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Posts Tagged ‘family’

Grampa is at peace. We lost him the other night, which was absolutely what was best for him, given the circumstances. It’s a small comfort to those of us left behind, as we would prefer to cling to him here, but that’s not fair, either. So we let his body go and all keep with us the pieces of the man who helped mold each of us in different ways. For me, I will always remember the grandfather who bounced me on his knee chanting about the duckies; introduced me to my love of theater; was my first minister; spanked me, my older brother and cousins when we got into mischief; took me to the top of Mount Washington; and welcomed us at the Cape. He furrowed his brow as much as smiled, and we loved and will miss both.

I apologize to all those who’ve commented on how silent I’ve been lately. It’s really been an overwhelming two weeks – in a totally different way than the preceding ones. From Mother’s Day when Grampa had his stroke, we’ve spent at least part of every day at the hospital, luckily surrounded by family. Tara rightly pointed out that one small silver lining was the timing of all this, in that at least with this happening during this point of my recovery, I was able to be there for him and my family, which certainly helped me. (None of us ever thought we would – or wanted to – know the Longwood district and all the hospitals so well. But we’re constantly thankful to be in Boston with some of the best hospitals in the world!) Now it’s planning and preparation for his service this weekend (details here). I’m doing a write-up on him for the funeral home’s web site, but struggling: it’s the hardest thing I’ve ever written. And I am beyond touched that Ginny and the rest of the family decided to direct people to donate to Dana-Farber for breast cancer research in lieu of flowers.

At the same time as all of this was happening, I also was running across the street from Beth Israel to Dana-Farber and Brigham and Women’s for my appointments. I had my first physical therapy (PT) appointment, which both felt like progress and hurt. I’ll continue PT twice a week for the next few weeks, in addition to my exercises at home. Also in the hurting category: I had my first tissue expansion injections with the reconstructive surgeon. The four giant syringes intimidated me at first (uh, do I really want boobs that bad???), but the process was fine, not nearly as bad as I expected. (I closed my eyes, although my mom was brave and watched.) Mom warned me not to get too excited about not hurting, as they gave me numbing stuff first. And boy was she right! I am still in pain that almost rivals the original surgery – no wonder he’s spacing these injections out to every four weeks! The highlight for me (in addition to now having slightly larger mounds where my breasts used to be) is that I am tentatively cleared to go back to work on Monday, June 4 – I really can’t wait. I will just need to take time off as necessary for all the appointments/additional surgeries and for when (if – as I am still dreaming I won’t be) I am sick from the chemo, which will now begin on June 12.

Also this week, my Dad and Maggie surprised me by driving up from Tennessee (where they went after I left them in Florida). My father was close to my grandfather and wanted to be here for him, as well as for me with all of this fun cancer stuff, and to help my 100-year-old Nana with things around her house, now that she is (momentarily) willing to accept a bit of help – boy do I know where my stubbornness comes from! (As well as some of the strong, independent woman DNA, although I am lucky to have that on all sides of my family!) It is comforting to have them here – and simply always good to see them, as it was when my brothers were both here last week.

This has definitely all been a reminder on the importance of family – including your closest friends who you consider family. Nothing is more important than spending time with the ones you love. You may not always see eye-to-eye, you may have knock-down, drag-out fights, you may not always be able to stand each other. But when it matters, you’re there for each other. And hopefully in the days in between you spend time together. It doesn’t matter what you do, as long as you’re together. Some of Nick and my favorite times were sitting on the deck at the Cape, simply talking with Grampa and Ginny and whatever aunts, uncles, cousins were around. Those are moments we will always treasure, and wouldn’t trade for the world. We love you Grampa , and miss you so already.

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In a way, my grandfather and I are in somewhat similar places. We both have to do things we don’t want to do in order to live. Of course, right now, he doesn’t have any choice in the matter. I don’t really feel I have a choice, either, although I at least am fully aware of what is happening to me. With Grampa, we’re not really sure how much he understands.

It is still early, so soon after the stroke that they’ve classified as major/severe. He has had many ups and downs in the few days: shown signs of understanding by attempting thumbs up, wiggling his toes and nodding when mom asked if the shoulder that he fell on hurt; had some heart issues; now has pneumonia, which they are controlling; and exerted his frustration by one day pulling the tubes out of his mouth/stomach and the next pulling out his catheter. Sometimes he looks at us like what the heck are we doing, prolonging his life by letting them do all this, but we’ve told him, he’s really breathing on his own and we haven’t done any special life-saving measures, because we know he doesn’t want that. We just want what is best for him, and if he is here, to be comfortable and to have hope that he can completely come back.

It will be a long time until we know for sure the extent of the brain damage, which they say could be extensive. He doesn’t always respond in the same way I mentioned before, but we know sometimes it’s just Grampa – if he doesn’t like a witchy nurse or uptight doctor, he won’t do a thing for them, and then when someone he likes asks him to do something, he tries and sometimes succeeds! It is all in God’s hand – and up to Grampa’s will. So we take it one day at a time, and they tell us that it could be weeks, even months like this. We have a big family, many who are here (I’m writing this from Beth Israel) every day, and we will soon probably start to rotate so someone is with him every day, but not everyone. We are thankful my older brother Steven, who lives in Florida, has joined us for a few days. He is a respiratory therapist in a trauma center and has been able to translate quite a bit for us – and catch some things others haven’t.

For me, I thought the worst was over, but now I’m thinking I’m wrong. At my appointments yesterday (how convenient Dana Farber is across the street from Beth Israel?) we learned that I am not quite as lucky as I thought I’d be. I thought cutting off both my breasts would do the trick. And it did, from what they can tell. However, because of the cancer found in my lymph nodes and my being young for this, I need to have all the follow-up treatments: chemo, radiation AND tamoxifen. Ugh.

I am not happy, but I’m also not about to fight it. I figure I have done everything so far to make sure I never have to deal with cancer again, I am not going to stop now. I’ve already begun regaining my strength – the daily hospital visits to see Grampa and family have helped both my mind and body. Next Tuesday I start physical therapy to really get full range of motion back in my arms, and that day I also meet with the reconstructive surgeon and may begin the expansions, depending how I’m healing (although breast surgeon says it’s looking good).

The following Tuesday the real fun will start. Chemo. That will be most of the day, and then I will have one day of chemo, every three weeks for four rounds. After that, I will have a few weeks off and then start radiation, Monday through Friday, for five weeks. And then Tamoxifen for five years. I know I said it before, but ugh.

What I understand from others is that chemo won’t be too bad at first, and then will get worse each round. The first time I may be sick for a day, the second round for two or three days, the third round for a few days to a week and the final round for a week or two. But everyone is different and I already have prescriptions for meds to combat the nausea and other bad side effects. What is really hitting home is the fact that I will lose all my hair – probably about a month from now, around two weeks into treatment. Argh! It took me so long to grow it, and I actually like it now. Not fair! But what among this IS fair?

I guess what is fair is that I get to live. I was lucky enough to find the lump, pretty much just in time before it spread further, and so what, I had to have a bilateral mastectomy? I do get two new ones, eventually. So what that it’s painful, I’m limited for a while and I have to go through PT? At least I’m young and strong enough to  push through it. So what if I have to go through those treatments and lose my hair? They will eventually be over, there are drugs to combat the side effects and my hair will grow back. And I actually, unlike Grampa, get to plan this all out and understand what I am facing. So I actually think I have a lot to be thankful for…

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Sunday, May 13, 2012

I know, and am incredibly thankful for, the unbelievable amount of prayers being said for me daily around the world. I would appreciate it if you could add to those a bit: we spent today at the hospital with my grandfather, who had a stroke early this morning and fell down the stairs. My instinct, of course, is to pray for him to live, for us all to have more days with him. While he has lived a good, long life – tomorrow is his 82nd birthday! – none of us are ready to say goodbye to him. Who ever is?

But that may be selfish. He is an active, energetic man, in both body and mind, and would hate to be confined to a bed and to not have control over his body – he’s a bad patient, as one of my family members said today. So I am praying for God to do what is best for Grampa – whether that is to take him home to heaven, or to grant us some more precious time with him – and that he hopefully will be well enough to be at his Cape house with all of us this summer, as we’ve planned.

What’s interesting is that through last night’s insomnia, I prayed quite a bit – more than I have in a very long time. It occurred to me that one of the things I have not done enough of lately is pray (yes, you can say ‘duh’). And to not necessarily pray for what I want. I think there’s a lot of truth in Garth Brooks’ song Unanswered PrayersRemember when you’re talkin’ to the man upstairs, That just because he doesn’t answer doesn’t mean he don’t care, Some of God’s greatest gifts are unanswered prayers. So I usually leave it to Him to determine what is best. Even though I don’t always know why some things happen, I do believe they usually happen for a reason. And praying, and putting my concerns in God’s hands, simply makes me feel better.

Interestingly, I prayed last night for today to be different since I’m starting to go stir crazy in my house, but I didn’t expect the hospital to be my change of scenery – although it was nice to be with many family members I haven’t seen in so long. (Why is it that it often takes tragedy to bring people together?) It was very tiring; many encouraged me to go home and rest, but I had a make-shift bed in the waiting room and could rest there as well as I could at home. (And thank you, Nick, for going home to get my pills – couldn’t have made it through the day without them…) It really was an exhausting day. Another thing I prayed for last night was to no longer have insomnia but I didn’t expect a long day at the hospital to be what would tire me out – I do believe I will be asleep before 2 a.m. for the first time since I was being drugged to sleep each night.

With my grandfather, we do have hope. I left him just a couple of hours ago. Throughout the day he went from completely unresponsive to now moving quite a bit in bed, squeezing our hands, opening one eye off and on, and nodding in response to some questions. He can hear, understand and acknowledge us. But he still has a very, very long way to go, should God chose to let him stay with us for a while more. There may be another blood clot, and he is having heart issues on top of the stroke. So thank you for adding him to your powerful prayers and positive thoughts. I know he and my entire family will appreciate them as much as I do…

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