Monday, April 21, 2014

"No news, is Good news," so I guess this aint' such Good News!




We've been running a liver marathon over the past year and hopefully THIS TIME we can cross the finish line. We are so freaking close (excuse my language Grandmas). We have truly appreciated the way in which everyone has been sensitive to our situation.  We have felt each and every prayer and sweet thoughts on our behalf. Everyone has treated us with the perfect amount of respect (letting us know they are concerned but not asking us all of the time). We are very aware that Alec's health issue doesn't just affect myself and Miles.  The effects are far reaching and for that we are sorry but also grateful to have your hearts in sync with ours.  



It's been a very weird  year.  Lots of ups and downs. The best way I can describe what we have been feeling is emotional whiplash. Kicked around when you are already down on the ground.  It's amazing just how much of a beating Alec has taken as well as myself for witnessing what he has had to go through. I am very proud him.  No one else could go through what he is going through with such courage, faith, and optimism.  Our doctor just came in and asked Alec how he was feeling.  Alec responded in his little hospital bed, "Terrible."  I was completely shocked with his response. I told the doctor that if my husband said that he felt terrible he means it! Because usually he says, "I'm ok."  The doctor replied, "I know. We all know. This guy is as tough as they come." It has been a whole year living poorly and the kid needs a break.  Hopefully its coming soon.  I can't tell you how wonderful it feels to have doctors treat you that truly knows you.  You don't have to repeat the same stuff a billion times to ten different people.  They have been with us every step of the way and for that we are so grateful.  Talk about Heavenly Father having our backs.  I can't imagine going through this in a different state, or even hospital.  We are so impressed with our doctors sharpness and love.  I think it is very rare. 

                                       
People often ask us, "How are you guys doing?" We typically reply with, "We're hanging in there."  I think we decided to stick to that answer because it was just getting to hard to tell people the details of our lives and watch their reaction.  So much sympathy, compassion, and heartache in their eyes for us.  We live this life everyday. Some days better than others. Sadly, we have become accustomed to our new life. But, others have not.  It hurts to watch others hurt for us. We would rather not worry others, especially those who are far away. It's a circumstance that is beyond our control and yours. But, now you are lucky (or maybe not lucky) because I feel like telling you what has gone on over the past year, especially recently.  Alec has been on a feeding tube (called TPN that comes from a port in his neck) for a little under a year.  This gives him 100% off his daily calories and nutrition.  He has had such a poor diet (no diet at all) that this really acts as his life support.  He's a skinny guy averaging around 145-150 at 6'2". I don't even want to think what would happen if he didn't have this intravenous feeding.  He's been eating ice chips and popsicles for the last 2 months about.  He throws up at least once a day. He is nauseated all day long.  He is weak. He has lost pretty much all of his muscle mass.  He gets dizzy.  He can't drive. He has shortness of breath. He gets muscle cramps. He needs a babysitter (i.e.) to watch over him everyday.  His mind is foggy.  He sleeps allllll the time.  He has short term memory loss. He moves from bed, to couch, to bathroom, to couch, to a chair in the sun outside, and back to bed.  He is plain and simple: exhausted.  And why wouldn't he be? So, with all of these symptoms creeping up a little more intensely just in the past couple of weeks and especially the last 2 days, it was time to go back to the hospital.




Yup, we had to come to the hospital last night.  Although Alec's main problem is his liver, his kidneys have taken a beating in the process. So, we are back giving them a lil' TLC. We just had some of the team come in and give us an update on Alec's x-ray and ultra sound.  I shared the information over the phone with Alec's father Vince. He is such a stinking smart man, and I'd rather relay his response on Alec's diagnosis than my own.  His way makes more sense.  (Also, please excuse my poor grammar and sentence structure.  Half of the problem is that the English language is not really in my skill set. Even though I graduated College, I still believe I capped out smart wise around the 8th grade. 1/4 of the problem is because i come from a generation of knuckleheads that changed the english language to fit in text message form. And, the last 1/4 is because I am so stinkin' tired and I won't proof read this).  Ok. So. This is Vince's text message that he relayed to his kids after talking to me.  "Megan can correct this if it's off base, but I understand the situation to be this. Alec's docs have decided to hold off on dialysis for now. Instead, they will administer Coumadin, a blood thinner (generic name: Warfarin, the principal ingredient in rat poison, but that's another story) to alleviate congestion in a main blood vessel passing through the liver.  This will also hopefully aid in normalizing the kidney function, but the big pay off will hopefully be to spike the INR component of his MELD score (already at 29). That's right they finally have a diagnostically-defensible reason to give him what he needs to qualify  for transplant priority."
Pretty much, we are on the right track toward our end goal to receive a transplant.  You never know when it will happen though. Alec has been on the transplant list for a little over a year. We hope its right around the corner. So in your prayers and in your hearts ask for a happy ending because we are "over it!"      
 I have to give the Easter lesson in church  and so last night  Alec and I read a beautiful talk together given by Elder Wirthlin.  It couldn't have come at a better time because we had just gotten to the hospital and we were both feeling frazzled, discouraged, and tired.  We did not want to be here.  And then on top  of it, everything was different about the hospital floor we have come to know.  When the level 10 button was pushed in the elevator and the doors opened I didn't recognize "our floor."  They refinished the floors from carpet to tile.  That upset me.  (I mean, I know it's cleaner and all, but don't go changing things that I have become familiar with).  


Then, when we asked if our favorite Nurse Jason still worked on the 10th floor, they replied nope. He works in the ER now.  I lost it! I started to bawl.  Somebody give me some familiarity here! As I looked around I didn't recognize any of the nurses that we have come to know and love.  My anxiety levels raised through the roof and I felt a panic attack coming on and realized I had forgotten my inhaler. Alec used the restroom and I told him that Jason wasn't here.  We both held each other and cried.  We needed that one person that calms us and lifts us up here.  Later that night, we had a nurse we knew, Ashley. She's a gem. We felt a lot better. And then, when Alec pressed the nurses call button and cute little Cathy answered we looked at one another and smiled.  She has the sweetest little voice that just reminds us how a grandmother talks to her grandchildren. So tender. With all of these little blessings to show us that we were watched over and comforted, we started to accept the fact that we needed to be here and that it was right to be here. We settled in and read Elder Wirthlin's words: 

Sunday Will Come

BY ELDER JOSEPH B. WIRTHLIN
Of the Quorum of the Twelve Apostles

From an October 2006 general conference address.                                

The Dark Friday of the Crucifixion

I think of how dark that Friday was when Christ was lifted up on the cross. On that terrible Friday the earth shook and grew dark. Frightful storms lashed at the earth.
Those evil men who sought His life rejoiced. Now that Jesus was no more, surely those who followed Him would disperse. On that day those men stood triumphant.
On that day the veil of the temple was rent in twain.
Mary Magdalene and Mary, the mother of Jesus, were both overcome with grief and despair. The superb man they had loved and honored hung lifeless upon the cross.
On that Friday the Apostles were devastated. Jesus, their Savior—the man who had walked on water and raised the dead—was Himself at the mercy of wicked men. They watched helplessly as He was overcome by His enemies.
On that Friday the Savior of mankind was humiliated and bruised, abused and reviled. It was a Fridayfilled with devastating, consuming sorrow that gnawed at the souls of those who loved and honored the Son of God.
I think that of all the days since the beginning of this world’s history, that Friday was the darkest.

Sunday Will Come

But the doom of that day did not endure.
The despair did not linger because on Sunday, the resurrected Lord burst the bonds of death. He ascended from the grave and appeared gloriously triumphant as the Savior of all mankind.
And in an instant the eyes that had been filled with ever-flowing tears dried. The lips that had whispered prayers of distress and grief now filled the air with wondrous praise, for Jesus the Christ, the Son of the living God, stood before them as the firstfruits of the Resurrection, the proof that death is merely the beginning of a new and wondrous existence.
Each of us will have our own Fridays—those days when the universe itself seems shattered and the shards of our world lie littered about us in pieces. We all will experience those broken times when it seems we can never be put together again. We will all have our Fridays.
But I testify to you in the name of the One who conquered death—Sunday will come. In the darkness of our sorrow, Sunday will come.
No matter our desperation, no matter our grief, in this life or the next, Sunday will come.
 
I would like to add my testimony to Elder Wirthlin's.  We have all had our fridays, but just as we know the sun will rise the next day we know that there will be relief to our heartaches.  How our hearts have been tugged in this past year. We are grateful for our Testimony knowing that the Savior Jesus Christ has risen.  We know this to be true.  I don't want to step on anyones toes here, so know that this is my opinion and it is completely out of love.  But really think about this, Someone had to created us.  There has to be a designer.  This designer designed man as His best creation.  Do you really think the end game is death? That We come here to live our lives, work in some of our crappy jobs, take the same route home to and from, eat some yummy food, have some good laughs, meet great people, some weird, learn some spiritual lessons and then thats it? I know that this can't be true.  We are here to progress, to grow, to learn all that we have, to share all that we have with others just as the Savior Jesus Christ did on the cross and through his resurrection we all have the chance to live again.  And be free with out pain and Liver disease!!!! This gospel message gives me so much hope. 

I am so grateful for the little miracles we have received thus far in our lives.  It truly comes from a watchful and concerned Heavenly parent. Out of all the things that have gone on through out my life I am most grateful for the huge heart i have been given.  My capacity to love is what makes me happy.  I love meeting new people and learning their stories.  I love diversity.  Its what makes us all so beautiful.  We are the same though however in that we are all God's children. We all need each other.  (Even Karl Malone:) 








Ill leave you with this message that Alec and I read which also calmed our hearts and gave us strength and peace for the things in which we will have to go through in these next coming week/weeks. It is because of all of you and HIM that we can do this and do this well and with a happy heart. Thank you all! And have a happy easter weekend!! we will keep you posted. Please share with whomever. We could use the love and prayers:)
xo Megan and Alec and Miles


Elder Marvin J. Ashton (1915–94) of the Quorum of the Twelve Apostles discussed how we can fulfill the Lord’s commandment to feed His sheep:
“Jesus said, ‘Feed my sheep.’ (John 21:16.) You can’t feed them if you don’t know where they are. You can’t feed them if you give them reason to resist you. You can’t feed them if you don’t have the food. You can’t feed them if you don’t have charity. You can’t feed them if you aren’t willing to work and share. …
“Those who need help come in all age brackets. Some of His sheep are young, lonely, and lost. Some are weary, afflicted, and worn with age. Some are in our own family, in our own neighborhood, or in the far corners of the world where we can help with fast offerings. Some are starving for food. Some are starving for love and concern.
“If we give His sheep reasons to resist us, the feeding process becomes difficult, if not impossible. No one can teach or help with sarcasm or ridicule. Dictatorship or ‘I’m right and you are wrong’ will negate all efforts to feed a wandering sheep. A wall of resistance will be built, and no one will benefit. …
“By our actions we show our love. Expressions of affection are empty if actions don’t match. All His sheep need the touch of a shepherd who cares” (“Give with Wisdom That They May Receive with Dignity,” Ensign,Nov. 1981, 91)











Saturday, December 28, 2013

September 2013

It's been 4 1/2 months since we've posted so here's some smaller posts to hopefully catch up. 
September consisted of no changes in my health really and some run drives to take in the last of summer and the slow transition into fall. 
It has been such a blessing to enjoy some relatively good energy in order to spend time as a family. On the many days when I had no energy to go out, Megan coped and relieved stress by demolishing our basement so that we can hopefully make it a livable area. 
She's an animal, and has done more than I could ever imagine as our own family contractor and as our mother, wife, nurse and care-taker. She's amazing!
So yeah, September was good to us. 

Monday, August 12, 2013

Us

I ran into a couple of people this past weekend who didn't even know that I was out of the hospital. So considering that I've been out of the hospital since Miles' birthday (June 28th) I thought we'd actually post an update on us on the blog and maybe a few more people can get a nice surprise. 
As I said I left the hospital on Miles' birthday at the end of June having had my kidneys fixed almost completely. The docs were pretty surprised by how well my kidneys rebounded, and Miles celebrated with a cupcake. The only problem with my kidneys doing so well meant that I was no longer on dialysis which kept me high on the liver transplant list. Now I am barely on the list, but am still listed and still not feeling even close to 50% of myself. So even though I am lower on the transplant list than I was when I was actually listed, I feel nowhere as good as I did when I was listed, if that makes sense? The listing system is a messed up system in a lot of ways, but we'll live with it and be grateful we have a system period that provides the opportunity to have a life saved. I feel good almost everyday now, but I have little or no energy (especially by the end of the day), I have no muscle mass at all, and my diet is a work in progress as I try to introduce new foods every day and see how my system tolerates each one of them. My staple is fish and rice, so that's good. 
It has been amazing to be home with Megan and Miles. It has come with its challenges since Miles is an amazing but also busy 2 year old, but the more time I am away from the hospital, the more I don't ever want to go back there, except for the actual liver transplant of course.  
In the meantime, we "wait" without really waiting for the phone call with a new liver to come, meaning we're not on the edge of our seats right now but are trying to live our lives as normally as possible, not knowing at all when I'm going to even get sick enough to qualify for a new liver. We keep pretty busy though. 
Megan has been doing a lot of biking, both road and mountain, of which I am super jealous, but it keeps her sane and happy, as do her projects around the house, like putting new flooring in our laundry room. 
We've spent good time with family




And we've done a whole lotta sitting and relaxing, since that's about the extent of my activity these days. 



And below is a photo of all that was left of Miles' waffle with strawberries and cream from Bruges. I had none. 
Well sir, that's us for now. Sorry to anybody who didn't know that I was out of the hospital but, I am! And it's been great! Keep the prayers coming our way if you can. They are definitely working and we need them!











Wednesday, July 3, 2013

Fundraiser Success!

This is actually everybody's liver patient Alec giving a quick report on how well the BBQ Silent Auction fundraiser went last week!  While I was so sad that I couldn't make it to the party (especially since I was suffering at the time with some severe abdominal pains) I was so happy to hear about the great turnout we had and more importantly the great time everybody had at the event. 
We can thank all of you enough for coming and contributing in so many different ways. Whether it was donated items for the auction, preparing goodies for the bake goods sale, and all the hands that went into organizing and carrying out the fundraiser. 

A special Thank You needs to be made to Michael Holton, and worked so hard and was constantly in communication with Megan getting everything together. Of course I need to thank my sweet Megan. She would spend nearly every minute of our times together out at the hospital working on different aspects of organizing for the fundraiser. She has always been such a dedicated person to anything that needs to get done, and she'll work like crazy until it gets done, but was still always so sweet to come and visit me every day and give us our time that I always need in the hospital. She is the most amazing wife, mother and person I have ever known. 
So the fundraiser was a huge success and we able to continue to raise money for our astronomical medical bills.  So again, thank you, thank you, thank you for all of your support! We feel so blessed to know so many loving, selfless, caring and generous people. You are all literally saving my life and our family. The prayers and fast never go unnoticed, and I cry for joy to be connected to so many amazing people. We love you all!

With all this, we continue to wait for a new liver to become available. While the waiting has been difficult, we continue to focus on the fact that we can't pray for a liver to become available now. Rather, we pray for patience and to be accepting of God's timing for us. We remain confident that The Lord will bless me with a new liver, and recognize that it will be on His timetable -not ours. 

As I said before, we love you all, and are grateful for your continued love and prayers on our behalf. 

Until we post again!
Alec







Wednesday, June 12, 2013

Rampton Fundraiser


Come and Join us for a

 Potluck BBQ and Silent Auction
to benefit
 Alec Rampton

Alec is suffering from a liver disorder and is currently awaiting a transplant.  His disease is called Primary Sclerosing Cholangitis (PSC). However, Alec and Megan prefer to call it "the jerk," because that is how it treats them:) All proceeds will help his family with medical bills caused by "the jerk."

Friday, June 21st, 2013-6:30 P.M.
Monument Park 14th ward pavilion
2255 South Wasatch Drive


Contact Michael Holton to contribute food : holton83@hotmail.com
Or to donate an item(s) to the Silent Auction contact: ramptonstrong@gmail.com

The Silent Auction bidding will begin at 6:30 P.M. and close at 7:30 P.M. Winning bidders can collect their items that evening. There will be “BUY NOW” items available such as #RAMPTONSTRONG wristbands, baked goods, jewelry, original artwork cards by Megan Rampton, etc.

For those who are able to donate an item(s) for the Silent Auction, please email ramptonstrong@gmail.com with the following information:
1.Your name and contact info;
2. Item(s) to be auctioned;
3. your minimum bid;
4. whether you need (or want) to bring the auctioned item to the event earlier at 5:30 p.m.; or
 whether you would like to drop off the item at another date/time for your convenience.

*Please bring item(s) to the pavilion (2255 S. Wasatch drive) on Friday the 21st, at 5:30  p.m.

Thank you all for showing so much love and support to the Rampton Family!  
Hope to see you there!
For more info about Alecs’ progress : alecandmeganrampton.blogspot.com


If you would like to order a RAMPTONSTRONG wristband please contact: jwhunter9@hotmail.com or get them at the event!

please R.S.V.P to holton83@hotmail.com so we can plan accordingly for food! Thanks!

Friday, June 7, 2013

My Honey is Home!

Alec was able to bust out of the hospital this week! We are so happy to have him home with us. Just to be clear. . .Alec has not yet received a transplant. After 3 weeks in there it was time to get out of there!  The Docs felt that he was well enough to return home but under a watchful eye.  We have a nurse that comes to our house several times a week to do labs. Alec goes to the Intermountain Dialysis center every Monday, Wednesday, and Friday for dialysis.  It is very taxing even at home but at least he is now waiting at our house instead of the hospital for a transplant. We would still like to treat his return as if he were at the hospital.  He is extremely tired and fatigued and needs to rest as much as possible. So, at this time we aren't able to have visitors. The texts, emails, and cards are awesome! We appreciate them sooooooo much. Because honestly what else can you do when you are sitting in a chair all day long?!  I'll write more later but as for now we are going to bed.  Goodnight! xoxo

p.s. Thank you Bonneville Mortgage for your awesome card. Alec LOVED it!!

Has anyone ever noticed that the 13th floor doesn't exist at the hospital? Superstitious much? (I guess I wouldn't want to be on the 13th floor. Oh, and also, they don't have rooms with 13 in them either).


 I tried to feng shui his hospital room. I rolled his bed around so that instead of him staring at the wall he would be able to stare outside his window. Not bad eh?
 All of the nurses loved coming into his room because it was colorful and filled with happy photos. Besides that, they LOVED Alec.  (Who doesn't though really?!)  One dude nurse loved Alec so much that he tried to switch with his co-worker. He told him that he would take 2 of his patients if he could give him Alec. How sweet is that?!

 When Alec got a little down and discouraged, my cousin and I made this poster and hung it in his room.  This is definitely our new motto this time around (Thank you Winston Churchill).  Last liver go around it was, "Just keep swimming." You know what? I'm done swimming. . .throw me a rope people!


                    The day we busted out of that joint! That was our nurse Nathan. He is awesome!

 Thanks for the great card Bonneville Mortgage! There is nothing like Seinfeld and Simpsons quotes to cheer you up!


                                                           Alec and some of his fam

                                       Chillin in the only shaded spot of our house that day

                                                              Home Sweet Home.

Dialysis trip