Kathie Harrington's World

Cushing’s Disease Anniversary

June fourth is the third anniversary of my second surgery for Cushing’s Disease. This is monumental to me because my team of doctors at Cedar’s Sinai Medical Center’s Pituitary Center (where the surgery was completed) told me that I would be 100% back to normal by my three-year anniversary.

The second surgery, June 4, 2007, removed my entire pituitary gland, along with the tumor. I’m living proof that one can live without a pituitary. But am I back to normal – I like to think so but I know there are deficit areas that remain a bit foggy. Most Cushing’s patients are in their 20′s and 30′s, I was much older than that at the time of my initial diagnosis and subsequent surgeries. Thus, one would expect my recovery to take longer.

Because of this website/blog and written articles, I have received phone calls and E mail from other Cushing’s patients or people who suspect Cushing’s in themselves or a family member. The stories are sad ones and often fill with professionals who will not listen to them or who refuse to do the right testing in order to diagnosis properly. I offer advise but I know how lucky I was to have a doctor who recognized the characteristics of Cushing’s in me right away.

So on the eve of my third anniversary, am I 100% back? No. Physically, I tire easily and take power naps about three times a week. I don’t like loud, crowed places because it makes my head “full.” I can’t listen to more than one person talking at a time and really pay attention, and conversation often tires me out. I lost weight at first but have gained some back. I continue to have a word finding problem at times, especially if I’m tired. Because I’m a speech pathologist, I know how to substitute many words and try to “hide” this language disorder. I don’t plan to overdo too much in any given day ~ if I do, I pay for it the following three or four days. I continue to get those deep, deep chills that only four or five blankets and a nap can cure – but not nearly as often.

BUT, when I compare where I was three years ago, I can only put the palms of my hands together, close my eyes, and thank God for my family, my faith, and my courage to pursue so desparately those things I knew I had to in order to get to where I am today. I’d put me at about 90%.

I’ll leave you with this thought because I like it and it says a great deal about anyone who has dealt with any disease:

“What lies behind us, and what lies before us, are tiny matters compared to what lies within us.”

~Ralph Waldo Emerson

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Cushing’s Disease ~ Pituitary Surgery

Endonasal Approach to Pituitary Surgery

My surgeon, Dr. Adam Mamelak, from Cedars-Sinai Medical Center wrote a great article for their recent newsletter about pituitary surgery. He discusses transphenoidal pituitary surgery and the two most commonly used approaches: sublabial and endonasal. I underwent the endonasal approach for my two surgeries nearly three years ago. I did not experience any pain with this approach. (I understand that the sublabial approach can be very painful and it is often necessary to pack the nose for up to three days.) Lesson here is to be sure that your pituitary surgeon is very skillful and familiar with both approaches before you decide what is best for YOU.
Cushing’s disease occurs in about 1-2 people per million! However, it is extremely common in dogs.

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Cushing’s Disease Awareness Day

Cushing’s Disease Awareness Day is April 8, 2009.
Could YOU have Cushing’s Disease and not even know it? Could someone you love have Cushing’s Disease and neither of you know it?

Cushing’s Disease is not nice. It is not fun. It is not cushy.
It can be deadly but more importantly, Cushing’s Disease can be cured.

Learn what the characteristics of Cushing’s Disease are. Look in the mirror with curious eyes and go to your doctor if you see what you hope you are not looking for. It could mean the difference between life and death.

Click on the Cushing’s page at the top of my website.
It could save your life or someone you love. Do it today!

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Rare Disease Day is February 28

The Cushing’s Foundation is teaming up with the National Organization for Rare Disorders (NORD) in promoting Rare Disease Day on Feb. 28th. Cushing’s disease is one of those rare conditions that needs attention and public exposure. Perhaps many diseases are not so rare as they are only unidentified or misdiagnosed (this happens often with Cushing’s). I am living proof that an early diagnosis and treatment is necessary in saving lives. If you have not already done so, go to the CSRF site on this blog and take a look at the characteristics/symptoms of Cushing’s disease. It could save your life. Also, read more about Rare Disease Day on the CSRF website.

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