Wednesday, December 26, 2007

Merry Christmas!

Ryan and Rachel

-opening one of many gifts-

Good evening!

I hope you all had a very Merry Christmas! It was such a blessing to spend the day with Rachel and Ryan and to celebrate SO much. We have much to be thankful for.

Rachel had Physical Therapy today, here in Centerville. After PT, they headed back to Nebraska for a family dinner and then off to Kansas City tomorrow for her HBOT seesion. Then tomorrow afternoon they will come back to Centerville for the weekend. She has gotten alot of road time with Ryan in his truck...she has definitely enjoyed the week off that Ryan has taken to spend the holiday with her.

Rachel hasn't used her cane or wheelchair in several days. She continually show progress. I would venture to say we see something different, new, improved...everyday. Rachel's speech is also continuing to improve. She starts singing lessons next week! We have heard that singing lessons is an excellent form of speech therapy. Probably because of the amount of vocal control it takes to sing. This will be a new adventure for her.

Thank you for all the prayers!
RuthAnne

Saturday, December 22, 2007

Nebraska!

Rachel and Nancy Baltensperger

Yummy!
Rachel, Emily and Anna


Rachel has been enjoying herself in Johnson with her future in-laws. Anna (Ryan's sister) write:

Note from Anna Baltensperger,
"This is the first weekend to have Rachel at our home since the first of September!!! We are delighted to see her continued progress and for her to be here this weekend! With Allyn & Emily also home, we feel very blessed to spend time together with family.
Yesterday, while the boys occupied themselves with outdoor projects, we girls were busy in the kitchen making "fastnachtchuchli". This is a holiday tradition for the Baltenspergers originating from our Swiss heritage. We spent hours rolling walnut-sized dough balls into paper-thin pastry and then frying the delicacies. (The rolling pin was part of Rachel's Friday therapy!) Though the fastnachtchuchli's take lot longer to make than to consume, the taste is worth it!"

Thursday, December 20, 2007

Going To Nebraska

Rachel is excited today. She is on her way to Nebraska to celebrate Christmas with Ryan's family this weekend. She has a HBOT session this morning and then she will head to NE. Ryan and Rachel will come back on Christmas Eve day and be here in Iowa to spend Christmas with us. I am SO thankful Rachel is home and able to have Christmas with all of us. What a blessing!

There has been some wedding talk...but no plans or dates set yet. They will wait till the first of the year to decide when to make this BIG day. They will check dates with the photographer and the church...we will definitely keep you informed as to when, where, and how to RSVP, etc.

I am sure I will have several pictures for you all. Anna, Ryan's sister is really good about taking pictures. And then we'll have pictures from the 25th.

Merry Christmas to you all!
RuthAnne

Saturday, December 15, 2007

More Winter

GOOD AFTERNOON!

We apologize if these updates are not timely as the weather has interfered this week.
  • It is snowing and snowing!!! Frosting all the ice with white. Winter wonderland if prepared.
  • We had no electricity from Tuesday to Thursday evening. Some are still without electricity within 5 miles of us! We had fun with kerosene lamps, cooking on our wood cook stove and plenty of hot water with gas hot water heater.
  • Rachel indeed is home. She begins her third week home today.
  • She is focused on continued improvement.
  • Her body keeps responding to her desire to be 100% recovered.
  • In this process of communicating to you how well she is doing, we ponder what words will give a true picture of her progress, her challenges and her limitations at the moment.
  • She DESIRES and is THANKFUL for your prayers! So thankful!
HOW TO PRAY?
  1. For her speech to return to normal. She does speak clearly, her voice is low with minimu, sounding like she is recovering from a cold. Listening closely to her for understanding her exact words or we break into laughter at what we 'think' she said and then find she was saying nothing of the sort. We are finding that in general, we humans have preconceived ideas about what someone is going to say before they finish their thoughts.
  2. For her right arm to return to full function. Her left hand's fingers can manage the piano and computer keyboard keys. Her right fingers are bumble-some and frustrating, but functioning individually (improvement as of the last couple days!)
  3. Walking to be normal. She walks with a cane by herself in the house or to the car. -She does need someone there to steady if she gets off balance or mis-steps. No wheel chair in the house. We only use the wheelchair to go to Kansas City for the HBOT (hyperbaric oxygen therapy) twice a week or shopping.
  4. For her coughing to completely stop when she drinks. It happens enough that it is frustrating to her.... it makes a mess and if you are in the line of fire when she spews and coughs at the same time...it's embarrassing for her. This frustrates her but she handles it well with laughter. But then she doesn't want others to think that she doesn't care that she does this, but what can she do? Cry? or Laugh? She chooses to laugh! It is easier on all of us and we know that this is something that will disappear soon.

WHEELCHAIR, CANE, WALKING WITH HELP?
Last night we had an interesting discussion about walking vs. wheelchair and the response that others give her. Her goal is to walk by herself, of course. Rachel's goal is to walk and do so without a cane or help from others.........well, when walking alone, she looks like the drunken friend or family member, so she should use the cane as the 'sign' to others of weakness....without a cane, well, she is perceived as having a substance abuse problem.

When in a wheelchair she is treated very well. People make concessions for her.

So it is just interesting. She is not opposed to the wheelchair but then must practice walking at home, using the wheelchair in public. This now answers the question for me why people who look like they don't need a wheelchair use one because it is better culturally to use the wheelchair than trying to be strong in standing but looking too weak or unstable to stand and too strong to sit in the wheelchair. So, our thinking is....she can walk into a public place with help. Since she is unsteady on her balance sometimes and sways, the looks she gets are not that of mercy (and previous to this I would have been no different in my thoughts either); but when in the wheelchair, accommodations are made for her. Walking with a cane is getting better, but she still needs one person to assist.

HBOT therapy is going well. Since she has come home her lung capacity measured by the inspirometer has gone from 500 to to 2000 regularly and 3000 when really trying. Our lungs, they say, hold 5,000. Healthy people can get the meter to read 3500-5000. Most people do not use more than 500 which is called shallow breathing. She has pushed the meter up to 3500 once or twice.

Ryan comes here to visit every weekend. He is the best therapy for Rachel!

We appreciate your prayers. We pray you will give thanks for all you are able to do and for all that Rachel has achieved since September 6. She is a walking miracle.

To GOD be the GLORY GREAT things HE hath DONE!

Crystal

Thursday, December 13, 2007

Ice Storm

Fun times in Southern Iowa. We have had enough ice to last us the winter. Some people got power yesterday and some didn't get any until today. The storm hit here Monday during the night. It's nice that Dad and Mom (where Rachel lives ;-) have a generator and wood heat! Josh and I stayed with them on the farm Tuesday night instead of staying in our cold apartment.

Rachel is doing well. The ice has been a challenge, one that she has taken on with courage. Walking on all the ice has been interesting, but she has done well with it. Today was Physical Therapy, he worked her hard for the full hour.

Rachel and I spent time this afternoon, when the power came back on, doing some last minute Christmas shopping online. I noticed that Rachel is able to type with her left hand and use a couple fingers with her right hand on the keyboard. I bet typing is still very frustrating since she was very quick at it before.

Tomorrow (Friday) Rachel goes to Kansas City for another HBOT. She missed Monday and Wednesday because of the storms that moved in. So, I'm sure she is ready to have another treatment, so she can finish up her 20 sessions, sooner than later. -they say it takes about 20 times to see a real improvement.

Thanks for understanding the delay in the update.
RuthAnne

Saturday, December 8, 2007

A Week Home

Good evening,

I just realized that it was Saturday, time for another update. Ryan is here for the weekend, he got in last night and will stay till Sunday evening. They both really look forward to the weekends together.

Rachel's week was good. She had her HBOT twice on Wednesday and Friday and will go 3 days next week as well. We had our first snow storm on Thursday, so she didn't make it into town for her PT session. It seems to be emotional on Rachel to be home. I know that she really enjoys being home and being in a familiar environment and surrounded by lots of people who deeply care for her. But, being home must be hard because it is a constant reminder of all the things that Rachel can't do, yet. Like walking through the kitchen, but not being able to make a meal for the family like she used to. Rachel said that it was hard to just sit there after a meal is over and not help clean up afterwards.

Rachel's right hand is still improving, she noticed yesterday that she is starting to regain control over her ring finger. Before, she couldn't move it.

Continue to pray for Rachel's spirits, we know that disposition one of the keys to health.

Thank You!
RuthAnne

Wednesday, December 5, 2007

HBOT

HBOT stands for Hyperbaric Oxygen Therapy.

We are excited to be able to use this therapy for Rachel. She will be going 3 days a week to have 2 treatments done each of those three days. If you 'google'. HBOT, you find neat information on how is has helped many people with several different types of problems. Here in the US, it is most commonly used for divers and burn victims. In other countries, they use it for stroke rehab and get great results. The closest place we found to do this is 2 1/2 hours away - northern Kansas City area. Anyway, today is Rachel's second day using this therapy and we are looking forward to seeing results. After her session on Monday, her breathing capacity increased and her speech became even more understandable. The experts say that it takes up to 20 treatments to see super significant changes, so give us a couple weeks and we will all be curious to the results.

Rachel's time home has been good. She gets to shower as often as she wants, choose when she wants to do therapy, and have great food to eat. Madonna's food was decent, but there is nothing that replaces food from home and smelling it cook. Rachel had her first Physical Therapy session with a PT in town, yesterday. It went well. He is really impressed with Rachel's progress in the couple months and has been following the story even before he knew he would be her Physical Therapist here at home. Rachel was proud of her bodies ability to do whatever the PT asked her to do. Her right arm was able to perform well and even was able to give some resistance with it. Yeah! She'll have 'official' PT twice a week. But Rachel is very motivated and does alot on her own at home.

I am thinking that soon Rachel will be able to update her own blog :-) and share with you all her thoughts, prayer requests and achievements.

Let's pray for quick results with this HBOT!

~RuthAnne

Saturday, December 1, 2007

HOME!

Ah, the day has arrived. Rachel is home. Everyone is all smiles and enjoying having her in Iowa with us. The trip went well, an uneventful, 4 hour car ride from Lincoln to Centerville.

There were several tears from the staff at Madonna as they told Rachel goodbye. Her smile will be missed in the hallways and gym.

Wednesday, Rachel walked 250 feet without stopping and then another 100+ feet all in one session. Because her activity level has increased, the doctor said she can go off of blood thinner. She is now medication free!!!

Thursday she did her last set of therapies. Mom and I went to lunch with Rachel and 3 of her therapists. It was considered 'therapy' (or maybe just a good reason to hang out together one last time). Emily (Ryan's sister) was there Thursday and Friday to see Rachel off.

Carol -PT, Rachel, Katie -Speech, and Stacy -OT

Friday we packed up her room and were checked out by 10am. Joyous! Rachel walked out the door of Madonna. Go girl. 8 weeks ago, they asked Dad and Mom what our goals for Rachel were upon her dismissal. Dad said he wanted Rachel to be talking and walking by that time. The case worker looked at him in disbelief and kept her comments to herself. Clearly she thought our expectations were too high.

Rachel and RuthAnne -(due in 4 weeks!)

Leaving Madonna!



We got home mid-afternoon. Did some therapy, hung out as a family and Amy and Jonas (Rachel's brother and wife) brought over supper. It has been a long time since we have eaten together as a family. Ryan was able to come last night as well, he is so faithful to be with Rachel. I think they will be counting the hours each week, waiting for the weekends to come around. Rachel will get alot of good speech therapy talking on the phone to Ryan each night. ;-)

Esther-11, Emily -13, MaryAnne -5 and Rachel


Thank you for all your continued prayers! It is amazing to watch them be answered.

~RuthAnne