Morning Update

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It is not even 8:00 am yet and I have already taken my modified bath and changed pj’s. I do not think I lost much breath if at all while doing that. Just yesterday I was still losing breath during that activity. I am so glad to breath with only a little wheeze. When my mother gets here later, I think I will have her come with me and I will do a few laps in the hall way. That should be a good test on how my lungs are really doing.

Fortunately, since I do not have an IV stuck to me all the time, just the catheter that is only used when I need medications, I can wear normal pj’s and not the hospital’s gowns.  Otherwise I might end up looking like this guy…..

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Have a good day, Neighbors!

ps. my morning blood sugar was 239, best reading yet since steroids were started.
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Oh What A Good Hospital Day!

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I could not have asked for a better day in the hospital.  My breathing has remained better all day, and with the four different insulins, my blood sugar has stayed under 300 most of the day, just now it was 316.

This morning after the PA from the pulmonologist office came over and gave me her news, the hospitalist who is doing my diabetes management said that the fourth insulin that he added seemed to have really helped a lot.  He said it was the first 24 hours that my blood sugar had not spiked way out of control.  So had a shot of that extra insulin again and he is going up another 10 units on my lantus (the long lasting insulin).  He thinks with all the steroids that I have had, even though my blood sugar is high, that we are keeping as good of control over it as we can.

Then a doctor from the pulminologist office came by and he actually gave me a tentative go home date.  Tomorrow, as the PA discussed we are going to reduce the IV steroids a little more, and see how I tolerate that.  Then on Tuesday morning the plan is to not give me any IV steroids, just oral steroids, and watch me through the day.  If I do not have a set back then I get to go home sometime Tuesday afternoon, probably.

 I call that a good day, as far as being in the hospital goes.

Have a great night, Neighbors!!

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A Better Morning In The Hospital

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Hey Everyone!  I am still in the hospital, but I am feeling better.  I do not get as winded walking a short way anymore and I am not having to gasp for air as much when I am being still.  I have to say today is already turning out better breathing wise than it has been since I have been here.

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Based on what the Physician’s Assistant from the pulmonologist’s office just said, I am thinking I will be here at least through tomorrow, because they want to continue to wean me off the IV steroids.  They are not reducing the dose today, they do not want to take it down too fast and cause me to have a set back.  The respiratory therapist I saw this morning, said I do not have to be woken for the two in the morning breathing treatment anymore, but I am welcome to call if I need it.  She also reduced the amount of oxygen I am getting, not much, only down 1%, but that also is to get me weaned off of the oxygen slowly.  My blood sugar was 279, yes I know that is high, however, there is no way to achieve a normal blood sugar while on steroids, and the 279 is significantly better than it was yesterday.  It has come down around 100 points or so.  It only took four different type of steroids to achieve that. 

I had to have my IV redone last night.  I am not very good with IV’s, they are either hard to start, or hard to maintain, most of the time both.  It took two ladies three tries a piece, all together six tries before they were able to get it started, but it feels so much better than the first one did.  The first one was on the back of my hand, the new one is on my arm.

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New IV Site

I am being giving a shot of an anti-coagulant one a day, to prevent blood clots since I am not very mobile right now.  That means I am bruising pretty darn easy.

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 More to come in a bit! 

Have a wonderful day Neighbors!

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Good Morning!

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This is my dad slee…..visiting me last night! Shhh he does not know I took his picture.

Never enough sleep in a hospital. I have been awake since about 2:00 am. First it was to have my blood sugar checked, then it was to have respiratory therapy to come in and for me to have a breathing treatment, shortly after that, I had to have some insulin injections. At least I can get an early start on my blogging today!!

My blood sugar is still in the 300’s, so my wish right now is that the Hospitalist who is working on the diabetes part of things does not decide to put me on an insulin drip. If that happens, I found out that I would probably have to go to ICU.

I do have some good news though. I am only partially IV’d up now. I now need fluids,so that part of things was disconnected. I just have the IV needle in my hand with a small amount of tubing. They use it to give me the steroids. The only time I will have to be hooked back to the full IV thing is about five this evening when I get my antibiotics. When I was hooked up to oxygen I was given a huge amount of tubing so I can go to the restroom still hooked up to oxygen. So I just feel better now that I can move around more, and now that I am not having to drag my IV pole around, I am not losing my breathe as much.

My chest is still tight. I know that it will continue to improve.

Have a good day, neighbors!

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Diabetes And Me

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I am an insulin dependent diabetic.  What that means is that, among other things, I have to give myself insulin injections on a daily basis. 

One of the things I quickly learned after I was diagnosed with diabetes is that there is math involved in managing your diabetes.  The ironic thing is, I really dislike math, and now I am stuck having to do it every day, several times a day.  I keep thinking of all those math teachers who said I would use a specific type of math one day, and how I blew off what they said.   The teachers in my head are now saying “I told you so”. 

My day starts off with a stick in the finger.  Before coffee, before breakfast, before anything else I have to get some blood out of my finger and test it to see how high my blood sugar is.  I do not care how many 1000’s of times I have stuck myself in the finger, it still hurts.  A lot of times it hurts more than my insulin injections do.  


If everything, insulin, medications, and meal planning, worked out the way they were supposed to, my blood sugar in the mornings is around 110.  That is a good number for me.  Not to low, not to high, right on target for what I need to achieve.  


I am always so darn hungry in the mornings.  The whole time I am checking my blood sugar, my tummy is growling.  Some mornings it is so difficult to resist the temptation of going ahead and eating breakfast before I check my blood sugar.  The worst mornings are when I have not slept well and I wake up around three or four. 

After I check my blood sugar, I can go about the business of making coffee and breakfast.  I have to carefully account for every bit of food that I am going to put in my mouth.  It has to all balance out so that I am only taking in a certain amount of sugar and carbohydrates.  Breakfast has become my favorite meal of the day, because I can eat more then than at any other time.  What I usually do is combine my breakfast and my morning snack allowances into one meal.  I do this for no other reason but to have a bigger breakfast.  I told you I was hungry in the mornings.  Maybe I should have said that I was very hungry in the mornings.  

Before I can eat, I have to give myself a small insulin injection.  Usually about three units of insulin.  I have to do this because my depression medications have a tendency to raise my blood sugar slightly.  After the injection, the chow down can commence.  

After I eat breakfast I am already thinking about what I can have for lunch, planning it out in my head.  You can tell from my profile picture that I am a person who enjoys food.  I really enjoy food.  I like cooking, I like planning menus, I just enjoy everything that has to do with food.  One thing I have noticed though, is that ever since I have been diagnosed with diabetes I seem to focus on food even more than I used to.  Maybe it is because I have to spend so much time every day planning what I eat out, or because I have to always be so aware of everything that I put in my mouth, or because as much as I still enjoy food there is a part of me that views food as the enemy. 

After breakfast I have to take care of my feet.  Because a diabetic does not have the best circulation, their feet have to be taken care of extremely well.   One little injury has the potential to become infected very quickly and can result in the foot and/or leg being amputated.  So every day I have to check my feet for any injuries and put lotion on them.  One of my favorite things to do was to go barefoot everywhere.  I cannot do that anymore.  Too much of a risk.  

The lunch process is similar to the breakfast routine.  Once again, the dreaded finger stick.  Ugh!  I am so tired of having to inflict pain on myself several times a day.   There are some days I put off eating lunch as long as possible so I do not have to go through the whole finger stick thing right away.  


I won’t bore you with the whole procedure, injection, stuffing my face, already thinking about my afternoon snack and supper, more finger sticks at supper and another injection.  


Before I go to bed every night I have to give myself yet another injection.  This one is of a long lasting insulin and the dose is rather large.  Of all the shots this is the one I really dislike.  Because of the amount of insulin I have to inject, this one tends to sting.  Sometimes, a bubble of insulin will develop and I have to be very careful, and not let any insulin come back out.  


The next morning the whole thing starts over again.


I get so tired of it all sometimes.  I get tired of the finger sticks, I get tired of the injections, I get tired of all the things I have to remember to manage my diabetes.  It is a very tedious disease.  Always so much to do with it, always having to think about it, everyday the same thing, needles, needles needles.  Sometimes I think about just not doing it anymore.  

Before I started getting help with my depression, and I really did not care about living any more, there were many days when I did not do any of the things I needed to do to take care of my diabetes.  Now that I have a better mind set, I do not skip my injections, or my finger sticks, no matter how tired I get of the whole thing.  I have a family that cares about me and I care about them, I want to live, so I do what I am supposed to do, needles and all.


The pictures at the top, from left to right
glucose meter (one of the types I have), insulin pen (same type as I use), needles for insulin pens (similar to what I use)

ummm Yeah….Do You Remember me?

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We live in a small town.  A very small town.  There are no banks, no grocery stores, no traffic lights, there are only a few antique shops.  To the immediate north and south of us there are bigger towns.  The one to the north of us is in a different county than we are, the one to the south of us is in our county and that is where we tend to do most of our shopping and get most of our medical care.   

The town to the south of us also happens to be where the hospital is that I was taken to after my suicide attempt in May, and where the crisis team had me go after they had come to my house.  It is not a very big hospital and between those two visits and other visits for different reasons, I had become very familiar with some of the staff at the hospital.  I had developed a “reputation”.


It is a reputation based on my crazy, screaming, violent behavior after I tried to kill myself in May.  Behavior that I still have absolutely no memory of.   It is also based on my angry pissed off behavior after I went there because of the crisis team.  


Now that I am on the right mix of medications, and I am further along in my recovery, when I think back to both of those times I was admitted into the hospital, I get rather embarrassed and ashamed of myself.  I really did not want to have to go back to that hospital and its emergency room ever again.  


Of course, as things usually go, the choice to go back to that hospital any time soon, was taken out of my hands.  The Saturday before Christmas I developed a nasty wheeze in my chest and had to go to the emergency department at the hospital.  I could just picture in my head what it was going to be like when I got there.  Some of the nurses would recognize me, some would stare, waiting for me to freak out.  The nurses who did not know who I was, soon would, as the facts about me and my craziness were passed around.  I could also see the doctor’s reaction to seeing that I was there again.  I had built up in my head a very terrifying experience, as well as a very embarrassing one.  


The reality was actually some what different.  I was taken back by the triage nurse almost immediately.  That is a common thing when you go to an emergency room with a breathing problem.  I had seen this particular nurse several times, so she was very familiar with my past visits.  I shared with her that I was rather nervous and afraid to be there because of what happened the last two times I had gone to the emergency room.  Her response to that was very sweet and quite surprising.  It put me at ease.


What she said to me that night was that the past was the past.  She said she did not make judgments about people or their reasons for being in the emergency room, and that she could tell that I was doing so much better than I had been doing before.  The final thing she said was that it was her job to take care of me for what I was there for that night and that I should not let what happened before prevent me from getting the help that I needed.



I ended up being admitted to the hospital.  Surprise! Surprise!  The doctor who was my treating physician while I was in the hospital, was the same doctor I had when I had tried to kill myself.  He was the doctor that dealt with me when I was being violent and had to be restrained.  He remembered me.  


It was at this point I realized I had two choices.  I could be a flake, and let my anxiety about being in this situation be in control, or I could use this as an opportunity to show the nurses and doctor that I am doing better and that at this time I am not acting like a crazy person.


I decided to go for the more positive of the two choices and show them that I was doing much better now.  I made sure that every morning when I woke up I gave myself a quick sponge bath and did other things to show that I cared about my appearance.  I talked with the nurses when they came by my room.  Asked questions, and looked up information about my treatment on the internet, staying engaged in my own treatment plan.  It was easier than I thought it would be.  


I ended up having to stay in the hospital several days longer than I thought I would have to.  The IV steroids that I had to have for my breathing, caused my blood sugar to be incredibly high.  At one point the doctor tried to take me off of the IV steroids and my breathing got bad again.  I was put back on the IV steroids and from that point on, my blood sugar had to be checked every four hours, night and day, and I had to have insulin injections every four hours.  My long lasting insulin dose was changed from 30 units to 72 units.  


Several times the doctor changed my other medications, took me off of one, and added a couple of new ones in the mix.  So I was having to keep up with the changes and keep up with why the doctor was making so many changes to my medications.  It seems my ability to keep up with all that the doctor was doing, and the questions I was asking, went a long way with the doctor.  He was able to see me for the intelligent person I am, instead of the raving, mad woman he had experienced before.  As a result I was allowed to go home Christmas Eve, with a very detailed set of instructions to follow. 

I learned a couple of things from this experience.  The first thing I learned is that for the most part, the staff in a hospital really want what is best for their patients, and truly believe in not holding past experiences with a patient against them.  The other thing I learned seems to be something that I have to keep learning over and over again.  That lesson is that very often my own anxieties make a situation worse in my head than the reality of it is.  One of these days, I hope, that lesson will stick with me and I will learn to not get so anxious about things.  

Diabetes and Me – My Diagnosis Part I

Most of the time I blog about my depression. I think it is because it is the illness that is most affecting my life right now.  Since November is National Diabetes Month, I thought over the next few days I would blog about diabetes and the effect it has had on me, same facts about diabetes and some myths about diabetes.  

I was diagnosed with Type 2 Diabetes in May of 2008.  I was 38 years old.  When I was diagnosed with Type 2 Diabetes I felt completely blind sided and devastated and oddly enough a little bit relieved at times.

About 10 months before I was diagnosed with Type 2 Diabetes, I had been diagnosed with Asthma.  From the time of my Asthma diagnosis, I never felt good.  I had frequent Asthma attacks that required emergency treatment and I felt so very tired all of the time. I attributed the fatigue to the Asthma.  

If I had the usual symptoms you have when you have untreated Type 2 Diabetes, I never noticed them.  I already urinated more frequently than most people, and because of some medications I was on, I was always thirsty anyway.  I do recall in the last few weeks before I was diagnosed with Type 2 Diabetes that I was even more thirsty, but I did not think anything of it.  The only thing I really noticed was the constant fatigue.  

One Friday in May, I began having some difficulty breathing.  I used my nebulizer several times, but it seemed to have no effect.  Since my breathing was getting worse, I decided that I needed to go to the Emergency Room and get some help.  When I got there, I was taken straight back and the triage nurse performed her assessment.  I was also started on a breathing treatment.  

The doctor came in and told me that my blood pressure was incredibly high. I sort of laughed and said I was not surprised considering how many breathing treatments I had given myself before I had gone to the Emergency Room.  The doctor did not appear to be as amused as I was.  In fact, he insisted that he do some blood work.  He was concerned that I had congestive heart failure because of my breathing difficulties and the high blood pressure. I agreed to let him run the blood work, I was not worried at all, as far as I was concerned there was nothing wrong with me except that I was having an asthma attack.  

I did notice that the nurses started treating me a bit differently, paying more attention to me, going out of their way to make sure I was comfortable, I was moved from a curtained bed area to a room that was much more private.  I still did not worry about anything “not good” showing up in my blood work.

The doctor finally came back to my room. He sat down.  It was at that point that I actually began to worry.  I knew by his demeanor something bad had been found in my blood work.  I was preparing myself for a diagnosis of congestive heart failure.  When doctor told me that I did not have congestive heart failure,  I was so happy that it did not really register that he went on to tell me that my blood sugar was 442 and I had Type 2 Diabetes.  It finally began to sink into my brain that even though I did not have congestive heart failure there was still something very serious wrong with me.  Initially, the doctor thought about admitting me into the hospital so that my blood sugar could be monitored. In the end, he agreed to let me go home because I happened to have a glucose meter that had belonged to my father.  He told me he was going to give me a prescription for glucophage and that I needed to see a doctor about the Type 2 Diabetes as soon as possible.  

While I was happy that it was not congestive heart failure, my brain could not completely wrap itself around the fact that I had Type 2 Diabetes. Even though I had several family members who had Type 2 Diabetes and knew I was at a higher risk to develop it, I never thought that I would.  

Shortly after the doctor left my room, a nurse came in with a syringe. She told me she needed to give me a shot of insulin either in my thigh or stomach.  I promptly burst into uncontrollable tears.  You see, shots/needles are a phobia of mine and the thought of having to get a shot in either my stomach or my thigh totally freaked me out.  The nurse calmly talked to me and told me she could give me the injection in the back of my arm.  The arm was a location that appealed to me because it was a place where I was used to receiving injections so I agreed.  After I was given the injection I was sent home, I was told to monitor my blood sugar, but I was not given any clear instructions about how or when to do that.

That weekend was a very tense weekend for me and my husband. We were constantly checking my blood sugar. At the time we had no idea when the best times were to check blood sugar so we were checking it every hour.  The glucophage upset my stomach.  I was halfway convinced that the diabetes diagnosis had to be a mistake.  We were also wondering if I would be able to get an appointment with an Endocrinologist on Monday.

I knew that once again that my life was going to take a drastic turn due to an illness, but I had no clear idea how this change was going to manifest itself.

To be continued…….Diabetes and Me – My Diagnosis Part II tomorrow

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 Diabetes Facts and Myths

information from American Diabetes Association

Facts – Type 2 Diabetes

Type 2 Diabetes is the most common form of Diabetes

In Type 2 Diabetes, either the body does not produce enough insulin or the cells ignore the insulin

Being overweight is one of the leading risk factors for Type 2 Diabetes.


A family history is one of the strongest risk factors for developing Type 2 Diabetes.


Fiction

Myth: Diabetes is not that serious of a disease.
Fact: Diabetes causes more deaths a year than breast cancer and AIDS combined.  Two out of three people with diabetes die from heart disease or st
roke.
Myth: If you have type 2 diabetes and your doctor says you need to start using insulin, it means you’re failing to take care of your diabetes properly.
Fact: For most people, type 2 diabetes is a progressive disease. When first diagnosed, many people with type 2 diabetes can keep their blood glucose at a healthy level with oral medications.  But over time, the body gradually produces less and less of its own insulin, and eventually oral medications may not be enough to keep blood glucose levels normal.  Using insulin to get blood glucose levels to a healthy level is a good thing, not a bad one.