Our journey of faith and difficulties as we struggle through the various diseases that have rampaged our family. Specifically multiple sclerosis and muscular dystrophy.
Thursday, December 31, 2015
L G Squared
I thought about making a list of how we had been loved and cared for this past year. Because man, we have been loved and cared for over and over again. God has provided to us over and over again through ordinary people. But the list is so long, I would never finish! And...I might leave something out because my brain is mush! But if I did, it would look something like this...house keeper, meals, counseling sessions, massages, cards and gift cards, monetary gifts, visits, phone calls at just the right time, errand runners, allergy shot taxis, furniture purchaser and installer, personal home renovator (aka Noel), happies delivered to our door .... the list goes on and on.
So I decided I would think forward into next year. I have no clue what details life will bring. We know we continue to stand in a fight against MS. And we know more chemo is on the horizon. We know more heartache is inevitable! But there is something that I think will be our life mission for the next year. We are going to try to live every day at the Smith House with more love, more grace and more gratitude!
More love...our love lately has been very conditional. As we embark on a new year, I pray that we would love like Jesus. We would love with no strings attached. We would love with pure hearts! We would love God, love each other, and love others like crazy...crazy love!
More grace...our children didn't learn to be judgmental all on their own accord. After all, God's grace is sufficient for each of our needs! So if God is filling us up with His grace...why won't we demonstrate grace to others around us? As we enter 2016, I pray that grace would abound. I pray that our judgmental spirits would be replaced with grace for others. I pray those unrealistic expectations we place on those around us, would be outlined with grace. I pray that God's grace would continue to sustain us each and every day.
More gratitude...we have days where we are grateful and thankful. Well, maybe I should say we have MOMENTS where we are grateful and thankful. A lot of other moments are not filled with gratitude! They are filled with dissatisfaction and complaining. I pray that we would learn in 2016 to see God's hand in everything. I pray that our hearts would continually be filled with praise. I pray our attitudes would show Jesus in us!
If we can simply remind ourselves over and over L G Squared. Love, grace and gratitude! All year long! No matter the heartache, no matter the situation, no matter the disease. L G squared. Love, grace and gratitude!
Sunday, December 27, 2015
Glimpses into our Christmas
Secret Santa delivers gifts early sometimes. At least he did last year and again this year. Really, I haven't even been able to talk or write about this topic very much. When I think of this Santa, I really struggle! I've heard everything my friend has told me about Secret Santa and receiving love and I try to apply it but then I find myself right back at those unworthy and uncomfortable struggles. Still working on processing that one! But it was a VERY special evening as we opened and remembered our Santa. And if Santa can hear and see this...it might give a glimpse into what we felt!
Homemade cinnamon rolls, pumpkin and banana bread, egg casserole, biscuits and gravy ushered in our Christmas morning! Yum yum! And then onto a new excursion for us on Christmas day. We felt led to purchase gift cards and just deliver to some people who were working! It was quite a fun experience other than the horrid rain and flooding!! When we gave the gift cards, the employees would just look at us with wide eyes like they couldn't believe we were doing that! Every one of them very gratefully received. They were excited to receive on top of that! There was much for me to learn in that experience. I receive gratefully sometimes...but I don't know that I am ever EXCITED to receive! The joy on their faces were so special. And then we did something else. We took two big pans full of home made cinnamon rolls to the ICU where Zine spent a week. We all thought it was a great idea! But oh my goodness, I stood right outside his room at the nurses desk as we chatted about our thankfulness for all they had done for us! And emotions totally OVERWHELMED me. I walked out of that hallway to the elevator and the tears began to flow. And they flowed on and off all day long! I don't think I was ready to do that! Zine and I talked about it later...we called it Post Traumatic Stress!! It was definitely a trigger point for me! I was telling a friend about it and she wanted to know if it was healing. And I still don't know the answer to that. It didn't feel like healing...but...then again...maybe it was!
This was our second year to not be with our family! It is indeed still difficult for me. Zine seems to be content and I think grateful to be just us. A sweet phone call came as a FaceTime and I got to chat for a minute with my family! For that I was super grateful. Somehow it came up later and I asked Krisann if she would rather have Christmas here or in Arkansas. The answer was here. I asked her why and she said because Santa comes here. I asked her if she remembered when Santa came to Arkansas and she has no memory of those experiences. It made me incredibly sad! I have two kids who have been raised with lots of family around and have such sweet memories. But Krisann...this is now normal to her! At four she was still small enough to not carry those memories forward! And it made me think of all the memories Conner and Chloe will have of life pre MS and how much Krisann will never know. Gut wrenching! I tell Conner and Chloe they have to tell Krisann about the things dad used to do! And over Christmas I watched Conner do something for Krisann that ushered in lots of memories. Krisann got tired walking and Conner reached down, picked her up, and put her on his shoulders! This was one of those moments that melted my heart. You see, that was what Zine used to always do with our children and Krisann has never been on his shoulders! The other two got many miles up there on his shoulders!!
Even through Christmas, it has pricked my heart to cry out more to Jesus. Yes, I have been mad at Him...(sort of). Not sure mad is the accurate word! But definitely knowing that He is the only One that can take this heartache of MS away and He has chosen not to! So sometimes I do get frustrated when I know beyond a shadow of doubt He can take it all away! But through the Christmas season, it has pressed me into a deeper heartfelt request and longing...Jesus please take this MS away! Please please and please. Please please and more please. I remember looking at our pastor one day and saying I just want it all to go away! I think I may have even had pleading eyes and asked him to make it all go away! Sometimes, there's just a desperate feeling to be rid of MS! We are in one of those seasons!
But...even amidst all this...as I reflect on our Christmas...there are many fond memories I hope will stick with me. I loved the blessing others on Christmas morning. I loved our secret Santa time on Christmas Eve. I have LOVED having Advent Family devotionals for the month of December. Those have created many sweet family moments! So amidst the struggles, there have definitely been some sweet sweet moments!
But yet here comes Monday, and we embrace this MS stuff again with a doctor appointment with oncologist. It is never ending.
Tuesday, December 22, 2015
Conquered
Wednesday, December 16, 2015
Blood Out and Blood In Is Wearing Us Out
Monday morning we began our day early for a surgery to put in a central line. |
Friday, December 11, 2015
Yes! We survived today!
Today Dr. G gave us lots and lots of details about our upcoming adventure. We have a definite plan but that definite plan is up for changes at any point. We are planning for a treatment on Monday, Wednesday, Friday, Sunday and Tuesday. However, there are many complications that are possible. We are starting outpatient but very much understand there is a chance that we could end up admitted at any point. We understand that Zine's platlets can drop and if that happens then the whole schedule goes out the window. We understand that we are looking at various IVs to replace some things that will be lost or damaged in the process. We understand the risks. But amidst all of the scary things we heard, Dr. G looked at us and said, with as much comfort as I've ever seen him exhibit, I have never lost a patient in this process. We will cling to that over the next couple of weeks as a piece of comfort for sure!! He also said to us, I would love to come be with you during this process but often it is when I am seeing patients. But I will do my best to get to the hospital and see you as you go through this. But assured us that he was the one making the decisions and he would be informed each time before the process began and he would be the one deciding if we proceeded or if we didn't. So...I felt like we saw a different side of Dr. G today. We saw a great deal of compassion from him today!
We then walked to a different hospital building and met with the vascular surgeon. We both really liked him. He and his nurses were super nice to us as well. He explained that they would put in a dual central line. Compared to the port this is a large tube. He wants to try to keep the central line away from the port. If an infection were to set in, if they are close together then they would both be at risk. So the hope is to put the central line on the left side if possible. But that could change when he gets Zine to surgery and actually threading the tubing to where it needs to go.
So all that took us 5 hours!!
On Monday, we will be at hospital at 7:30 where they will do an outpatient surgery and insert the central line. When we are done with that procedure they will send us to where he will have his first blood process done. So we are prepped to be there all day long on Monday.
I know that God is with us. It is no coincidence that this is Christmas season when we often refer to Christ as Immanuel--God with us! So that has really stuck out in my mind today. God is with us. Definitely don't want to walk this path. Nope nope and nope. But as I told someone earlier, I might shed lots of tears between now and then but come Monday, I will put my brave face on and I will embrace our day. Kinda like telling your children to be brave before they get their 4 year old shots. (which by the way I think are the absolute worst)!
I asked Zine how he felt about everything so I could put it in the blog post and he didn't come up with any feeling words. He grimaced and said, it's another surgery! He also said I hope it helps. So I think he's pretty disengaged from the situation right now. He is in function mode. Doing what needs to be done!
I am personally very tired tonight. Krisann and I both are struggling with loads of congestion. I have been teary eyed today. And feeling overwhelmed at times. But yet I am calm. There's no frantic feelings. There is an apprehension and a bit of fear about what's to come. But I think there's a peace as well. God is with us and that promise I am resting in and if I'm not resting in it, I am speaking it to myself!
We do cherish your prayers the next couple of weeks.
Thursday, December 10, 2015
The New Adventure
At 9:30 we meet with the oncologist and receive nitty gritty details of this season of our life.
At 11:30 we meet with the vascular surgeon who will explain even more details to us!
We will have a busy weekend of trying to finish up Christmas shopping, choir practices and Christmas musical, and a bit of fun for our kids hopefully, before chaos ensues.
Monday Zine will have an outpatient surgery where they place a central line! Yes, he will then have a port and a central line. Just sounds like a recipe for disaster to me! But...we trust in the doctors making the decisions!! And then after the line is placed he will have his first procedure with his blood of removing his attacker cells!!
Please pray that we would be able to process the needed details tomorrow. And pray for our emotional stamina.
And really, for me (Karen), I don't think I have ever had a season in my life where I feel as alone as I do right now. The aloneness is often very overwhelming. I know there are a lot of people loving us and praying for us, but that doesn't remove the smothering aloneness I have felt the past several weeks. I try the majority of the time to hold my head high and march on with life! But I have my moments and the past few days, I have had many moments! But I am doing what I know to do, I am begging God for Him to do in my life what He desires to do in me!
As far as Zine, he is dreading yet another surgery. But he is such a trooper. I would complain loudly over and over again! And he really doesn't! On occasion, he will complain! But when he has a plan and he knows what has to happen he is the best patient ever. So that's where he is. Dreading the surgery but resigned to this is the way it is and he just "wheels" forward!
Let the New Adventure begin! An unknown Adventure, uncertain of the outcomes, and unsettling the insides. Intimidating and scary. Reminding ourselves to trust in the One who holds all the details of our lives in His hand! And continuing to trust that our doctors are working for our best interest!
Tuesday, December 8, 2015
The Blue Day...rails, chairs, and days of wondering
Thursday, December 3, 2015
The Next Two Steps
At our oncology appt two weeks ago, the oncologist brought up something that Zine nor I ever had heard of. And we didn't share that information with anyone as we wanted to wait until we met with Dr. L. As it turns out, Dr. L had mentioned it as an option before but Zine nor I neither one remembered.
In light of the fact that traditional methods nor chemo have worked, we will begin a procedure that is not done often in the United States. We are in the waiting mode while doctors communicate with each other. Zine's blood will be taken most likely from his port, it will be ran through machines and the cells that are attackers in his body, will be removed from his blood and then his blood will be given back to him. Until we hear back from Dr. G at The Cancer Center we definitely do not know all the logistics. But we do know Dr. L expects it to begin possibly as early as Monday. Until just recently, this procedure has required a two week hospital stay but in the last year some doctors have begun to do this procedure outpatient. We believe that this will be outpatient for us as well. If it is outpatient, it will require us to go every other day for two weeks for this procedure to be completed. But once again, we will not be certain of details until we have communication with Dr. G. It was a blessing for us to have two very important doctors to agree that this was a great trial to see if it might help. This does not treat the disease, but if it could help with some symptoms then that would be good!
Step number two is chemo! Which one was the question? We had our list of questions that we had developed as we researched. And as always, Dr. L was very good to answer each of our questions and concerns. The final decision...step two is that Zine will take a 5 day chemo. He was scheduled to get this chemo in November but due to the blood clots, we missed it! There is over a year long waiting list to get this drug. However, we will not have to wait nearly that long. We expect to have the weeklong treatment by February.
We have come to understand that I am going to become very good friends with the nurses at Dr. L's office!! This is a process and details will evolve on a daily/weekly basis as needed. So although we like plans and dates on the calendar, this is one of those situations where we will have to walk through very loosely! But we know for certain these are our next two steps and the logistics will be worked out as needed.
With the chemo, because of risks of autoimmunity, infusion reactions and some kinds of cancers, we will be put into a restricted program called the REMS program. (Risk Evaluation and Mitigation Strategy) This chemo is only available at a handful of locations across the United States and has only been approved in the past year. We are very blessed that our dr was the first doctor in the US to administer this drug. So although, it will require a week long stay at Cullman, it's not like it is forever away! And we are able to get it with a doctor that we already have a relationship with.
Now as Dr. L stated, I don't want to give you any false hopes. This drug nor the other chemo drug, that will follow a few months after this 5 day one, will come with any great amount of hope or research that it will change Zine's progressive disease. The drug that came with the most hope, didn't work. But these two things are the only things we have left to battle with. And it is a battle. We will expend all battle weapons that we have to fight with. And this is part of the battle plan! We fight not with a hope that these drugs will work. However, we do fight with a hope that there is Great Physician that has the power to heal at any moment! And we fight knowing, that even drugs that aren't expected to make a huge difference, that the Great Physician could choose to use one of those to bring His healing! So the battle is worth fighting! If we were old and our kids were grown, we might feel differently. But for pete's sake...we have a 6 year old, a 15 year old, and a 17 year old! The battle is worth fighting!
Thank you all so much for praying us through our day. I have many details that I can share but those will have to come in future posts. This does not even begin to touch the emotions or the relationships involved in these decisions. I have just wanted to get an update of facts to you as it relates to our next steps. And I feel bad that it has taken me this long. But we were needed to be with our children as they process this information which is very difficult information to process. We know beyond a shadow of doubt that we were prayed for all day! Thank you!
Continue to pray as the next adventure of our lives unfold before us! We are very tired! We are pretty emotionally spent right now. A simple hug from a friend brought tears to my eyes a few minutes ago. An hour in a counseling office brought a dumb truck load of tears today! But we are walking in complete confidence that our doctors and us have made the right choices and there is great peace that we are in the middle of God's plan for our lives at the current time. That in no way makes this place an easy place, but we walk with a peace and confidence in the decisions and path ahead!
Thank you for journeying with us and we hope that even in this post you see the great struggle but also the great faith we have! And may God use our words in the middle of your darkest struggle, that you would know there is still a hope and a faith in the One who loves and cares for us so much that He began our lives with a kiss a breath from his heart to ours!
Tuesday, December 1, 2015
Wednesday is a Big Day
We then meet with the neurologist later that afternoon. Yes, we have several hours to kill between the appointments. So...we are taking an unexpected little adventure.
We are taking all three children with us tomorrow! We will do our school in the waiting room while Zine has MRIs done. Then we are headed for some lunch out and fun family time. Zine and I will return to doctors office and we will let Conner bring the girls back home and then head to church. Conner's not driven from Cullman to our house before. But we have great faith in his driving skills! And talk about kids having to grow up fast...Conner has most certainly had to do that!
At the appointment with the neurologist we will be discussing information from the oncologist and comparing notes with neurologist. We are praying for great wisdom on the next step. We do know a different chemo is going to happen. We have two more to try. So the question is...which one do we try next. That decision will be made tomorrow! We think we know what that is...but...everything is always up for change when we walk into the neurologist office!
Whatever that decision, our lives are about to change again. And everyone in this house struggles with change! But we are walking confident in the promise that God will never leave us or forsake us. God is always working His good in our lives And lastly, it is when we are weak that His strength is made perfect.
Thanks for praying for us through this journey and especially as you pray for us through our day tomorrow.
A side note...Zine is adjusting well to his new wheels. He's still not a proficient driver yet...but he's doing fantastic. I think I've had a harder time than he has. I had adjusted to seeing him in his manual chair but the power chair...it messes with my insides!! That's just wrong to see your husband in a power chair!!!! And...I am going to be totally lost and not know what to do not pushing him around. I will have to find a new identity I'm afraid!! :-)
Another side note....I came in this evening from picking Chloe up from art class to a laundry room with water in the floor. My washer apparently decided it was ready to leak! But you know, I didn't freak out, I didn't fall apart, I simply gathered towels, dried water, moved my washing machine out to dry water from underneath it. It was a calm moment for me. For that I'm grateful. However, in moments like that, I really hate my hubby has MS! I still remember the day, before we had iPads and smart phones, watching Zine walk from the study to the laundry room to the study to the laundry room. I finally asked him what he was doing and he said I am fixing the washing machine. He was watching a video a section at a time, then going and fixing the washing machine! And guess what...it has worked perfectly ever since! But now...there's no Zine taking my washing machine apart! I wonder...can I watch you tube videos and fix my washer?? I might be caught trying it this weekend! But I'm not thinking about that stupid washing machine until we get through our day tomorrow. First things first!! And as I am going through my day tomorrow I will remember this scripture verse. And I know I've posted it before, but there's a song that speaks to my heart often called We Will Not Be Shaken.
Saturday, November 28, 2015
Let the seasons change
Currently, we are making decisions about the next chemo we are going to try. Wednesday the decision will be made! The struggle is relentless. Conversations of long term side effects, short term side effects, possible results, timing of treatments, etc. seem to infiltrate discussion after discussion.
Relationally, a year ago, we had a sweet relationship with each other. However, over the past year, the relationship has struggled. Especially in the past three or four months marriage has just been exceptionally difficult. And for the past two weeks, we have lost count as to how many serious conversations/discussions we have had. And those discussions are physically draining. Healing and mending relationships take time! We have to remind ourselves we didn't get to this place over night! But at same time, so grateful for the improvements that are taking place and the healing that is in the works!
One of the things I have told Zine since we started dating is that he gave the best hugs!! And he did!! I have melted in his arms more times than I care to count! That's been my safe place! But...I think we need lessons on how to give hugs from a wheelchair. They just aren't the same! There's something different about your husband pulling you to himself and holding you than there is for me to bend down and let him put his arm around me. Just being real here....
Our children have become more impacted by MS over the past few months as well. And they all struggle so differently!! I'm sure the home environment has played a part. I think just accepting reality has played a part. As a parent, to watch your kids struggle is very difficult! I can't imagine the pain it must be for Zine to watch his kids struggle because of his disease! But I remind myself constantly and I remind Zine on occasion that these struggles make them the person they are today. (And I happen to love each one of these persons just the way they are!!) These struggles are preparing them for the plan God has for their lives. And we must remember it is not our job to be God in their lives! Our job is to love them through this season! It's God's job to protect them from unneeded pain!
Anyone who deals with a long term illness, understand this...your friends often disappear. They get tired! You get tired of needing things. Relationships just struggle. Friends don't know what to say. And if they do say something, it is sometimes greeted with frustration! You begin to feel that you are simply someone's mission project at times. Keeping relationships in tact is simply put...difficult. There is always a grief when I think of changing relationships. If I could only learn to just hold on during those times of change. God always is providing but I just don't want relationships to change.
I love the phrase that a sweet friend used to tell me all the time....this is for a season Karen and the seasons always change! I am so grateful for that truth she poured into me over and over and over again! Sometimes when we see the season changing, its scary! Sometimes we see the season changing and we're grateful. But there is one thing that remains constant even as the seasons change, and that is His presence is always with us! He goes before us, He stands with us, He walks behind us (and gives us some pushes periodically), and on occasion He simply shows Himself to us in very real and tangible ways.
So I am watching the seasons change these days. A relationship that was good, then struggled immensely, and now is working it's way back to more steady place. From changing sheets three and four times a night and lots of trip to a bathroom to a permanent cath. A disease that did not respond to chemo, but it did cause blood clots, and now a new chemo is on the horizon. From kids that have been accepting and loving to frustrated and angry. From kids who sometimes seem to have it all together to other times they are falling apart. From kids who didn't really understand to a time of intriguing questions and thoughts as they seek to comprehend. From feeling connected to feeling disconnected. From having time to focus on others to having to focus inwardly. The seasons are definitely changing!
Saturday, November 21, 2015
The Week that Went and Went and Went
After our visit to Madison Hospital, I then made it to Birmingham for my one month follow up from my surgery. Now...when I first came home from hospital I got to do physical therapy with this stick every hour. And let me just say...it was torture. My mouth indeed did not open to that marked line, until about try number 5 or 6. I was supposed to do these exercises 10 times for a count to 10 every hour. And then at 2 weeks post op, I was able to go to 5 times a day! I was so sure that when I went back this time, he would say I could stop! But oh no!! It didn't work that way at all! Scar tissue is beginning to form and things were not opening like he wanted. So I'm back to the stick every hour! Arghhh!!! I have been very diligent to do these exercises because the thought of having to do that surgery again because scar tissue built up definitely doesn't warm my heart!! So...the stick and I are getting to be very good friends.
I left Birmingham late afternoon and travelled home to have a painting night with these fun ladies.
The rest of Thursday was spent in counseling session with Chloe and I. It was one of those sessions where I walked away and went...wow I didn't know we had THAT much going on in our lives. To summarize the counselor said in closing...let's think about this...1, 2, 3, and she continued to count to 7. 7 major things that are going on in your lives. Well, when she put it in summary like that I saw for the first time what all was going on. When you live in chaos...you just function. You guys think all the time, we have so much going on! But that's not how we feel about it the majority of the time. We are just in the middle of life, making schedules work, finding time for rest, fun, work, etc. Just like normal people. Except ours usually has numerous medical appts on regular basis. And when it is summarized 1 thru 7 it didn't sound too normal! But just when you think wow, our plate is full...there's this phone call.
Mr. Smith is to report to an ophthalmologist office in Cullman at 7:40 Friday morning! YIKES!! This wasn't on my to do list either!! He had been to the eye dr here in Huntsville. There was some concern about one of the tests that they did. The eye dr called Dr. L, our neurologist. And then called us late on Thursday afternoon and asked us to be there the next morning to see this specialist. They did have equipment to do some testing that most do not. As it turns out the test the dr was worried about here....well...it turned out fine. But what we did learn, the issues with vision are actually not related to his eyes. They are all neurological! The doctor said he was almost certain that Zine had a lesion that had developed across his brain stem. That so far things were still communicating but they were a lot slower to communicate. Many of you may have noticed that you can talk to Zine and it appears that he's not looking at you. His eyes do not work together...they actually work against each other. When his eyes aren't working together it also makes his depth perception way off. Which we notice this difficulty the most with driving!! Making driving decisions or rather when is it time to not drive can be VERY difficult. For those of you that maybe have older parents you can sympathize. However, the difference between an older parent and Zine is he's young. He still desires to work for as long as possible. He is needed to help with kids. So this is an area that doesn't have cut and dry decision in. The eyes technically work. But the problem is everything is slower to connect. And depth perception is off. The dr. did say to give plenty of space between you and car in front of you! But he definitely didn't say no more driving either! But this is one of those areas that I pray about everyday. That God would give us great wisdom to know when the time has come that driving is no longer safe. And when that day comes...it is going to be a VERY SAD day in the life of the Smith Family.
Zine is scheduled for an MRI on Dec. 2. And then we are scheduled to see the neurologist that afternoon. They will be able to tell from that if there is a lesion across his brainstem. But we are pretty certain there are many new lesions so we don't really need an MRI to confirm that! Chemo hasn't worked and that's obvious! Now we move forward to next drug. That decision will be made on Dec. 2. So we know we are in for life changes again. But I have to admit, not having chemo looming over our heads while his lungs have healed has been very nice reprieve.
By the time Friday night got here...I was past going! I really thought I might be sick. I got in the bed at 8:30. That never, I say NEVER happens!! But my body was done!!
So...we are glad this week is almost over!! And we are praying for God to strengthen our tired worn out bodies! We are continuing to pray that our angel encounter will make long term changes in the relationships in our home. That God would continue to give wisdom as needed. Praying that God would fill our home with peace and joy and contentment despite the difficult circumstances that exist. And extremely grateful that God chose a simple person to communicate big things to us this week. Pretty sure I will NEVER forget that experience! Also grateful that the week that went and went and went some more is almost over!
Monday, November 16, 2015
Unexpected Appointments
I have come to believe that when the Satan chooses to act, seeking to steal, kill, and destroy with his plans; the ×™ְהוָ×”, Who is our God, cheers as His good for us is revealed to us, correcting our concepts regarding ourselves and Him. Is that wordy enough? Let me try to explain with an occurrence from today.
I have a relatively new shower chair (~1 week). A wheelchair shower chair. It is very impressive almost to the level of intimidating. With Karen's help, I have discovered a way to transfer, dry off, get dressed, etc. to use this new inevitably thing. Last night I determined to find a new method for one small point that was disturbing me about it. The chair needs to be pushed further into the shower after I have transferred onto the changing bench. Previous to last night I had simply pushed the chair while seated further into the shower. inevitably it was pushed too hard and would run into the end of the shower with a wonderful 'THUD'.
It was time for that to be corrected. Rather than following protocol, I adventured to follow a different method that would 'place' the shower wheel chair in the shower rather than push. This would remove the 'THUD'. I had a great idea. It would work! It would be PERFECT and everyone would be happy and I would be impressed with myself! What could go wrong? Murphy. Murphy is what could go wrong.
In my planning I forgot that the floor would be wet, the grab handles would be wet and my hands would be wet. Those three things do not play well into my wonderful plan. Plan broken. Idea undone. Pride crushed. Fall taken. Bad. Bad. Bad. Then Satan had stolen (self concept of worth), killed (my hope), and destroyed (my desire to not impact my wife with my disease).
Taking blood thinners now since the wonderful days of hospital stay (24 hours post chemo) now creates issues with any fall. The fall wasn't what I would consider far or hard, but I did have a mark and a bruise last night. Karen marked the extent of the bruise with a sharpie and checked it again right before going to sleep. Nothing looked too troubling.
As the day began today Karen was very interested in the area that I fell on (my lower left hip). She noted that the bruise on the surface was not appreciably bigger but that there was a significant knot and it was very warm to touch. Calls were made. Conversations were had. (Not really including me, mind you, but between Karen, the doctor's nurse and the doctor. I really shouldn't be included in those conversations given my past.) I was given an appoint for today for an X-Ray to be taken to determine if the bleeding was anything that needed to be dealt with. Yeah, another medical thing. Another schedule impact for Karen on a busy day. Another drain on finances. The reason? The person typing and the disease he has. Steal. Kill. Destroy.
I was at the Imaging Center for the X-Ray today. I expected to hate the whole thing. I didn't want an X-Ray. I didn't want to cause Karen's day upset. I didn't want to spend the money due to my stupidity. Karen checked me in and within minutes we were called back for registration. ID. Insurance card. Standard questions regarding advanced directive. Lame joke from me about how much better Karen's life would be with out me. Standard stuff from me to pass the time. The lady typing wasn't impressed. She called me out for my words and how my words caused great pain in my wife. She called me our for what I said and believed about myself, my wife, my family and my God. She looked me in my eyes and told me that she could see the hurt, pain and anger that I kept in my heart. She looked me in the eyes and told me that I was loved. I was loved by my wife. I was loved by my family. I was loved by God. God loves me. She repeated several times that I was loved. I was loved. I was loved.
I sat there and cried like a little girl. This was not what I had appointment for. I came to have an X-Ray for a mistake I made. God had an appointment for me that was different. He had placed a sister in Christ to speak his words of truth and life to me. Truth that I wasn't willing to receive from my family or friends. Truth about who I was. Truth about what I was doing when I did not believe my wife and her love. How she needs me and wants me to be with her for as long as possible. I am not a weight on her or a trouble. I was hearing my Father speak audibly through a 50 year old African American lady who did not know me but knew me deeply.
I have never experienced my God that way before. I am overcome by what I was told, how I was told and how I was encouraged. My God loves me. My family loves me and I am not a weight on their life. I am a blessing to my family and they like me around. God loves me. God likes me. I am important and not a burden.
Not the appointment I had scheduled for today.
Saturday, November 14, 2015
Inside the House (Behind Karen's Walls)
Inside the House (behind the walls)
I wrote this quite some time ago but it never got published. By some time ago I mean November! The truly sad thing is that I could have written it this week with only minor changes.
You have likely been reading here for a while and have gotten a fair view from Karen about the life she lives and a lot of the struggles of our home. The struggles are deep and ongoing. Sometimes Karen and I are not on the same page and that makes the struggles almost overwhelming and hopeless. We get on different pages when I have a particular view of what is best and least impactful on the family and Karen has another.
Discussion. Discussion. Discussion. All of us who are married have heard this advice for marriage unity and happiness. Like most married couples, we forget this wisdom until everything comes to a head and the wisdom must be applied or the union falls apart. I thank God that we have never let the union fall. Though it is often the hardest action taken, responding to an olive branch offer of open conversation with the one you love positively is the greatest act of growth and healing for the marriage union.
We found ourselves there again recently. I missed the first olive branch (that I know of). Thankfully she was loving enough to present another. I don't see what most would consider obvious. She has taken much time and effort over our entire relationship to help me see. This time I received and engaged in a very difficult discussion about our union, MS, what I see as the war against MS, the collateral damage from how I was fighting that war, what Karen sees as the war, how she sees fighting the war and what we can do to defend the union together in this war. I had done deep damage to her. I had taken damage from her.
Like all damage, healing doesn't happen in a moment. We are now both damaged people, damaged by each other but who love each other deeper than the damage. It is very difficult for me to recover from causing damage. It exceptionally difficult for me learn that my way isn't the best for me, others, or anyone really.
It is really difficult to attempt to change course when the changes that you think you have made are not observed or trusted. That makes for a hard relationship to grow and heal in. Thus the long and difficult road of unity. I know that this road isn't a dead end. I know that I have a companion that is committed to the journey. This gives me hope.
Sunday, November 1, 2015
Good or Not Good Part 2
First, I totally lost it. I called a friend after I found out I was going to have surgery and she told me later she sure was glad she had caller id as she had never heard me that frantic. It was bad!!!
And...it didn't get better. It continued to bad. The more I tried to settle down the more of a wreck I became!
I was MAD that I had to have surgery. I looked at my family one day and said please understand I am not mad at you. I know it probably feels like it but I'm just mad!! And when I am mad, I just want be alone! Unfortunately, I live in a house with 4 other people. Alone rarely happens!
My friends who would normally be caring and loving were all in a difficult situation and didn't have the time nor energy to encourage me. I talked to one of my best friends on the phone the night I found out I had to have surgery and she was so emotionally spent herself she didn't even remember I had gone to surgeon that day. I wasn't mad or hurt over that at all. But it did lend itself to where I went in my life.
I went into do it yourself mode. My friends are all emotionally spent. They don't have time to care right now. I just want to be alone. I want to figure out how to make this all work all by myself. And then all of a sudden...God was not good again! What about all those things I learned? Well, they were easily forgotten and I went back to God is most definitely NOT good!! So therefore my other post sat in my blog just waiting for me to publish it for a LONG time!!!
But then what God did when I was at the end of myself was pretty amazing!
My pastor took time to encourage, love, and speak truth. I will forever be grateful for a pastor who loves well. And some days I'm grateful for a pastor who speaks truth. Sometimes...not so much!! But he called my hand on my self reliance that day! I think I even told him I didn't want ANYONE to help me! It was a bad moment for Karen Smith! But it was quite an honest moment.
I will forever be grateful for a pastor's wife who loves well and who cares greatly for others! Geesh, I'm sicker than a dog and she loved me well in the middle of that! And I will be grateful for the time they spent with Zine and I loving us well. I want some time with them when someone is NOT sick! I think we deserve that!
But then...that was just the beginning of God's gifts.
I had an aunt that unexpectedly called and said she wanted to go with me to Ohio. Two months previously she had had surgery and she understood exactly some of the pain I was going to have. When you can't hold your hand up to dry your hair...it's pretty desperate folks. Especially with frizzy hair like mine!!! Grateful for a last minute phone call that says I'm going with you! Wow!! What a gift! I don't even want to imagine what my hair would have looked like if she had not been there. When she left and I tried to dry my hair I realized what a blessing that had been! Not to mention that Chloe was about to have a nervous breakdown about going with me!! And that phone call calmed her spirit in a half of a second! That was a good gift for sure!
I had another aunt who stayed at my home and just blessed us all tremendously that week! Truly a gift from God.
But let the gifts continue...the surgeon told me that it was going to be excruciating to fly and that sucking on hard candy might help. Did I ever get hard candy...nope!! But guess what at the check in counter there were bowls of peppermints! Really? God did you really just do that??
Oh wait that's still not all!! On the first airplane I met an old friend who helped us in the Atlanta airport and showed us exactly where to go. Even took extra stops along the way with us to show us elevators. Wow! What are the chances of that happening?
Well, it's no fun to have surgery and to have to recover. But at least I got to recover the week that I was already scheduled to be off work. So I didn't have to take another whole week off for recovery. I was able to recover and Ohio it at the same time. So thankful for that!! What a gift! Not an easy task to say the least but a gift when it comes to being off work!
So when I step back and look at these things...I have to say God is really good! I didn't ask for my pastor and his wife to take care of Zine and I the day of surgery, I didn't ask an aunt to go Ohio, I didn't ask for peppermints, I didn't ask for a tour guide of the massive Atlanta airport and I sure didn't schedule surgery so that I could recover in Ohio!! I did ask an aunt to come stay here but she went way beyond anything I would have ever asked for while she was here! Hmmm....things that you don't ask for but you receive. Doesn't that sound like a gift? And weren't those good gifts?? And since I didn't ask for these gifts but God made sure I had them doesn't that mean that God is good if He desires to give good gifts in the middle of chaos?
Once again, I was brought to the same conclusion...God is good and He cares for our simplest needs! Now...I need to learn to not doubt His goodness. That shall be the hard part. When chaos comes, to not let that alter truth about God. And I need to learn to gladly accept those gifts...and that's an even harder part of learning!! It is a constant battle I shall not tell a lie! Simply just being honest with a friend tonight was hard! It's much easier to just walk around and say we are okay than to be open with my heart and receive comfort and care!
God gives good gifts. But I often just refuse them!
God is good! But I often let truth become clouded!
Wednesday, October 28, 2015
Choosing to See Today
"You have a type of MS that there is no treatment for. There are no real clinical trials going on for your type of MS. The shots that you give yourself daily, they really aren't of any use. In 5 to no more than 10 years you will be in a wheelchair full time."
These words sent our world spinning out of control. I chose to write updates everyday for those that wanted to follow our journey. Today as I go back and read notes, there is one thing that comes glaring out at me...God's fingerprints were all over our lives at the time. Some of the time we recognized His touch in the moment, others weren't obvious until sometime later.
Most recently, as we have had our world totally fall apart again in November and in December and in May and in August and in October, I think the same is true. Sometimes we have recognized His touch in the moment. Other times we haven't seen His touch. But just because we haven't seen His touch doesn't mean He was not there!
I actually think it has more to do with what we choose to see! Zine and I don't always choose to see the best. We don't always make the best of a bad situation. We would rather turn our heads to pain than let God work in those moments. We would rather function in our own strength rather than letting God work His will in our lives, especially when it involves other people fulfilling His will. Zine often says, I'm going to die anyway so why bother?! I sometimes say, I am done! We both often wonder, how we can keep enduring and keep moving forward. Weariness is a common place we visit!
But today as I have reflected on the past five years and very much recognized all the fingerprints he left in our lives that week, I have prayed that God would help me choose to see His touch in my life everyday! I have prayed that as Zine and I continue to walk a very difficult road, that God would help us choose to see Him at work in our lives and respond to Him in the right ways! I have prayed that in the next month as we make a big decision regarding the next step that His calming presence and His loving touch will be ever-present in our home and in our lives. I have prayed that our children, who each struggle in their own way, would experience God's fingerprints in their lives and that they would choose to see His touches! May we not walk past moments and write them off as coincidence. May we not avoid pain, because it's easy. May we not walk in pride but rather complete humility. May we not let fear control us! May we not let anxiety overwhelm us. May we not waller in the the mud pit of pity. May we just choose to see in the midst of chaos that God is there and His fingerprints are everywhere if we will only choose to see! And may we be thankful! These prayers are not a one time prayer. These prayers are a daily prayer!