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I wanted to share a couple of photos I have of being bald. I was bald alot. I loathe fake hair. While going through chemotherapy it was still winter so I stayed in the house alot. My friends wore the wig more than I did =)
I hated the wig. Did I mention that? It was itchy and uncomfortable. Mainly because I had gotten ripped off buying it. Stupid me waited to get the wig until after my second round of chemotherapy. I was tired, feeling sick already, and my hair was falling out in the store. I was pushing back tears and the manager took advantage of me and sold me a piece of crap for over 400 bucks!! I just wasn't thinking. There was so much going on - I left everything for the last minute. So with all of that - I rocked the baldness, instead. I would highly advise falling in love with your facial features and trying the same.
Now I know there are places you have to wear the wig. I tried to avoid wearing it as much as possible. But for my best friends birthday, this may, I went out for the first time rocking the synthetics.
s and I would count the stares or faces people would make. Like I was ruining their day, or I was the entertainment. I couldn't believe some peoples reactions and manners. I guess in their mind they think: BALDNESS = CANCER = DEATH. They would assume I was dieing and didn't know how to react. So they would either stare or look down and walk away. Didn't want me to catch them staring! But it was worse when I caught them trying superhard to ignore my bald elephant in the room. Im sure some of you have encountered this. What is the right way to react?
I know staring and people looking down made me feel uncomfortable- but then again, so did the wig. So what do you do? A question I asked myself ALL OF THE TIME. There was no answer. So what is the better reaction then? I guess no reaction at all, would be nice? It shouldnt be so unheard of. Us chicks just ROCKING THE BALDNESS!!! How can we change that? I mean - There is even a disease called: Alopecia. This is a disease of spotting baldness in both males and females. It occurs in 1-2% of humans and 90% of those who have the disease have their hair grow back. But 10% of those who have it- It never does. And yet these people are also made to feel they have to wear a wig.. FOR THEIR WHOLE LIVES?!? No Way! Ladies.. One day when you're feeling good - Get dressed up, put some makeup on, toss the wig in bathtub and go out without it. Go out with a loved one or good friend- Because again, people will stare. It will make you want to go home and stay home!! But go out and do it anyways!!!!Waiting for the intial results.. a cancer 'Yeh' or 'Neh' if you will- was agonizing. I was emotional and positive all at the same time. When the doctor finally called he asked if I wanted to come in to hear the results and I told him just to tell me over the phone. (But at least he asked) He went on to tell me Hodgkins Lymphoma and how it was a "great kind of cancer to get if you're going to get cancer" AH.. The things some doctors will say to try and comfort you..
He referred me to an oncologist (cancer doctor). Now this guy is worth writing about. He reminded me of a nutty professor. He spoke quickly and with an accent. I can't place where he's from but it was almost german-ish. He had glasses and fuzzy grayish hair popping off of his head. His shirt was always untucked and he ran around his office like a chicken without a head. But he was smart, super-cautious, and had an excellent track record with head and neck cancers. So I was sold. My mom laughed when she met him. She didn't believe my description I guess. You know us youths today- always over exaggerating. =)
I cried alot the first couple days. It was sporatic and wouldn't last very long. I would break down. realize I was breaking down and stop myself. It was alot to take in. I am 21 and I have to go through chemotherapy and radiation for a disease that can kill me. And on top of that I was faced with more wonderful news. Being that my cancer docter was very cautious he wanted me to see a fertility doctor about harvesting eggs. He explained to me that I did have a chance after treatment of not being able to conceive and have a baby. This I'm sure everyone has been told that has gone through treatments.
Now guys- when you freeze your swimmers you have a great chance of being able to conceive in the future. But as for eggs- The fertility specialists explained to me that there was a 10% chance of a baby with each egg. But if they had an embryo (swimmer + egg = embyro = frozen baby) I would have a 30% chance of conceiving with each embryo. And they would usually try with two embryos to increase your chance to 60%. So to sum up : In two weeks time I was told I had cancer and my boyfriend of 3 years and I had to decide whether we wanted to have children. Basically--A bit much to take in. But my boyfriend is amazing. He signed away his dna for me in a heartbeat and I was onto hormone self injections. I want to get more in detail about this treatments but I will leave it for another post. I want to gather others experiences as well.
So i was onto 'The Pre Tests' Among all of the bloodwork, MRIs, Xrays, Biopsys etc. I had to do heart scans, and a bone marrow test. The MRIs are not that bad if you can relax. The heart scan was interesting. You can actually see your heart pumping. It was quite entertaining. But as for the Bone Marrow test.. YIKES. Ok- it hurts. But not in the way you would think it hurts. My cancer doctor had me on 2 perkecets, 1 xanax and actually double dosed the numbing shots they put around the area and into the spine. The intial needle- and I was ok. But sometimes if you have strong bones =) they have to rub or shake or whatever he was doing back there. Well- thats what hurt. I wasnt in crying or in screaming pain.. It was just a quiet little "muthafucker" out of my mouth and then he was done. My cancer doctors assistant was hysterical. She looks and sounds like Wyanda Sykes- So I was being distracted, loopy from drugs, and trying not to think about it. I would suggest to do the same.
Biopsy #2 was a surgical procedure. 'Out Patient Surgery' is when you have whatever you're getting done- and get to go home. It was like a little surgical factory. They had a locker room where you put your stuff down and got into your gown and booties. You then enter a room with a bunch of beds in a row with curtains seperating them. The nurses take your blood pressure, temperature etc etc. And you're hooked up to an IV drip. You see your doctor, are taken into the surgery room and night night. Thats it. A piece of cake. I did this twice. Once for the second biopsy and again for the installation of the port.
GET A PORT! If you have the option which most of you will or have. They will check your veins and let you know whether you would need one or not. But I would suggest asking for one anyways. They cut your treatment time in half!!!
Well- I believe Im just writing away- So Im going to cut myself off.
I will get more into details in future posts. But I really want to hear from you. Please email me at YOUNGANDCANCEROUS@YAHOO.COM
Thank you for reading- and I hope you can check back often.
Stay Strong. -Megan