Showing posts with label gratitude. Show all posts
Showing posts with label gratitude. Show all posts

Thursday, April 19, 2012

Day 19: CHANELLE in her own words



Take a look at the story of my friend Chanelle, a darling and daring Cushie survivor. I admire her so much for her courage, positivity, wisdom and fighting spirit.  This girl has *moxie*; so much, in fact, that it will take several posts to tell her beautiful story.

late 2006 

9-20-07 (1st pit surgery)

 
Early 2009





September 2010

November 2010

January 2011
November 2011
February 2012





































Early 2006 - I was a happy, healthy 16-year-old cheerleader at my high school. I made great grades, had tons of friends and had just won Wildcat Idol, a singing competition at my high school.  I enjoyed writing poetry and even won a contest for an essay I had submitted, also, for my school. I was in chorus and advanced academic classes and just loved being involved in activities like a normal teenager would. Overall, I had a pretty busy and fun life with my major problems being remembering to study for tests and what outfit I would wear.

Towards the end of the year, though, I started noticing that my clothes were getting a little tighter and by the holidays, my dad and close friends were commenting that my face looked different and that I looked like I had put on weight. Now, since I have danced since the age of two and had the typical "dancer body" all my life, I was shocked to hear anyone say I looked different. I could always eat whatever I wanted and never gained weight, so that was devastating. I soon found myself putting away my normal jeans and wearing simple t-shirts and my mom's old pants to school. I soon had to stop cheering since I had zero energy. School was no longer fun since I had no desire to put effort into my appearance or socialize. On top of my ever-changing looks, school and learning, which I always found enjoyable, were becoming impossible. I found myself up at all hours of the night with insomnia, struggling to write essays that I would usually complete in an hour or two. Needless to say, 2006 was not a good year for me. To add insult to injury, both of my grandmas passed away, a great aunt of mine died and one of my old pastors also passed within months of each other, leaving us to take in two of my cousins who lived with my grandmother on my mom's side. So, within a year, my looks, my health and my life changed and I thought my life was falling apart. 

By 2007- I knew that things were terribly wrong. I was struggling to just make it through each day with my depression, insomnia and myriad of strange symptoms. I started keeping a log on MS Word of all the things that would happen to me every day: new stretch marks, sudden outbreaks of acne, tiredness, rashes, hair falling out, etc. I kept that log with the hopes that my doctors could see a pattern and hopefully fix me. At this point, I was also seeing a psychologist, a psychiatrist and my primary care physician who were keeping me on anti-depressants, acne medications and other things to try and repair my quality of life. (Of course, as we know, Cushing's can't be cured with pills and creams... but I had yet to discover my disease).

So I carried on with my treatments and my miserable life. I would simply go to school, come home, take a two hour nap from exhaustion and then be up all night until the next day of school, every day, getting a little heavier and more depressed. That was my existence for months.

Mid-2007- By this time, I had gotten so tired of people not recognizing me (since I had gained about 30 pounds) and went to my primary care physician who literally told me she had no clue what was wrong with me, so she would refer me to a specialist (and her mentor), a pediatric endocrinologist. So I went home and (by the grace of God), I happened to turn on the TV and flip to the Discovery Health channel where Sharmyn McGraw's episode of Mystery Diagnosis was playing. I finally saw someone who had the same thing as me. I didn't know what it was, but when the episode was over, I researched Cushing's disease, printed out pages of information and took it to the appointment with the endocrinologist. Of course, when she first met me and saw me, she knew something was wrong, too. I suggested Cushing's disease and she thought I could be on to something: all I needed was an MRI to prove it. 

After that, the rest is kind of a blur! In August 2007, I got the MRI that showed a 6mm tumor in my pituitary. I had my first brain surgery at John's Hopkins on September 20, 2007. I ended up getting diabetes insipidus with my first surgery, but I felt it was worth it to take care of my health. 

I missed the first semester of senior year with my friends because of the surgery, but it was totally worth it to finally attack that tumor! A few months after, I started losing weight and feeling better, so I went back to school second semester and graduated from high school with honors in 2008. Unfortunately, I only dropped about 10 pounds, and my weight began to creep up on the scale. I was feeling miserable again. In my heart, I knew my Cushing's had come back. 

Through the pediatric endocrinologist, I was able to be put in a medical journal and also spent time at the NIH to be in a Cushing's protocol where regrowth of my tumor was found. By January 16, 2009, I was having my second brain surgery and got out of John's Hopkins again on inauguration day (go Obama!). But sadly, after the second surgery, I never lost a pound and none of my symptoms went away. I knew that it was time to do something different.

By 2010, I was fed up with being sick and started exploring my options. I was considering two treatment options:  radiation or bilateral adrenalectomy (BLA, removing both adrenal glands). When my cortisol levels in my UFCs were coming back greater than 1200 and 1300 with a reference range of 16-50, I knew I had to do something extreme to fix my extreme cyclical Cushing's.  So I opted to have BLA on April 23, 2010.  It was the best decision I ever made. From that June to December 2010, I lost 50 pounds. 


By 2011From then to now (April 2011), I've lost an additional four pounds, bringing me to my lowest weight of 129 pounds. Besides the weight loss, my skin is perfectly clear, my hair has grown back, and my stretch marks continue to fade. I have enough energy to have a part time job while going to school. I don't need to take two hour naps each day. Of course, I take hydrocortisone and other drugs to regulate my hormones, but I do it happily knowing that the alternative is pure hell. 

Although I wouldn't with Cushing's on my worst enemy, going through this journey from 2006 to now has changed me and given me opportunities that I would have never dreamed of. I was even featured in my local paper!  It has also helped me realize that I want to go into the medical field and that I can do anything I set my mind to. Friends call me their hero, and that is an amazing feeling! 

So for all of that, I have to thank Dr. Lorelle Bradley (former primary care physician), Dr. Catherine Christie (first endocrinologist), Dr. Alfredo Quinones-Hinojosa and Dr. George Jallo (AMAZING neurosurgeons at John’s Hopkins), Dr. Ashish Behari (urologist), Dr. Michael Bryan (current endocrinologist), and all the nurses and staff at John's Hopkins, Kaiser Permanente and Washington Hospital Center for getting me where I am today... but I also thank God for speaking to me through Sharmyn McGraw and Mystery Diagnosis so that I would have my "aha!" moment and basically diagnose my own condition. 


February 2012: a birthday photo shoot. FUN.
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1) How are you now- what can you do now but couldn't before
I'm great right now! Since my BLA, I have gone from 184 pounds with sore joints, painful feet and almost 0 muscle strength to 129 pounds and being able to shop in the misses section of stores again! I also have enough energy to have a part-time job while also being a full-time student. I don't take naps every day because of my increased energy, my hair is looking beautiful and my stretch marks are getting lighter and lighter each year. I also enjoy time with friends and am no longer ashamed to see people for fear that they won't recognize me or comment on how different I look. I plan on working for a while to make money for school and transfer to Virginia Tech next Fall, but for now I'm just a happy, and much healthier student and employee!

2) What you hope to do differently as deal with patients because you had Cushing's, etc. 
As of now, I want to get my undergraduate degree in nutrition (which I became very interested in while at John's Hopkins for my first brain surgery), and I may decide to take the test to become an R.D. afterwards. 

I also dream of going into Endocrinology after my Bachelors (and if I don't want to continue with nutrition). If I were a doctor, I know that I would NOT give up on my patients and also, find the best recourses for them if I couldn't figure out what was wrong with them. After all, that is what saved me. Of course, I would have an extra level of compassion for them, but most of all, I would encourage the ones that have been battling Cushing's for years NOT to give up. I come across a lot of Cushies today that want to throw in the towel and it makes me sad.  If I were their doctor, I wouldn't let them give up. 


My friend Chanelle. I'm glad Cushing's brought us together.

Saturday, March 31, 2012

236,892 Page Views & Counting

April is my favorite month of all. I think about it all year!

It's Cushing's Awareness Month.  On April 8th, we honor Dr Harvey Cushing's, the father of modern neurosurgery and the namesake to this terrible disease I have. We don't blame you, Harvey. We like you!
I wanted to let you in on a project I've got going. In appreciation of where I am in my journey and all the close friends I've made along the way, I plan to blog every day through the month of April. Maybe, just maybe, a few patients suspecting Cushing's will see enough information to reach out and stand up to the MDs that are blocking their way to treatment, cures, and ultimately, reclaiming their lives.

Now, back to the writing and daily blogging for a sec. For someone so scatterbrained, exhausted, and unreliable as someone with Cushing's, even agreeing to a challenge strikes fear in me. Eek. That's a lot of commitment, and Cushing's makes us so flaky, I really hate that part. All I can do is try, right?!

This blog has been an important part of my life since its inception in May 2008. It was a special place that I created where I could talk about Cushing's in any way I wanted, any time I wanted. For the past three years, I have shared as much and as often as I could of myself, my experiences, and tidbits of knowledge I accumulate along the way. Bringing more awareness to others is critical to how I have made sense of and come to accept this haunting disease.

So for me, this challenge is very personal.

As a pre-disease perfectionist, I always wish I could do more here.  I wish I could blog every day. I have so much to say Cushing's and how it changes the trajectory of my life each day.  However, I struggle to maintain the energy for myself and my family. For this one month of April, I really want to work to balance my focus on Cushing's and my focus forgetting Cushing's enough so I can be present with my family.  I hope I can hold it all together. I can only do my best.

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I always wish this body and mind would let me do more or not hold me back.  I feel so trapped in this body.  It is also so important to my self-identity to combat this reality of me being stuck inside the house all day.  I realize I can be sick with Cushing's and still contribute something to this world. With this blog and these numbers, I sorta kinda maybe see the impact I have already made in my little corner of the Cushing's world.  

I think of all the Cushing's patients -- fearful, lost, defeated -- that have come to me by way of this blog, and I am thankful that something I have done could help another kind soul in this world. I always wish I could spend more time with each person who writes me--four people last week!--but I am without a doubt always rooting for them. That's what I see in this counter, and it always makes me smile. 
Seeing that graph below makes me feel pretty, pretty, pretty, pretty, pretty certain that there are many more undiagnosed Cushies in this world than any doctor would ever care to admit.  That’s fine by me.  While I can’t control the doctor side, I can do my part to educate and advocate for the patient side.
Hope you stick around in April for a fun month, as we learn more about facing Cushing’s with Moxie.

Bye for now.  Melissa

Saturday, June 20, 2009

FAQ YOU: MELISSA'S MAIL BAG

From Sweet Sue in Houston, through Facebook:
Melissa, if you can see this, hope you are doing okay with good thoughts and prayers your way. Let us know if you need something.

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Hi Sue. Thanks for checking on me. You are so sweet. I am doing well. I am trying to write stuff up to post on my Cushing's Moxie blog. I'm trying to get a follow-up email set up, too. People may be wondering how I am, and I don't want them to worry.

I am doing well, better than expected. I have to remind myself though, it is all synthetic. My body is not making cortisol/steroids on its own, and any good feeling now will soon be replaced with severe withdrawal symptoms as they lower my dose of hydrocortisone week by week.

BUT I am happy.
I feel more in control.
Grateful.
Pensive.
Appreciative.
Wistful.
Optimistic to be moving forward.
Happy to be me.
Happy to have my husband, miracle baby, family, and friends.

It's all good. :)

They must have pushed through an extra dose of clarity with my anesthesia last week.

~Cushie Melissa