The Girl Who Lived ~ by Sam

17 years ago today, on March 28th 2000, I was 29 years old.  Gosh, it seems like a lifetime ago.  Shane and I lived in the upstairs apartment at the back of our building of six units, which faced another, identical 6-unit building.  Our daughter, Justice, had recently become a big sister for the first time, to Hallie, who was born at 11:58 pm on March 17th ~ St. Patrick’s Day! ~ on the front seat of our Honda Civic in front of Kaiser Permanente Hospital’s Emergency Entrance in Woodland Hills.  We almost made it to the hospital in time, but, what can I say?  Hallie was in a hurry to be born on St. Paddy’s Day.

When I think about that little baby, my first impressions are of a strong, alert child, right from the word, “go!”  I had a hard time, hemorrhaging and requiring a couple of courses of pitocin to get the bleeding under control upon being transferred up to a recovery room, but not our little baby.  Hallie was eager to nurse, wide-eyed, alert and responsive.  I remember lying on the sofa the day we brought her home, with Hallie resting on my belly.  She just wriggled her way up my body all by herself, like a tiny little mountain climber.  I know, I know ~ babies do this ~ but we were so impressed right from the start by her strength, her grip, and how awake and aware of the world around her she was.  She just seemed interested in everything.

On the evening of March 28th, baby Hallie was just 11 days old.  Justice was asleep her room.  She would have been 2 years and about 4 months old.  Shane was working at his desk in the living room, and I was napping on the sofa.  Hallie was asleep in the cradle my dad had built, which was in the room with us.  We always had our babies sleep wherever we were.  So, we kept the cradle in the front room.  I learned later that Shane had somehow become aware that something was wrong with Hallie.  Maybe it was the absence of breath sounds.  Maybe it was a choking sound.   Maybe he saw something out of the corner of his eye.  I don’t know, but I thank God that something alerted him.  I awoke to the sound of him yelling her name.  He was holding her, her face was bright red, mouth wide open, like she should be screaming, but there was no sound.  I could see the terror in both of their eyes.  I don’t even think I was fully awake before I was across the room whisking her away and saying, “Call 9-1-1!”

Having worked in a preschool classroom, I had, at least, been trained in infant CPR.  I went in to auto-pilot.  It’s hard for me to put in to words what happened next.  I can remember it all so clearly, like I am watching a movie, but it’s difficult to articulate.  I remember checking her airway.  I remember running through all of the steps in my head ~ which I remembered then, but don’t now ~ I remember performing the infant Heimlich maneuver, and feeling a tremendous sense of relief when she coughed up a huge chunk of mucous…and then a renewed sense of panic when, instead of starting to breathe, my tiny little baby went limp and blue.

I remember that Shane was on the line with the 9-1-1 operator by this time, and that she remained on the line with him until we left for the hospital.  I remember that, at some point, little Justice was awakened by the commotion, and wandered out.  I remember that the paramedics from the nearby fire station arrived within two minutes that felt like an eternity.  I remember.  I remember loosening her clothes, jiggling her limp little limbs, begging her to breathe.  I remember Shane’s voice pleading with her to breathe.  I remember repeatedly thumping the soles of my baby’s tiny feet, so she would gasp for air, and hoping against hope that, eventually, those tiny little gasps would “catch,” and she would start breathing regularly again.  And I remember that, eventually, miraculously, she did.  Right before the paramedics arrived.  She was breathing, albeit shallowly, by the time they got there, but, since she had not been, of course, a trip to the ER was still in order.

I remember when the paramedics explained to me that I couldn’t hold her on the way to the hospital.  That I had to hand her over to them.  That she had to be transported by them the way any patient would, but I could ride inside the ambulance with her.  Shane and Justice could follow in the car.  I remember the look on Shane’s face when he realized he had to let them drive away with his baby.  I remember how tiny she looked inside the ambulance on that huge gurney.

I remember sitting at the hospital while they checked her over and over and questioned us about what had happened, and found no explanation.  No explanation.  And just…sent us home.  I remember the diagnosis.

ALTE

A.L.T.E.

I remember searching for information to try to understand what had happened to my child and finding that it stood for “Apparent Life-Threatening Event.”

As if we couldn’t have guessed.

I remember months later when I had to fight for the insurance company to cover that ambulance ride and hospital visit, because, they told me, the incident “wasn’t life-threatening.”

*ahem*

“Please refer to doctor’s diagnosis.  A.L.T.E. – Apparent Life-Threatening Event.”

I remember how, at about two months, she suffered another episode of the same type.  Still with no further explanation.

I remember how, years later, she developed asthma, and often suffered respiratory complications such as bronchitis or pneumonia.  I remember the time she had croup, and developed stridor, and her little chest would cave in, instead of expanding, when she took a breath, and my heart would ache for her.  I remember other parents thinking I was being “overprotective” when I said it was important for her not to be exposed to respiratory ailments because she was at high risk for respiratory complications.

But, more than anything, on this day, I remember my child’s beautiful eyes, smile, voice.  I think of all of the amazing things this almost grown person has achieved.  I think of the art my child has created, the roles this young actor has played, all the music and dances and stories…and everything yet to come.

Hallie was due on March 27th, born on March 17th, under rather unusual circumstances.  Then March 28th came along and did its best to wrestle her away from us.  Every year at this time, I can’t help but pause and count this particularly incredible blessing.

 

Cold Hands, Warm…muscles? by Sam

One day last week, while I was making dinner, my hands suddenly turned bright red and felt as if I had poured bleach all over them. Thinking I must have come in contact with some allergen, I immediately stopped what I was doing, and thoroughly washed my hands. The redness and irritation greatly subsided in 15-20 minutes, but my hands remained irritated, and the skin was peeling, as if I’d had a severe sunburn. Over the next few days, the symptoms recurred, so I contacted my PCP via email, including a photograph of the initial reaction. I supposed there were three possibilities:
a) the CRPS was spreading to other parts of my body (rare, but not unheard of)
b) these symptoms, ‘though not like any I’d experienced with it in the past, might be related to Raynaud’s (to be fair, the symptoms were not exactly like CRPS, either, but it does involve both redness and burning pain)
c) this was something entirely new and unrelated to any of my previously existing conditions
     We played phone tag for a few days until I finally got a call from a nurse on Monday of this week. My doctor felt it was most likely that the symptoms were, in fact, a more extreme manifestation of Raynaud’s than I’d experienced in the past, and that, as my symptoms seemed to be getting more severe, it might be time to consider medication.  Hence, I was referred to a rheumatologist. That appointment occurred on Thursday of this week.
     As luck would have it, the medications used to control symptoms of Raynaud’s Disease are blood pressure meds; and, because my blood pressure is low, my doctor doesn’t want me to take them.  You see, unfortunately, they could cause my blood pressure to drop even lower, and this could result in dizziness and falling. Falling has already been rather a chronic problem for me, and it has been deemed an unnecessary risk, as has dangerously low blood pressure.
     So, I have been given recommendations to step up my efforts to stay warm. These include things that might seem obvious, like using hot water bottles and heated gloves/socks/blankets, warming creams, taking warm showers when I come in from being outside, making sure to keep my hands and feet covered and protected, even when I don’t feel cold, and keeping my core warm. They also include things that might seem a little less obvious, like increasing my salt intake, in hopes of raising my blood pressure, and building muscle mass. The challenge, here, my rheumatologist pointed out, will be striking a balance in which I work out to build muscle mass, but am careful not to accidentally lose weight. This will involve adding protein-dense calories to my diet, which means adding food to my diet.  (I know.  This doesn’t seem like brain surgery.  Stick with me.  It’s trickier than it seems.)  I started working on this as soon as I got home on Thursday. I immediately baked a loaf of peanut butter bread, replacing part of the flour with almond flour.  Then I made myself a peanut butter and jelly sandwich with it.  I figured, that way, at least I am getting lots of protein (and lots of calories ~ yay!)  Because that working out and not accidentally losing weight thing?  Believe it or not, that really is a challenge.
     I know. This all sounds sort of stupid. But…food is hard.  I mean, I have had food issues for a long time.  First and foremost, there are the lingering eating-disorder-related issues, which will always linger; but, on a more basic level, there are all of the food allergies and sensitivities.  I am allergic to milk protein (and elderberries, and echinacea, which don’t come up much, so that’s okay, really.  Oh, and shellfish ~ which never comes up, because I’m vegetarian, but does somewhat complicate eating at restaurants, or buying some prepared foods).  I also have IBS, and, while it seems to be fairly mild most of the time, it can rear its ugly head at any moment, and, at those times, it is triggered by: eggs, white/refined carbs (so, any bread, pasta, or baked goods made with that, white bread, white rice ~ basically, I do better with whole grains and more fiber in my diet), and fried foods.  Then, there are times when I think it is triggered by food.  Oh, also, stress.  It is also triggered by stress.  Then, add to that the fact that I am on a medication that makes it hard for me to keep on weight, even when I am not working out.  So, now, I am trying to eat the right things that won’t trigger my IBS, so I can be sure not to lose weight while doing PT, so my CRPS won’t flare up, so I can then work out enough to build muscle mass to try to keep myself warm ~ but not so much that I accidentally work off any of the extra peanut butter I ate.
     Because then, maybe I will be buff enough to haul in some firewood and build a big fire, and then we will all be warm.  By “we,” of course, I mean me, and all of my fingers.  And my toes. My toes are also cold, but I don’t see them often, because they are very far away, and usually inside several pairs of socks. I miss my toes.
     Ah.  But we have a gas fireplace.  So, forget about that firewood.  I’ll use my muscles to lift more peanut butter sandwiches, instead.
     On Friday, I didn’t manage to do much working out, but I ate pretty well.  I mentioned this to Hallie, adding my concern that, if I keep doing this, I won’t build any muscle, and all that extra protein will just be converted to fat.  “Well…fat will keep you warm,” Hallie responded, quite correctly.  And, so, I guess we’re good.  Because, the truth is, fat will keep me warm, and I really, really need to stay warm.  Nevertheless, I have always dreamed of being sort of buff.  Warm, and buff.  It sounds kind of dreamy.

     I guess I’ll keep working on the muscle-building thing.  To be perfectly honest, I was already working on that.  Which sort of makes me wonder if I should feel a little bit insulted at the implication that I need to build muscle mass.  Except…well, I really do need to build muscle mass, and I know it.

I guess I needed a New Years Resolution or two, anyway.  Y’all watch: by 2018, I’m gonna be stronger than I’ve ever been.  And warmer, too.

How Bad Is it? ~ by Sam

Last night, my foot went out.  I don’t mean it had a pleasant night out on the town.  It’s done that, with me in tow (if you’ll pardon the pun), but that was not the case last night.  Last night, my foot just sort of ceased to work.  I call this “going out,” as in, “My foot’s gone out again.”  You know, like when your transmission goes out.  This happens in a number of ways.  What I mean by this is that it simply freezes up and refuses to move.  Sometimes, it sort of seizes, and assumes an usually grotesque position before freezing (often folding vertically in a way that feet don’t actually fold, so that my big toe rotates in to a position that is under or over the rest of my foot).  Other times, it just sort of flattens and becomes stiff, like a boot, all the way through the foot and ankle.  In any case, it is useless, and it feels freshly broken.  No, scratch that.  I would say it feels more painful than a break.  It feels… hmmm… It feels like it was broken, and then…I don’t know…something else happened to it.  Like, maybe it caught on fire, and got slammed in a door.  Yeah.  I’m gonna go with that.

But that’s a mouthful; so I just say, “My foot’s gone out.”

It goes out a lot lately.  I think I should buy it some fabulous jewelry.

Anyway,  this is a CRPS thing, and, yeah, it has been happening, so I guess I had better call my excellent Pain Management doctor, because his job is, after all, to help me manage my pain.

But, see…

It’s hard, because I can’t think of myself like that.  As a person who has a Pain Management doctor, and a chronic pain condition that needs to be managed. Coincidentally, just yesterday, Justice was asking me if I considered myself to be disabled, due to fibromyalgia, CRPS (and a host of other health concerns that have cropped up recently, I suspect), and I told her I don’t.  Of course I don’t.  I am able to get around and do what I need to do.  …pretty much…  I might not feel great, but I get by. …most days…  I mean, I had to quit my job, but I am still able to do a lot of things.  …usually…  I am even able to do things I enjoy.  …sometimes…

And then, here we are, on a day like today, when CRPS has brought me, literally, to my knees.  I am not looking for sympathy.  I am not making excuses.  The thing about CRPS, for me ~ where I am with it, anyway ~ is that I have been advised to just keep using my foot as much as possible, no matter how much it hurts.  I just have to keep making myself use it, even when it feels like it’s broken, and on fire, and someone slammed a door on it, because, if I don’t ~ if I let that stop me, and it stops me for a day, and that day turns to 10 days, then a month, then 4 months, then a year…well, then, eventually, I might lose the use of my foot.  And that  would be unacceptable to me.  I think, perhaps, I am writing today to figure out where it is I stand with all of this.  (Again, if you’ll pardon the pun.  There are just far too many foot puns.)

So, last night, when my foot went out, I took my Nortriptyline, like I always do.  I struggled to get my jeans off and pajamas on over my stumpy boot-foot.  I used the ketamine gel that I only use when I really need it, because, frankly, it’s just too expensive to use more often.  I ran through my exercises.  I cussed while doing all of the above, because, frankly, it hurt like a motherfucker (you can consult the  McGill Pain Index to see exactly how much a motherfucker hurts, if you are curious ~ it’s a lot).

(Sorry.  That was rude.  I probably apologized last night for cussing, too, even though Shane was the only one in the room, and he was asleep.)

This morning, I got up and made coffee, and didn’t help much with getting kids ready for school, and drove Kaia to school.  Then I went to the store, because I had to.  I mean, I probably didn’t have to, but there were a few things we needed, so I did it.  At one point, as I was pushing my cart, a man said to me, “Oh, come on now ~ it can’t be that bad,” and I thought, “Fuck you,” but I didn’t say it, and I think he’s kind of lucky I didn’t say it, because, really, just a little bit, fuck him.  I mean, I get it.  He had no idea what I was going through today.  He has no idea what my life is like.  In fact, I have no idea what his life is like.  He might have a terrible time, for all I know.  But, you know what, it is that bad.  Sometimes, it really is that bad, and I guess, this morning, maybe that was evident, in my demeanor.  I know I was limping.  I know I was using my cart for support.  I can assume I was obviously not having a great time, or he would not have commented.  And yes, as a matter of fact, it really was that bad.  I guess, I’m lucky he didn’t ask me to smile.  Or maybe he is.

On the way out of the store, after I had paid, I noticed a woman walking directly behind me with her shopping cart.  “I’m sorry,” I said, as we made our way through the automatic door, “I’m very slow.”

“Oh, that’s okay,” she replied.  “So am I.” After a moment she added.  “At least we have our carts to lean on. I don’t know how I’d make it without that.”

“Yes,” I agreed, “that does help, doesn’t it?”

We walked very slowly to our cars together.

So, I’ve come to the end of this entry, and I haven’t figured out anything ~ except, perhaps, that, sometimes, it’s enough to know that someone else understands.

I Ate a Sandwich – by Sam

The other day, I was out shopping, running some errands, picking up dry-cleaning, and I realized, at about 11-ish, that I hadn’t eaten more than the sample of cranberry bread and coffee at the grocery store.  So, I decided to stop and grab a sandwich at a nearby sandwich shop.  It’s funny, I think, that it was a sandwich.  By “funny” I mean, “coincidental,” or, perhaps, “unintentionally ironic,” because, you see, I am periodically told that I need to “eat a sandwich.”  Really.  This comment usually comes from rude strangers who have decided that, for some reason, it’s okay to make comments about my weight or my body because I am thin.  It’s okay, they think, to tell me that I “look anorexic,” that I need to “get a little meat on my bones,” that they “prefer women with curves” or even to ask me if I think I look attractive like that, or what example I think I am setting for my children.  Yes, these are all comments that have actually been made directly to me by strangers.  Once, a few years ago, I had a guy at a bar tell me that I was so skinny I looked like a Cancer patient, after I turned down an advance from him.  At that point, I was probably actually sick, but really?  Because, a second ago, you were interested.

What’s even weirder to me is when friends say things like this to me.  It happens.  I understand when they express concern.  They tell me I am getting too thin. They ask if I am okay.  I get that.  I mean, that’s cause for concern.  Some of them know my history.  I’m an eating disorder survivor.  So, yeah, okay, that’s reasonable.   Even if I they didn’t know that, seeing someone lose weight…well, I guess it can look unhealthy at a certain point.  They know my health, in general, is an issue.  I can see why it would worry them.  It’s still hard, when it happens, but it’s reasonable.  But that “sandwich” line?  That’s gotta go.

The problem is, right now ~ and, as it turns out, maybe for a long time ~ I have to be on a particular medication.  I have to be on it. I don’t really want to go in to detail about what’s going on, but it’s nothing terribly earth-shattering.  The end result is that I have to take medication daily, which solves the problem, and the only caveat is it affects my weight.  It has caused me to lose weight.  It increases my appetite, which is awesome, but it does make it difficult for me to gain weight, which is not great.  However, under the circumstances, I can’t worry about that.  So, I guess I should take this opportunity to assure those close to me that I am not relapsing into my eating disorder.  I’m actually doing quite well, and eating better than I have in years.  I feel pretty great.  But I am very thin.  I’m sorry.  I know that might look frightening to some of you, particularly those who have known me for a long time.  I know it might be hard to understand.  I am going to ask you to try.  To trust me.  I’m doing okay.

I will ask my friends to please avoid the “eat a sandwich” line.  Maybe you think, by saying something like that, you are keeping it light, but still addressing the issue?  It’s really just kind of mean.  That just doesn’t need to be said.  Frankly, sandwiches aren’t my favourite, food is a bit of an issue for me, my weight is always going to be a sensitive subject, and I am very self-conscious about it.  Besides which, it’s just not the kind of thing on which people need to comment.  Aren’t people taught not to make personal comments anymore?

As for the strangers who make those kinds of comments to anyone: stop.  Just stop.  Whether you are saying these things in person or online: stop it.  Why do you think you get to do this?  Who cares what you like?  Keep it to yourself.  You’ll tell me you have a right to your opinion, and sure you do, but here’s the thing: that person you’re talking about might be very thin for any number of reasons.  Maybe they actually are anorexic.  Did you ever stop to consider that?  Why is that term thrown around like an insult?  You know, its an actual illness.  It’s not a choice people make because they are trying to be cool, or they think it’s beautiful.  Maybe they’re just naturally thin, in which case, who do you think you are telling them how they should look, and that they are setting a bad example, or that they are unattractive, just because they look the way they do?  Maybe they have some kind of health problem that causes them to be very thin.  What if that person you just said looks like a Cancer patient actually IS a Cancer patient?  Aren’t you a freakin’ rockstar, now?  I mean, whatever happened to “if you can’t say something nice, don’t say anything at all?”

This brings me back to the sandwich shop.  I was really very hungry, so I ordered my sandwich, with all the toppings I wanted, and the guy behind the counter asked me what size I wanted.  I had no idea.  I just thought they had the one size.  He explained that they had three sizes: 7″, 10.5″ and 14″.  I chose the 10.5″ sandwich.  He paused.  I waited for him to ring up my order.

“Um,” he said, finally, “Are you sure?  That’s about as big as this bag.”

He was looking down at me from behind the counter, showing me the bag, so I could fully  understand the gravity of my decision.  I was sure.  I wanted a really big sandwich.  For godssake, I can measure.  I mean, I’ve been using standard 12″ rulers since grammar school.  I buy 12″ subs all the time.  I can guess roughly how large a 10.5″ sandwich is! Now, I’ll be honest, I had a lot of errands to run, and I didn’t really plan to eat the whole thing all in one sitting, but, while he stood there judging me and my sandwich, I didn’t see any reason to explain that to him, so I just said, “Yes.  Ten and a half inches.  Please.”

“Okay,” he said, still sounding skeptical.  It kind of pissed me off.

You guys, I can’t win for losing.  I’ve got people telling me to “eat a sandwich,” and people telling me I couldn’t possibly eat THAT sandwich.  If a larger person comes in and orders the small sandwich, does he say, “Oh, I think you’re gonna need a bigger sandwich, buddy,” or does he judge them in another way, and offer them the lettuce wrap?

I guess I’ll never know.  I sat outside and unwrapped my sandwich.  A guy who looked exactly like George Lucas walked by.  I like to think it was George Lucas.  I mean, not many guys look exactly like George Lucas.  I ate 5.25″ of sandwich, then wrapped up the rest to eat during my errands.  It was a very good sandwich.  A very large, very good sandwich, even though I was a little pissed off about the guy’s attitude.  I ate it.  And I am still thin.  I still have only very minimal curves.  And I still don’t give a rat’s ass what some stranger prefers.

Needles to say… by Sam

**Yes, I know that says “needles,” instead of “needless.”  I did that on purpose.  If needles are a problem for you, RUN NOW.  I still love you.  Oh, and they’re a problem for me, too; but, sometimes, you have no choice.

Well, I certainly do know how to keep ’em hopping! This morning I went in for what was supposed to be a routine nerve block. Routine for me, that is, because, while most people are told to fast and not drink water before the procedure, I am told to drink water and a cup of coffee before mine, since I have a tendency to faint. Oh, and, yeah, nerve blocks are pretty routine for me these days. Now, usually, this procedure takes about 15 minutes.  Shane drives me to Kaiser, I register in the Pain Management Department, and, within in a few minutes, they call me back.  We have learned to make sure I am well-hydrated (and have had a cup of strong coffee) when I arrive; that I am given oxygen during the procedure, and that my vitals are monitored throughout.  You know, and that there are smelling salts handy.  No, it shouldn’t be this hard.

When I arrived, my blood pressure was already low, so the doctor decided to start an I.V.  I warned him that a) my veins are tiny, and b) I am a great big baby.  Every time I need to have a blood test, I lead with, “I tend to faint.”  They have me lie down, and, as a result, I hardly ever faint.  This morning, I was sitting in a chair when the I.V. was inserted.  It honestly did not occur to me to ask if I could lie down, even though I have fainted with I.V.s before.  The doctor put in the I.V., and he did a great job.  Got it right in on the first try, and I remember thinking, “Wow, that wasn’t bad at all.  I barely even felt it.”

And then I was coming to.  They were hooking me up to all kinds of monitors and giving me oxygen.  Poor Dr. Pastushenko.  I am always doing stuff like this.  Well, since I was already there and hooked up to an I.V. and everything, they decided to give me fluids and monitor me until my vitals were back to normal.  This took some time.  Poor Shane was sitting in the waiting room with absolutely no idea what was going on, so, once I was settled, I asked the nurse if someone could let him know that I was okay, but it was probably going to take a little longer than planned.

After about 45 minutes, I think ~ it’s hard to tell, as I was a bit hazy at the time ~ my vital signs looked good, so I was moved in to the room and prepped for a lumbar sympathetic nerve block.  These nerve blocks aren’t especially entertaining.  First, you’re lying face down on a table with a pillow under you, so your bum’s in the air.  In my case, you’re doing this while attached to all kinds of tubes and wires, and the pulse oximeter keeps slipping off your tiny fingers and setting off alarms until the doctor, in a stroke of genius, clamps it on your thumb.  Problem solved!  Oh, but before the doctor comes in, they open the back of your gown and pull your pants half down.  So, face down on a table, hooked up to a bunch of crap, setting off alarms, with your half-naked bum in the air.  So, maybe I’m wrong.  Maybe it is entertaining.  It’s like your typical wild party.  I mean, if that’s the way you party, I guess.

Luckily, the I.V. fluids and oxygen helped a lot.  Also, I found that picking a spot in the distance to focus on while taking deep relaxed breaths helped.  I didn’t even have to close my eyes.  Why I usually have to close my eyes is beyond me.  It’s not like I can see my lower back while lying face down on a narrow little table.  The actual nerve block was par for the course.  First, you are numbed locally.  They do this, I think, to lull you in to a false sense of security, because, the truth is, when they administer the actual nerve block itself, you can still feel it.  Well, I can still feel it.  I have no idea how it is for anyone else.  But, you know, then it is over, and, though it is not the way I would want to, say, celebrate my birthday, I know that, in the long run, it will lessen the pain in my foot and leg, so I can continue to use them more normally, and that’s important to me.  It’s been flaring up a lot lately, and the pain now travels farther up my leg than it had, so something had to be done to try to halt it, at least for a little while.

I am monitored until the I.V. fluids are gone (not all of the I.V. fluids in the hospital, just the ones that were already hooked to my arm), the doctor evaluates me, and I am cleared for take-off.  Very slow, walking, on the ground take-off.  No lifting, pulling, driving…or, you know, actually flapping my arms and flying, I suppose.  Already, my leg feels better.  When I walk on it, I am aware of the difference.  Pain doesn’t shoot up through my knee with each step, and that is a vast improvement.  My feet are the same temperature ~ which is still probably colder than normal feet, but better than when the CRPS-affected foot is markedly different in temperature than the other one.

So, now, I rest.  Since the procedure took a couple of hours longer than anticipated, Shane called in and took the rest of the day off.  I hate to make him miss work, but I am glad to have him here, so I can just rest all day.

The verdict, in the end, was that the I.V. helped enough that we are going to have to make it part of my protocol.  From now on, however, we are going to make sure I am lying down with my feet up when it is started.  Everyone is always surprised that I have so much trouble with needles, when I have so many tattoos.  The thing is, no one ever tattooed into my veins.  I can take other kinds of needles.  I pierced my ears with pins ~ CHILDREN: DO NOT TRY THIS AT HOME.  It was a really stupid idea, and I am lucky I still have ears.  I actually have a pretty high pain threshold. I think I must just have a very low “vein threshold.”  I don’t really even like talking about my veins, or seeing them through my skin.  *shudder*

So, I have to figure out how to get over the whole fainting with I.V.s thing.  But not right now.  Right now, I’ll just read a book.  A book that’s not about veins.