Tis The Season…..

….to have all sorts of things churned up.  I don’t really get ”depressed’ over the holiday season, but more a vague sense of being overwhelmed since there are a lot of ‘anniversaries’ around this time.  This year added a new one with the death of my amazing, crazy companion- my miniature schnauzer Mandy, who died on December 27, 2012.

I’m still crying pretty much every day when I think about her, and especially about that last day.  I’m very thankful that that ‘end’ part was pretty fast.  And she was in my arms.  At first, she whimpered enough to alarm me, and from that point until she was actually gone, no more than 15 minutes went by.  After she  peed, and then froze in her tracks, she seemed confused, and not sure what to do, so I just held her and told her how wonderful she’d been.  Her breathing slowly stopped as I held her on my lap.  The ‘new normal’ of not hearing her come running when I mess with the dishwasher or clothes dryer (she had a thing for appliances), of her not leaving the room when I sneeze (or even said the word ‘sneeze’), or escorting me to the door when I got my keys to get the mail.  I didn’t have to say anything; she just knew.  I miss her more than words really can describe.  She was my only companion here in this city, for the past 10 years.  I talk to my dad every day; I saw my dog 24/7- especially since being on disability since April 2004.

Then there is the whole issue of being disabled.  It is somewhat worse in the winter months since everybody has the heat on. I don’t tolerate heat- to the point I shaved my head again (well, I had a professional do it; I wanted to avoid slicing my ears off).  With my ‘normal’ hair (mine is really, really thick), I can’t tolerate the heat it retains. Think dead animal on my scalp.  I also have to see a surgeon this next week about some (more) cysts on my scalp that are painful.  They need to go, so the poor doc has to be able to see my head.  The other issues with disability include being in more pain when it’s cold outside, and my joints just not liking getting in and out of the car.  Sounds wimpy.  Maybe it is.  All I know is that I have to manage it the best I can- so whatever I can get delivered to my door (Schwann’s frozen foods, Walmart for laundry and paper goods, Amazon for miscellaneous stuff, etc), I do.   It’s still very painful just grocery shopping for the dairy/fresh items, but it definitely helps to get stuff delivered when possible.  I’m thankful that those things are available.

Early January is rough for anniversaries.  January 7, 1978 my figure skating coach’s six kids were murdered by her then husband.  I was 14 years old, and it rocked me to the core. I can’t imagine how she has done.  I think about her often, and have always prayed that somehow she’s managed to have a life after that.  January 10, 1987, I was raped and ‘tortured’ (word the newspaper used- don’t want to sound overly dramatic on my own) for 6 hours when the uncle of a baby I took care of regularly lied his way into my apartment… he did things to me I’d never heard of, being very naive…and a virgin.  I’ve never let anybody get close to me since then.  I’d always thought I’d have a family of my own.  That day changed a lot- but I survived.  And I’m thankful for that.

In 1982, the semester that started in late January was a bad one.  I was in the midst of some serious eating disorder stuff, and the depression I only get when I’m starving and purging.  I ended up getting sent to a psych hospital (no eating disorder ‘treatment centers’ back then) for several months.  That was a bad year. I ended up attempting suicide the next semester when I returned to the university.  I was in a coma, and then shipped back to the psych hospital for many more months, once I woke up and was medically cleared.  Things weren’t done in a week to 10 days back then.  I spent about 8 months altogether at Forest Hospital (Des Plaines, IL) in 1982.  They were good to me; I did do better, but the eating disorders were on-again/off-again for decades.

This is the first winter since early 2010 (when I was diagnosed with acute promyelocytic leukemia) that I haven’t been on chemotherapy or waiting for the built up amounts of toxins to leave my body.  I’m still dealing with the weight gain and changes in my blood sugars and insulin doses, as chemo messed that all up.  The diabetes is getting better faster (great endocrinologist with a Joslin Diabetes Center affiliate here in town). I wasn’t on steroids long enough for that to be an issue- it’s ‘just’ the arsenic, tretinoin (ATRA), methotrexate, and M6Mercaptopurine.  They rearranged my chromosomes (literally…. they ‘re-translocated’ the arms of 15 and 17). I guess it will take some time to get my body back to ‘normal’.  I hate the weight.  I’ve had a long history of eating disorders, so can’t just do some crash diet and hope for the best- it could easily trigger a relapse that I just can’t afford.  But I’m going to turn 50 in late 2013; I don’t want to  look like this when I turn 50.  I didn’t want to look like this at all… but it was chemo or die.

And yet, I have a lot to be thankful for. I’m alive- that’s the big one; people with APL sometimes aren’t diagnosed until autopsy (and I know of 2 people just a few months ago who only had one and two days from the time they were told the diagnosis and the time they died; one was 11 years old).  I’ve survived being raped, and other stuff. And, with my health, I am glad to just have a day when I can get the basics done around here.  I’d like to be around people more, and am hoping to get to that Bible Study I’d mentioned in another post; last week (the first meeting of this topic- Ephesians) I wasn’t feeling well- that doesn’t mix well with indoor heat, even with my ice vest.  A childhood friend who I’ve reconnected with on FB came over one Saturday, and helped me with some generalized clutter (result of not being able to unpack after the last time I’d packed to move BACK to Texas), and is coming again- that has been a huge help.  I want to get this place puppy-proofed for the new puppy I hope to get this spring.  That helps, too.  I can’t imagine not having that hope for a new little companion to fill the dog-shaped hole in my heart.

2013 isn’t starting badly… just ‘complicated’ by past and present stuff mixing together.   There is still more good than bad.  I still have a lot of interests, and while I can’t physically do a lot, I do find things to keep me happy and make me laugh, especially online.  Blogging has been a great way to blow off steam, and some days that makes  a big difference.  🙂

Schnauzer Heart Failure

I’ve seen several search engine topics involving schnauzers having symptoms of heart failure, and fainting, even when asleep.  I’ve been there with two of my schnauzers. My last one just died 12 days ago… always consult your vet with questions, but here is my experience.   I’m also an RN (disabled, but got my license 28 years ago and still have it).  I was cued in to abnormal breathing and behaviors, which helped me know that I needed to get both of my dogs who had heart failure seen by their vets.

My first schnauzer to have heart failure was Hannah.  I got her in 1988 as a 6 week old puppy. To make a sweater for her (there weren’t many options for puppy clothes back then) I cut holes in one of my socks.  She had some episodes that were called seizures, but with how things turned out, she probably had some heart issues starting at about 18 months old when she fainted (and twitched) for the first time. By the time I got her to the vet, she was fine. She had those episodes now and then, until 2000 when in one night she fainted 7 times (I stayed up with her all night). I thought I was taking her to the vet to be put to sleep that next morning, but he got her on some medications and prescription dog food and she lived another GOOD year.  I vowed to not make her live just so I didn’t have to face the loss of her.  As a single woman with no kids, she was my family.  I wanted the best for her, but when she died, it was really hard. She had done well up until the last couple of days; when she quit eating, I knew that was it.  I had decided to get another dog before she died, so that kept me going.

Then I got Mandy.  She did very well until she was just about 11 years old.  She fainted.  Her breathing got too ‘hard’, and I knew what was going on.  I took her to the vet, and with an exam and x-rays (showing an enlarged heart, displaced trachea- from the size of her heart, and some lung congestion) she was also diagnosed with canine heart failure.  She was put on medications, and did fairly well. She only fainted 3 times total- including one time when she was asleep.  The last ‘episode’ wasn’t the same, but it was similar, and she died in my arms within 15 minutes.  I still cry every day missing her.

Something huge to remember is to not give the dog ‘people’ food because of the salt content, unless it has no salt (which means that most processed foods are out).  I got freeze dried peas  (meant for toddlers) for Mandy, and she also loved freeze dried bananas (NOT the fried ones in the grocery store).  Those items had NO added ingredients.  She also liked pieces of raw apples. The only commercial treat she could have was “Charlee Bear”- because of the sodium content being low enough (I e-mailed the company for the answer re: sodium content, and then cleared it with my dog’s vet- please check this out with your dog’s vet as well 🙂  Towards the very end, Mandy didn’t want to eat. She had lost weight, so I tried various things- ground beef, ground turkey, scrambled eggs, rice, potatoes, oatmeal, baby food fruit and veggies…. that last morning she had two Swedish meatballs that I’d adjusted for her (low sodium and baked instead of fried- like the Christmas party meatballs were).

It’s heartbreaking to see them get older and struggle.  I made some mental notes as to when it was ‘enough’- though with Mandy it was a bit less clear until she just had a brief episode and then was actively dying in minutes.  But I was prepared to have her put to sleep.  Hannah died in my arms as she was euthanized. She knew I was there. That was important to me- I couldn’t have either of them think I’d left them.  Mandy looked scared until she just collapsed in my lap.  Then it was just a few minutes before it was over.  I talked to her, and scratched behind her ears as I knew she liked.

Please feel free to use the comments to share your experiences or ask questions.  ❤

I’m Grumpy Today

I’m not sure what my malfunction is, but I’m sorta grumpy.  I got up way earlier than usual (I’m one of those who is usually up half of the night and then sleeps until noon).  I’ve got a vague headache, but that’s nothing all that new. I have chronic headaches.  Christmas was really good- I got to see (and meet) family, and talked to my biological mom and half-brother on the phone, which is always good.  I got to spend time with family at the Swedish Christmas party since I’ve got the ice vest to wear when I leave home and don’t have as much chance of being overheated because of the dysautonomia. And yet, I’m a major dud this morning.

My 11.75 year old schnauzer with heart failure was so eager to eat some ‘meatloaf’ I made for her yesterday (with controlled sodium), and this morning she won’t touch it. I’m running out of options.  She started refusing the prescription dog food weeks ago, and prior to that had been eating a minimal amount (which wasn’t all that unusual for her- but she managed to keep her weight up). So now I’m trying to figure out other ideas… have been through ground beef/turkey/chicken, oatmeal, mashed potatoes, brown rice, white rice, baby food veggies, cooked carrots (gag), baby food applesauce and oatmeal,  and various combinations of the above.  She normally likes all of those things. Now, I’m lucky if she eats some of her Charlee Bear dog treats- they have minimal sodium, so she can still have them.  If she weren’t still alert and very interested in what is going on, as well as physically mobile and showing no signs of pain, I’d have her put to sleep…but I don’t want to ‘kill’ my best friend if she’s still getting some enjoyment out of life.  It’s a fine line right now, so as long as it’s not blatantly obvious, I’m holding out… but that time is coming.  There’s only so much I can do, and I think I’ve pretty much hit my limits. 😦

I’ve been extremely irritated at comments to news stories on various online sites and publications. So many people are so heartless and cruel.  Or pathologically immature and even psychopathic.  Responding that they’re ‘happy’ about an article where five people were made homeless by a fire that destroyed their home? How do people get that way?  Who dropped them on their head?  Or burned them?  And then there are the other ‘less’ disturbing posts that are just plain nasty and/or cruel.  Or ignorant.  I’m actually very thankful I don’t know those people or have to spend any IRL time with them.  A click of the back button takes them out of my life.

The onslaught of horrible stories that are on the news constantly is also a major bummer. I feel really badly for those folks and what they’re going through, but what good does it do anybody to have it dissected in the media for days to weeks on end?  I’ve been a crime survivor of a high profile case (before the 24/7 media, back in 1987).  It wasn’t helpful to see it on TV for days or see the newspaper coverage over and over.  The people who knew about it, and were my actual friends/family already knew what happened, and face it: most people really don’t want to know about real life horrors that happen to other people.  Or they don’t know what to do with the information, at least to the persons’ face. Behind their back, the chatter won’t stop. If people would have just asked me straight out what happened, or even if I wanted to talk about it would have been much  more helpful than days of media coverage  (without any input from me- I was an object).  I had one ‘different’ neighbor that responded to meeting me with “I never thought I’d meet you ! ”  Really?  Meeting someone who has been raped and beaten was a life goal?  Step away from the strange one !

I’m extremely disgusted with my weight, and have my food diary set up to start on January first. I don’t want to look like this on my 50th birthday next November.  I don’t want to be grotesque and repulsive going into the last third to half of my life. I have to restrict food. I’ve tried the ‘normal’ calorie amounts I’ve been given from the doctor and diabetic dietician, and that doesn’t work…so I’ve got to go lower. I can’t do much exercise because of the issue with passing out when my heart rate goes up or I get overheated, and my knees and spine issues.  So the calories have to go.  A slippery slope for me, so I’ve got to be careful- but I have to DO something beyond what I’ve been doing.  I didn’t look like this before chemo… and I want to lose any remnants of those days.

Losing weight will also save me some time before having to have my left knee replaced (I had the right one done in late 2006, and it was a very unpleasant experience with some complications and ‘dull’ response time by the doc and nurses to a bladder infection). I had to go to a rehab place for the medically defective. It was a good rehab facility- great care, but set up where people stayed in their rooms like a hospital between therapies (no common area), and since I was infective, I was in a private room- not a horrible thing, but friggin’ isolated. It’s not like there was a big risk of someone coming into contact with my pee.   My left knee has unrepaired, and questionably healed ACL and medial meniscus tears, done when I turned over in bed back in 2009- about a week before my closest friend from here in this town died suddenly (following several complications from a KNEE replacement). She’d moved to a different state to be closer to one of her daughters, but we were in contact by phone daily, even when she was in the hospital or rehab.  I was supposed to have the left knee replacement done, but then got leukemia and everything was put on hold to survive that.  Been a weird few years.

I’m frustrated that I don’t feel that people understand why I’m like I am.  I’ve got diagnoses that people haven’t heard of.  I ‘look’ like I’m capable of working, and I miss being a nurse SO much- but too much standing or walking, and the whole heat/heart rate thing = one unconscious middle-aged RN.  I’ve been an RN for nearly 28 years.  I’ve been on disability for 8 years.  But I still keep my license, because I still AM an RN.  I worked hard for that thing.  And I loved working with it…  And those days are done.  When people ask me what I’m doing to get back to work, it hurts- there isn’t anything that can be done by me or anyone else. Some things CAN’T BE FIXED !  SO those perky, blessed-to-be-clueless people need to shut up and go target someone who has some stuff going on that is treatable. I’ve been dealing with much of this since 1996- and worked until 2004- I held out as long as I could.  I fought to keep working.  QUIT asking me if I’m going back to work. NO, I can’t !

I was raised in an evangelical church, and am a born again Christian, without some of the judgmental drama that can go with those two things.  I hate the passive ‘I’ll pray for you’ stuff- prayer is wonderful, and I do it often, but if someone wants to help, some action would be really amazing ! Prayer is about as passive as a person can get and rationalize to themselves that they’re ‘doing’ something– and while I do believe in prayer and that it is a very positive and powerful thing (and pray for people on the news all of the time since I can’t do anything else), it’s not the be-all end-all answer to really being of use to someone.  It’s definitely better than nothing, but it really doesn’t show much in terms of actively supporting and helping someone. Sometimes it’s all people CAN do- and that’s appreciated.  But remember the ‘faith without works is dead’?  I’ve sensed a lot of dead.  I wish I could do more for others, and feel guilty about that.  Not like I know many people around here to be available for… back in the home where my heart is, I could be more useful, even if I’m not that physically ‘able’… I could drive someone to the store, or appointments.  I could water plants when they were gone, or change out cat litter. I couldn’t walk dogs or watch kids… but I’d do what I could.

I’ve contacted my ‘old’ church (from when I grew up and it was an amazingly positive experience) to find out about women’s Bible studies and other things in the past, and have been essentially blown off. I guess I’m not good enough for the ‘elite’ evangelicals anymore. My checkbook may not be deep enough or something.  I’ve tried again, and will hear back after the 31st when the contact person returns. I had really looked forward to going back there when I moved back from Texas.  I found it to be cold and a bit pretentious.  If someone can’t go back to the church they grew up in, where should they go?  Where is the ‘real’ message in that?   It hurt.  There were some really nice ladies (who I’ve known since I was a kid) who invited me to a type of ‘grief’ group, but I don’t want to sit and talk about dead family.  If that works for them, I’m really glad they have somewhere that feels right for their grieving process.  My mom is dead. Sitting in a room with folks who need that type of support doesn’t work for me.  I guess if I want to connect with anybody there, I have to be bummed out.  Not something I’m interested in.  I’m hoping the Bible study that starts on January 9th will work out- otherwise, I’m done trying to get back in to the church I grew up in. It shouldn’t be a ‘project’ just to find somewhere to fit in there.  The singles group wasn’t my bag – I want some ‘study’ group type thing.  🙂

Anyway, that’s a bit of what’s rattling through my head today.  I’m a little less grumpy now.