Update from Daniel's Mom

Thank you for your prayers and words of encouragement.
The Drs are thinking Hannah was low on potassium and some other
minerals....and because of this (her body being depleted) her blood levels
dropped after dialysis.
I am thankful she was listening too her body & how she was feeling.....
She had a headache, was shakey, and just not feeling right. When she arrived
at the hosp. her blood levels were low....in the 7's & have since risen up
into the 8's on their own! We are very thankful for this.
The kidney Dr is working to figure out what all went "wrong" or is still
needed.
She will stay another night at the hospital and have dialisys there.....just
to watch how her body responds to the dialysis.
Her Mom & Dad are with her and learning more about her diet needs and other
health concern/ needs as well.
thank you

Back to the hospital

Hello Friends,

Please pray for Hannah. She went in for her first dialysis treatment since leaving the hospital at a dialysis clinic in Leavenworth. The dialysis went really rough...Hannah felt terrible the whole time and just thought it was the dialysis, but as soon as the dialysis was finished, she still felt terrible (tingling through her whole body, bad headache, extremely weak, etc.) This really concerned her and those who gave the dialysis, but the nurses didn't know what to do, so told her to go into the ER at Olathe Medical (where she had been staying before).

She, Daniel and our parents (just back from Africa) went in to the ER this evening. They found that Hannah has a Urinary Tract Infection (because of the dialysis).When Hannah had previously been in the hospital, the doctors had not wanted to see her blood count go below 8. This evening Hannah's blood count had dropped to 7.4, so she had been readmitted to the hospital. She is going to be getting another transfusion either tonight or tomorrow and put on an antibiotic for the UTI. They are also still waiting on the results of the CAT scan they did because of her headache.

Even though this is somewhat discouraging, Hannah was very blessed because she was able to have her former hospital room (the only room on the floor with just one bed in it so that she doesn't have to share the room with another patient). This also means that she has the nurses that she already knows.

We're not sure how long Hannah will have to be in the hospital. I'm guessing that it will depend on her blood count going back up.

Will update you as soon as we know more. Thank you so much for praying!

-Chloe

Hannah's going home!!!

Hello friends!

I want to share some exciting news with you all! Hannah gets to go home this afternoon!!!!

The doctors have been monitoring Hannah's blood count the past couple days. The numbers have continued to rise (this morning was something like 9.2), so she finally gets to leave the hospital!

As you can imagine Hannah is very, very thrilled about this news. Our family is flying in from Africa tomorrow, so this is perfect timing as Hannah will need lots of help once she's back home.

I know that Hannah is going to have to continue going in for dialysis treatments three times a week (Tuesday, Thursday and Saturday) but at this point in time I'm not sure how long she'll have to do that. We will keep you updated on this.

Please pray for Hannah's transition back to home:

-that her blood count keeps going up, and stays up

-that her kidneys continue to mend

-that God gives us wisdom in how to best address Hannah's Lupus and Lyme's disease

-that the home is filled with peace and grace as Hannah transitions back into being a full time mommy again

-that Hannah doesn't get overwhelmed with all the medications she will be taking, but that she is able to understand and know how to take each one

One of the other main areas you can pray is about Hannah's diet. We talked a little with the dietician yesterday, and it looks like Hannah is going to have to be on a pretty strict diet. My Mom will probably be the main one figuring this out and cooking for Hannah, so please pray for her. Also, for those of you who have dealt with kidney failure diets, we would so appreciate some good recipes or meal ideas (you can send those to me – please understand if I can't respond to your messages).

Thanks so much to all of you who have personally messaged me, sharing your care and concern for Hannah. I'm so sorry if I'm not able to respond right now...please know that we SO appreciate you taking the time to express your love. I daily call Hannah to share all of your sweet notes with her. :)

Isn't this all so amazing!? Our God is mighty!

Rejoicing,

Chloe

Update from Hannah

Hello All!

Its me - Hannah! I know Chloe just sent out an update here recently, but I thought I would say Hi to everybody and give you all a peek into my world here in the hospital.

I have been feeling so much better these past couple days. Dialysis has definitely brought down the swelling and is getting my body back to normal. With all the extra pounds of fluid on me it was so hard to walk around or do anything, so with it coming off its been great!

Boy, what an experience its been in the hospital! These past three weeks have been a whirlwind, but God has just been pouring out blessings all over the place...

I have so enjoyed seeing my kiddos everyday. Adonia (almost 3 yrs old) acts like she owns the hospital. When she comes to visit, Daniel says she insists on taking the lead and walks right through the entrance door, through the lobby, elevator (she knows what buttons to press), winds her way through the hallways....straight to my room! Her and I love doing manicures together, so everyday she comes in, hops up on the bed and we get a new nail color on. She had a big growing up moment the other night when she got to paint her toenails by herself for the first time. She did such a good job that I let her paint mine and Chloe's too...but had to draw the line when she asked to paint Daddy and Creed's toenails. :) She is so helpful in kissing all my boo-boo's and praying for me...and she always wants to make sure I get my intake of animal crackers for the day. Creed is my little happy “chunky monkey” (as we call him) and bright smiling sunshine! It seems every time I get to see him he is bigger and bigger. He loves to stick everything in his mouth and I hear he has adjusted well to eating lots of varieties of food since I haven't been able to nurse (because of all the steroids I'm taking).

On to Daniel.....my most AMAZING husband ever! This experience has totally brought us to a whole new amazing level in our marriage. We have bonded like never before. He has been the best support and encouragement to me and has such a servant's heart. He is constantly by my side asking if he can do anything for me, helps keep my room tidy and gets me anything I need. He reads to me, prays for me, and makes me laugh. Its been nice having him able to sleep here at the hospital with me so we get our evening together. Its amazing the little things that mean so much. The other night we were getting settled in together to watch our tv show for the evening, when I had the sudden craving for popcorn...so we sat trying to figure out how we could get some from somewhere. He then suggests he couldn't get me that, but that he could take me on a “date” to the vending machine. I got overly excited at the thought of treats (since I have been on a restricted diet we were actually going to have to sneak it in)....so we walked (or he walked...I waddled) to the vending machine where he spent several bucks getting me whatever I wanted! I was so excited - like a kid at the candy store. He is the best! Another night we had an funny memory together in the bathroom. I really needed to wash my hair and I had to be extra careful, since I can't get my catheter (that's near my neck, in my chest) wet, so I was on my hands and knees on the floor with my head hovered over the shower drain, Daniel was standing next to me with the shower hose, attempting to wash my hair. He got some shampoo and put it in, realized it wasn't enough, and went back for more. He ended up going back to get get shampoo four more times before I said "Daniel, I have a MANE of hair....GLOB IT ON!" We sat there laughing just thinking of how we looked getting my hair washed. I told him we don't have to worry about how we'll do together in our older years , because we are already experiencing it, with him helping me with getting dressed, washing my hair, and taking care of me. :)

I have so enjoyed my beautiful room! I have what I call my "garden" in the long window sill of my room, a row of the flowers you all have sent. With all the cards that you have sent, we have strung and hung them all over my room! Its so beautiful and every time I look at them it makes me smile to think of you all taking the time to pick out, write and mail your love to me! The nurses come in all the time and say "Wow, this is the prettiest room ever!" :) Thanks to all of you!

Speaking of the nurses (and doctors, too). They have all been amazing! Other than the thousands of needle pokes and surgeries that they have administered to me, they have been so sweet and helpful (not like the surgeries weren't helpful, but...). Since being in the hospital for this long I have become super good friends with lots of them and I know will stay in touch.

Sleeping here as been quite a time in itself. I have to get my vital signs checked through the night and get blood drawn in the early morning, so a full nights rest is out of the question here. Also, since I am on steroids I have been feeling pretty awake. Getting a good solid three hours of sleep is great for me and I wake feeling very perky and rested. If I get to bed at midnight, I can be up and wide awake at 3 in the morning ready to go! So God and I have had some wonderful times at those hours in the early morning together. I am reminded of the verse in Psalm 119:148 "My eyes stay open through the watches of the night, that I may meditate on your promises." And the steroids have definitely helped for that! :) I am so glad God is available for me 24/7. :)

I can't wait to have my parents and siblings back in the states !!! We are so excited as we make plans and arrangements to get them settled in with us in our house. It will be a full house and a ton of fun going on for sure...and it will be soo wonderful having their help as I get back on my feet in the next months.

I know you all have heard the great news that I will be getting out of here soon, and of God's healing of my body. Yesterday when I got the news my heart was so full of joy and excitement...I was jumping and dancing around my room like crazy, just celebrating what God had done! (and hoping one of the nurses didn't pop in and think I was going out of my mind!) When I was first in the hospital I was so bummed to think that I would be spending my month of August here, feeling like I was stuck and missing out on life. But God has given me one of the greatest months of my life. I wouldn't trade it for anything! I have so grown in my faith and trust in God, I have come to an amazing deeper level in my relationships with my husband and family, I have been so blessed to realize how so many people care and how powerful prayer is, and I have deepened my relationships with some people that I never would have had the opportunity to do if it wouldn't have been for this experience, and made tons of new friendships. Its been an experience I will never forget and would never want to take back. God has given me the best gift ever!

I just want to say thank you for your continued prayers. It was such a great encouragement, especially when everything was really going rough with my intense swelling, pain, surgery recovery, and just feeling very overwhelmed with all the news and diagnosis and information being poured into my little mind. God is teaching me to take everything a day at a time. And He will take care of the rest! I know its going to be a journey ahead adjusting to my condition and changes in lifestyle and just knowing my body can't take as much.... but I am confident in the verse of who God says I am, (Psalm 139:14) "I will give thanks to You for I am *fearfully* and *wonderfully* made. Wonderful are your works: and my soul knows it very well."

I hope I haven't rambled too much...I know my writing skills aren't anywhere near Shakespearean. ;)

I just can't even express how much you all mean to me!

Love you all!

~ Hannah

Isaiah 41:10 "Do not be afraid for I am with you. Do not be dismayed for I am your God. I will strengthen you, I will help you, I will uphold you with my victorious right hand."

Good, good news!

In the middle of the night about a week ago, Hannah was awake in her hospital bed, crying out to the Lord from the depths of discouragement. The doctors had told her she only had 2/3 a chance of living in the next five years. The doctors had told her that she would probably never be able to lead a normal life again....that she would probably have to take chemo-like medications...that she may have to deal with these medications and dialysis the rest of her life...that she may not be able to have any more children. Overwhelmed with fears of what the future held, crying out the question, “God, and I going to die?” she flipped open her Bible, hoping for some word of encouragement. She looked down at the pages and her eyes rested on these words, "I shall not die, but live, and declare the works of the Lord." (Ps. 118:17)

Yesterday afternoon Hannah's Lupus doctor (the one who had been the most sober about her situation and future) came into Hannah's room and – fighting back a smile – told her that that day, August 24^th, marked the beginning of her path to living a normal life – yes, a NORMAL life! He told her that she would probably be able to get completely off of dialysis. He told her that she would probably be able to leave the hospital within a week. He told her that it looked like she would recover and be able to be a lively, active wife and mother for the rest of her life.

Yesterday evening Hannah shared this miraculous news with us and, beaming, shouted, “I shall not die, but live, and declare the works of the Lord!" (Ps. 118:17)

We praise You, Father!!!

Hannah is continuing to respond very well to the dialysis. Her blood count is gradually improving. Hannah had been given her first major Lupus medication a few days ago, and to the doctors surprise, hadn't experienced any side effects (this specific medication normally always comes with pretty major side effects). Her blood pressure is finally beginning to go down.

We are overwhelmed with joy. We are overwhelmed by your fervent prayers...by your deep love and concern. We are overwhelmed with awe as we worship our God who sees, whose hand is not too short to save.

We know this journey is not over, and will continue to keep you updated as Hannah recovers.

Much love to you ALL,

Chloe

Hello dear friends!

I know you have all been anxiously awaiting an update on Hannah, and I first want to apologize for how long its taken me to write this. Between being a new mommy to a 2 ½ week old daughter, to frequent hospital visits to see Hannah, I'm swamped! Thank you so much for your patience, and please forgive any delays in response or updates.

Now to the update! (I apologize in advance for the length)

DIALYSIS
Hannah has been doing dialysis daily, and this is an area that we have really seen prayers answered. Her first couple days of dialysis were quite rough, but things seem to be going more smoothly now. It seems like Hannah's kidney function is stabilizing, if not getting better, and with each dialysis treatment, the swelling is going down...there are still 20 lbs of extra fluid on her body that we hope the dialysis will address. The plan is to continue to do dialysis daily. Once Hannah is out of the hospital, she will be going in to get dialysis three times a week.

BLOOD COUNT
This continues to be the biggest prayer need. Hannah's body is still rejecting the blood in her body. She had a transfusion the day before yesterday, and they are looking at doing another one soon. Until this improves, Hannah cannot leave the hospital. Thank you for continuing to pray that Hannah's body stops fighting itself, and accepts the blood that the hospital is giving her.

HANNAH
Thank you all SO very much for praying for Hannah's encouragement – I have personally seen the effect of your prayers the past couple days I've gone to visit Hannah...she is noticeably more upbeat and cheerful (more like the Hannah we all know and love). The nurses at the hospital are all delighted by how cheery Hannah's room is. Your cards, gifts, flowers and posters have made Hannah's room so fun and cozy...I know this helps brighten each of her days.

VISITORS
Especially since dialysis has started, Hannah has been extra worn out, so Daniel and I feel the need to reiterate some guideline for those who would like to visit Hannah. Please make sure to call or text Hannah or Daniel at least an hour before going to visit so that we're not interrupting Hannah's dialysis, naps, or visits from family. Most importantly: while visiting Hannah, please keep an eye on the clock, and keep your visit to strictly 15 minutes or less. **Hannah may seem chipper and talkative, but is much more tired than she seems**. Hannah is so thankful to each of you who have taken the time to visit Hannah – I know this has cheered her up a lot.

BIG NEWS
For those of you who don't know, mine and Hannah's parents are currently living as missionaries in Mozambique, Africa, along with our younger brother (18 yrs) and sister (16 yrs old). Due to the high cost of airfare (about $3,000 a person), they have been unable to come back to the US since Hannah's been in the hospital. As you can imagine, it has been heart-rending for them knowing the things that Hannah has been going through and not being able to be here with her in this time. Just this week their home church told them to come home, offering to pay most of their airfare. This has overwhelmed and blessed us beyond words. My family quickly bought tickets, and will be arriving this next Sunday (the 28th). They will be staying for 6 months (but will be able to change the date if necessary), and will be living with Hannah and Daniel, helping care for Hannah, prepare healthy food, and take care of the kids and house. If Hannah is still in the hospital when they get here, my Dad will be taking an active role in talking with the doctors and sorting out all the medical advice so that we can better decide the best way to help Hannah. My mom will be making sure that Hannah is eating much healthier (so that she recovers faster), and being there to comfort her like only a mother can. My parents will also be helping out a lot with the kids. After praying about it, we feel this is an opportunity for you to give financially if this is on your heart. If you would like to give, your gift will first go to covering the rest of my family's airfare, and then will go towards other expenses my family will have while they're here including gas (trips to the hospital, doctors, etc. and food for them and Hannah and Daniel's family).

If you would like to contribute toward this, you can make checks payable to Daniel Maddux (Hannah's Dad) and your gift can be sent to:
Daniel Maddux
1124 E Westerfield Place
Olathe, KS 66061

Or if you would like your gift to be tax deductible, you can make checks payable to Daniel Maddux and your gift can be sent to:
B.E.A.
c/o Thomas and Linda Ledford
31625 Summit Ridge Dr.
Crystal Lakes, MO 64024

HUGE thanks in advance for your generosity...this deeply blesses us. One last prayer request would be for my parents as they're swamped trying to get ready to leave Africa on such short notice: packing, getting ministry and finances in order, etc.

I'll bring this long note to a close now. May God richly bless your hearts as He has ours. You all are treasures!

Much love from us all,
Chloe (Hannah's sister)

Dear Friends,

Daniel, Hannah's husband, just called me with an update. The doctors came in this morning and told them that Hannah's kidney's have been getting worse. I've been wondering if this was the case since she seems to have been getting more and more swollen. Her kidneys are now only functioning at 10%, and their guess is that she has about 30 lbs of extra fluid on her body.

They just started her on Dialysis. Please continue to pray.

Please pray that her Lupus "calms down" so that it stops attacking her blood. This is the main reason they're having to keep her in the hospital, because her blood count keeps going down so fast that they have to keep doing transfusions.

Thank you - every single one of you - for praying. Even as things seem to be getting worse, we continue to look to our Mighty God for help - He is so worthy of our praise!

Just one last note about visitors. At the moment Hannah is very weak and tired. If you are wanting to visit, please call Daniel or text Hannah at least an hour before hand to make sure they're up to visitors. Also, please do your best to keep your visit short (around 10 minutes)...Hannah loves people and its hard for her to ask her visitors to leave, so let's keep it short and sweet. We want to make sure that Hannah gets plenty of rest so that she has energy when her children come to visit in the evenings. Thanks so much for honoring us in this way!

Much love to you all,

Chloe (Hannah's sister)