Wednesday, December 16, 2009

Successful Feeding Tube Replacement

The feeding tube was replaced with ease and no complications. Thank you for your prayers!

Andrea is starting a new routine of physical therapy and occupational therapy at home. Dialysis is at home, too, on Monday, Wednesday and Fridays. She still goes to the Speech Therapist near Southwest Memorial Hospital, goes to MDA for blood draws on Sundays, and sees her MDA primary doctor there once a week. Antibiotics seem to be working and she sees that doctor next week for a change in medicines.

Andrea misses shopping this time of the year but at least we are out and about to enjoy the decorations everywhere. Betty and her friend, Missy, put up the tree and decorated J and Andrea's house. So sweet of them!
Have fun and be careful traveling and all during the holidays. We think of you all.

Sunday, December 13, 2009

New Physical Therapist

Today a new Physical Therapist from Memorial Hermann came to the house since Andrea has been released from TIRR. Next appointment for her is Wednesday.
On Tuesday, plans are to change out the feeding tube in Andrea's tummy. Supposedly it is routine as the feeding tubes wear out often. She will need to go under anethesia, so please keep Andrea in your prayers at 6:30 a.m. Tuesday!
The antibiotics are making Andrea feel a bit better.
Thank you for your faithful prayers, and we remember your needs, too.

Tuesday, December 01, 2009

Meds Working

The internal medicine doctor prescribed one more antibiotic this past week, which means Andrea is taking 4 antibiotics to clear her lungs. We can see good improvement this past week and she is gaining some strength back. We worked out on the exercise mat for an hour and a half this afternoon and she stood in her wheelchair for 30 to 45 minutes. I really do not think I am biased when I say that I admire Andrea's spunk and tenacity.
Please keep the prayers coming as we pray for you all, too.

Friday, November 20, 2009

Close Call but Okay!

The infection in Andrea's lungs is causing her oxygen levels to go down. Her doctor wanted to admit her into MDA from the emergency room, but Andrea convinced him to give her the medicine she needed and send her home because she likes the care she receives at home over the masses of nurses and doctors as in-patient who may have the flu. Her doctor reluctantly agreed, and the pulmonary doctor saw to it that she got an oxygen bottle to use at home should she need it again. So, with new medicine and as-needed oxygen, Andrea is up and trying to get better again. She is also receiving dialysis 3 times a week now which should help clear the lungs.
Your faithful prayers are soooo much appreciated.

Thursday, November 19, 2009

Emergency Room

EMS took Andrea to the MDA Emergency Room last night because her oxygen levels kept dropping to an unsafe level. As soon as Andrea got oxygen from the EMS, she was okay, so hopefully she can get oxygen to bring home today and not have to be admitted.
Please pray.

Wednesday, November 18, 2009

Identified Secondary Infection

We got a call from MDA today that there is an infection in Andrea's lungs. Right now they are trying to see if they can send the medicine home or if she will have to go back into the hospital. For those of you who have been to Andrea and J's house, you know home is a better hospital than MDA, so it is just a question of getting the right medicine to treat the infection.
Please continue your steadfast and immediate prayers and remember that we pray for you all too.

Sunday, November 15, 2009

Hanging in There

Andrea is enjoying the new wheelchair and the ability to stand up in it every day. I had to excuse myself as a "student driver" when trying to manuever tight spots at MD Anderson and that way I get to laugh at myself and everyone else can laugh too.
The doctors had Andrea take an MRI of the abodmen this past week hoping to find an infection that is causing her white blood cells to be elevated. They didn't find anything amiss. However, they do know there is an infection somewhere, but no fever, which is frustrating because it is hard to treat. Broad range antibiotics have such a hard affect on the liver and kidneys. Andrea was especially sad to miss one of her best friend's wedding because of this latest pesky problem.
Please pray for this nerve disruption to pass and the infection to be resolved.
We think of you all each day in our prayers.

Wednesday, October 28, 2009

Very Encouraged

Have you seen the cartoon movie "The Incredibles"? I really liked it because the leading man was a guy named Bob! Also one of the movie's highlights is most people's tortured feelings when it comes to actually using their insurance plans.
Well, we've gone through insurance trials during these past 4 years, but right now all I can say is that Andrea is driving a motorized wheelchair that also goes into a standing position when she wants or needs it to. It gives her independence in her own home, endurance in the standing position, and she can do so many of her physical therapy motions while she is in the wheelchair. She has been very encouraged by this new form of assistance and we are very pleased.
Thank you for your prayers, and please know that we pray for you too.

Monday, October 12, 2009

New Responses

This past week the TIRR physcial therapist applied nerve stimulation to Andrea's right leg (which has been pretty much numb) and got some really good response. Since then Andrea has been able to slightly kick it, move and bend it more. yeah! The therapist says it is a good indication that Andrea will be able to walk again.......however, we know that could take a long time. TIRR occupational therapist mainly works on Andrea's right arm and hand which is showing some movement. The speech therapist continues to work on Andrea's muscles in her mouth and speech even though the feeling has not returned.
In the mean time Zeus loves being in his new home and welcomes Smokey (Betty's dog) or Tito (Bob's dog) very often and they all provide plenty of entertainment for the weekends.
Andrea still requires dialysis which makes her fatigued and is a real drag that limits shopping time or going places.
We are still asking prayers for the kidneys to restart and the hypeintensity to go away so the numbness will dissapate in her face and lips.
You all are so kind to read this blog and we think of you all daily because we know you have ups and downs in your lives, too.

Saturday, September 26, 2009

Healing, but slow

It has been a while since the last posting, but more of the same has been transpiring with doctor visits, dialysis, and TIRR rehabilitation physical and occupational therapy. We are so busy that the weeks fly by quickly.
Andrea is regaining strength but is still frustrated with the numbness in her lips and mouth. Still, she pushes on for healing each day and I am encouraged by her willingness to push forward in the midst of headaches or fatigue.
Thank you for your continued prayers. We think of you daily, too.

Friday, September 04, 2009

Stronger but continued frustration

Andrea is doing well at TIRR and has become strong enough that they arranged for her to try out a motorized wheelchair that also moves into the standing position. She is just now trying it out, so it will be a while before she decides on which one will be the right fit for her.
As she becomes stronger it is just so strange that Andrea's mouth has become numb. The neuro doctor said that even though the MRI showed improvement of the brain scan, the hyperintensity is resting over the sensory part so that would explain the numbness in the mouth and face.
We just keep on praying that this nerve disruption dissapates quickly, and thank you for yours.

Saturday, August 29, 2009

Step by step

Andrea continues to try to improve each day with each doctor's, physical therapy or dialysis treatment. She can even con me or Betty into shopping for her and J's new house on the way home from these visits. Any distraction from these very difficult times is a treat as they build a more comfortable home for themsleves. We all admire her and J as they strive each day for a physical health.
The last MRI showed great improvement overall, but the hyperintensity over the part of the brain that controls motor skills is there, so we need to pray that it dissappates quickly. The neuro doctor said it may take 18 months or longer for all of this to occur, and it has been 7 months so far. Please pray for total healing......The TIRR therapists are so encouraging and rejoice at every improvement Andrea makes.
Your prayers are so important, as we pray for you all each day.

Monday, August 24, 2009

Busy Schedule

Andrea has her ups and downs but is continuing to get a little better overall. Her determination comes from faith, hope and prayer that she will be able to eat and walk again. She has appointments every day of the week. When the lungs get clear enough our first hope is that she can drop the Tuesday and Saturday dialysis. Even on Sundays we go to MDA for a blood test and lung x-rays, which are improving.
Thank you for your continued steadfast prayers.

Sunday, August 16, 2009

With Your Prayers

With Your Prayers, Andrea continues to get a little stronger each day. It is very hard for her to realize, but over a 2 week period, her TIRR physical therapist say that she is doing really well and they are very encouraging for her to go to the next level. As long as Andrea is on a firm surface, like her exercise mat, she can sit on her own for at least 15 to 30 minutes or more. Then she exercises her arms and legs. We are so very encouraged by her determination and abiltiy. We are scheduled to go to the MDA doctors his week, too, so hopefully they will have good news about her lung xrays.

Please continue to pray for her swallowing ability as she prays for each of you and your daily hurdles.

Friday, August 07, 2009

Standing Chair

Andrea is getting a little stronger everyday. At TIRR this week, they put her in a special chair, then pumped it up to a standing position. It was tough work for her but she was so mentally charged and happy when it was all over. She can hardly wait to go back. Andrea continues to go to her speech therapist and MDA doctors. We have great hope that the speech therapist can help the nerves in her throat swallow properly again.
Thank you for your prayers as we remember you, too.

Sunday, August 02, 2009

Starting TIRR

Andrea is excited about being accepted as a TIRR out-patient. She will be going there 3 days a week for an hour each time. The young lady physical therapist was very optomistic, nice and has immediate goals for Andrea to accomplish.
She is also seeing the MDA doctors this week about her cricopharnyx, so please pray that they, too, can help Andrea to heal more quickly. We appreciate all of you and think of you and your needs daily, too.

Saturday, July 25, 2009

Swallow Test

The speech therapist is really good and the doctor who did the swallow test gave her the information that she needed to help Andrea's cricopharynx respond properly when swallowing. Betty and I got to observe the x-ray/barium swallow test and it was amazing. I even found out that we have a floating tiny bone in our throats that is held in place with muscles. All of this is such a detailed process, so please continue to pray that what is done will help the neurological condition to heal.

Andrea is really fighting fatigue but we know it is really her body working overtime to heal. We continue to go to many appointments each week, but the one we are anticipating the most this week is the TIRR (The Institute for Rehabilitation and Research - the leading in-patient and out-patient hospital for neurological or neuromuscular injuries that Memorial Hermann runs for UT Medical and Baylor College of Medicine). Hopefully (and prayerfully) Andrea will be accepted there as an out-patient.

Thank you for your faithful prayers. We continue to the think of each of you in your daily activities, too.

Sunday, July 19, 2009

Moving in the Right Direction

Even though Andrea has to have dialysis for a while, J got it set up at home so at least Andrea can be in the comfort of their own home for 4 hours every Tuesday and Saturday. Please continue to pray that the kidneys heal so that she does not need dialysis or a transplant in the future.
There are plenty of other appointments, but the most promising is the speech therapist who is working with Andrea on her swallowing mechanism. Andrea will have a swallow test this Friday, so please pray that she improves enough to eat something. We think of each of you often and hope you are staying cool enough throughout the summer.

Sunday, July 12, 2009

Mega Appointments

Almost everyday this week Andrea sees several doctors or therapists each day. We count these appointments as blessings because it gets us going early and keeps us moving in the right direction of healing!
I think the most enticing appointment for Andrea is the speech therapist because she gives Andrea all kinds of tastes and stimulation in her mouth to help her learn to swallow without aspiration into the lungs. Again, it is such a fine balance on what and how to do it that it is really amazing to watch and try to help do the same thing at home when we leave.
Please continue to pray for the neurological condition to resolve and for her kidneys to improve so that she does not need dialysis. Twice a week Andrea's blood is drawn to determine if she needs dialysis. We went to MDA this Sunday afternoon and will find out tomorrow if she needs to go for dialysis Monday afternoon.
We do think of you all daily and pray for you too.

Thursday, July 09, 2009

Seeking a fine balance

Andrea spent 4 crazy days and 3 crazier nights at the MDA emergency room last week. At least she got home for the July 4 weekend! Her kidneys seem to be rebounding, but not just enough yet to keep her off dialysis totally. So, the kidney doctor was trying some medications that threw her blood levels all off which made her end up in the emergency room. It is so hard to find the fine balance with all the medications. Andrea has been so active, just going to all the different doctors, dialysis and the most promising - her speech therapist who is trying to help her rebuild face, neck and throat muscles to swallow correctly again.
Thank you for your prayers for Andrea's swallowing mechanism and her kidneys. We think of each of you often.

Thursday, June 25, 2009

Home and Healing

Sorry, blogspot temporarily blocked me out, don't know why, but at last I get to report that Andrea has been home since Friday June 19 and getting better every day. She has a long road to recovery but at least we can help her in the comfort of her and J's home. We have been back to the MDA kidney doctor for a check up and to the speech therapist to help her regain her swallowing ability. We go back to MDA tomorrow to see her primary doctor and to back to the speech/swallowing therapist on Friday. The physical therapist came by the house today to do the assessment and will most likely come to their house twice a week to help her figure out the best exercises to help her regain balance and mobility.
Please keep the prayers going for the neurological condition to improve. Things are looking up for Andrea! Thanks to all of you for your care and concern.

Sunday, June 14, 2009

HOME Wed, Maybe??

Andrea has been improving...and they are thinking of letting her go home on Wednesday June 17, but with so many variables....., we must ask of your prayers for:
her neurological condition to improve,
dialysis to be a non-issue
and overall strength to boost her up and home.
She is doing all that she can do to gather up strength and courage to get out of the bed each day with our help to try to get stronger. She had a visit from her 5 month old nephew, Levi, this weekend which gave her such joy! We pray next posting will be from Home!
Thank you for your continued prayers!

Wednesday, June 03, 2009

Seeing Progress

Andrea is in a regular 11th floor room (accessible through elevator F for those who can visit) at MDA and is working through "issues" so she can go home again. The first thing she wants to know when waking up is "what are the day's goals and schedule so she can get strong enough to go home again". Dialysis is usually 3 times a week. This past week she had a thoracentesis to pull fluid off around the lung to alleviate pain and let her lung expand again. The side pain did not go away as we had hoped and ultrasound she had yesterday showed an aggreviated gall bladder. The doctors are putting their heads together to proceed on that one, so we will let you know how that turns out.
I told J. today that I have never seen such pain, determination to get better or courage as I have from Andrea. I also have never seen such love, coaching or support as the Martin family are to Andrea.
We thank God for such supporters as yourself to read this blog, pray for Andrea and want you to know that we pray for your needs each day too.

Thursday, May 28, 2009

Out of ICU!

Andrea left ICU about 7 p.m. last night. It was good to sleep in a quieter room on the 11th floor without hearing all the alarms beeping from other rooms. Many nurses came by as she was coming in to say "you go, Andrea, we are here to help you get back home". That was just so supportive of them to do that! She is also getting her trache adjusted tomorrow so that it should be easier for her talk, and for us to understand. Today Andrea was already sitting in the neuro chair and sitting up on the side of the bed with the help of the physical therapist. Every bone and muscle of her body aches, but she is limiting pain meds so she can move about and get going again.
Thank you for your prayers. As our regular doctor was leaving rounds this a.m., Charley, a pastor from Second Baptist came in and led a powerful, thankful prayer for Andrea leaving ICU and improving. It was perfect timing as all of your visits are just when Andrea needs a boost. You must know too, that we do feel YOUR prayers from wherever you are. We thank God for you.

Tuesday, May 26, 2009

Talk of leaving ICU

Progress has been slow, but steady. Andrea has been in a chair, sitting up and trying to communicate as best as she can with a trache. I have to admit it is hard to try to read her lips because everyone knows how Andrea like to talk, and she goes too fast for us sometimes. They will change the trache to one that is easier for her to talk, and we are just waiting for them to do that, and then maybe they will release her to a regular room so we can get physical therapy and get back home. That week home was just soooo good, and Andrea wants to be there so much.
Thank you for your faithful prayers. They really, really do mean so much to Andrea and us, too.

Tuesday, May 19, 2009

Let the Healing Begin - Again

Andrea had a trache put in her throat Monday night. She passed her breathing test this morning and they took her off the ventilator and is on a low level of oxygen. She is much more awake and we are all looking forward to get out of ICU now. Again, she has amazed some doctors who have not seen her before.
Thank you for your faithful prayers. I read the blog notes, cards and letters to her and she is so appreciative.

Sunday, May 17, 2009

Path Forward

After several days on the breathing ventilator and medicines, Andrea's lungs have cleared except for the left bottom lung that was not crystal clear the last time doctors declared her "clear". She is also breathing more on her own, has been weaned off the pain meds and is awake more during the day.
The doctors plan to put in a trache early this week to prevent Andrea from aspirating and getting pneumonia all over again. The trache will need to stay in several months to allow time for the neurological condition to continue to improve. We were seeing signs of improvement when this second round of aspiration pneumonia set in.
It was wonderful that Andrea was honored as the Shining Star recipient at The American Cancer Society Gala last Saturday night. Lindsey did a great job speaking on her behalf. Thanks, Lindsey!
As always, thank you for your prayers.

Monday, May 11, 2009

Broncoscopy and Breathing Ventilator

Andrea said she was "exhausted" from her breathing rate and how hard it is to breathe from having pneumonia. This morning her heart showed slight stress, so the doctors decided to put her on a breathing ventilator and that also gave them the opportunity to do a broncoscopy and find out if they could give her more specific antiobiotics to kick the pneumonia.

Some of her other blood numbers improved since yesterday, so we are still hopeful that she will continue getting better day by day.

Andrea needs your continued support and faithful prayers.

Friday, May 08, 2009

No broncoscopy for now

Once Andrea got to ICU, they found a urinary infection and started her on a wide range of antibiotics which could clear the lungs, too. So, one step at a time ....... and as frustratingly slow that is for her, they are monitoring her closely and could decide to do something else at any time. Please pray for clear lungs, eradication of the infection they found, but most of all for the neurological condition to heal completely. Thanks so much.

Wednesday, May 06, 2009

Please Pray Tonight

Please pray tonight for Andrea's lungs. She was admitted to ICU earlier due to the pneumonia in her lungs. This afternoon she was short of breath and very uncomfortable. Her doctor decided it would be best to monitor her all night in ICU. They are planning to perform a broncoscopy tomorrow under close supervision. This will give the doctors the information needed to treat her lungs and the ability to remove some of the junk in her lungs. Thanks in advance for all the prayers.

Tuesday, May 05, 2009

Hospital.....again

Nice try, but after one week at home, Andrea was remitted at her one week check up Monday because of a low grade fever and really bad pain on her right side abodmen. She told them while in the hospital last week of the pain but after CT scans, they could "see" nothing, so they allowed her to go home on a reduced scale of antibioitcs and so now they figure something is brewing and they need to find out what that something is.......
Well, home was just toooo gooood, so we need to figure out what this something is so we can get back there by the weekend.
Please know that we continue to think of you and your family as we go through this latest trial.

Wednesday, April 29, 2009

Home! Monday April 27

Andrea came home from the hospital Monday late afternoon just before the big 10 inch rain came across Houston. It has been wonderful to be home, and very, very busy trying to find all the right spots to put things into the new house. She continues to get just a little bit stronger every day with exercises and visits from friends who help her. The home health care nurse has already come for her weekly visit and a physical therapist should be by soon.
Many nurses said "unbelievable" when we took Andrea home after almost 3 months in the hospital, but we say "All things are possible with God".
Thank you for your unending prayers, as we can see that God has answered our prayers the way we asked for again. She still has a lot of recuperation to accomplish. She wants so much to walk again, and it may take months for the neurological condition to improve. Love and prayers to all.

Thursday, April 23, 2009

Home Monday??

Plans are being made to go home Monday, April 27, but Andrea says that with reservation because she does not want to "jinx" anything thing in the works. However, with prayer, we are making plans that it will happen. The swallow test today was better than that one month ago, which means the neurological condition is improving even if it is slow. She is still having problems with high blood pressure which the kidney doctor attributes to blood vessel leakage rather than kidney function. The kidneys are trying to do their part....somewhat!
Your part in prayer is very critical, so thank you very much. We continue to remember you and your family in our prayers.

Saturday, April 18, 2009

Plans

Yeah, feeding tube working again! No more disruptions! We are still making plans for Andrea to go home but do not have a date yet. Please keep those strong prayers coming!

Friday, April 17, 2009

Closer, but not there yet

Andrea is getting stronger and we all keep talking about going home, but in the wee hours of Friday morning her JG feeding tube clogged. They put meat tenderizer in it to clear it, but it did not clear. As of Friday afternoon, she is still on the waiting docket for Interventional Radiology to do something about it. Urrrrr. We are so encouraged by your prayers, and it has been very routine for us to pray for you all daily, too. Oh yes, those dogs do keep us laughing, don't they!!

Tuesday, April 14, 2009

Biopsy results

Biopsy results showed healing taking place in the "tubes" of the kidney and just a little scar tissue. The filtering part of the kidney was not inflamed. The doctor did not think Andrea would be on long-term dialysis. Since there is swelling in her legs/ankles, he thinks it is blood vessels leaking fluid. This is just one of the many specific details of figuring out how to help Andrea get well. She is still exercising as much as she can, trying to gain strength to sit up and maintain balance.
The fun part is that she did get to see Zeus over the Easter weekend and Mary's new French bulldog puppy.
We appreciate your prayers as we pray for your families, too.

Thursday, April 09, 2009

Kidney Biopsy

Andrea had a kidney biopsy today and she could not stay on her "getting well" routine of physical therapy and exercises for now. We will not know the results of the biopsy until Tuesday, but they are suspecting the kidney to be the one not functioning up to par and causing the high blood pressure. Based on the findings, they will adjust treatment one way or the other. Please continue to pray for the neurological condition to improve, as it slowly has. Prayers work! We also pray for you and your household.

Friday, April 03, 2009

MDA day 57

My, how time passes quickly even when it is not so fun. We are constantly busy trying to piece the puzzle together on how to help Andrea get better and go home. She started exercises to make the muscles in her throat stronger so she can swallow properly again. The headaches keep popping up which make it hard to work out in physical therapy as hard as she would like to. The kidney doctor today said he thought the high blood pressure may have to do with the kidneys, so we will be looking at an ultrasound and maybe a biopsy this coming week.
On a sadder note she will be missing Chris and Alicia's wedding which she wanted - oh so much - to go to. She sent hugs via J. since he is in the wedding.
Please continue to pray for the neurological condition to improve, as we feel like that is the biggest hurdle. We continue to pray for all of you dear friends and family too.

Friday, March 27, 2009

MDA day 50

Well, it is day 50 here and we are not "supposed to" be counting anymore. But, that is a way that Andrea knows just how long it is taking her to recover from this aspiration pneumonia gig. We do now know from tests this week that she can aspirate just from normal saliva each day, most likely when sleeping or even nappping when Andrea cannot grab the suction tube to get the stuff out of her mouth before it goes down into the lungs. She has started coughing, (that is good) otherwise it would go straight to the lungs. That is what aspiration is .....when any fluid goes to the lungs instead of the stomach. Anyway, Andrea is getting better, but the steps are smaller than she would like. So, we continue to pray for aspiration to stop and the neurological condition to improve.
Thank you for your prayers as we continue to pray for you and your family too.

Tuesday, March 24, 2009

MDA day 47

Good things are happening, like seeing Zeus on the outside benches of MDA this past weekend. Oh, relatives were visiting too, which was a great bonus as they could actually talk! But, the visits were good and uplifted our spirits. Andrea also had a "wheelchair fitting" yesterday so she can be more comfortable as she is trying to be more mobile. She is being unhooked from all the meds every day for a few hours so rehab can work with her in their facility at MDA. We are starting talk of "going home" even though no one knows when that will be. A swallow test will be performed tomorrow, so hopefully that will be another step forward in figuring out why this aspiration pneumonia occurred and what can be done about it.
Thank you for your prayers as we remember to pray for you and your families.

Friday, March 20, 2009

MDA Day 43, Spring

Today is the first day of spring and after 43 days, Andrea happily got to go outside in her wheelchair for "real air and sunshine". She is doing better each day with physical therapy. We are real glad that she is sitting up, but she is hard on herself because she is not sitting up "straight". We know that it will happen as she becomes stronger, but it's hard for her to not be able to do that now. (You all know her "can do" personality.....) I am now waking up with a "to do" list for the day, and that makes me happy : ) We think dialysis will either be 2 or 3 days a week, but I'm predicting it will be less sooner rather than later.
Thank you for your prayers as we remember you and yours, too.

Tuesday, March 17, 2009

MDA Day 40

March 17 Happy St. Patrick's Day. It was one year ago Andrea received her 2nd stem cell transplant from her sister, Kristin. She's as anxious to get out this time as last year. Andrea had a really good morning. Her bed can be manuvered to a sitting position with her feet dropped down. She stayed that way 2 hours this morning and then the PT and OT came in and moved her to wheelchair. She used her left arm to help the therapist push the wheelchair around the 11th floor. She continued sitting in the wheelchair for a shampoo and stay there until well after lunch. I think she will be sore from so much activity, but knowing Andrea she will count it as gain because of using muscles she so desperately wants to use. The lungs are improving and please continue to pray for the neurological condition.

Wednesday, March 11, 2009

MDA day 34

I'm sorry it's taken me a week to get back to this blog, but we have been working real hard with Andrea. I had a bad feeling when Andrea was bleeding from the dialysis catheter insertion. She also had too much fluid removed in dialysis that same day and it caused her blood to desaturate (not enough oxygen in the blood). She had taken 5 steps forward in recovery, then with this desaturation, she took 10 steps back. Her goal is get out of the hospital and it is not happening as quick as we would like for it to. Please continue to pray for the neurological issues to clear.

Wednesday, March 04, 2009

MDA day 27

When I told Andrea it was March 4 today, she said "Wow, I've got to get out of here". Her attitude is refreshing. The lung x-rays are improving, but still showing some pneumonia. Respiratory therapy is helping a lot.
Andrea had a permanent dialysis catheter put just below her collar bone this morning. She was receiving dialysis right after the procedure for putting the catheter in and there was extra blood that a mom gets nervous about seeing, so it was a good time for me to leave so I can be refreshed for my night time shift. She may not need dialysis every day, but at least the catheter is there if she does need it. Andrea is weak but will push herself to the limits for physical therapy. She has some real good PTs.
We are seeing some neurological improvements and those can only come from your prayers. Thank you for your faithful prayers.

Saturday, February 28, 2009

Still Struggling

Day 23 at MDA (Sat.), Andrea is still struggling to get her lungs clear. Respiratory therapists are in and out of her room a lot. She is weak, but she will still gather her strength for the physical therapists to help her move about and exercise. It takes about 2 to 3 hours for dialysis each day and it has been helping quite a bit.
Please remember to pray for the neurological condition to clear. We are so grateful for each of your prayers.

Tuesday, February 24, 2009

Finally!

Finally, about noon today, Andrea had a tube put in lower tummy so she can receive nutrition. She told us yesterday, "let me eat and I will get well". So, by late this afternoon, Tuesday, she can get some formula into her tummy so she can get stronger and help her beat this congestion in her lungs. It really is a difficult battle, because it is hard to have strength to cough up what is in her lungs. She is a resiliant young lady who has your prayers to call upon God for healing, and she definitely thanks God for you all daily.

Sunday, February 22, 2009

Last 4 days

These last few days Andrea's kidneys have been responding well to dialysis. However, her lungs are still on a roller coaster of looking better one day and relapsing the next. Tomorrow (Monday) the doctor plans to put a tube in her lower tummy to feed her until the swallowing reflex gets stronger again. Even though she is weak, she insists on physical therapy. That's our Andrea......go for it! We appreciate your prayers so much, especially for the lungs to clear and become strong again.

Wednesday, February 18, 2009

Regular MDA room

Late yesterday Andrea was able to go to the Stem Cell Transplant floor at MDA. They will concentrate on clearing her lungs, helping the kidneys along with dialysis, figuring out how to feed her since she still chokes some when swallowing and physical therapy. She is encouraged so much by your thoughts and prayers. Thank you, thank you, thank you.

Tuesday, February 17, 2009

ICU Tues 2/17

Andrea received dialysis all morning today. She coughed a lot last night which is "good" because the lungs are responding to treatment but it did keep her wake most of the night. The doctors are saying she'll go to a regular room "soon". Thank you for your prayers!

Monday, February 16, 2009

ICU Mon 2/16

Andrea started talking yesterday afternoon and this morning she is telling us about all kinds of events. Some of them are very factual and others we have had to tell her that it was just dreams she's been having over the past week. Last night we had the dr. give her Ambien because she has been in such a half wake/half sleep state that she really was sleep deprived.
Today they are taking her off some antibiotics, increasing her tube feedings, and giving her dialysis to help her kidneys. She's been coughing a lot of stuff from her lungs, so they will be watching that too. They want to more comfortable with her lung and kidney capability before they let her go from ICU. I know Andrea is "back" with us because this morning when I was massaging/exercising her feet and ankles, I asked her where she wanted to walk to. She said "Home". I told her everyone is praying for that and it will happen as soon as the lung/kidney function gets in sync. Your prayers are being answered in the way you are asking and what you are asking for. Thanks.

Sunday, February 15, 2009

ICU Sun 2/15

Better today than yesterday, but not well enough to leave ICU. Each day's progress brings us hope that not only are Andrea's statistics better but that she actually feels better. She is moving her arms and feet around this morning because she remembers the repercussions of being in bed for too long of a period of time. She still seems very tired and it is hard to get rest in ICU with all the machinery and tests being run in the wee hours of the morning.
Thank you for your prayers.

Friday, February 13, 2009

Prayers Heard

God heard your prayers to clear Andrea's lungs. They are not perfectly clear, but so much better than yesterday. She woke up this a.m. trying to tell me something but I didn't get it, so she leaned forward for me to discover one of the blood pressure cords was between her and the bed. They will try to start weaning her off the BiPap machine today and will start the tube feeding again. She was shaking her head and seemed really concerned about that, but the nurse explained to her that she would only get about a teaspoon an hour and they would be checking to make sure it would not aspirate into the lungs. Andrea is listening and comprehending everything we are saying. It is good to get a definite "yes or no" head shake today for what is going on.
Please continue to pray that the after effects of chemo continues to clear in the brain as we pray for all you in your daily lives, too.

Thursday, February 12, 2009

ICU Thurs 2/12

The potent antibiotics kept the pneumonia from getting worse. Andrea can respond by blinking for yes and shaking her head for no. She is on a BiPap breathing machine that supplies both pressure and oxygen, so hopefully the result will be somewhat related to what the doctors were looking for in the hyperbaric chamber by adding pressure and oxygen in the blood stream. We are being reminded of the blood gases and acid in the blood that we all deal with every day and are never aware of because we just feel okay.
Please keep up your kind prayers because we feel she is better today than yesterday. Prayer is THE very best thing you can do for her.

Tuesday, February 10, 2009

ICU Tuesday

The tests revealed blood urea nitrogen levels and creatine (kidney) ratio way off plus this bad infection in Andrea's lungs are the main reason for her unresponsiveness. However, she has responded to some light and some voices today but is not able to speak yet. We believe she will respond to the "big guns" antibiotics and prayers will be answered again.

Monday, February 09, 2009

ICU

The doctors moved Andrea to ICU today so they could run more tests in a quicker fashion. Her lungs did not respond to the antibiotics like they had anticipated they should on Saturday and Sunday. They are looking at some sort of renal (kidney) failure or other infection that could be sending her blood numbers askew. Thank you for your faithful prayers.

Sunday, February 08, 2009

Critical Monday

Monday will be very critical as the MDA team of doctors decide to (or not to) put a feeding tube in Andrea's tummy until this nerve disruption subsides which is causing her to choke on liquids and escape to her lungs. The brain doctor says he sees an indication that it will subside and she can recover from this fully. She is still in the hospital and resting not so comfortably, but as always, Andrea is a real trooper and tries her very best. She sends her prayers and love to each of you, because she is so grateful for you praying for her.

Friday, February 06, 2009

Hospital, again

The pain block in the face trigeminal nerve seems to have worked, but since Andrea is supposed to taper off the pain meds for it, we won't really know until Monday or Tuesday.
The last two days has been strange, though, because this chemo nerve disruption has caused Andrea to cough or almost choke when eating or more especially drinking fluids, which most of you know she tries to have a water bottle around all the time to help her kidneys.
Today we started out at physical therapy at MDA, had lunch, went shopping for some Puma tennis shoes, went to an MRI, then to the Brain & Spine doctor. He examined her and personally pushed her wheelchair to the MDA Emergency Room to get all the tests they needed on a Friday at 5 p.m. (He knew there was no other way to find out what he needed to know at this time of week day.) As he suspected, Andrea has infiltrates (- fluids-) pneumonia in the right side of her lungs. She can't eat or drink until Saturday when they find out if she can eat or drink without it going to her lungs.
Again, all this just seems unbelievable, but we keep praying. Thanks for yours.

Wednesday, January 28, 2009

Pain dr. says

The pain doctor says he can do a temporary pain block on Andrea's facial trigeminal nerves on Thursday, Feb. 5. It's categorized as another "minor surgery", which we know are never minor and is supposed to last about a month, so that is long enough for her to get through the hyperbaric treatments which have caused the nerves in the face to be so painful. Her blood pressure has been really high the last few days, so we are to see her regular MDA doctor tomorrow. This is in addition to daily hyperbaric treatments, and M-W-F physical therapy so if feels like we are just running from hospital to hospital all day. We have faith in God for her healing.
Please keep praying all this works for Andrea. She's in quite a bit of pain.

Monday, January 26, 2009

Hopeful

After 16 hyperbaric treatments down at Memorial Hermann, we can see movement in the Andrea's right hand again. We are still going every day Monday through Friday. MDA physical and occupational therapists will be working with her motor skills on Monday, Wednesday and Friday. It is unbelievable how quickly the nerves deteriorated and how hard she has to work to bring them back. The nerves in her face are still painful especially on her right chin and jaw, so it hurts even more when she eats. We will see the MDA pain dr. on Wednesday, so we will finally get his view on everything that has been going on.
We really appreciate your prayers as we remember all of you too.

Thursday, January 22, 2009

Physical Therapy

MD Anderson Physical Therapy will try to help Andrea next week with the facial trigeminal pain which she experiences several times a day, and some days almost all day. They have a lot of good exercises and equipment to help her. Our schedule there is Monday, Wednesday, Fridays.
Andrea will continue going to Hyperbaric at Memorial Hermann Monday through Friday from 12:30- 3:30. She's doing all that she can to plow through this downturn.
Thank you for praying for Andrea as we also remember you and yours.

Monday, January 19, 2009

2 weeks down, 4 weeks to go

Please pray that Andrea can finish the hyperbaric treatments. Her headaches have turned into migraines and there is limited pain medicine because her kidney function is not good. The pain medicine she can take increases her dizziness. We realize each of us have daily struggles and we pray for you all, too.
2 weeks down and 4 weeks to go

Monday, January 05, 2009

Hyperbaric Chamber

Andrea will go into the hyperbaric chamber every day Monday thru Friday, about 2 hours a day for 30 sessions, then they will assess her situation.
The Hyperbaric and Wound Care Center's doctors, nurses and technicians are super nice and understanding. It took all morning to check in and to be seen by the doctor, but at 1 p.m. Andrea took her first dive in the chamber. To me it looks like a small submarine with seats lining each wall. It lasted about 1 hour and 40 minutes. She said the stabbing pain in her cheek hurt a lot and more often in the chamber, so tomorrow they will try a mask instead of the helmet. The doctor at Memorial Hermann believes the cheek pain is trigeminal neuralgia, so we will return to MDA at the end of the month to see if the pain doctor agrees with her. The Hyperbaric Doctor said that in the past 19 years she has seen only about 12 patients with close to the same case study as Andrea's. Some cases improved and some didn't get worse. We appreciate your prayers for the best outcome possible, as we pray for the total healing from God.

Sunday, January 04, 2009

Need Powerful Prayers

Since the last posting Andrea and J have become Aunt Andrea and Uncle J.! It was wonderful to welcome Levi into this world Dec. 22. Andrea's sister, Kristin, (who has been Andrea's stem cell donor twice), is doing well and I got to spend the first week with Kristin, James and Levi when they came home from the hospital. Levi is such a sweet baby boy.
Over the past two weeks Andrea has experienced progressive nerve damage on her right side. The doctors have run blood tests, spinal taps, and MRIs. Thank goodness some doctors work during the holidays.
Thank you God that all tests are CLEAR.
The diagnosis is nerve damage from the combination of radiation/chemo.
Even though Andrea hasn't had chemo since October, it is the long term affects of the treatment that is causing headaches, shooting pains on her right cheek, occasional nausea, and even additional balance problems that started this past week. Her kidneys are still having a hard time, too.
Tomorrow, Monday, we go to Memorial Hermann to see the Wound Care Unit where, hopefully, Andrea will be put in a hyperbaric chamber that will increase the oxygen flow in her blood stream that promotes healing. The MDA doctor said there were two cases in Israel that matched Andrea's case study that had marked improvement from the hyperbaric chamber. He thinks it is possible to stop this progressive nerve damage.
We know that with God it is possible (Matt. 19:26, Mark 9:23, 10:27), and we are so, so thankful for each and every prayer you lift up for Andrea.
Again she needs powerful prayers.

Monday, December 15, 2008

More Tests

Last Friday Andrea's neurology doctor at MDA printed out some MRIs for us to see how the this "chemo effect" is changing and evolving. He said it may take 18 months for it to diffuse. He also stressed again the importance of nutrition - we are what we eat! Right now the main issues they are trying to help her with are daily fatigue, headaches and shooting pains.

As we pray for each of you in your daily lives, Andrea is encouraged so much from your prayers.

Friday, December 05, 2008

Getting worse before getting better

Even though the numbness in the arm subsided a bit, Andrea is experiencing the stinging/prickly feeling in her cheeks and a stiff neck. The preliminary report on the MRI tonight was okay.
The brain doctor suggested foods to help re-build the nerve damage from the chemo. The headaches come and go often. Since she no longer takes steriods, the fatigue forces her to take naps. She is so good at doing everything in her power to get better.
As usual, we ask for your prayers.

Thursday, November 20, 2008

Doing Good

This week Andrea's main doctor was pleased that her left arm is less numb than before. He said sometimes with neuro chemo, it goes away completely and other times it does not. Her blood tests showed improvement except with her kidneys. She really needs prayers for her kidneys. They are working about 30-40% capacity. They start dialysis when patients are at about 10% capacity. Andrea is still drinking loads of water a day, and her diet was almost exactly what the kidney doctor wanted her to be eating; however, he said all of us could probably benefit if we cut down on salt intake.
Andrea sees the brain and spine doctor on Monday, but we do not anticipate any more input, so have a Happy Thanksgiving.
We all are so blessed.

Thursday, November 06, 2008

Keep on keeping on

Sorry I haven't posted lately but we were waiting for test results.
Andrea's kidney levels came down close to normal so they gave her a half dose of contrast on the MRI this time. It still shows a high intensity in the medulla of the brain which they continue to attribute to chemo. They are still concerned that it may be an infection or otherwise. So they ordered a spinal tap without chemo and it came back clear, just as it has before. Plans are to continue monitoring. Her left arm has become less numb and she can write again.
Andrea had her flu shot, but she still caught some bug that made her throat feel like golf balls had lodged during Tuesday night. She got a prescription to deal with that, so hopefully she'll be okay tomorrow.
Thanks for the emails, calls and asking about Andrea. You all are a wonderful support group praying for her, and we thank you for that.

Wednesday, October 15, 2008

A Bigger Hiccup

With the higher kidney levels, Andrea started feeling more fatigued and nauseous last week; however, her greatest concern was when her left arm went numb. MDA ran an MRI of the brain and a spinal tap with no chemo on Monday. The good news from the spinal tap is that there are no cancer cells, but the MRI showed a new high intensity spot in the medulla of the brain. Basically, the neurologist said Andrea has had too much aggressive chemo which is causing the spot in the brain, numbness in her arm, throwing her kidneys off balance, and giving her massive headaches . We are meeting with a renal nutritionist tomorrow to help her plan a diet to combat all these issues. I think it is safe to say "No More Chemo"!
Let's just say with Andrea being left handed, she can recover from this quickly.
You know what's next.....pray, pray, pray. : )

Tuesday, October 07, 2008

One More Diversion

Andrea cannot have the spinal tap this month because her kidney function numbers are not in the normal range and her blood pressure has been a bit high. She feels good, but it is one of those silent obstacles that can be picked up from drawing the blood and monitoring the blood pressure. Her main doctor is setting up an appointment with a kidney specialist so he may have added suggestions other than taking her off as many drugs as they can.
We really appreciate your prayers.

Friday, September 19, 2008

3 More To Go

Today the spinal tap with chemo went well so far. Andrea is sleeping through the medication this afternoon. We just pray for no headaches or back pain when she awakes. The advanced practioner nurse was talking to us before the procedure and was surprised/happy when Andrea told him that after today, there are only 3 more scheduled spinal taps. We are all looking to the end of spinal taps and a great new year of 2009 with no more chemo. Her hair has grown back to a "boy cut" length, which I think is cute even though I know she prefers longer hair!
Thanks for checking this site and for your prayers.

Saturday, September 06, 2008

Continued progress

Andrea went to her main doctor Thursday with the jab to the arm vein for all the blood tests. Some nurses are just better at jabbing than others. Her "numbers" are looking good now, but she does need to keep more hydrated. She has become conscientious about how many plastic bottles of water she was using and we have been trying out a variety of reuseable plastic bottles while using the filtered water from home. While in hospital beds along with recuperating and watching HGTV does have an affect on your views of a 'green earth'! An outing to a Home and Garden Show in Katy with Carter Oosterhouse, host of 'Red, Hot and Green" was fun this weekend. Reuse and recycle was the theme.
Andrea is feeling better and we appreciate your prayers.

Tuesday, August 19, 2008

4 More To Go

The spinal tap/chemo went well on Friday. Andrea has only 4 more of those, once a month through December. She has swollen ankles and appears to be retaining water, so we saw the main doctor Monday and he agreed with the pain management doctor to drop a medicine to see if that is the reason. Otherwise, she is feeling okay now, thank goodness!
The brain MRI was good, spinal tap fluid clear and bone marrow is 100% donor cells. We appreciate everyone's encouragement. It has been such a long process, and we are beginning to look forward to fall and cooler weather since we've been having a good dose of rain.

Wednesday, August 13, 2008

Friday is the Day

Andrea goes in for blood tests on Thursday, and if everything checks out good as it did Monday, then she gets the methotrexate chemotherapy in the spinal tap on Friday morning. Like I said before, she just wants to get on with the prescribed treatment and be done with it because she is feeling better. She does feel tired and fatigued, but that can be attributed to the chemo effects that last quite a while after it is given. Her MRI of the the brain this week looks very good, so they are confident the headaches were from low red blood cells. Thanks for your prayers, God listens!

Monday, August 11, 2008

More Rescheduling

The doctors are trying to get together again to reschedule more chemo since Andrea's white blood cells returned to normal, and even though the red blood cells and platelets are low, they are not so low that it would inhibit her from having the spinal tap. They also think the headaches could be from low red blood cells but have ordered an MRI to make sure they are on track. Please continue to pray that Andrea gets a boost in her red blood cells. We think of each of you wherever you are and pray for your families, t0o.

Friday, August 08, 2008

Well.....

I didn't think we'd be disappointed to NOT have chemo, but Andrea is at the point she would like for everything to go as scheduled so it will be fininshed. Today she could not get the scheduled spinal tap with chemo because her red blood count was too low. Most probable causes for this are the chemotherapies of the past, so we go in Monday to see what the blood counts are. We ate liver at Luby's at lunch to see if the iron in that boosts her system, and more yummy proteins this weekend are in store.....so we'll see what comes of it. Otherwise, she is feeling okay, so we'll be praying for a boost in her white and red blood cells.

Monday, August 04, 2008

Gaining Strength

Andrea is feeling better and gaining momentum.
However, today was a bit exhausting just in the waiting game to have blood taken, get a bone marrow aspiration, and see the doctor. Total time for all of those takes about 30 minutes, but we were at the hospital today for 6 1/2 hours, all without Andrea eating during that time because she has the bone marrow aspiration with sedation. We were glad to get home!
On Friday, she gets the once a month spinal tap with chemotherapy. So far, those have been going well and we pray for the same. Thank you for your continued prayers. God listens!

Monday, July 28, 2008

Continuing Improvement

Today is J. and Andrea's first wedding anniversary and we are so happy for them that they are celebrating it with a positive health outlook. The doctor dropped more medication, so Andrea is taking about 11 pills a day now. She has her major burst of energy in the morning and usually has a list of things to be done, then rests some in the afternoon. Andrea has even driven her car some on streets near her home, which shows boldness for any driver! Thank you for your ever-continuing thoughts and prayers.

Sunday, July 20, 2008

Getting Better

Andea is off the immunosuppresant drugs and her platelets have returned to normal. What a relief! Her kidney creatinine level function is still little high, so the main doctor is not going to give her the Vidaza shots now. So, Friday they removed the Central Venous Catheter line that was just below her clavicle. With that line out, it is just so much easier to take a shower. She still needs to drink at least 3 liters of fluid a day, and is taking about 14 pills a day. With all that said, Andrea is 'on the mends' and feeling better. Thanks for your continued prayers.

Thursday, July 10, 2008

Seeing past the discomfort

Tomorrow, Friday, is the day for the once a month methotrexate chemotherapy spinal tap. We somewhat have that routine down now and can anticipate what will happen and how careful Andrea needs to be the next few days.
Monday the plans are for her to take the Vidaza shots once a day for 5 days. She's been drinking as much water as she can so her creatinine levels are good in order to take those shots, so we'll see what the blood tests reveal tomorrow. As with most of us, a good motto may be: "work in progress".

Wednesday, July 02, 2008

Trade Offs

It has been a relief not to report to MDA everyday to receive meds and fluids. However, that means that Andrea has to drink at least 3 liters of water/fluid a day. Anyone who has actually measured that out knows it is one of the greatest weight loss or weight control measures of all time. It is difficult to be hungry enough to eat at meal time, and she needs to gain weight. Plus she is still taking about 20 pills a day. She has a good outlook on what she needs to do each day and is trying to eat healthy meals.
Even though Andrea does not have to go to theATC, she is still at MDA often to test her blood levels, have the Vidaza shots 5 consecutive days each month, and the spinal tap chemotherapy once a month. The spinal tap chemotherapy should be finished by the end of the year. The MRI of the brain came back normal again, so the spinal tap chemotherapy is a reassurance of no relapse.
She was happy this week when they said she could eat salad again. Great gains and great hope. Thank you for your prayers.

Sunday, June 22, 2008

100 Days

As 100 days from the stem cell transplant approaches on Wednesday, June 25, Andrea continues to feel better. They have her reporting to M.D. Anderson once or twice a week instead of every day to check her blood levels and take care of any other health concerns that arise. Also this marks the time that they reduce the immunosuppressant drugs so she can start building up her own immunity system. We're hoping the amount of pills taken a day drops from the 20's down to the teens. She is still receiving medicine through the central venous catheter. It is a long process that takes time and lots of patience.
Thank you for your continued prayers as we realize this is a long time to keep praying!

Monday, June 16, 2008

Wouldn't you know

Wouldn't you know as soon as I said that Andrea had not needed blood or platelets, she needed a red blood infusion on Friday. I noticed that the red blood cells she received stayed good until July 10, so they do not expire as quickly as platelets do. Anyway, if anyone wants to give blood or platelets, just tell MDA you are giving on behalf of Andrea Martin. She is feeling better and is working hard recoup.

Thursday, June 12, 2008

Grateful

We have so much to be grateful for and your continued prayers and support are part of the top of the list. If anyone in Houston wants to give blood or platelets on Andrea's behalf, M.D. Anderson is ready to accept them at 1515 Holcombe, 2nd Floor, near Elevator A. All you need to do is call 713-792-4531 to make an appointment and they will tell you what medicines you can and cannot be on to give blood. It struck a heart string to know Pi Phi sisters (who may not even know Andrea) are interested and praying.
Praise God that Andrea didn't need any this week because she sustained the minimum that she needs. If Andrea does not use any blood donated in her behalf, just know that the blood you donate is going to our fellow Ambulatory Treatment Center friends or to the surgeries that they perform daily to battle these awful cancers.
Andrea is feeling better even though her energy level is low. Her stamina will grow with God's help, your prayers, time, good food and the TLC she has been getting.

Monday, June 09, 2008

Small Gains

Even though Andrea's blood count numbers are low, she gained a few points from the 30's last week to 41 platelets today. We are encouraged that she made her own platelets. The spinal tap went okay last Friday and did not cause extreme pain like it has before. This week she takes the Vidaza shot every day Monday through Friday and is taking infusions of extra daily fluids to be able to take the drug.
Please pray that this new treatment will work in her favor.

Tuesday, June 03, 2008

Steady

Although the platelets are not normal, they have held steady for a week and a half, and Andrea has not required an infusion. This is good news but low platelets causes extreme fatigue. Andrea is not in pain, but has a very low energy level. She is just so grateful not to be hurting that she does not complain, but she wants to do so much more.....You know her....... Please pray for her to make her own platelets!
Also she has to have the chemo spinal tap on Friday, so special prayers would be appreciated for healing and no pain then, too.

Friday, May 30, 2008

Forward

After a long frustrating day last Friday of receiving meds and platelets, Saturday was the turning point when Andrea did not have pain. She didn't have it all this week either, so when the tests came back with no detection of the viruses yesterday, Andrea was doubly relieved. Her platelets continued to drop this week but at a much slower pace. She does not have to have the continuous hydration 24/7 and is free from the pump and bag of saline. What a relief! So now, with God's help, onward with healing.

Monday, May 26, 2008

Better than Last Week

Andrea is feeling better now than she did last week. She received platelets on Friday and they seem to have "stuck with her" through the weekend. She will be having tests this week to determine if the viruses are still lurking and how much additional medicine will be necessary. Without the additional meds, she takes between 25-30 pills a day. So, prayers for her platelets and strength are so much appreciated.

Wednesday, May 21, 2008

Bacteria Down, 2 Viuruses to Go

MDA protocol keeps plugging on, as Andrea strives to feel better. After 2 "all clear" test reports, we can safely say the bacteria is gone.
Tomorrow and Friday are her regular days for treatment of the 2 viruses that are so pesky and take all day and then some at MDA hospital Ambulatory Treatent Center. Pain management has helped with the side effects of the viruses somewhat. However, side effects of this helpful medicine include dizziness and loss of concentration, which Andrea makes into a joke at times that us both laugh at what could be a crying situation.
Your prayers help the best, so please keep them coming!

Friday, May 16, 2008

Baby steps

Andrea had to receive blood and platelet infusions today since both were very low. Her kidney function level was slightly high, so they would not give her the once a week treatment for the virus. She will receive fluids and meds at home this weekend and they will try to see if her levels improve enough by Monday to get the virus medicine.
On a more positive note, the new medicine from pain management has helped enough that she is not in constant pain. There continues to be a dull pain, but she can sleep for a couple of hours at a time without interuption....which is at least an improvemtent.
Thank you for your prayers.

Wednesday, May 14, 2008

Pain Management

Andrea went to the MDA Pain Management Doctor today to see if he had anymore suggestions to ease the pain she is faced with. He actually had a different medication to try and had some moral support since his wife is undergoing treatment for cancer at this time, too. It is a really tough road to go down right now, but I truly believe Andrea can turn that corner to feel better soon.
Your prayers and support are so much appreciated.

Sunday, May 11, 2008

Ups and Downs

One day "this" is feeling better, but then "that" is not, then the next day "that" is feeling better but "the other thing" is not. So, "there" is the life of healing day by day, baby step by baby half step. This transplant is especially hard on Andrea, and I am amazed how she is braving through it. The advanced practitioner nurse and her doctor are keeping close tabs on her daily progress as she goes to MDA each day, but that does not ease the pain she goes through. She had to have platelets on Friday and blood infusions on Saturday at MDA.
Just please keep praying because God listens to us and we believe His miracles prevail.
We had a nice Mother's Day at our house and are blessed by our children.

Wednesday, May 07, 2008

Powerful prayer request

With the immune suppresant drugs Andrea is taking for the stem cell transplant to take place, she is fighting 2 viruses and a bacteria that are trying to take over her system. We need powerful prayers as she goes into MDA tomorrow for new drugs and the will to fight these adversaries. She wants so badly to feel good again; and with God's will, her tenacity and your prayers, we know it will happen. Thank you for your powerful prayers.
Matt. 7:7-8 Ask, seek, knock. For everyone who who asks receives; he who seeks finds; and to those who knock, the door will be opened.

Sunday, May 04, 2008

This past week has been very difficult for Andrea. The virus continues to cause discomfort and for her to loose sleep. The doctors have a plan to help her get rid of this but it is causing pain in her kidneys. Please pray for this to clear up. She also received a spinal tap with chemo this past Friday. She's really been going through a lot and is exhausted.
In addition to all this, Andrea is in a new clinical study in which she will receive the new Vidaza shots Monday through Friday.
We appreciate all your prayers.

Sunday, April 27, 2008

The good news and the bad news

I really hestitate to post good news because of so many other things going on. But.....
There really is good news, like Andrea making her own plateltets now, (and thank you to all those who contributed, because of privacy laws we do not know exactly whose platelets she got, but she got a real boost from some of you who I KNOW were in there on particular days....). Andrea is above 100 platelets and has been making her own for the last couple of days now, which Great News. (140 platelets is normal, so she still has a few more to go on her own.)
Her bone marrow biopsy also came back very encouraging with all donor cells in 40 percent of bone marrow. (Yeah!)
But, she is having difficulty in some other areas she did not have during the last transplant process. Some irritations and viruses are popping up that are causing havoc, so she continues to really need prayers for comfort and healing. The itchiness, burning or sleeplessness is awful. Any and all of these are "normal" for stem cell transplant patients, but that does not really help when there is no real relief other than "time".
We do thank you for each and every prayer.

Sunday, April 20, 2008

Hey, how about that?

I just mention the possibility of Andrea getting to take home her backpack of fluids, everyone keeps praying for her, and it happens! Andrea had been going through a routine of receiving platelets and gradually losing them by "15" each day until she hit bottom and needed them again. Well, Friday for the first time since her transplant, Andrea gained "3" instead of losing "15". So, that meant that she did go home and J. became the one in charge of hooking up bags of fluid and medicine with a battery powered pump over the weekend so Andrea could stay at home instead of reporting to MDA.
She is slowly regaining strength each day and we appreciate you thinking of her.

Thursday, April 17, 2008

One Month Down

Today is April 17, and Andrea received the stem cell transplant on St, Patrick's Day, March 17. One month down, and she feels awful in many ways but the doctor and nurses say that she is doing Good. But, then they want to know how, when and where the yuckiness is and how bad, so they can determine how they can help. This is the ritual for the next two and a half months which make up the 100 days release time out of the hospital, which was April 1. No fooling. Last time I counted, Andrea was taking 24 pills a day, which did not account for the IV fluids she is hooked up to. They are talking about sending Andrea home Friday with a backpack of fluids with a pump to sustain her so she will not have to tumble out of bed Saturday morning to come to the hospital. We'll see....
So, please keep praying, as we do believe in the power of God over all.
We send love to all who keep reading this blog and keeping positive thoughts coming our way.

Monday, April 14, 2008

Rough Week

We haven't posted any progress because it really has been much of the same pains and all the strength Andrea can pull together to get up each morning and go to MDA for the whole day receiving the meds and fluids she needs.
But, Sunday night she had a major rash outbreak from her ankles to the back of her ears. Her main Stem Cell Transplant doctor made a special visit during his regular clinic lunch hour to the special MDA unit Andrea goes to each day to verify that he thinks it is the "graft versus host" syndrome that transplant patients need in order for the transplant to work. It causes extreme itching which they can try to control with medication. They also took a biopsy of her skin which will help confirm it is "graft versus host". We are just hoping that this, too, will pass with the best results possible and total healing.
We continue to keep Andrea updated on your prayers and comments. They are such a comfort.

Monday, April 07, 2008

+21 days

On this 21st day from the stem cell transplant, Andrea is experiencing bone pain (maybe from stem cell grafting) that was bad enough for her doctor to prescribe 2 more medicines. On the last transplant, she was still in the hospital with a pain pump and nurses and doctors around the clock. This time, she is working it through with us and about 5-8 hours at the hospital each day getting fluids and platelets while a nurse monitors the blood draw numbers and calls the doctor when medicine needs to be prescribed. It has been a week since we saw a doctor and tomorrow we finally get to actually see him again. She is still in a lot of discomfort tonight. We pray for better days ahead!

Friday, April 04, 2008

Encouragement

Thank you all for your encouragement. Andrea's stomach, head and bones are still very sensitive and anything (or who knows what....like medicine, the rest of the chemo in her body, or grafting cells) can set off a an adverse reaction. She has averaged platelets every other day in the Ambulatory Treatment Center 10th floor outpatient unit. It really is like a full time job going to it all day to receive fluids and meds, then returning home at night. She even has to go over the weekend. BUT at least Andrea gets to sleep in their own bed at night and that alone is worth A LOT.
It is great you keep praying for her strength each day. She feels it.

Tuesday, April 01, 2008

No April Fools!

No April Fools joke: Andrea is at home tonight, getting to sleep in her and J's own bed! The new doctor "on rounds" saw Andrea when she was out this morning doing her exercise walking and was impressed by her spunk even before he got to her room to do her assessment. He looked at her blood draw numbers, nurses' reports and by what she was telling him that she felt better today than yesterday, he let her go home.
Now, she has 100 days of returning to MDA each day for fluids, meds and assessment to really get well again..... but at least she can go home each night to sleep peacefully.
Thank you all for your continued prayers and an extra thank you for those who gave platelets because Andrea is still receiving those platelets and will be assessed each day to see if she needs more. You ALL are terrific!