We originally created this blog to keep family and friends updated about our little man Jacob, who was diagnosed in the summer of 2011 with a rare, life-limiting genetic disease called Niemann-Pick (type A/B). Jacob earned his angel wings on November 15, 2012, but remains our daily inspiration and constant reminder that we must live in the moment and fill each day with JOY, LAUGHTER and an abundance of LOVE.

Tuesday, April 9, 2013

Back To Work I Go...

Tomorrow is my first day back to work after being off on maternity leave for five months. I have serious mixed emotions about it. Five months seems like a lifetime ago, in fact, it was a lifetime ago...Jacob's.

Five months ago, I had absolutely no idea what my life would be like caring for a child with a life-limiting illness and a new baby. I constantly wondered how I was going to manage caring for both children, while Josh went back to work full-time. On my last day of work, my heart and mind were filled with so many emotions. GRATEFUL that I chose an education and career in health care because I truly feel that it helped me to better navigate the "system" and care for Jake. I was NERVOUS and yet, filled with EXCITEMENT anticipating the arrival of our baby girl [Kelly]. I felt JOY in knowing I would get to spend my days with my favorite little man, and yet I felt immense FEAR of the unknown. I left work on the 9th of November not knowing whether I'd even be able to return to work. My priorities were and always will be my children. At the time, I wasn't sure how/if working would be feasible and I worried how we would keep our insurance coverage. How would we pay our bills? The only thing I knew is that I was exactly where I needed to be...HOME!

At that point, Jacob's health had been steadily declining and we were really struggling with managing his seizures. Knowing that Jake's care needs were increasingly demanding, we began the lengthy process of obtaining coverage for respite care for Jake. This would allow us to have a licensed health care professional to help me with taking care of Jake for several hours each week -- it was not what I wanted. I am not one to ask for help and more importantly, Josh and I wanted to be the only ones caring for Jake. I did not want some stranger caring for my son because I knew they couldn't care for him as well as we did. Realistically, I knew I needed the help in order for Jake to receive full-attention and the best overall care possible.

On my last day of work (a Friday), I had absolutely no clue that Jake would only be with us less than a week. The Thursday before my last day, I had put Jacob on a portable oxygen machine for the 1st time (outside of being hospitalized) because of his labored breathing and he remained on oxygen for just one week before taking his very last breath. Ever since Jacob's diagnosis, I had hoped, prayed and wished with every single bit of my being for a miracle that would take away his illness...a cure...any sort of treatment that would at least give us the gift of time. However, I truly feel with all of my heart that we experienced a miracle. Jacob was our miracle boy who persevered through so much. He had one week of supportive equipment and pain medication at our home where he was most comfortable. The fact that we did not have to see him suffer through some of the awful stages of his disease for a long period of time was a miracle. Life is about quality, not quantity. As much as I wish with every fiber of my body that Jacob was still here, I am beyond grateful that we did not have to witness him suffering any longer. The pain of watching your child suffer is an indescribable feeling.


My last day of work I took Jakey with his portable oxygen tank to his grandparent's house to visit his new cousin Alexis

Fast forward five months and my life is entirely different now. I have an amazingly sweet and smiley baby girl Kelly who fills my days with so much joy, but life as I knew it is forever changed because Jakey is no longer here. My daily routine that involved a full-time work schedule, yet revolved around caring for Jacob and loving him -- feeding pumps, medication administration, scheduling doctor appointments, infant development therapy, ordering medical supplies, giving my little man a comforting bath in his special bath chair, snuggling and holding his little hands for hours each night before he drifted off to sleep -- is no more. Things are just so very different.

I am fortunate that I have had the past several months to focus on my family and myself; to navigate my way back into a very different life and to refocus my energy on that what brings me joy. Being a stay-at-home momma has been my greatest joy and truly makes me happy. Thankfully my employer is allowing me to return to work on a part-time basis temporarily so that I can ease back into things and have more time with Kelly. Time stops for no one and time has pushed me forward into this new chapter. It's going to be a big adjustment. One foot in front of the other and one day at a time. Wish me luck!!

On a side-note...please send some special healing thoughts and prayers to our little buddy Riley (NPA) who is currently in the hospital with severe pneumonia, which is collapsing his lung. Riley is a fighter, but he and his family could use a little extra love!!

6 comments:

  1. You are an amazing woman, and an amazing mother. That doesn't seem to cover it. The short time I was around you and Jake was profound. Your love, and Josh's love, for Jake was beyond a perfect example of how parents can love a child beyond words :) I am glad your little lady has the opportunity to have such selfless and loving parents. Thinking about you guys (and Jake!) often. Good luck :)

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  2. Sarah - your ability to adjust to each new "normal" as it comes along for you astounds me. I've never met you, but I know enough to know that you are an amazing mama, super-woman wife, multitasker extraordinaire, and a shining example of love and compassion. I just know that you will move through this next chapter with your usual grace and courage. Sending love and good thoughts for a smooth transition - xoxoxo

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  3. What a tough decision to make to go back to work. You have so much courage and strength and I'm so happy to know you have had a wonderful experience at home with your new daughter. She is just thriving! You and your family have been such an inspiration to others. Sharing Jacob's life has left such a wonderful gift and legacy. Your work seems very supportive and I know your transition back will be just fine. Your little girl has the best big brother Angel to watch over her and he will always be around to give you that extra push and all the love you need on those rough days. Take Care!

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  4. You are such a special person. You have so much love and support from family and friends around you. Lean on them if u feel the next step may be a bit hard. I admire your strength and determination through this tuff journey. You are an inspiration to me. I'm sending you lots of love many prayers to you and your family. I wish for only happiness to fill your hearts! With much love, the Chavez Family!

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  5. You are an inspiration Sarah. A wonderful mother balancing the gifts that your daughter is learning and showing you, while missing and honoring little jake everyday. We are here for you always. Much love xoxo

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  6. what a beautiful and heartwarming post. I am too so glad that Jacob did not have to suffer. He had such a beautiful and peaceful life. I am so glad that Kelly is here, what a beautiful lovey. I know it will be hard to leave her, but I am so glad you had so much time with here just you two!!! sending you so much love, Chelsea

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