Subtitle

Just Like You... But A Little Different!

What's gweedlife?

gweedlife is a blog about our lives. Some people use "Honey", "Dear", "Sweetums" or even "Babe" as terms of endearment. But as you will find out, Bob & I don't do things like most people! "Gweed" originated when Bob & I were dating. I started calling Bob "Gweedo-Schmeedo", which was eventually shortened to just "Gweed". Being the super creative individual that he is, Bob decided to call me the same thing! So we both call each other "Gweed".

Bob Herman & Julie Anderson met on an old porch in downtown Grabill in August, 1981. Something must have happened that day, because we have been married for 26 years (!!!) & have 5 kids to prove it. We’ve lived in Grabill, Leo, South Bend & Auburn, Indiana, as well as Birmingham, Alabama & Edwardsburg, Michigan. We currently live just south of Auburn.

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Tuesday, November 13, 2012

Audacious Prayer

This morning as I read from my Bible, I felt the need to write down & share what the Holy Spirit was teaching me.

I started reading Luke 11:5-13.  “Then He said to them, ‘Suppose one of you has a friend, & goes to him at midnight & says to him, “Friend, lend me three loaves; for a friend of mine has come to me from a journey, & I have nothing to set before him”; & from inside he answers & says, “Do not bother me; the door has already been shut & my children & I are in bed; I cannot get up & give you anything.” I tell you, even though he will not get up & give him anything because he is his friend, yet because of his persistence he will get up & give him as much as he needs.

‘So I say to you, ask, & it will be given to you; seek, & you will find; knock, & it will be opened to you. For everyone who asks, receives; & he who seeks, finds; & to him who knocks, it will be opened. Now suppose one of you fathers is asked by his son for a fish; he will not give him a snake instead of a fish, will he? Or if he is asked for an egg, he will not give him a scorpion, will he? If you then, being evil, know how to give good gifts to your children, how much more will your heavenly Father give the Holy Spirit to those who ask Him?’”

The thing that God pointed out to me was verses 8-10.  In the parable, Jesus said that the man with the bread wouldn’t get out of bed to help someone who was his friend.  But because the man who had the unexpected guest kept knocking on the door, kept asking for his friend’s help, because of his persistency, the man eventually got out of bed & gave to his friend as much as he needed.  The key was the persistency of the man in need.

The word “persistence” from verse 8 means “recklessness; audacity; shamelessness; disregard of considerations of the man making the request; one who knows no restraint; no deference; imprudent in one’s relationship with another”.  (From Lexical Aids to the New Testament, Spiros Zodhiates, Th. D.)  The man banging on the door was secure enough in his friendship with the man who had the bread that he shamelessly kept bugging him until he opened the door & gave him what he needed. 

In verses 9 & 10, Jesus told us to do as the persistent man did - KEEP ON asking; KEEP ON seeking; KEEP ON knocking.  EVERYONE who does those things with persistence will receive, find & have doors opened.
From Luke 11, I next cross-referenced to Luke 18:1-8.  “Now He was telling them a parable to show that at all times they ought to pray & not to lose heart, saying, ‘In a certain city there was a judge who did not fear God & did not respect man. There was a widow in that city, & she kept coming to him, saying, “Give me legal protection from my opponent.” For a while he was unwilling; but afterward he said to himself, “Even though I do not fear God nor respect man, yet because this widow bothers me, I will give her legal protection, otherwise by continually coming she will wear me out.”’ And the Lord said, ‘Hear what the unrighteous judge said; now, will not God bring about justice for His elect who cry to Him day & night, & will He delay long over them? I tell you that He will bring about justice for them quickly. However, when the Son of Man comes, will He find faith on the earth?’”

Jesus was illustrating that we are to pray & not “lose heart”.  Just like the man who need help from his friend, the widow in this parable was persistent!  She “kept coming”, relentlessly making her request for protection.  The unrighteous judge who had no concern for the status or character of a man, was worn down by this widow.  She kept bothering him & he got tired of seeing her & hearing her case over & over again, so he relented & granted her request just to get some peace.  Jesus tied it all together by saying that if an unrighteous judge who doesn’t care about anyone but himself would give this little widow lady what she asked for, even more so God, who loves the world & everyone in the world, will hear our requests & will bring about justice.

What about that last sentence in verse 8?  “However, when the Son of Man comes, will He find faith on the earth?”  Faith in this verse refers to faith like the persistent widow.  Will God find that I have a persistent, relentless faith that has the audacity to come to God over & over & over again with my requests, expecting Him to answer my prayers in His timing? 

So many times I’ve heard teaching on prayer that makes it out to be something mystical, something difficult, something rote.  I believe that prayer is actually quite simple - so simple that a child can do it.  It’s merely communicating with our Father.  Prayer is talking with God.  Prayer is reading His word & listening to the Holy Spirit’s teaching about what was read.  Prayer is interceding for others’ salvation.  Prayer is the cry of our hearts when we can’t find any other way to express ourselves to God.  Prayer is also “reminding” God of our needs & asking Him to provide in His time.  God WANTS us to come to Him in prayer.  Yes, He already knows what we’re going to pray before the thoughts even form in our minds.  But He still wants us to go through the process of prayer.  He wants to be our hero, the one who swoops in & rescues us.  He wants to expresses His great love & concern for us by meeting our needs & answering our prayers.  He wants our awe, our overwhelmed gratitude, our worship of Him.  

God wants us to have the audacity to come before His throne of grace & ask Him to work in our lives.  He wants us to pester Him in prayer!  Now more than ever, I am committed to being persistent in prayer, bringing every need I can think of to His attention & begging Him to intervene so that He can receive glory, honor & praise for His amazing work.

Saturday, March 10, 2012

One More Time...

The PleurX System Soon to Be A Part of Bob's Body
Thursday Bob had follow-up appointments with his doctors.  Before Dr. Sowden saw him, he had an xray of his chest performed to check for fluid.  Shortly after the xray was done, Dr. Sowden entered the room & said only a few words.  Two words, actually.  “It’s back.”

The xray revealed a significant amount of fluid which had accumulated in the lower lobe of Bob’s left lung (“And today’s program is sponsored by the letter “L”...).  Dr. Sowden hypothesized that since the pericardial windows were wide open, the fluid, which apparently originates from his heart, flowed directly downward into the next available cavity - the lung.  His right lung is dry as can be, which is great. 

Dr. Sowden told Bob he would have to install a PleurX tube only on his left side, to drain his left lung.  The tube will remain until Bob has no more drainage whatsoever.  Since no one has ventured to speculate why he even has fluid at all, no one has a good theory about how long he will be draining.

On Tuesday, March 13, Bob will be sent to la-la-land via Versed one more time.  An Intervention Radiologist will insert the PleurX tube, instead of Dr. Sowden.  The procedure only takes a few minutes.  Bob will be observed for the rest of the day & then allowed to go home in the evening.  Then, on a schedule determined by Dr. Sowden, a home health nurse will visit Bob & drain the fluid that has collected in a little bag taped to Bob’s side.

Other than this snag, Bob’s recovery is nothing short of miraculous!  He has no pain, not even in his sternum.  He is walking the neighborhood already, which no one should be surprised by.  He continues to have family with him during every day but is now sleeping at home alone, save the 3 furry puppies that worship the ground he walks on.  He has had many, many amazing meals prepared & served, which he is so grateful for.  And many people have sent cards, called & visited to check up on him.  He is profoundly grateful for all of the amazing love & support he has felt from you all throughout this long illness. 

I will update again when we know how the procedure has gone.  Thank you for your continued prayers!

Saturday, March 3, 2012

Home At Last!

Well, it FINALLY happened!  Friday evening Bob was released from Parkview!  He had a pacemaker place on Thursday by Dr. Mirro, the very highly regarded & esteemed heart “electrician”.  The procedure went without a hitch & he was back to his least favorite room in the world before he was awake.  The biggest pain he said he had from it was that he couldn’t use his left arm for a while.  Thankfully, the Versed he was given for the procedure helped him to sleep for most of the day.

Prior to putting the pacemaker in, Dr. Sowden “yanked” his chest tubes - all 3 of them.  His chest X-ray showed very little fluid, so he felt comfortable removing the chest tubes.  My dad was SO glad to get rid of those tubes tethered to that little box he had to carry around with him everywhere!

As you know, sleeping had always been a problem while he was hospitalized.  Thursday night wasn’t much different than any other night.  But he awoke Friday morning with the hope that he would soon be free again!  More chest X-rays showed that everything was where it should be (or wasn’t where it shouldn’t be!) & showed that his heart, which had been the size of a football, was back down to the size of a fist!

Friday afternoon he was told the great news of his impending departure.  As always, it took some time to get his discharge paperwork & prescriptions prepared, so he didn’t actually leave until evening.  His sister, Pam Norton & her husband Grant got to chauffeur him.  He wanted real food before heading home, though, so they made a stop at his favorite restaurant - Golden China!  He couldn’t eat all of his food, but what he did eat he thoroughly enjoyed.

Connie spent the night with him last night.  He kind of had the expectation that he would sleep perfectly in his own bed, but he didn’t sleep that well because of the pain from the pacemaker procedure.  Of course, he won’t take anything for pain because of how crazy it makes his head, so he has asked that you pray that God will be gracious to him & allow him to sleep deeply & comfortably tonight & onward.

Now that he’s home, he is much more comfortable & feels a little more himself.  Neighbors, he isn’t up to walking the neighborhood right now, but if you are able, he would love it if you would stop in & get him caught up on the news of Bay Shore Heights!  He is very ready for visits, but requests that they be kept short & sweet so he’s not worn out by them.  He won’t be at church tomorrow, but hopes & prays that he will rebound from his ordeal quickly so that he can rejoin fellowship with his church family.

Your prayers, visits, cards & other forms of encouragement have meant very much to Bob.  He realizes that God has kept him here for His good purpose & he is willing to stay as long as God has work for him to do.  Praise God for all he has done in the past 13 days!  He alone is worthy of praise!

Thursday, March 1, 2012

Growing Weary in This Temporary Body

Wow!  What a beautiful day we had today!  We almost hit 70° in Indiana on February 29th!  Everyone hated to tell Bob how beautiful the weather was, considering the fact that he was still a “prisoner” in the hospital.  Unfortunately, it looks like he will be there for another couple of days, too.

This morning he had a chest xray to see if fluid had accumulated in his pleural cavity.  Strangely, not much fluid was there!  Because there wasn’t a significant amount of fluid, Dr. Sowden is still contemplating whether or not to install PleurX drainage tubes.  He plans to have another xray tomorrow morning to see if things have changed & then will make his decision regarding the PleurX drainage tubes.

Overnight, Bob had irregular heart rhythms again, despite the medication Dr. Mirro prescribed in an attempt to control his rhythm.  This morning he strongly recommended that Bob needs to have a pacemaker put in.  Bob really balked at this suggestion, because he didn’t think it was that big of a deal.  In an effort to illustrate to Bob just how serious the situation is, Dr. Mirro had the records of Bob’s heart rhythms for the past few nights brought in.  He showed him in black & white where his heart stopped beating in the middle of the night, every night.  One time his heart completely stopped for 4 seconds!  Seeing those records convinced Bob that he better listen to the counsel of Dr. Mirro.  He signed all of the necessary papers & will be having the pacemaker put in tomorrow afternoon.

It’s a relatively simple procedure that they will perform in a cath lab at the Heart Center.  Bob will be given Versed, which will knock him out - something he looks forward to!  The procedure shouldn’t take much time at all, & recovery from it is relatively short.

Today was a long day for Bob, just sitting in a chair in a small room with an uncomfortable bed & a few chairs.  The only thing that made today bearable was the many visitors who were kind enough to take time out of their day to visit him.  Many people prayed with Bob, which really encouraged him.  His sister Kim Culbertson was with him much of the day & commented several times about the loyal, committed, loving friends that Bob was so fortunate to have. 

The specific prayers I would like to ask you to pray for are:

  • For the Holy Spirit to come upon & in Bob in a very powerful, overwhelming way.  Bob has some crucial decisions to make regarding the care of his body.  It is difficult for him to see past his emotions right now to make the best decisions.  He needs God to impress upon him what His best course of action to take regarding the tools that are being offered for the care of his heart.

  • That fear & anxiety will be forbidden from influencing Bob in any way at all.  Those demons are attacking Bob when he is weak & causing much confusion for him.  Pray that God’s holy angel army will surround Bob’s room & guard Bob personally from the fiery darts of fear & anxiety that Satan launches against him.

  • Pray for Dr. Mirro & Dr. Sowden to have wisdom that comes from God as they care for & advise Bob.  Pray that they will not be swayed from pursuing what they believe is in Bob’s best interest, no matter how stubbornly he grouses about it.  Yes, Bob Anderson can definitely GROUSE!  He can GROUCH, too!  He is very discouraged about his current situation & that discouragement is sometimes clouding his reasoning.  Pray that he will trust God to use his physicians to accomplish His will.

Thank you, all of you who have invested in Bob during this trial, either by visiting, praying, sending a card or just reading this blog.  We, his family, believe that God still has much service for our dad to do, for the glory of our beloved Father & Saviour.  Thank you for believing these truths along with us!

•  •  •  •  •  •  •  •  •  •

“For we know that when this earthly tent we live in is taken down (that is, when we die & leave this earthly body), we will have a house in Heaven, an eternal body made for us by God Himself & not by human hands.  We grow weary in our present bodies, & we long to put on our Heavenly bodies like new clothing.  For we will put on Heavenly bodies; we will not be spirits without bodies.  While we live in these earthly bodies, we groan & sigh, but it’s not that we want to die & get rid of these bodies that clothe us.  Rather, we want to put on our new bodies so that these dying bodies will be swallowed up by life.  God Himself has prepared us for this, & as a guarantee He has given us His Holy Spirit.

We are always confident, even though we know that as long as we live in these bodies we are not at home with the Lord.  For we live by believing & not by seeing.  Yes, we are fully confident, & we would rather be away from these earthly bodies, for then we will be at home with the Lord.  But whether we are here in this body or away from this body, our goal is to please Him.”
2 Corinthians 5:1-9

Tuesday, February 28, 2012

Trying His Best to Get Through


Another day in the hospital.  Another day of learning to let God be God.  Another day being cooped up in a tiny room.  Another sleepless night.

Sigh.

As you can expect, Bob is weary of his surroundings.  He didn’t sleep well last night, but has actually taken a few catnaps in his chair.  He even laid in his bed & took about 1/2 an hour nap!  We’re telling him that sleep may be hard to achieve at night, so take it whenever you can get it throughout the day.  He knows that sleeping won’t be a problem at home, which makes him want to get out of here even more!

Dr. Mirro visited him today to report that his heart is having episodes of atrial fibrillation, especially at night.  He has tried several medications to get the “electrical circuitry” of his heart functioning properly, but he believes he will eventually exhaust the medicinal options available & will put in a pacemaker.  We (his daughters) just want them to put the thing in!  But our father wishes to allow Dr. Mirro to do what he deems is best.  So, there’s nothing for us to do but wait.

Dr. Sowden rounded later in the day & had come to a decision about the PleurX chest tubes.  Bob only had 80 cc of fluid drain overnight, but so far during the day as he was more active, he had an output of over 300 cc, which is WAY above what he should be expelling.  Because of this, Dr. Sowden plans to put the PleurX tubes in, maybe tomorrow (Wednesday).  He will have to undergo general anesthetic again, which will mean his eye will be unable to focus again for a while.  Dr. Sowden shared his opinion about the pacemaker - he believes it is inevitable.  However, he’s the “contractor” & Dr. Mirro is the “electrician” of the building that is Bob’s body, so Dr. Sowden officially defers to Dr. Mirro about the pacemaker.  We all wish we could find the “plumber” of Bob’s body so we could get to the bottom of why he has the fluid retention in the first place.  We keep being told that we may never know.

He had a nice day with his sisters, Betty, Sandi & Kim, Kim’s son Taylor, Bob & me.  There were several visitors throughout the day, which really lifted his spirits.  He especially enjoyed his visit from Phil Chapman & Marc Davidson.  He has a kindred spirit with them & was very touched by their time in prayer.

Things to pray for are that he will have a spirit of peace & tranquility come over him, that his vision will clear so that he can read again & that his body will heal according to God’s timetable. 

Those who have visited, thank you!  You are what he looks forward to every day.  Those who are hesitant to visit, come on up.  Bob gains strength from positive, discussion & encouragement from people.  We only ask that you be brief in your visits so that he is able to get appropriate rest.

Several of you have contacted Kim Culbertson, Bob’s sister, about providing food when he gets home.  Thank you so much for your kindness!  If you haven’t contacted Kim about preparing meals for Bob when he’s home & you want to minister to him in this way, you can reach Kim at 260-925-3213 or email her at luvruby007@gmail.com.

God is working in Bob’s life right now to prepare him for all of the ways He wants to use him in the future.  God isn’t finished with Bob yet!

“Answer me when I call, O God of my righteousness!  You have relieved me in my distress; be gracious to me and hear my prayer.  But know that the Lord has set apart the godly man for Himself; the Lord hears when I call to Him.  Tremble, and do not sin; meditate in your heart upon your bed, and be still.  Offer the sacrifices of righteousness, and trust in the Lord.”

Psalm 4:1,2,4,5

Monday, February 27, 2012

A long, frustrating day

Catnapping in the Lobby

It’s been a really discouraging day for Bob.  He’s one week post surgery & he’s still hospitalized, which is not how he envisioned his recovery to go.  Contrary to what he was told on Saturday, he did not have a pacemaker implanted today.  The doctor who is rounding for Dr. Sowden this work is Dr. Mirro.  Dr. Mirro decided to wait to go to a pacemaker because he wants to let the heart adapt to the new pig valve that was installed & hopes that things will work themselves out. 

Another reason why he is still hospitalized is that he is draining way too much fluid every day.  Today he drained over 300 cc of fluid in an 8 hour period.  That is the amount of fluid he gave out right after the surgery last Monday!  As of now, there is no doctor who is willing or knowledgeable enough to investigate & discover why Bob is creating so much excess fluid.  There is some cause!  But no one wants to try to find out what the cause is.  This frustrates us all tremendously!

He was prescribed Coreg, which is a beta blocker.  He has been very withdrawn & sullen, which is so unlike him.  He still isn’t sleeping well, so he catnaps while he sits up in his chair.  We are hoping that he will finally sleep better tonight.  He has a fan, which helps provide white noise to drown out the racket in the hallway.  Please, please, please pray that he will “sleep in heavenly peace” tonight!  Also pray that we will find someone who can shed light on why he is producing so much fluid.  He would enjoy short visits & phone calls.  He needs something to make his day go a little faster. 

Thank you for your prayers & support!

Saturday, February 25, 2012

Some Bummer News

Illustration of Pleural Drainage Catheters
Day 6 of my dad’s hospital experience was a little bit better than previous days, to say the least.  Today was the first day he didn’t wear his hat!  That’s because he was able to wash & dry his hair.  He got a clean gown, clean PJ pants, clean socks...  It was nice for him to feel presentable again.  AND he was able to sleep better than he has so far, which is a blessing from God!

Very early in the morning his cardiologist, Dr. Kelley, paid him a visit.  He was not bearing the best news.  Bob has a telemetry monitor attached to his body with leads.  The monitor is very sensitive & very accurate.  Somewhere on the 2nd floor of the hospital, there are nurses whose job is to continually watch computer screens that display the activity of a patient's vitals via the telemetry monitor.  Overnight, Bob had several “flutter” episodes.  His heartbeat was irregular.  Because of those “flutter” incidents & the occurrences of some v-tach episodes, he put an external pacemaker on Bob & scheduled him to have a short surgical procedure on Monday to install a permanent pacemaker.  This news was a bummer, since Bob really wants to get out of the hospital!

Connie spent the morning with him, working away on her computer trying to get everything ready for the opening of Parkview Regional (aka the Emerald City).  I got there at around 2:00 & I brought some contraband with me.  KFC fried chicken breast & mashed potatoes with gravy, baby!  My dad really enjoyed having food that actually tasted good.  Just before Connie left, Dr. Sowden came into the room.  He also had some discouraging news. 

The fluid from Bob’s pleural space is continuing to drain at a significant pace.  At this point in his recovery, he should be draining less than 100 cc of fluid in an 8 hour period.  He is currently draining over 300 cc of fluid in an 8 hour period.  This causes Dr. Sowden concern.  The longer the chest tubes are left in, the greater risk there is of infection in his sternum.  Since there is still excess fluid in Bob’s pleural space, Dr. Sowden plans to install pleural drainage catheters on both sides of Bob’s chest.  I’ve placed a picture of what this will look like so you can get a better understanding of the procedure.

The procedure is performed under general anesthesia. Dr. Sowden will tunnel a chest tube into place under Bob’s skin & into the pleural space.  The fluid accumulated in the pleural space will drain through the chest tube & into a bag taped to Bob’s side.  Every so often, a home health care nurse will remove the fluid from the bag.  This will continue until fluid ceases to be produced & drainage resolves. 

The problem with excess fluid build-up is more concerning to the family than the pacemaker is.  We know why he needs a pacemaker.  We don’t, however, have any idea why Bob continues to create & carry excess fluid in his pericardium, his lungs, his ears & other spaces.  No doctor has been willing or able to get to the root of this fluid problem.  This is a matter that we really would like you to pray about.

Since Bob isn’t going home on Sunday like he would prefer, he will be in room 354 at Parkview Main & would LOVE to have some visitors!  He is much more able to cope with having visitors as the anesthesia dissipates from his body & his mind becomes more clear. 

Friday, February 24, 2012

Halucinations, Security Guards & Restraints - OH MY!

Today is February 24.  19 years ago I was in this building, on the 2nd floor, giving birth to my son Colson Robert Herman!  He was a big boy, 9# 1oz, & he has grown to be a tall, handsome man.  What a great memory for me of my time spent at Parkview.

Last night however is a night my dad never wants to remember again!  He had a terrible night, to say the least.  I’m not totally sure of the timeline of events, but it all began at 10:00 pm.  He took 2 Benadryl & 1 Xanax to help him sleep at 9:30.  Within half an hour it took effect & caused Bob to experience great confusion.  He said he woke up at 10:00 & thought he was in a basement somewhere.  He tore off the bandage that covers where his chest tubes exit his abdomen & began to try to pull out the chest tubes.  His nurse, Nikki, intervened at the right time & got in his face.  She calmly but firmly explained to him that he was hallucinating, that he was a danger to himself & others & that she was not going to allow him to do that.  She is a tiny woman, but she stood right in his face & didn’t back down.  She called Connie & told her to come help get him under control.  She also called security.

In his paranoid state, he was completely out of control.  He was rebuking the devil, praying loudly, throwing things & tried to leave his room.  Standing outside his room was a wall of 4 security guards that stopped him dead in his tracks!  Then he looked over them & saw Connie standing in the background with a stern look on her face.  Nikki, the security men & Connie were able to coax him into his bed, where they promptly restrained him by tying his arms to the side rails of the bed.

He fell asleep for about an hour & woke up panicked again.  Nikki was able to calm him down again & he slept for a couple more hours.  He woke up a 3rd time & was less confused.  It dawned on him that all of the things that had occurred were not a dream as he had supposed, but they were real events!  That horrified him!  He felt so bad for Nikki!  He was very embarrassed (although he’s been telling everyone who visited him today about this story) by his lack of control, but Nikki said following a major surgery where a patient has been under anesthesia for a long time, this type of episode can occur.  Nikki said he was the nicest paranoid patient she’s ever had!

Pray that God will allow my dad to sleep peacefully, restfully & soundly. 

He made every effort to stay awake all day so that he would be really sleepy tonight.  He walked the halls a couple times, at a brisk pace I must say.  He sat up in a chair all day, which is good for his lungs.  He even had Rachel take his chair out of his room to the end of the hallway where there were big windows.  He sat in the clouded light for a while.  He watched some TV, but not much.  He never took a single pain pill!

He had a nicely paced day of visits.  Bob stayed with him for a while, as did Connie.  I was with him in the afternoon & evening.  Ray Harrison faithfully visited him & prayed with him.  He went across the hall to visit with Merle Mullett & his family, which was a nice time of sharing & laughing.  Two ladies who set up Home Health nurses visits stopped by to talk with him about what to expect when he gets discharged.  As it turned out, one of the ladies, Michelle Rhodes, had him in 6th grade at Leo Elementary!  She still has the term paper she did for Science class.  She did it on Polar Bears.  He graded it & wrote “Beary good!”.  The other lady with Michelle is named Rhonda.  Rhonda has cousins Pat & Peter Johnson, who also had him in 6th grade.  He really enjoyed talking with Rhonda & Michelle.

Dr. Sowden came around in the late afternoon to check on my dad.  He asked if he was in pain, & he told him not at all.  He said he hurts sometimes, like when he coughs, but he’s not in pain.  Dr. Sowden told him that he is still draining a lot of fluid from his chest, which is not what he had hoped would be the case at this point.  Tentative plans are to release him on Sunday.  If he is still draining a lot of fluid, Dr. Sowden will install semi-permanent intravascular catheters that will exit his body on his side.  Home Health nurses will come several times a week to drain the accumulated fluid.  Hopefully, the draining will stop by Sunday so that Bob doesn’t have to worry about it any more.

Jack Clark came in & prayed with Bob.  Bob has a tremendous respect & love for Jack.  Then my dad was invaded by his sisters, Sandi & Kim.  They had stories to tell about his doggies & what they are up to while he is away.  Next Kristie & her current boyfriend Jeff came in.  A couple minutes later, Bob came back with Josiah & Colson.  Next Jason Eckes & Kirsten Meadows squeezed in the room.  Rachel came next, but there was no room in the inn.  We took that as our cue to leave.  So Bob, Rachel, Colson, Josiah & I said goodbye & left to go celebrate Colson’s 19th birthday.

Saturday Bob would really love to have brief visits from friends.  He’s ready to interact with people again & could use your encouragement.  Students from LPCS, he has really appreciated the cards you made for him.  They decorate his hospital room!  Please keep praying for Mr. A.  He wants to be back at school with all of you as soon as possible.

Food for thought: 
We have had several wonderful people asking us about preparing meals for Bob after he gets home.  He doesn’t have any dietary restrictions.  If you provide a meal for Bob, we would appreciate it if you could deliver it in small containers that can be used in the refrigerator, freezer & microwave & then can be thrown away.  Please include instructions of how to reheat the meal.  During the first 2 weeks he is at home following his hospitalization, he will have a caretaker with him 24 hours a day.  He will need 2 meals a day, one for lunch & one for dinner.  Please include enough food for both Bob & the person who is keeping an eye on him each day during his recuperation. 

Bob’s sister, Kim Culbertson, will be creating a calendar to organize meal schedules for the weeks of February 27th - March 12th.  If you wish to prepare a meal, please either call Kim at 260-925-3213 or email her at luvruby007@gmail.com.

Thursday, February 23, 2012

Full Circle

Today seems to be the turn-around day.  This morning was terrible for Bob.  He was very irritable, frustrated & somewhat angry.  To say he wasn’t himself is a gross understatement!  We’ve never seen him like he was.  Nothing could soothe him.  If asked a question, he acted irritated because you asked him anything.  If he seemed to be wanting something & you asked what you could get for him, he would bark his answer at you.  He acted so out of character, it was surreal. 

In spite of his poor disposition, he did walk the entire STICU & did it at a steady, quick pace.  He has a good appetite & ate all of his meals.  His heart rhythm became more regular, which was encouraging. 

At 2:30, Connie cornered his nurse, Peggy.  She’s an amazing nurse!  She spoke with Dr. Sowden about the problems we were concerned about & he decided that Bob was experiencing anxiety brought on by a lack of sleep.  He prescribed Xanax, which reduces nervous tension & anxiety.  It can also be used as a sleep aid.  When he took the Xanax @ 2:45, Connie, Bob & I left to allow him to sleep. 

When I went back to his room around 4:45, he was sitting in a wheelchair & his nurses were packing him up!  He was moving on up!  He is now in a regular room, #354 on 3 West.    His attitude was completely different!  He was relaxed, talkative, able to speak in sentences & give complete answers.  I beat him up to his room & got things arranged for when he got here.  The only problem with the room is there is only one chair!  We told his nurse that he will need at least 4 more chairs.  They are looking around for unclaimed chairs for us!  Shortly after settling in in his new room, he had a very pleasant visit with Ray & Arlene Harrison.  Ray read some very appropriate scripture & prayed with us before leaving. 

As I am writing this he’s sitting on the edge of his bed, watching TV & doing his breathing exercises.  He’s doing wonderfully!  Connie & Kristie are coming up in a little bit & he told them he wants a big slice of chocolate cake!

As far as visitors go, we don’t want to bombard him with people coming in & out.  He isn’t physically or emotionally strong enough for a lot of stimulation.  So for Friday, lets just have family visit.  Sisters, please come!  Grandkids, he wants to see you!  As always, pastors are always welcome to visit.  Hopefully he will do well with guests on Friday & we can expand the scope of visitation.  We are being so protective of him because we are concerned for his health.  We want to protect him from fatigue & exhaustion.  Thank you for respecting our visitation “rules”.

Please pray for him to heal physically, emotionally & mentally.

Wednesday, February 22, 2012

Gangsta in STICU

Bob tries out his gangsta look.  Not very intimidating!
Day 3 of the Great Recovery has been challenging.  Bob has done well with his appetite and although he’s restricted to a full liquid diet, he’s cleaning off his tray.  Yesterday his appetite was nonexistent, so this is a good sign.

He has been bothered often throughout the day by the respiratory therapy team.  For some reason they insist on keeping him breathing!  He is doing very well with his breathing exercises & the crackles in his lungs from yesterday are gone.  Breathing deeply when you have just had your chest sawed open can be pretty painful.  But he’s a tough guy & he’s doing his best.

This morning he took a short walk in the STICU.  It wore him out quite a bit.  This afternoon he sat in a chair for 4 hours, which is good for his lungs.  Tonight he got in a chair for dinner & he’s been sitting up for 2 hours so far.  He really wants to get a good night’s sleep tonight, so he wants to get really tired.  In the above photo, he’s sitting in his chair.  You will notice that he still has an open port in his jugular vein.  They won’t remove that until they are certain that his heart is responding appropriately.  He’s wearing a sock hat because his hair is messy & he’s wearing his sunglasses to ease the pain in his bad eye.  He still has 3 chest tubes draining, so that kind of gets tangled sometimes, but he’s really moving so little that he can’t really make much of a mess of it all.

We thought that he would be out of the STICU by now & be upstairs in a non-restricted environment, but because of some quirks with his heart rhythm, he’s been kept here for now.  His heart is responding beautifully to the new valve, but there are just a couple hick-ups that the doctor says will work themselves out eventually.

This evening Dave & Lauri Carnahan dropped off some cards that kids in Power Plus (@ LPCS) made for him.  He looked through them & we thought it was funny how many of them had ties on them!  Mr. Anderson is known for his flashy, unique ties!  He really appreciated those cards.  If you want to send him a card, too, send it to Parkview Hospital, 2200 Randallia Drive, Fort Wayne, IN 46805 Attention:  Robert L. Anderson, patient.  We hope he will be released by Sunday, so if you’re going to send a card to the hospital, please do it soon. 

Until he is released from the STICU, he is limited to immediate family visits only.  He’s had several clergy visits, which he welcomes & enjoys.  Clergy - Keep Coming!!!  But other than that, his visitors are limited to Connie, Kristie, me & Bob.  Since the surgery, his personality has been quite subdued by the pain & recovery process.  He really doesn’t want to talk much or answer questions.  Because of the vent tubes in his throat, his voice is very soft & hoarse.  Thank you for your thoughtfulness in respecting the limitations necessary for his health.  Soon enough he will be upstairs in a regular room & able to received short visits from friends & family. 

Tuesday, February 21, 2012

Baby Steps in Recovery

Monday night after I had posted my update, God again graciously blessed Bob by freeing him from the ventilator.  It all began when Kayleen Schlegel (Rachel’s girlfriend) stopped by during her break.  She works as a tech in the ER.  She talked a minute or two to him & got a little smile out of him.  His nurse, Millissa, told him that he had to be able to lift his head off of the pillow & control his head before they could begin the

At around 9:45 his nurse, Millissa, began the “trial” that is required in order to remove the vent.  The respiratory therapist turned the vent way down, so that it wasn’t really doing anything to help his breathing.  He was receiving oxygen, but that’s it.  He did fantastic during the trial, so at 10:45, Millissa called Dr. Sowden to get permission to remove the endotracheal tube.  Sowden gave the OK & within minutes, he had the tube removed.  As soon as he was free, the respiratory therapist had him do some exercises to help clear out his lungs.  He had to cough, which made his chest really hurt.  Clearing his throat hurt.  Blowing to have his lung capacity measured was hard, too.  But he made it!  He was the only heart surgery patient to get off of the vent on the same day as surgery!

Tuesday morning he was visited by Dr. Sowden, who is very please by his progress.   He had them pull the tube out of his femoral artery, which is another sign of progress.  After removing that tube he had to lie still for 6 hours.  He is still groggy because of his pain meds (Dilauded & Vicodin), so he doesn’t really talk a lot.  Yes, that’s a really weird experience - Bob, speechless!  He ate some Jell-O & has been sipping water & diet pop all day. 

In the afternoon his nurse Peggy had the job of detangling a lot of his tubing because they discontinued several of his medications.  It took her at least 15 minutes!  I asked her if she is the one who gets stuck detangling Christmas lights.  She laughed & said yes!  Bob’s day was pretty much sleeping with short periods of awakening with a little conversation.  If we ask him what he needs, he doesn’t know.  If I ask if he wants to take a drink, he doesn’t know.  “I don’t know” seems to be the answer he goes with most of the time.

There was shift change at 3:00 & he got his night nurse, Kim.  She’s a very competent nurse who watches her patients very, very carefully.  All of his nurses have been fabulous!  At 6:00, when his femoral artery had had enough time to close, Kim came in & started moving stuff around in the room.  She put a blanket over the chair, moved IV poles, shifted tubes here & there & told him it was time to sit up.  He told her he’s been getting himself ready for this all day.  Kim brought in 3 orderlies to help move him.  It was painful for him to sit up for the first time.  He became very dizzy & severely nauseated.  A little Zofran helped calm his stomach, but he was still quite dizzy.  He started coughing, which really hurt.  But after he settled down, he was able to sit in the chair for 30 minutes!  While he sat in the chair, Don Schlatter dropped by.  Don & his devoted wife Jewel are long time missionaries in Thailand who are retired now & live in the Leo-Grabill area.  They attend Grabill Missionary Church, where Bob also attends.  Bob was glad to see Don.  Don prayed with us, a gift that means the world to my dad.  He was so grateful for Don’s ministry to him.  Shortly after Don left, Bob began feeling weak & dizzy & decided he needed to get back into bed.  That isn’t an easy task either, so the orderlies came in again & it took over 5 minutes to get him back in bed. 

I spoke with Kim, his nurse, to get her assessment of how he’s doing.  She said that her only concern is that he has pockets in the base of both lungs where he’s not breathing deeply enough to get oxygen to those areas.  She wants to work with him on taking slow, deep breaths to remedy the situation.  He does have a slight fever (101.6), but his stats look great.  Tonight she plans on getting him in the chair a few more times, exercising his lungs & keeping a delicate balance of pain control.  She wants him to have minimal pain without drugging him so deeply that he can’t respond or cooperate with her directions. 

“Praise the LORD.  Praise the name of the LORD; praise him, you servants of the LORD, you who minister in the house of the LORD, in the courts of the house of our God.  Praise the LORD, for the LORD is good; sing praise to his name, for that is pleasant.  For the LORD has chosen Jacob to be his own, Israel to be his treasured possession.  I know that the LORD is great, that our Lord is greater than all gods.  The LORD does whatever pleases him, in the heavens and on the earth, in the seas and all their depths.  He makes clouds rise from the ends of the earth; he sends lightning with the rain and brings out the wind from his storehouses.  Your name, LORD, endures forever, your renown, LORD, through all generations.  For the LORD will vindicate his people and have compassion on his servants.”                     Psalms 135:1-7, 13,14

Monday, February 20, 2012

God is Gracious Again


Bob's Tower of IV Medicines

It’s been a long day already, & it’s not even evening yet!  Kristie picked my dad up at 5:00 a.m. To take him to the hospital for his surgery.  It doesn’t sound like he slept all that well.  How could you?  As soon as he got here they started prepping him for the surgery.  Connie arrived & said he got kinda loopy from the meds they give him to relax him.  I was almost at the hospital at 6:55 when my sisters called & told me they already took him back.  Drat!  I wanted to pray with him before he went to the OR. 

Connie, the Wizard of the Emerald City, was able to interpret the information on the surgery screen, so we knew when they started anesthesia, when they had everything prepped, when the surgeon started cutting... 

We got the call to go into a consultation room at around 12:30.  Dr. Sowden walked into the room with both thumbs up & a smile on his face!  The surgery went without a hitch.  He looked at the aneurysm & noticed that it was smaller than first stated.  He measured it at 4.5 MM.  Typically he wouldn’t do anything to an aneurysm that is smaller than 6 mm.  He said he wasn’t sure he would even call it an aneurysm.  He called it a post stenotic dilatation, which is caused by the bad valve.  Theoretically, once you fix the leaky valve, the dilatation shrinks & become a non-issue.  Dr. Sowden also cut two large holes in the pericardium, to drain the fluid amassed around his heart.  He hopes these two windows will remain open so that any fluid that forms between the pericardium & heart wall will be able to drain effectively.

What great news!  He expects him to make a swift, full recovery!  Praise God for His healing power!  The rest of today is going to be critical.  He is in the CCCU for the first 24 hours post-op.  We went back to see him.  The first thing we had to do was fix his hair!  As we were warned, his face was puffy & his skin was an odd color.  He was covered completely except for his face.  He had a endotracheal tube from the vent machine that was helping him breathe.  It was taped into his mouth.  He was surrounded by tube after tube after tube!  His IV pole was more like an IV tower!  So much stuff attached to him from all sides.  As we talked with his nurse, he heard our voices, opened his eyes & tried to talk.  His blood pressure shot up, so we tried to soothe him & calm him down by holding his hand, stroking his arm, talking to him & reminding him that he’s OK.  We told him he had to go back to sleep so he could rest.  I said he needed to sleep so he could dream of his one true love, my mom.  Slowly he settled down & went back to sleep. 

His nurse told us that he will be weaned off of the vent this evening with the goal of having him breathing on his own again before night.  He has an external pace maker right now, just as a precaution.  The doctor will have that removed when he is confident that his heart has reached a stable rhythm.  He has 3 chest tubes to drain blood & fluid from his chest cavity. 

Please continue to pray for Bob as he recovers from surgery.  We know he will be in significant pain for a while.  Pray that he will be patient with himself & the healing process.  You know how he hates to be out of the action!  I will provide periodic updates about his recovery.  To ensure that you are notified when I make a new post, please go to the bottom of this page & click on “SubscribeTo:”

Thank you for your prayers on behalf of my dad & his family.  We are so grateful that God has given us at least a little more time with our father!