Well, much has happened in one week...... Since John was released from the hospital we have gotten all the necessary equipment and meds to help fight off any future lung congestion. What a relief!!! We were also able to get hospice care in place which will now oversee our care, our meds and also will provide extra help for some of the daily tasks we have been doing. We are all very relieved and encouraged by their involvement. It also became clear as we considered what the next couple of months will look like that I needed to be home full time in order to care for John and to make the most of the months we have together as a family. I am so grateful there is such a thing as the Family Medical Leave Act which allows employees up to 3 months of leave, while paying their insurance, and holding their job for them. Right now I will be taking off through the holidays and then will reevaluate if I should go back to work on a more reduced number of hours. For now, its been a real gift to have this time together as a family! We could not be more grateful.
Wrote this one day later..........I'm so slow at posting :(
We are now officially in hospice care as we have met with the lady who will be our primary nurse and a social worker. They are seeing about getting a CNA....nurses aid, to come 3 mornings a week to do the morning routine for us. This would be an incredible help to us, so we're praying they have the available folks to be able to do it. We will find out soon. Additionally, our nurse Leslie will come twice a week to check in on John and monitor his status. In the short time we have been with them, we've been overwhelmed by the amount of support we have received.
For many years we have had the tradition of going out with our good friends Steve and Vikki Cook to cut down our Christmas trees after enjoying a breakfast feast together. Well, after a few cold and rainy years and the Cooks moving away to Minnesota we began to go and purchase trees that had already been cut down. This is then followed by lunch at Red Robin restaurant. Last year the ALS association provided the lift van allowing us to do this family tradition. Thanks to your contributions and support in the " Walk to Defeat ALS" they will once again be providing a lift van so we can continue our family tradition.
We continue to be incredibly blessed and humbled by the care we are receiving from so many of our friends and family. The delicious meals, the calls, the gifts of money.......Amazing! Sunday night about 40 people came to our house for what has become known as " Bringing church to Johnny". It was such a rich and encouraging time for John and the rest of our family. The scriptures that were shared, the songs that were sung and the prayers that were prayed.........really helped us to redirect our focus not on ourselves and our trial but on our savior who suffered the ultimate suffering, death on a cross.
John loves visitors but sometimes does not know his own limits :) So, please give Amanda or me a call before you stop by for a visit. A - 240-676-0257, K - 240-676-4921. Even is you are scheduled, its always a good idea to call. Somedays are better than others. Thank for your understanding!
Have a wonderful Thanksgiving!
Love,
Kathy
Thursday, November 18, 2010
Saturday, November 13, 2010
Home from the Hospital
We are relieved and grateful to be home from the hospital. The necessary treatments to clear out Johns lungs were very helpful and made him feel much better. Sleep or rest however was another story . After being there one night and one day, we felt we'd recover better at home so asked to be discharged. Friday was the day we were scheduled to go to the ALS clinic for our 3 month "check up", but couldn't make it because of being in the hospital. While in the hospital however, they did perform the lung capacity test which showed that John's number had dropped from 40% in August to close to 25%. The progression is moving at a much quicker rate than we expected. The reality of the disease and its affects hit us afresh and have prompted us to get many things in order. Doctor Mays our doctor and friend is caring for us so well, ordering meds, machines, and also will be getting the ball rolling with Hospice Care next week which will be a welcome relief for our family. In addition we now have oxygen, a nebulizer, suction machine and BPap ..... scattered around our bedroom. All things considered, we are doing well and are looking foward to enjoying precious times with friends and family. God continues to encourage us through his word and assures us we are not alone as we go through this. We covet your prayers for our family that we would glorify God as we walk through the next few months. Your notes, meals, calls, and visits all mean very much to us. We feel so loved and cared for and are so grateful for each of you.
Psalm 9:9-10...The Lord is a stronghold for the oppressed, a stronghold in times of trouble. And those who know your name put their trust in you, for you, Oh Lord, have not forsaken those who seek you.
Romans 8:18...I consider that our present suffering are not worth comparing with the glory that will be revealed in us.
Love,
The Spiros
Psalm 9:9-10...The Lord is a stronghold for the oppressed, a stronghold in times of trouble. And those who know your name put their trust in you, for you, Oh Lord, have not forsaken those who seek you.
Romans 8:18...I consider that our present suffering are not worth comparing with the glory that will be revealed in us.
Love,
The Spiros
Friday, November 12, 2010
#2 Update
Hey so Amanda here =) Okay so Dad is still in the hospital and is looking to be discharged. He spent the night here and was cough free. He had a nebulizer treatment around midnight and after that was put on the hospital's BPAP machine and tried to go to sleep at 1:45. At 3:30 he woke up and realized the machine wasn't working properly and we called the respiratory man. We ended up hooking up our BPAP machine with their mask, since we forgot our mask earlier that night. He had one more nebulizer treatment and was ready to go back to sleep at 4:45. Doc Mays greeted us in the morning and let us know what was going to happen today. Dad's breathing is doing much better and all the congestion is out of his lungs. This is mostly to due to the nebulizer which Doctor Mays ordered for us to have at home. Right now we are in the process of getting him discharged. We are waiting on his flu and pneumonia shots. The process of getting him discharged can take 5-8 hours, so we are trying to get thing moving so dad can get home to his bed and have a good night's sleep. This morning I was blessed by texts and emails from friends just encouraging our family with scriptures and many, many prayers. Thank you! God is in control of this situation and he remains faithful throughout this time. These texts and emails of encouragement have hammered those truths further into my heart and that is the biggest demonstration of care.
Hope you enjoyed the photobooth pics! We got a couple of 1 am laughs out of it.
Love,
~Amanda
Thursday, November 11, 2010
Update on John
As many of you have heard by now.......early this afternoon on the recommendation of our Doctor
( Doc Mays ) John was brought to the hospital to get some chest X Rays to determine if he had Pneumonia or not. For the past several days he has had a hard time coughing up mucus in his lungs. But, because he has little muscle allowing him to cough , he has a hard time getting his lungs cleared. They are doing many different respiratory treatments on him to loosen things up and clear out his chest. We're doing well and feeling a God's grace and peace. Our good friends the Fortiers are in the same hospital awaiting their son Eric's tonsils removal. We seem to do everything together :). While I stayed with John, Chris Fortier and Amanda went out and brought back pizza for all of us, so its been a real party in the ER. While we wish he was home, we're glad he is in such capable hands and they can treat the problem better than our family could. They are giving him a Nebulizer treatment every 4 hours, which has already made a huge difference. Thank you to everyone for their texts, emails and prayers. They are much appreciated! We feel so loved and cared for as we continue to walk through this season of our life. So comforting to know God orders all our days, for our good and for his glory!
( Doc Mays ) John was brought to the hospital to get some chest X Rays to determine if he had Pneumonia or not. For the past several days he has had a hard time coughing up mucus in his lungs. But, because he has little muscle allowing him to cough , he has a hard time getting his lungs cleared. They are doing many different respiratory treatments on him to loosen things up and clear out his chest. We're doing well and feeling a God's grace and peace. Our good friends the Fortiers are in the same hospital awaiting their son Eric's tonsils removal. We seem to do everything together :). While I stayed with John, Chris Fortier and Amanda went out and brought back pizza for all of us, so its been a real party in the ER. While we wish he was home, we're glad he is in such capable hands and they can treat the problem better than our family could. They are giving him a Nebulizer treatment every 4 hours, which has already made a huge difference. Thank you to everyone for their texts, emails and prayers. They are much appreciated! We feel so loved and cared for as we continue to walk through this season of our life. So comforting to know God orders all our days, for our good and for his glory!
Thursday, November 4, 2010
Walk to Defeat ALS
Wednesday, November 3, 2010
Amanda here =)
Well as you know we aren't that amazing at blogging. Today is a very special day, it's my Mom's birthday!! I figured this is a perfect opportunity to use this wonderful blog to share about what an amazing woman she is.
My mom is my best friend. It hasn't always been this way. Through the ages of 12 and 15, I was a walking terror. I was running after the world hard and having "fun". All though I wanted nothing to do with her, she wanted everything to do with me. And I was not happy about it. She pursued me with all the strength the Lord had given her. She basically never trusted me, which was very wise. She continually would check up on me and try to talk to me and seek me out. I hated it. I hated the fact that she always had to be involved. I hated even more that she was always right when she would confront me on what I was up to. I hated that she would tell me no. She loved me so much, that she cared more for my soul than she cared about what I thought of her. She knew that challenging me to do things God's way and not the worlds way, would make me dislike her. Glorifying God was more important to her, then having my approval. There were tough times, lots of fighting, screaming, arguing and crying. She took her calling as a mother seriously, she knew that this time in my life she couldn't always be my "buddy" but had to parent me.
I am now eternally grateful for the sacrifice she made for me in my teen years. Thankfully God has saved me! I am so happy God used my mom in my life for his purposes. It grieves me how much I hurt her and how many times she would go to bed crying. Now we are best friends and are able to have a biblically based mother-daughter relationship. I am provoked by her daily example of laying down her desires to serve others. Ever since I was ten she always had me serving at the church, for mothers with kids, conferences, and at home. I love her so dearly and I am privileged to be her daughter.
We are now watching my dad suffer with ALS, it has been more than difficult and testing. However watching my mom earnestly seek the Lord daily and seeing her grow in her love for her Savior is such a blessing. God is strengthening our friendship even more through this trial and I am undeserving to have such a wonderful best friend. Thank you Lord for giving me such an amazing example and for giving her life. Happy birthday mama!!!!!
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