joke nearby but they actually have it backwards! It’s because I am so sick that I can smile and laugh every day.

Some days I have to laugh so I don’t cry… some days I laugh in the midst of level 10 pain… some days I make jokes to convince my family that I really am doing okay… some days I just don’t know what else to do.

No matter the reason, the ability to smile through the pain has benefited me in my everyday life more than I can even say. Keeping my heavy life lighthearted and fun isn't always easy but it reminds me that I am so blessed. I have a loving family who understands my craziness and self proclaimed hilarity but many people just don’t understand.

What would they have me do? Constantly moan and cry out protests from the pain? I’ve tried that… it doesn't work!  

So I laugh and I joke. I joke about my interstims being trackers, fax machines, iPods, and garage openers. I joke about wetting my pants: “if peeing your pants is cool, consider me Miles Davis”. I joke about being on Medicare at 26.

I guess my favorite part about this unique gift is the peace it gives my loved ones. It is a lot of pressure to know what to say and how to act around someone who is chronically ill but when I smile and laugh, I give them permission to do the same which breaks down walls around them.

IC is a part of me and in some ways I’m thankful for it. The gifts it has given me almost… ALMOST… outweigh the pain and agony of the disease.

Then today was Day 5 and the assignment was to make a list of things that your thankful for and then hang it in the bathroom (where a lot of our pain happens) to remind us that we are blessed. So I did this...


Yes that's written on toilet paper... I thought it would be fitting! :o)

I'm enjoying all these challenges that make us think outside of ourselves and our IC while spreading the word about IC! 

One more thing I want to share... my husband works for a big company in downtown Seattle and they put a bit article in their monthly newsletter about IC Awareness Month, complete with an awesome description of IC and the official slogan with  picture! So cool! 

Monday, September 2, 2013

The Weed.

Happy IC Awareness Month!!! 

Every day in September I will be writing something to spread awareness of this horrible disease that is impacting more and more people every day! I know of a 7 year old little girl who was just diagnosed and I know 60 year old man who was as well and lots of women in between! This disease is not prejudice, it affects anyone it please! 

Yesterday the challenge was to name our bladder and thanks to my clever husband we came up with El Vejiga Diablo (the devil bladder in spanish). 

The assignment for today was to write a poem about how IC has POSITIVELY impacted my life... Poetry always makes me feel very vulnerable and I don't share much but here it is for all to see! 


The Weed.

The weeds in a garden 
Must seem like its enemy 
Constantly encroaching 
And hindering growth 

Keeping tulips and tomatoes
From flourishing
With ease and fertility

But how fresh and abundant
Would that garden be
That flourished in spite
Of weeds and hardship

As a young lady growing 
Into the woman
I have become
IC was my weed

No gardener could hold this 
Particular weed at bay 
So it reared its heads
Yielding its thistly leaves 

I thought it was
Holding me back 
From growth
From life
From positivity 

Until one day I realized 
I may have not bloomed 
As a healthy girl may
As a carefully weeded garden might 

But my roots were deep 
My stem was strong 
I persevered
I grew. 

I blossomed
With prickly weeds entangled 

I became more than a meer flower
I became a sturdy, enduring woman
The IC made me stronger
Just like weeds makes
Any resilient flower

Now as a woman,
A veteran of the battles:
Good vs evil. 
Weed vs flower.
IC vs life. 

I know I am who I am
Because of my daily battle
With this encroaching and hindering
Weed of a disease.

I will continue to flourish amongst my IC
Using it to strengthen me
The flower will do the same with the weeds.
We will both produce abundantly




Friday, August 23, 2013

Give me a break!

If you haven't read the last blog I posted entitled "change of plans" let me summarize... 

My husband and I have been trying to get pregnant for 4 months but since I've been suppressing my period since I was 12 (except the year it took to get pregnant with our almost 2 year old son) it's been tricky. My doctor put me on a scheduled hormone plan to induce my period. In spite of all the hormones and things that go with it... the dag blasted thing wouldn't start. 

Then due to a bunch of reasons described throughly in my last blog, we decided to stop trying and go ahead with a hysterectomy. So I got off the estrogen immediately since it was wrecking havoc on my body in other ways. 

That was a week ago and guess what happened... My period just started...

I've been suppressing it for this long for a reason! It's hell. Yep, I said it... Not h-e-double hockey sticks. Hell. It's deep, dark, scorching and torturous. 

Each time I got off the hormones trying to induce a " withdrawal bleed" I booked out a whole week so I could suffer in peace. I knew what I was getting into, the first period after almost 3 years was going to be brutal. But. It was for a baby. I would endure it for this cherub known only in my heart. 

Now I'm just filthy with pain. Covered in it. Head to toe. With no purpose. In fact now we have to deliberately be careful and protected so I don't get pregnant... 

It's just cruel. 

For a normal person a period is annoying, for a person with interstitial cystitis a period is painful, for a person with endometriosis a period is brutal, for a person with both... There is no word. 

I won't even attempt to explain the pain that's happening right now... A very snarky pipsqueak in high school called me Webster because I like to use big, expressive words. But I have no combination of words to describe the sheer agony. 

Can I just give you a run down on my last month.... It started with a uti and intense nausea that wouldn't go away. Then I had an allergic reaction that caused seizures and sent me to the icu for 5 days. Then I couldn't walk and kept falling as I recovered from the seizures. Then I found out I should never be pregnant again and decided to go ahead with the hysterectomy. Then I got another uti. Now my period is full on. Next I have my Botox surgery on Monday. 

Home girl needs a break! I'm not saying a lavish vacation or extravagant dinner out... I'm saying a day to sit outside under the shade tree without my heating pad or fear of wetting my pants, and to be able to get up and walk whenever I see fit. 

I'm sure I'm going to look back on this last month and laugh... Well maybe not actually... 

I'm no stranger to hardship and pain but this month has really raised the bar! Good thing I have support from loved ones as a ladder and strength from God, I can still reach and hang on to that bar! (This hallmark moment brought to you by raging hormones) 

I'm really trying to not having a pity party but things have been grim around here lately... I better go eat some ice cream, that will help.

Ugghhhh... The emotional and physical pain of this unexpected period is wearing me down... I just had to vent. Thanks for letting me dear readers!

Sunday, August 18, 2013

Change of Plans

I have dedicated myself to this blog and my readers. Never holding anything back. But I have to tell you out of all the doozies I've written... This will probably be the hardest. 
I'm sorry for not posting lately but don't think I haven't been writing. I've been slowly documenting my journey trying to get pregnant while battling my ferocious interstitial cystitis and endometriosis. 

What a journey it's been. It's been 4 months of taking different combinations of estrogen and progesterone trying to get my period to start that I've been suppressing medicinally since I was 12. The last real one I had was the cycle I got pregnant with Titus on. 

But as you may or may not know hormones exacerbate IC and Endo like you wouldn't believe. Picture Endo being a garden that's planted and carefully watered, it grows quite well on its own. But then you dump some ripe fertilize all up on there and you're having salad for days! Of course when the Endo is acting up, the IC gets mad and tries to steal the spotlight back. 

Being the stage that they're both trying to hog has been exhausting and more painful that I could describe. 

So there's that going on. Plus I've been getting UTI's (urinary tract infections) literally once a month and I have a general sense of nausea 24/7.

I don't think I've told you that story... Well. I had hyperemesis gravidarum while I was pregnant with my son, Titus. It was constant, unrelenting nausea and vomiting. I literally threw up every day from the day of the positive test to the day he was born. 

It got so bad around 16 weeks pregnant I passed out from dehydration. So they put me on constant IV's, pumps that administered zofran (the go to antinausea med), and eventually gave me a PICC line (which is a central line that goes from a vein in the arm to a vessel near the heart that can stay in for long periods of time) that administered meds and fluids around the clock, all while taking phenergan (another antinausea med) by mouth and sometimes as a suppository when I couldn’t keep it down. And I still threw up daily and was nauseous all the time. 

I lost 20 lbs by the time I was 20 weeks pregnant but miraculously and thanks to the medicine I ended up with a sweet, chubby cheeked 7lb 11oz baby, Titus James.

Unlike most people with HG, my nausea and vomiting didn’t stop after I had him... It continued while I nursed him for 14 months leaving me around 45 lbs less than I was when I got pregnant. (The only advantage to vomiting for 2 years)

When I stopped nursing it reigned in a little bit. I was rarely vomiting but still the nausea lingers to this day. Oh and by the way I've gained 15 lbs of that weight back. Darnit. 

Another fun fact about my broken body... When I take a particular drug for a long time my body eventually rejects it with a very dramatic allergic reaction. (My body is all go big or go home.) 

So. As of a few weeks ago I was down to only one antinausea med that I could take, phenergan, but it doesn't just make me tired. It makes me sleep the sleep of... Well... My husband. (Imagine a bear that took Tylenol pm before he headed for hibernation.) 

So while I was at some random doctor for yet another UTI I asked if she knew of any other antinausea meds and she basically said "by George yes there is, Tigan!" (She was wearing a Scottish sash, it was all very strange.)

After a bunch of rigmarole at the pharmacy about it being a super old school med, having to call around to find it, and having my sister pick it up… I finally had the new medicine and new hope. 

The next day I woke up with my usual pain and nausea so I happily took my trusty dilaudid and this new tigan stuff. 

Next thing I knew my toes were clenching up all on their own. I had a dystonic allergic reaction to compazine (another antinausea drug) when I was 15 so I knew what was happening.

I was on hold to talk to a nurse when my calf muscle froze up too. I hung up the phone and waddled to the car in my cupcake pajamas, my mom loaded Titus up in his dinosaur jammies and we sped to the hospital. 

By the time we got to the ER my whole body was contorting as random muscles tensed up on their own. My head was literally being forced as far right as it could go. It was like some serious exorcist business... So they rushed me to a room and pumped me full of Benadryl, steroids, muscle relaxers and fluids.

Pretty soon my body had relaxed and they sent me on my merry way. I came home, ate a little bit, and then crashed from all the meds. 

An hour later I woke up, still really drowsy but my toes were clenching up again! We once again sped to the local hospital and went through all the same motions. 

Except this time it didn't work... It just kept getting worse and worse. My muscles were locked up so hard I was shaking. Next thing I knew one very important muscle was flexing in the wrong direction. My tongue. It was closing my throat. Then my pulse went soaring up to 180.

They pushed me to the trauma room and I vaguely remember words like “intubate” and “paddles” being tossed around.  

They quickly decided I needed to go to a bigger hospital, more equipped to deal with this crazy reaction and I needed to get there soon. 

The next thing I remember I was laying in the back of an ambulance seeing the flashing lights and faintly hearing my husband’s voice mixed with the sirens. I mumbled a joke to the medic about my husband being thrilled to be riding shotgun, sirens blazing before another attack send me unconscious again. 

Next thing I knew I was in a big, dark room that I later found out was the Cardiac ICU at a hospital in Tacoma. I was having full on seizures at this point except they weren't considered that simply because I was technically conscious. Whatever. They called them episodes (don't get me started on the word episode... an episode is 30 minutes of Friends not flailing about choking on my own tongue).

I don't remember much about that part... I remember a phase when a doctor told my family members to hold me down when the seizures started and I knew they were trying to help but it hurt so much worse. I could barely communicate. I wasn't allowed to have any food, water or even ice for fear of choking during an "episode" They kept the room quiet and dark as to not over stimulate me. A lot of times I'd open my eyes after one, I would see my loved ones crying and I'd try to say that it was okay. I could never figure out where I was, what day it was, where Titus was, who Titus was with. There was a suction tube on my bed for when I choked on my own saliva and tongue. My Mom and husband used it on me several times. They wouldn't give me a catheter because of my high risk of infection yet they were pumping me full of fluids so I almost constantly had a bed pan under me and still wet the bed dozens of times. My husband slept in a chair not fit for a long meeting much less sleep. My very not touchy sister in law rubbed my leg. I told off a few doctors who tried to say I shouldn't have visitors. I was told I was loved a lot. I somehow knew I was going to be okay.

Other than all that I don't remember much... My family has filled me in on more stuff but I think this story is best told from my perspective. (Expect I’d be remiss to not tell you I was apparently seeing mice playing cards regularly and a parrot on my dear cousin’s shoulder.)

One thing I remember clearly is being thrilled when I was rolled to a bright room with a lovely view in the critical care unit 2 days later. My vitals and blood work had leveled out and though I was still having episodes, they were shorter and further apart. 

View from my room in Critical Care
My husband finally got a cot, I could have water and ice, and the nurses were very friendly... It was much better. Still scary but better. 

The next night they considered letting me go home but I hadn't been able to eat solid food and was still having occasional episodes. Since I was doing better my husband went home to sleep, he had to go back to work the next day. I was only a little bit scared to be there by myself and was thankful to have a very sweet, young nurse on duty all night… Who gave me my first sponge bath and somehow made it not as awkward as it should have been.  

I made it through almost all night without an episode and though the next morning I threw up the bite of blueberry pancake I tried, I was able to drink some odwalla juice and eat a few pita chips. So guess what! I was sent home Monday afternoon! Five days after the nightmare had begun.

I was on strict bed rest for a week and not to be alone for the first few days and not alone with Titus for several days. But most of all... I was never, ever allowed to have any form of antinausea medicine again. I was now considered allergic to it all. The only thing I can do for my nausea from now on is a scopolamine nausea patch, I think it’s usually for sea sickness but it does take the edge off.

I was sent home 2 weeks from tomorrow. Yesterday was the first day I was actually able to walk on my own. My muscles were so sore and weak from the constant tension and thrashing that they would just give out. I fell dozens of times, it was so weird! It wasn't like a big dramatic fall, I'd just be standing and then I wasn't anymore. I said to my sister, "It's not falling; it's just sitting when I don't want to." Sometimes it looked like I was doing some weird gangsta walk and other time it was more like a chicken dance… but I’m so thankful to have my mobility back. THAT was annoying.

More than the exhaustion, soreness, and weakness the hardest part of my recovery has been the constant pain in my heart.  A few days after I got home I realized something… how could I possibly be pregnant for 9 months without any medication to ease the nausea and vomiting? It’s true… it might not be as bad as last time. What if it’s worse though, most people with hyperemesis each pregnancy just get worse. Would I be able to sustain a pregnancy? Would I end up miscarrying? Or what if my body gave all its nutrition to the baby and put my life at risk? 

But if I chose to not risk it… that left me with the alternative… Be a family of 3. Make Titus an only child. Never be pregnant again. Never nurse again. Never have the chance of having a daughter. Never hear my kids laughing in their room when they’re suppose to be sleeping. No one for Titus to commiserate with about having a sick mom. Oh the list could go on and on.

My sister is only 13 months older than me and has been my best friend my whole life. I have done everything with her… I wouldn’t be Deni without Jeny. My husband, Zach’s brother is only 15 months younger than him… they are still inseparable. How could I not give Titus that giant, blessed gift of a sibling?
Oh how my heart was breaking. My arms, my heart, my soul… yearned for another baby of my own.
I kept praying for God to give me a clear answer what to do and then peace with whatever that is. I just felt pain. I just felt incompletion. I just felt disappointment.

While lying in bed sobbing, pleading to God I felt a sudden acceptance. My heart hurt so bad, my breasts hurt, my uterus hurt, my whole body hurt as I realized it would never create and nourish another baby but I knew it was the right decision for my body and my family.

I took it really hard at first. I sobbed for 12 hours straight. I mourned the baby I had never had, that God hadn't even knitted in my womb yet. I cried for Titus who would never have a sibling, for the chance of having a daughter, I cried because I wanted to have a daughter with D name like my Grandma, my Mom and I. I cried for not knowing my first pregnancy was my last- somehow I would have soaked it up more, I cried because I would never nurse again. I cried for my husband who had always wanted two kids. I cried for my family. I cried when I realized this has been God’s plan all along. I cried when I thought about how Titus would turn out being an only child. I just cried and cried…

The next morning I woke with EVEN worse pain than usual so in attempt to squelch it I took two dilaudid that morning instead of just one. Minutes after I took them I knew that was a bad idea without any antinausea meds. I threw up from 9:00am to 6:00pm… Each time I would try to eat a mere cracker or sip water it would come right back up. Titus cried every time he saw me sitting in front of the toilet even though I tried to tell him I was just looking for something in the potty. He was inconsolable. He just wanted me but I was miserable and so fragile. The slightest thing would send me back to the bathroom to vomit. I usually love our evenings with just his Daddy, him and me but I was counting down the minutes until 7 so we could put him down and I could just sleep. When 7 hit, Zach carried Titus to his crib but when he put him in there he just SCREAMED, like he was being tortured. As I watched him on the video baby monitor he climbed out of his crib for the first time.

No matter what we would try he would not stay in his crib… If you know Titus, you know he loves to sleep! He gets in his crib and goes right to sleep. No reading, singing, rocking required. We turn on his white noise and lay him down and he is OUT. He hadn’t fallen asleep in our bed since he was 4 months old. But I didn’t know what else to do. So I sang to him and rubbed his back, he laid there with his eyes wide open but real still. Every time I would stop he would sit up and said “gin” (again) and I would keep rubbing and singing. He moved around fighting sleep until he finally fell asleep on top of my feet at the bottom of the bed while Zach and I whispered.

God works in crazy ways some times. He showed me exactly what I needed to see in one miserable day that ended perfectly. I got a glimpse of how it would be if I was sick without antinausea meds and with a sweet, sensitive toddler around. Then he showed me how much Titus needs me and how content we are as a family of three.

So Zach and I have fully accepted that this is God’s plan for us and I even feel at peace with it… the sadness does still linger… I’m sure it always will. There will probably be days that I’m thrilled with the way it turned out and days where I still yearn for another baby. But God had a different plan for our family than we did. He knows far better than we do.

The good news is now I am excited to hunker down and start treating my IC and Endo. I have pretty much put that on hold until I was done having and nursing babies. There is a medication called cyclosporine that is an immunosuppressant that my doctor has wanted me on so I’ll start that process soon. My interstims have been broken for over a year so we’ll get those up and going again. We’ll do the hysterectomy… It will be good. Hopefully between all of that my health will improve and then I can be an even better mommy, wife, daughter, sister, cousin, friend, aunt, niece, granddaughter…

So that is… I’m sorry to leave some of you in suspense… wondering what in the heck has been going on. It’s been the most tremulous, horrendous few weeks… Physically, mentally, and emotionally…  I couldn’t keep telling this over and over so I wanted to just write it out for everyone and also for myself.

For those of you that have struggled to get pregnant or miscarried you know the pain I was/ am feeling… I can’t do it justice. It’s just raw maternal pain. I know we are beyond blessed to have Titus. It’s not that he isn’t enough! He is MORE than enough. We are so very blessed to have him. He is an absolutely perfect boy, he is sweet and sensitive, he loves music and has some sweet dance moves, he gives fierce hugs and open kisses, he adores animals and pretends to be them most of the day, he is smart and contemplative, he is kind and loving, he has a wild temper but hates to disappoint people, he has bright blue eyes and white blonde hair, he is cautious yet adventurous… I could go on for days. He is perfect.
Titus and I have been doing lots of snuggling and watching Pooh lately as I recover. Love him so much!
Also I know a lot of you are thinking this… what about adoption? YES! I hope and pray that there will be a day that I am healthy enough to consider it. My cousins have fostered and are in the process of adopting two precious kiddos and someday we would be honored to do the same.

I’m sorry if you’re underwhelmed by all of this or if you think I’ve been overly dramatic and vague on facebook… I just needed prayer without explanation for a few days... and it helped so much! It’s just been an overwhelming time for me as I recover from the allergic reaction, my usual miseries, my nausea and vomiting without any thing to relieve it, now I have another UTI, I got off the hormones, and the emotions of making this huge, life changing decision to not only stop trying to get pregnant but proceed with the hysterectomy.

Not to sound like a rapper accepting a Grammy but… I’d seriously like to thank my family for all their support and prayers during this unbelievable hard time: my parents, my husband, all of my siblings, my in-laws, my grandparents, my aunts and uncles, my cousins, and some dear friends. Most of all I am thankful for how close I have felt to God the last few weeks… He answered my prayers quickly and thoroughly.

I’ll keep you posted on the new treatments as I try them!

….. Sorry for the excruciating length of this blog!

Love to you all!