Thursday, May 3, 2012

Progress Report


Waiting in the Doctor's Office

If there was one theme that covered this month’s progression appointment it would be stress. Just coordinating the day, schedules and prepping emotions leaves you frazzled and at times clouds your judgment. It seems lately that our family has just been attacked from all sides. There has been a great deal of change with my dad’s job, huge strains on personal relationships and just an enormous amount of frustration.  When you combine it all with the unknowns of ALS it becomes a volcano just waiting to erupt.

I am so grateful for family who sticks with you and offers support in time of need. My sister in law Shannon kept Ryan with her all day for a play date. Knowing Ryan was in such good hands gave me the peace I needed and the strength to focus completely on my mom. Dad is overwhelmed and didn’t attend the appointment. Quite honestly, I completely understand. I think hearing the summary from me and the extra time it allows to process everything helps make it seem bearable. The bond that we have all formed is incredible and although it’s a great burden to carry, to relay the information, and teach him about medical terminology and research it’s one I take with great honor.

Unlike the previous progression appointment mom went in with a few concerns. They all seemed to range in severity but I think she found great satisfaction in having herself heard. She wrote of issues we have experienced with the home care company APRIA. This is nothing new as they have been a nightmare to work with from the beginning. Unfortunately, all of mom’s supplemental feeding supplies as well as Bi Pap supplies come to us from here. Thankfully, we are now in the process of switching over to a new home care company. The hope is that she will receive better customer service and care.

In addition to housekeeping concerns she was very anxious about the “paralysis” in her face. As the doctor examined her it was clear that he was concerned at the severity of it. After asking several questions regarding time frame he told us with great care that he was concerned enough at the progress that additional testing would be required. Much to our surprise we were told that it is extremely uncommon for an ALS patient to have asymmetrical “paralysis” in the face and especially at this point in her ALS journey. He told us that it is most common to see symmetrical paralysis… that by looking at the person you would never know unless you were specifically looking for signs of weakness. Though statistics tell us that possibly 1% of ALS patients will experience the type of “paralysis” mom has its rare and her doctor has never really seen her type of case before. So- all that to say that he has ordered an MRI of the brain to rule out a brain tumor. It’s possible that what mom is experiencing is a completely unrelated issue.

We went in thinking this was just another piece of the ALS puzzle. What we were told was unexpected and came as a bit of a shock. But in all reality- we were more numb than anything. After all that we have dealt with thus far nothing seems to phase us like it used to. I can’t sit here and tell you that my mind wasn’t instantly flooded with thoughts of hope that maybe mom really doesn’t have ALS. For that split second I let myself begin to hope for something else. And yet, in just a split second I pushed that thought so far out of my mind. I can’t allow myself to go there. The realism in my personality refuses to allow myself to think that this has just been one bad nightmare.

The worst part of summarizing this appointment to the rest of my family has been that each one asked exactly what I thought. To hear my dad say: “So, she might not have ALS?” To hear my brother say: “you never know Tara” and to then have to tell them no. To explain that yes, mom does have ALS and this doesn’t change things… to watch those tears fall down my dad’s face… it’s the most heart-wrenching experience. I am so incredibly grateful that God has given me strength and grace to stand and hold us all together. That I can gracefully break the news, explain the situation, offer hope, be the physical strength for each one of them. I can’t explain the strength and peace that washes over me in each of these situations other than to say that it’s not me doing it. That strength completely comes from God and I’m so grateful that I can be the vessel he is choosing to work in to send peace and hope to my family. I cry and I feel pain, don’t get me wrong… but to have the strength to cry later- to feel the pain as I drive myself home is a blessing to the rest of them.

Mom’s stats have been hovering around the same as her last appt. Her breathing levels dipped from 51% to 43%. We are on the waiting list for the Diaphragm pacing clinic… at that appointment testing will be conducted to see if she is a candidate for the diaphragm pacer. She gained 2lbs- and the strength in her arms and legs has stayed steady.

Thank you all for continuing on this journey with us. As always, thank you for the prayers, cards, texts and support!

1 comment:

  1. Tara,
    It is neat you are taking on the role I played throughout my families ordeal with ALS and other illnesses. I was the one always in the middle. I believe He wanted me in the middle, so I could help others. I wrote a chapter in my book titled "Always in the middle" and asked my readers: Is it because you are the best vessel He has?

    I can tell you because I have been there not to get worked up while waiting for the results; is it this or that? Enjoy this week and love on her, be there for her, and hold her hand. Much love and blessing! ~ Judy

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