Thanks for stopping by my page and hello new followers!!! What a pleasure it is for you to read my thoughts. I’m amazed that you would spend your time reading my work.
I only blog as desired and my post are simply reflections of my thoughts at the moment. As we all know, moments change, so there may be conflicting posts!
I appreciate you for taking the time to read my work. I can only promise to stay true to myself in the moment, whatever that moment may be!
Today I will be the best version of me
I should graduate from my doctoral program May 2018; but there’s so many changes that will happen before that day.
Health, illness has caused major delays in my original plans but I’ve made progress also. If you’ve read my posts, you know that I have endometriosis and I’ve known for awhile.
I had a dream to receive a PhD so that I could not only teach at the postsecondary level, but so I could help others reach their goals. Believe me when I say that I don’t believe you need fancy degrees to help people and you certainly don’t need a PhD; however, there are some levels of access that are denied to many without the fancy degrees.
My pursuit of this degree is not for reasons of vanity but lies in the fact that it inspires many. Many groups are still underrepresented in the halls of academia so it’s not shocking that some individuals from those groups feel that dreams of having fancy degrees are just that, dreams. I am and will always be a symbol that those dreams don’t have to remain dreams. I look to inspire at least one person to pursue her dreams.
I am representing many underrepresented groups…I think I can achieve my dream of obtaining this fancy degree I’m in pursuit of in spite of the seen and unseen obstacles in my way.
Often I have to encourage myself to keep going because it feels like an uphill battle…but in a little over one year this battle will be won and I’ll prepare for the next one.
I believe I can do this and that’s a major part of the battle.
Being diagnosed with endometriosis in my adolescence was a blessing and a curse. I was glad to know that there was something wrong and it had a name. I was excited because I finally knew that I did not make up the pain; it was definitively real…with a name.
It didn’t take long for me to receive my diagnosis, considering that many individuals go years without a proper diagnosis. Endometriosis was always the suspected diagnosis from the very first time I experienced pain. The only delay in diagnosis was due to my age, my doctor didn’t want to subject me to an unnecessary surgery. We waited 1 1/2 years before surgery while trying oral contraceptives and so I could become an “official” teenager.
Once the official diagnosis came it was also a curse because I instantly developed fears about my future fertility and my future career.
I automatically assumed I was infertile and that NO man would want a woman who couldn’t bear his children. After reading information about endometriosis – most of which was provided by or recommended by my physician; I feared that I would never have a successful career either.
These thoughts, fears were compounded by my very premature mind, I was only a teenager – barely -and I tried to deal with a very mature problem. I wasn’t dying, but I often felt like dying was a far cry better than living In constant pain.
Today, I’m learning to put the brakes on as far as my fertility and career goes. No reason to worry about things that are not at the forefront. I’m currently working toward the career that I’ve always wanted and I’ve never tried to conceive so who knows what the future holds
Why do I not live in a place where fruits and vegetables are always in season? Many of my favorite foods are vegetables but so far frozen vegetables come up short. Sigh
I felt the presence of endometriosis in my body during my SECOND EVER menstrual period, I was nearly 12. Once I turned 12, I started my first set of birth control pills in an effort to address the menstrual related problems I was having…birth control pills didn’t help so I was referred to a gynecologist. In the referral documents, the pediatrician suggested endometriosis as my potential ailment.
I was so young at the time so the gynecologist tried a few other birth control pills and patches before deciding on the exploratory surgery. The surgery would confirm or deny the suspected diagnosis of endometriosis.
I was 14 when it was surgically confirmed that I indeed had a pretty bad (in terms of location and size of lesions) case of endometriosis.
For a moment, I was relieved…there was a medical reason for why I missed so much school and missed out on hanging with my peers that was no longer a mystery, it was endometriosis.
Then I remembered that my doctors told me that endometriosis had no cure. My relief flew out the window because now with diagnosis, I was the sick one.
Before the diagnosis I was just an adolescent who didn’t like school and made “excuses” not to go or to leave early in the day. After diagnosis, I had an incurable disease and no guaranteed surgical or medical relief.
Endometriosis officially made me the sick one…as an adolescent this was torture.