Saturday, November 19th, 2005

The Cruel Truth

Recently found out from a fellow hodgkin’s survivor that yet another has befallen the fate of death (they were both diagnosed around the same time I was and we still communicate on/off since remission). It was not the cancer itself that killed him. No. It was a drug that he was taking for an extremely rare side affect / complication from a bone marrow biopsy that was performed at the beginning of staging (I sense malpractice…), which caused complications and resulted in liver failure. They were only able to correctly pinpoint what was wrong with him in late March this year, 5 years after the bone marrow biopsy. He passed away exactly months later. I was shocked. We were all shocked. The way I look at it, cancer was the cause, directly or indirectly.

Sure, Hodgkin’s has a high cure rate. In fact, it is often referred to as “the best cancer* to get”. But there are still those who die from it or from the treatments. And it always seem like the strongest and most committed fighters lose in the battle.

He was one of those people. One who was always upbeat, never gave up, and never really complained about the unfairness of it all. One who’s there for you no matter what he himself is undergoing. One who truly believed there are more good than bad people. One who’s always looking out for you and ways to help you through with his knowledge and experience. He was only 44 years old. Leaving behind a beloved wife who is deaf.

He was also one who strongly believed in god, always prayed, for himself and for others. And asked that others pray for him and his wife as well. I just don’t get it. There’s no just and mercy. There’s only randomness and chaos.

It’s so unfair.

Once there was this someone who pretended to have hodgkin’s and was in the support group. She studied and understood all the terminologies and treatment protocols for various stages etc. She even went as far as meeting some other fellow patients for lunch and shopping, commiserating about their journey in cancer land. And shaving her head! Once she met a fellow patient at the hospital and told the mother that she was there for chemo treatment! Later on (not soon enough) it was discovered that she had some other illness, not life threatening ones, and was the reason for her hospital visits. Of course, she’s alive and well and people forgave her. After all, she was just a young adult seeking attention and belonging of some sort. Ha.

Some sick cosmic joke.

My 5-year hodgkin’s diagnose anniversary is coming up next week. Most days I feel as though it had happened to someone else. The whole thing’s very surreal. I remember the bedridden months, the puking until I was purple in the face weeks, the umpteen trips in/out of hospital. But really, it feels it was so long ago. Eons ago. The longer I’m in remission, the easier it is to talk about it. There are still times when it feels too much to handle and I have emotional breakdowns here and there, thankfully though, the pain and devastation have faded some. Occasionally I get jolted back to the inner most fear, especially when someone passes, or when someone recurs after 7 years or even 20+ years later. Truth is, the fear never really leaves. You know how close you came with death and it’s scary. You know it could all crash down again. And again. It’s like there’s this suspended sling with a huge stretched rubber band, ready to launch the biggest boulder any minute. There’s nothing you can do but breathe, and hope with all your might that you will be spared the unfortunates. With this, I relish everyday spent with my children and family, albeit the sleeplessness and frustration of taking care of 2 young ones. Because you never really know what’s going to happen in the future, distant or otherwise.

R.I.P. dear friend. I hope your faith has carried you to a far away disease-free place that is filled with laughter and happiness. I know you will watch over all of us, like you used to do.

* Most doctors, nurses, and just about anyone with/without oncology expertise will tell you that hodgkin’s is one of “THE best cancer to get,” if you are so unfortunate as to get any type of cancer at all. It is so because hodgkin’s has a survival rate of over 90% (meaning, surviving 5 or more years after diagnosis). So one should feel LUCKY** upon diagnosis instead…

** WTF???!!! That is the worst thing to hear, right after “I know So and So’s cousin’s girlfriend’s grandpa had cancer and they’re fine now” or “Lance Armstrong had cancer and he still won Tour de France, many times!”

5 comments » Filed under Misc. by Jennic at 0:38.

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Friday, November 18th, 2005

Regarding Feet Sizes

You know what they say about the size of a man’s foot, right?!

It is so untrue.

I’m just sayin’.

Leave a comment » Filed under Misc. by Jennic at 23:21.

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Tuesday, November 8th, 2005

Still Around. Just Very Tired.

It’s been a while since I’ve posted. I am just not finding the time or energy for it. Taking care of 2 little ones - even with help around - is difficult. The older one has the Terrible Twos from HELL, the younger one has acid reflux and on/off thrush thus requiring extra burping and holding and more attention in general. I find it hard to even get a bathroom break at times. I wonder how I will manage when the in-laws leave…

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I had a breakdown the other night.

One of hubby’s friends (from eons ago) who lives on the other side of the globe, who I met last year (shortly before I miscarried) suddenly messaged me. For backgrounds, he did know about my pregnancy, the miscarriage, as well as Fiona. We aren’t very secretive. Our lives is just one big open book. Anyhow, after the obligatory greetings, he told me that they had a baby boy in May. The same time that I would have had our baby, if I did not miscarry.

They waited 6 months to announce their news — and they didn’t tell hubby either. We didn’t even know she was pregnant.

I congratulated him. Then bursted into tears while typing that we would have had a baby around the same time, if not for the miscarriage, and that it’s still very hard for me to deal. He must not know what to say, because he passed the computer to his wife right away. His wife didn’t know what to say either, but managed to do a little bit of small talk.

I felt pangs in my heart. It was probably very childish of me, but I did not want to talk to them anymore. I just left that screen idling, staring at the lack of empathy and sympathy with my red, puffy, and wet eyes. I havent’ cried in a few weeks, and it’s been a little while since I felt that intense feeling of loss. But it all rushed back, with the same intensity as it was 13 months ago. I did not expect that. When does it become just a memory, a bad nightmare? Never??

Thank you Laura for being there to catch my fall.

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Today Miss Fiona is 9 weeks old. She’s growing up so fast. Too fast. She weighs 12 lb 5 oz, and is 23.5 inches long. She was very brave today and endured 4 shots. I wish I could have taken them for her. The poor little thing screamed until her face turned purple. Fortunately she did not get a fever.

I’ve forgotten how much fun it is to talk with a baby. You are the center of their world. And unlike a certain toddler I know, they don’t know how to say NO yet!!!

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I finally resolved the lumpy thing in my left boob. Apparently the ducts were completely closed in 1/5 of my boob. For almost an entire month. I thought it was still the infection working itself out after the antibiotic course. The ped, being a new mom (again) herself, she showed me ways to coerce the milk out. I heart her. My left boob heart her.

3 comments » Filed under Misc. by Jennic at 22:45.

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