Friday, July 13, 2012

Mail

Today's mail brought four envelopes from Gillette. Sam's vitamin D level dropped almost 20 units over the winter. Some other labs were off too. He is to take prescription vitamin D and more labs in three months. It was hard reading the transcript from the developmental pediatrician. Definite problems. I'm also second guessing the surgery. Hearing is fine. It is late at night and my mind is going.

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Trying to catch up here. this was written March 24 and not published as I had more I wanted to write. Now I'm not sure what it was. This past spring we had check ups for orthopaedics, endocrinology and neurosurgery. The above paragraph is about the endocrinology results. We have now finished the prescription vit D and retested with good results his levels are now up to 53.  We have to do a 24 hr urine catch still to complete that testing.

 Neurosurgery ended up postponed until late spring due to a problem Sam's brother was having.  When we finally got in things looked fairly good as far as the chiari goes. He is still having a few headaches a month, but that is livable. What surprised me there was being told for the first time that he has a lesion near his right optic nerve we need to watch over time. We went to a opthomalogist and he is a little nearsighted, not enough for glasses yet,  but otherwise OK. So he will have yearly MRIs, neurosurgery and opthomalogy appointments.

Orthopaedics threw me for a loop. It was a six month check up and I assumed all was OK. Well the lesion mid-shaft on his right femur had expanded and Dr Healy was now recommending a bone graft to force his body to heal it. This is kids of controversial as FD bone usually gets "angry" at a bone graft and comes back worse than before. Dr Healy knows this and has told me so. The reason he wanted to do this for Sam was that he had healed the two previous femur fractures so well with very little trace of FD in only one femur. I contacted a doctor in Des Moines, Iowa about it and finally decided to go ahead with it. I think I have told about this surgery else where in this blog.

Monday, July 9, 2012

So Behind...

I am woefully behind in updating my blog on things going on, things like recent appointments, good news, Miracle League, bad news and another fracture. We are currently in the hospital because Sam fractured his femur through the bone graft sight on Friday July 6.

God is amazing and brings things to me at such needed times. After yet another interruption, I had finally given up sleeping this morning at the hospital. It was around 6 am. Hospitals begin to wake up at this time. Night shift nurses make final checks, take vitals and change positions on bed ridden patients like my little guy. Residents come in to check patents before starting their day in clinic appointments or surgeries. The sun was also shining in the room making sleeping difficult for me, so I grabbed my phone and began doing some reading. I checked in with Caring Bridge and read up on some families I am following there. One shared an amazing essay about life with a special needs child. It can be found at http://www.whatiwouldtellyou.com/

What I Would Tell You

I sensed someone watching me as I comforted my daughter after a particularly traumatizing dentist appointment at the Children’s Hospital. I looked up and saw you staring at us from across the waiting lounge. I didn’t pay much attention, as I have grown accustomed to the curious eyes of onlookers. Our daughter was born 7 ½ years ago and after an abrupt lack of oxygen at birth, she changed the course of our lives forever. Perhaps, our lives unfolded exactly as they were meant to — they just didn’t unfold in the way we had imagined or planned.
I talked to my daughter, kissed her and hugged her. I was giving her a brief break before putting her through the next traumatic experience of the day ~ the car ride home. Having cerebral palsy is the least of her worries but this condition can turn a car seat into a torture chamber.
I stood up to gather our things, my daughter in my arms, and it was then that I noticed you were holding an infant. It was difficult to know for certain how old she was. I knew immediately, though, that you were one of us. I knew that only recently your life had changed drastically and you sat here in this Children’s Hospital wondering, “How did we get here?” I should have recognized that shocked stare because I once had it, too. And I assume that the man sitting next to you, looking equally tired and shocked, was your husband.
I made my way toward the doors and as I passed you, our eyes met and I smiled at you. You smiled back and for a moment I knew that you knew that I understood.
If I could, I would tell you although you might not believe it right now, you will be okay. I would tell you to dig deep within yourself because you will find the strength and resilience somehow and it will surprise you. I would tell you to honour your feelings and let the tears flow when they need to. You will need the energy for more important things than holding in emotions.
I would tell you that the man sitting next to you might cope differently and he might even want to run the other way. But I would tell you to hang on because he is scared and he really doesn’t want to leave you. I would tell you to look after yourself so that you can care for your daughter. Don’t underestimate the power of good nutrition, exercise, sleep, supplements and an empathetic therapist.
I would tell you that grief will come and it will confuse you because how can something that brings such joy also bring such sadness? I would tell you to let people into your lives to help you. Our children really do require a village to raise them. Access all of the services and resources available. Find someone who can learn how to care for your child so that you can have breaks and so you and your partner can go on dates… even little ones like a twenty minute stroll outside holding hands, sharing wine on the deck or even catching a movie.
I would tell you that you know your child best of all and no matter what you are told by the doctors and other professionals who will be a part of your life, YOU know the answers. You will teach them about your child. At times you will question the validity of your intuition but after a while you will become profoundly aware of how accurate your gut feelings are when it comes to your child.
I would tell you not to be a martyr. Caring for your child will require tremendous focus and unimaginable energy and it can burn you out and make you sick when you least expect it. I would tell you to let your guard down along the way so that you can stay healthy in your mind and spirit.
I would tell you to seek out other mothers like yourself. This is, indeed, the road less travelled and you will feel very alone along the way especially in the company of healthy children and their parents. Yes, you will feel very isolated but know that we are here. Sometimes you have to look a little harder but we are here. You can find us online, in support groups and wandering the halls of the Children’s Hospital.
I would tell you that you will know far too much about the human anatomy, neurology, gastro-enterology, feeding tubes, pharmaceuticals, and so on, than a mother should ever have to know. I would also tell you to do some research to inform yourself but be very careful not to be overwhelmed by the internet and all of the information available to you. Having some trust in what your child’s specialists tell you can be very grounding. Other mothers and fathers of children like ours can be a wealth of information.
I would tell you that this isn’t an easy life. It is tough: there is no doubt about it but you are very capable and the rewards are great. You may never see your child graduate from university, walk down the aisle or give birth to your grandchildren but you will feel pure joy when your child laughs for the first time at the age of 3 years and 8 months. You will celebrate the moment when you connect with your non-verbal child. You will call your spouse at work to tell him that she has gained 4oz. because weight gain is always a struggle with our children.
I would tell you that you will have to witness procedures and surgeries and suffering well beyond what any parent should ever have to bear. But, I would tell you that you will be courageous and comforting because your child will be experiencing far more suffering than any child should ever have to endure.
I would tell you that your life will not resemble the life you had planned. It will be as though you landed in Holland instead of Italy but after some time, you will adjust the dreams you had and this reality will be normal to you. You will dream new dreams.
I would tell you that you might find yourself staring death in the face during close calls. You will be asked to fill out DNR (Do Not Resuscitate) forms and although you might make decisions to not resuscitate in the event of a cardiac arrest, when the moment arises, you will panic to think that it could all come to an end. And I would tell you to not feel guilty in the darkest moments when you pray to God to take your child if it would mean the suffering would end. This might horrify you but know that your love for your child is so great that at times you will believe that death would be a blessing.
I would tell you that others will not get it. They can’t. This is a very unique and complex journey on all levels. We cannot expect anyone to get it. And I would tell you that people — the cashier at the grocery store or your insurance broker or even your hair stylist — will say stupid things like, “God only gives these special kids to special mothers” and “God will only give you what you can handle.” You will nod and smile but eventually you will look them right in the face and tell them that those simple maxims are a bunch of bullshit.
I would tell you that imagining your future will be bittersweet and may involve a Plan A and a Plan B. Plan A will be what you will do if your child outlives the predicted life expectancy set forth by the experts and Plan B will come into play if they do not. You will catch yourself casually discussing your future with the code phrases of Plan A and Plan B.
I would tell you that grief will creep up on you after years have passed and you least expect it like at a wedding when the father and bride have their first dance or when you hear a birth announcement. It will also creep up on you when you see yourself in a new mother who is just beginning this journey.
I would tell you that you will recognize her because she is you from 7 ½ years ago. And you will want to run to her and hug her and tell her that everything will be okay. You will want to save her from the pain and the hardship and the unknown.
But I would tell you that when you find yourself sitting at the Children’s Hospital and you see a new mom and dad who are just starting this journey, you smile at them and walk by as they have their own path to travel and it will be different than yours. It may be longer or shorter. It may be more or less complicated.
I would tell you that her searching eyes are looking for some sign that she will survive this. And you, smiling as you pass, with your child arching all over your shoulder, will let her know that yes, she will survive this and may even thrive.
Julie Keon
June 29th 2011

Not all of it applies to my life with Little Guy but the paragraph about witnessing procedures and surgeries and suffering had me in tears as I remembered Friday evening sitting in a waiting room that was 2 rooms and down a hallway from where Sam was being x-rayed and listening to his screams as they positioned him. He told the nurse afterwards "That was horrific!"

Within minutes of reading this and digesting it. I received a text from a dear friend. It was today's devotional from Jesus Calling by Sarah Young.

July 9

Stop worrying long enough to hear my voice. I speak softly to you, in the depths of your being. Your mind shuttles back and forth, hither and yon, weaving webs of anxious confusion. as My thoughts rise up within you, they become entangled in those sticky webs of worry. Thus my voice is muffled, and you hear only "white noise."

Ask My Spirit to quiet your mind so that you can think My thoughts. This ability is an awesome benefit of being My child, patterned after My own image. Do not be deafened by the noise of the world or that of your own thinking. Instead, be transformed by the renewing of your mind. sit quietly in My presence, letting My thoughts reprogram your thinking.

Do not conform any longer to the pattern of this world, but be transformed by the renewing of your mind. Then you will be able to test and approve what God's will is -His good, pleasing and perfect will.
-Romans 12;2

The two things coming to my attention within minutes of each other amazed me and had me blubbering away. I barely had contained myself before the resident came in. Now to shower and make myself more presentable for the day and myriad of people coming through the room before we will hopefully be able to go home today.

Thursday, May 31, 2012

Rotten Day

I have a lot to update my blog on. Maybe next week will slow down enough to do so, but I need to say this some where. FD is terrible. It so hurts to see your child hurting. It has been terrible watching him in pain through injuries and surgeries, but today was a whole new level. It was Field Day for Sam's school. Think track and field events turned into fun games for elementary kids. He is still in the wheel chair healing from the bone graft. There was not a whole lot he could do. One of the stations was inflateables. Sam was in tears and so upset he could not participate. He stuck it out longer and got to be the starter for some other events. When we got to the obstacle course in the gym he finally had enough and wanted to go home so I took him out of school early. I'm so broke right now I couldn't offer him much. Next year, I will make sure I have funds available to go to a museum that day or something instead of Field Day at school.

Tuesday, April 17, 2012


I have a quiet house this morning. Sam went back to school today. It is amazing how quick a child can bounce back. After Friday, my last post, he just got better and better. He is now down to just acetaminophen for pain meds and doing great.



Yesterday we went to the library and got Sam his own library card and a bunch of books. Then in the evening he went to his Cub Scout Pack meeting. He won the boot for best showing what a being a Cub Scout is all about!

Friday, April 13, 2012


What a couple of weeks. I am so tired but got some sleep last night.

Sam had his surgery on Wednesday. the day started with jello for breakfast and 15 minutes before the clear liquid cut off, Sam found a Girl Scout Cookie and took a bite. That delayed surgery from 11 am to 1:45.  Fortunately Dr Healy worked with us and was able to do it later in the day so we did not have to go through the whole process of getting ready for surgery again. Sam and I passed our time with some movies and playing games. Child life was able to bring us Candy Land (which Sam won twice), Connect Four (we both won at that one), and we were almost done with Chutes and Ladders when they came to take Sam to surgery.

Before surgery we had a good conversation with Dr. Healy about the emails I had been sending back and forth with Dr Lindaman in IA and what exactly does Sam have. Dr Healy was already planning on sending specimens to U of MN again. I mentioned Dr. Collins at NIH who has done lots of research on FD and Dr. Healy took his name down. Before surgery started Dr Healy was able to find contact information and called Dr Collins and left him a message. During surgery Dr Healy also prepared a set of specimens to send to Dr Collins also. Last I heard, Dr Healy still had not heard back from Dr Collins but is going to follow up and it. Got to love a doctor you can talk with and who will take information you bring to the table and act on it!!!

During surgery Dr Healy found the lesion to be very fragile, like and egg shell he said. It took almost nothing to break it and clean it out. he feels Sam would fractured that very soon had nothing been done. Dr Healy also cleaned up the scar on his right thigh that had keloided. It went very well, Sam was sleepy afterwards and it was 5:30 before we went up to his room. He turned into ravenous boy and consumed 5 Popsicles, chicken noodle soup, a sandwich before finally falling asleep again for the night.

It was a fitful night with meds and pain every couple of hours and trouble finding a comfortable way to pee. By morning we were on top of pain and he was doing better. We saw PT at 10 and were on our way to pick up his wheel chair by 1:30. His wheelchair. that seems like it deserves a post of its own but I will likely not get that far. It is so surreal to get a wheel chair for your child.  This one his special ordered and built for Sam. It is not a rental.the process began in January. The $6000 ticket will go to insurance.

We got some more sleep last night. The difficult first bowel movement began giving tummy aches last night and making him generally grumpy. That continued into this morning. He finally moved this afternoon and promptly fell asleep again all snuggled into the bean bag with his newest blanket from the hospital.

Thursday, March 22, 2012

8th Surgery

This month has been so busy with doctor and therapy appointments, not only Sam. Sam has seen endocrinology. I have not heard back about the labs yet, but everything else looks OK. Just more waiting and watching.

We got in to the nuerodevelopmental ped early due to a cancellation. There is definite concern in both home and school. But Sam is complicated with a lot of history at Gillette. He has already had some of the testing the doctor usually asks for, but there is some still to do. So we have opthamology and psychology to add to our list of doctors.

The fun bit there was the trip home. His big sister had her big wax museum project at school that day so I sent Daddy to see it while we were at the doctors. Then he had to get other kids after school so Sam and I took the bus home from St Paul. He was so excited but fell asleep on the way home!

Today we saw Dr Healy. you can see Sam's x ray above. The right femur has a lesion that looks about ready to break. Dr Healy wants to put a bone graft in and stimulate Sam's natural healing process to help heal the bone. That is surgery number 8.

It doesn't get any easier to hear your child needs surgery.

Wednesday, January 18, 2012

5 months headache free

I never did get back with pictures from Sam's birthday, sorry about that. Life is busy with 4 kids going all sorts of ways! Good busy!

I am here today because Sam had quite a headache last night. We were at the Dakota County Communications Center with his Cub Scout pack. He is loving Cub Scouts by the way! We were leaving the training room to a long hall way with windows where we could watch the call center in operation. Sam was at the front of the group with several boys who ran ahead to the lobby. Another parent went to bring them back. About 5 minutes later he told me his head hurt. I took him to the lobby and he laid in a chair for a few minutes. Then the rest of the group came out and one of the parents told me he had slipped with another kid on the highly polished floors.  At bed time his head was hurting agin and upon questioning he told me it started when he fell. I asked him to sit up so I could get a better look at his eyes and he said no it hurt to much. At this point he was almost crying, so i just let him go to sleep. he seemed better this morning.

I had to look up when his last headache was and this was the first since the first week of August. I think there have been mabey two mild complaints of a passing headach but they did not slow him down. He does seem to have a bit more of the fatigue than he did during the summer.

Today we are going to HandiMedical for a fitting for a wheel chair.