Gloria's Progress   Updates on Gloria's battle with Non-Hodgkin’s Lymphoma

 

 




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Current info of Gloria's condition.  Her regular appointments are every Tuesday.  I will update each appointment and during her week of treatments.

 

June 19, 2006:  I DO believe in miracles!

 

Mama had her bone marrow biopsy last Tuesday.  She called last Friday and was told the cancer in her marrow was 30-40%.  Mama was so disappointed.  It was too high to take Bexxar, (our only chance for a true cure) and the numbers had not changed much since the last biopsy.  Well, Dr. Beck’s office called this morning and the nurse she talked to said “Guess what?  I read those numbers wrong and the doctor wants to talk to you!”, so then , Dr. Beck got on the phone and said “They changed the form the usually put results on and the nurse read you the percent of bone marrow USED in the testing.  The percentage of cancer in your bone marrow is not 30-40%, but 0%!!”  They could not find ANY cancer in her marrow!  We cannot believe it (sort of) it is such a blessing!!  Her cancer is not the type you can just say they are in remission and get checked up every few months, because the cancer is still lurking and waiting for an aggressive re-attack (that’s what happened last time she was in remission).  They will start Bexxar as soon as they can schedule to start it, which will be hard on her physically but was our best option and chance for a cure where she could truly be cancer free and healthy once again.  Thank you again for all your prayers and thoughts… keep praying, the battle isn’t over, but praise God for this great news!!!!!!!!!!!

 

June 13, 2006:  Blood counts up!

All the blood counts are up in a good range.  Some are still a bit low, but not like they have been in the past.  It is a good indicator of how her marrow is doing, so maybe the biopsy she is getting today will prove her marrow below 18% so she can take Bexxar (you can read about this drug below).  Keep her in your prayers, please as we wait for results.  I will let you know when we found out anything.

 

 

June 8, 2006:  No news is good news…

 

Mama has had a little reprieve from doctor visits but will have another biopsy next week to see what percentage of bone marrow is cancerous to see what we will do next.  Remember those biopsies are very painful, please say a prayer for her and I will update in the next few weeks to let you know the results and any new plans.  Thanks!!

 

March 14, 2006:  More changes

 

Things have changed again already.  Instead of her taking a chemo after this round of four treatments of Rituxan, they are going to keep her off chemo for three months, I guess just to see what happens.  I haven’t gotten to talk to Dr. Beck myself or hear the reason or anything, so if I get a better understanding from Mama, I will explain more later on.  My theory is “fix her… and FAST”, but I know Dr. Beck is the expert and even with my extra doses of love, what I would choose to do may not be what’s best for her.  Just keep her in your prayers… she has been very tired and weak lately.  Thanks again!

 

 

March 13, 2006:  Spine/hips better, lymphoma not so good

 

Please forgive me for not being more efficient on getting her site updated lately.  I plan to be much better, so please keep checking!  She ending up NOT having staph again in her spine… it was bone damage from the earlier infection that was flaring up.  The bone marrow biopsy she had in early January showed her cancer to still be at 30% so they were unable to give her Bexxar.  Dr. Beck put her on Rituxan AGAIN and she is now in the process of completing 4 rounds (1 treatment per week) before he performs another bone marrow biopsy to see if the tumor burden is less than 18%.  If it is 18% or less, she will start Bexxar, if it is more than 18%, I believe he will start another chemo which will be very hard on her physically.  Bexxar is hard on the body too, so just keep her in your prayers.  Again, the biopsy’s are preformed without pain meds and is excruciating, and waiting for results are hard too, please just remember Mama and Daddy at this time.  I will update with those biopsy results as soon as I hear, should be in a few weeks.

 

 

December 20, 2005:  Pain returns…

 

I know it has been a very long since an update.  The reason is, she has been taking those 8 rounds (one treatment a week for 8 weeks) of Rituxan and hasn’t had any major changes, she has just been tired mostly.  Her last round of Rituxan was last Tuesday, December 13th.  She was so glad to have about 4-6 weeks off treatment with no biopsy, so she could take a breath and enjoy Christmas.  Unfortunately, over the weekend her lower back started hurting terribly.  Most likely the Osteomyelitis (staph infection in the bone of her spine) has returned.  She went to the hospital yesterday for blood cultures to be ran and has an appointment today with Dr. Beck.  This is really an intense pain that affects her sitting, laying, and walking.   Please pray that the doctors can get this handled quickly.  She will have another bone marrow biopsy in about 4-6 weeks to see if cancer burden is less than 18% so she can take Bexxar.  The last time they tested it was 30% in one hip and 50% in the other.  Thank you.

 

 

October 28, 2005:  A few changes

 

Dr. Beck is going to give Mama 8 rounds of Rituxan instead of 4-5.  This will at least give her a little reprieve from another bone marrow biopsy.  Dr. Beck thinks this will better her chances of the cancer being at the right percentage to take Bexxar.  Also, she has two large knots come up over this week, one on her shoulder and one under her arm that is causing a great deal of pain and sleepless nights.  She needs her rest and your prayers, thank you. 

 

October 22, 2005:  Disappointment

 

Mama got the results of her bone marrow biopsy that she received this past Tuesday.  The cancer had to be less than 25% of her marrow to begin taking Bexxar, which, although it is a powerful and strange drug, it was one that came with great hope.  The biopsy came from both hip bones… one showed 30% cancer involvement and the other showed 50%.  This was not good news because we not only had hoped to take Bexxar, we also hoped the cancer would have been beat back better than this.  The plan now, is to start back on Rituxan this next Tuesday, take about 4-5 rounds of it (once a week for 4-5 weeks), have ANOTHER bone marrow biopsy and see if it is less than 25% then.  This is hard on Mama because she has to wait longer to get the drug she was ready for and she has to endure more bone marrow biopsies which are utterly painful and the dreads them more than most of us could ever know. Please pray that the cancer WILL recede and she can begin treatment that will not just sustain her life, but really move toward complete remission.  Thanks.

 

September 21,2005:  What is up ahead

 

Right now, Mama is still in a waiting period.  In about 3 and ½ weeks she will have another bone marrow biopsy to see if the cancer is less than 25% of her marrow.  If it is, they will then schedule her (about 2 weeks from the test) to start Bexxar, which will be once a week for two weeks.  This is a radioactive treatment and will lower her counts and she will not be able to be around those pregnant or any children for two weeks, and she will have to limit activity around all others.  This is a new thing to us, and it is a bit scary, but we have to do what is our best option and this is it.  Please start praying that this will be a very effective treatment. You can read more about Bexxar at this link

 

http://www.bexxar.com/

 

(if link does not work, copy and paste)

 

August 31, 2005:  A few weeks off

 

Mama doesn’t go in for another checkup and possibly more treatments for four more weeks.  The type chemo she has been on for the past few weeks continues to work for months, so we do not have to fear that the cancer is re-growing as we wait.  She looks like she feels much better than she did a few weeks ago when she was so weak and had to be hospitalized.  We are still with great hope!  Thanks for your concern!

 

 

August 23, 2005:  Things are looking up!

 

Mama had chemo again today (last Tuesday as well) and this week, her platelets are WAY up and the red and whites are holding their own!  We are excited!  She isn’t feeling really good physically though.  Maybe the chemo is taking its toil.  Thank you for all your prayers, I will update again next Tuesday.

 

August 10, 2005:  Yesterday’s chemo and doctor visit

 

The Rituxan infusion was not as bad as last week, they ran it very slowly and I do not believe they gave her the entire dose.  It had to be stopped once for chest pains, but she was pleased that it wasn’t as painful as before.  Her blood levels are dropping a bit, with her whites back down to 2.8 and her platelets down to 26,000.  Dr. Beck seemed more concerned with the white count than the platelets, so we are trusting that things can remain alright with the platelets at their present level.  If anything should happen this week I will post it here and I will update after her visit next Tuesday.  Thank you all for your prayers.

 

August 7, 2005:  Home from the hospital

 

This will be a long one… I will give an update on this past week.

 

Last Tuesday, Mama received her Rituxan infusion, which was tough.  It took six hours to administer and caused terrible chest pains, but they were able to give her the whole dose, which is good.  This first dose is usually the worst, so that is now behind her.  Her platelets this day were at 37,000 which is a very low count. (normal platelets are 140,000-300,000)  Her red and white blood cells were low as well.

 

Wednesday, she went to Talladega hospital for a blood transfusion to help out her red blood count.  At the end of the transfusion, she developed a fever so they wanted to keep her for observation, Her platelets went down to 29,000 and her white count was down to 1.5 (normal 5-10).

 

Thursday, Her fevers were coming and going, the platelets now were 25,000 and her white blood count was .8, Dr. Beck told the doctor at Talladega to send her on to St. Vincent’s, that they had a room ready for her.  She was transferred by ambulance.  When she arrived Dr. Beck calmed her fears (and ours as well) and told her he could help her, to not worry.  He ordered platelets right away and a medicine to up her white count.  They were unable to locate any platelets today.

 

Friday, her platelets were up to 38,000 and she finally received her platelet transfusion.  Her white blood is down to .6, but our spirits were up that things would improve.

 

 

Saturday, her platelets still holding at 39,000, her whites are up to 2.6!  She looks and feels much better. 

 

Sunday, (today) platelets, again at 39,000, her whites a whopping 4.6!!  Thank you, Lord!  The doctor on call released her and she will go back for chemo and/or to see Dr. Beck this coming Tuesday.  Please pray her blood counts hold there own.  I will update after Tuesdays visit.      

 

July 26, 2005:   Confirmed Relapse

 

Not good news.  The lymphoma is back in the bone marrow at 60%, which is worse than when she was first diagnosed.  We aren’t sure if it is anywhere else right now.  Dr. Beck is concerned about the swiftness of its return.  He is going to give her four weeks of Rituxan, once a week, starting next Tuesday to try and get the cancer down and then give her an oral chemo + steroids to beat it down further.  The goal is to get the cancer beat back to less than 25% in her marrow so they can use a new promising drug called Bexxar.  She is disappointed and so exhausted, but we still have hope.  I will update each week to let you know if her blood count is rising and they will do another bone marrow biopsy after the Rituxan treatments in about four weeks and I will tell you what the marrow involvement is then.  Thanks.

 

 

 

July 25, 2005: Again… waiting

 

Mama talked to her nurse, Alan today and he said they haven’t gotten results back yet, but they will just see her tomorrow.  I am sure we will get the results then.  I am going with her and Daddy to see what Dr. Back thinks is going on and will update as soon as I get home. I am sure we will get the results then. Thank you.

 

July 23, 2005:  Still waiting

 

We didn’t get any results Friday, for those wanting to find out any news.  Mama’s nurse said they should have them this Monday.  We will only find out whether or not the cancer is in her bone marrow by this test.  We will find out much more Tuesday at her doctors appointment.  I will update Monday if we find out anything and then again on Tuesday.  Thanks for checking in.

 

July 20, 2005:  Bone Marrow Biopsy

 

Daddy and I insisted Mama go get her blood checked yesterday instead of waiting until next Tuesday.  She had gotten worse through the week.  When they checked her blood, all the rates have dropped even lower.  Her platelets are down to 37,000.  Instead of waiting until next week to do a MRI and then a bone marrow biopsy, Dr. Beck just bypassed the MRI all together and went ahead and did the biopsy right after her blood test yesterday.  This is a very painful procedure, so we hated she had to go through that AGAIN, but, we are glad the doctor is getting to the bottom of this quickly.  She should get the results for that by this Friday.  They are pretty definite she has relapsed.  Her nurse said that even if the bone marrow is clear of disease that, with her platelets so low, the lymphoma is somewhere in her body.  PRAY PRAY PRAY for Mama and Daddy, this is disappointing and so hard to deal with.  Also, Mama is so weak she has a hard time holding her head up.  Thank you.

 

July 12, 2005:  Concerns

 

I know it has been a long time since I have updated the site, but I was going on the “No news is good news” notion.  It really has been nice for Mama to be in remission and we pray it continues.  She hasn’t been doing really well the past couple of weeks.  The fatigue has been overwhelming at times. She had a couple of doctor visits with her oncologist put off for different reasons, but finally made it in today.  Her blood counts are all low.  The reds, whites, hematocrit, hemoglobin and platelets are especially low.  For example, normal platelets are between 150,000-400,000 with 150,000 being an “okay” low, and hers are 42,000. Her spleen is also enlarged.  This is frightening for us because all of this is what happened when she was first diagnosed, so we fear relapse.  Dr. Beck wasn’t very encouraging either, but he wants to wait a couple of weeks and recheck her blood levels and perform a MRI.  If the levels are still low, they will do another bone marrow biopsy to see if she has relapsed.  We are remaining hopeful that this is not the lymphoma but something else that can be explained.  Please pray for her these next couple of weeks while we wait to see.  Thank you so much.

 

April 19, 2005:  Prayers are answered!

 

Mama had her Pet Scan last Friday.  Today, she went to Dr. Beck’s to get those results and to find out where she was with the lymphoma.  She is officially in complete remission!!  No sign of cancer on any of the tests.  They could tell by the Pet Scan that the staph is improving as well!  This all is of course, is an absolute answer to prayer.  We pray the remission lasts for years and years.  I will keep this site updated as she goes back for check-ups and to let you know how she is!  Thank you everyone for all your thoughts and prayers! 

 

 

April 12, 2005:  Bone Biopsy results are in!

 

We have been waiting a week to get the results of Mama’s recent bone marrow biopsy to see where we are with her cancer now, to see what good the chemo did to the cancer cells.  We were supposed to get a percentage of how much cancer is in her marrow specifically and the answer is… 0%.  There is 0% cancer in her marrow!!  Praise be to God!  We are SO excited, as you can imagine.  Dr. Beck will not officially call it “remission” yet because she has to undergo a few more tests to confirm it, but, it is looking good!  She has a pet scan this week, and then she has another appointment with Dr. Beck next Tuesday and I will hopefully go with them to see what is going on and what will happen next.  Just a little over a week ago, Paul called and said he was moving back to this area and will help Daddy with the shop, which was wonderful news, and now, this news is even sweeter!  Mama is so happy… we all are!  Thanks for every single prayer and thought.  If we could just get this staph under control, she should be feeling great… better than she has in years.  I will update on her doctor report next week and let you know if she is in remission!  Take care!

 

 

March 31, 2005:  Watching and waiting

 

Mama had an appointment for a bone marrow biopsy to see where she is with the cancer but it had been postponed until next Tuesday.  Her blood counts haven’t been looking very good because her white blood count has been dropping but the counts concerning infection have crept back up.  We try not to be alarmed watching the blood counts, but we are afraid of her body not being able to fight this staph if her white blood gets too low.  Her red blood has been going down too, so she is feeling anemic and tired.  Please pray that her body just becomes stronger and stronger and starts to compensate the needed cells to fight the cancer AND the staph. 

 

March 14, 2005:   Curious blood work

 

I wish I had updated sooner because things have been looking so great.  Her pain was better about a week and a half ago, she went to the doctors who encouraged her about getting her next bone marrow biopsy and even thought, with her blood work, maybe remission was a possibility.  This past week hasn’t been so great.  Her pain has intensified again and her blood work doesn’t look good for the staph or the lymphoma.  Her next appointment is next Tuesday.  Her biopsy is scheduled for then, but she thinks they may postpone it because of the infection.  When she gets some info on her counts I will let you know what they say.  This is an emotional (and physical for her) roller coaster for us all.  Please keep her in your prayers.  My prayer is the blood counts go right back up where they are supposed to be.  Thanks for so much for checking and for your prayers.

 

 

February 7, 2005:  Not much improvement… yet

 

A week later, Mama says the pain is about the same.  (If you know her well, she isn’t a complainer)  She is fine as long as she lays perfectly still, but, to sit up or go to the restroom is a feat and it leaves her in throbbing pain for a while, but to even try to bathe and wash her hair by herself, has so far been impossible.  The home health nurse told her today that with the staph in her bones, there is probably swelling in her spine that is pinching nerves which makes the pain worse.  The staph is in the spine, but the pain extends down her hips and legs as well.  Please pray she sees a lot of improvement in the pain and mobility real soon.  Thanks so much.

 

 

February 1, 2005:  There’s no place like home…

 

Mama arrived home yesterday afternoon and looks like her spirits are up  a bit.  The ride home was very painful, but she is glad to be back.  Daddy got her a better recliner and Dr. Beck prescribed her a different pain medication, so we are hoping this will work better for her.  She is taking antibiotics by IV for three months and also by mouth for a while.  We pray she will start to see improvement with the pain in the next week or so while this antibiotic is working.  I’ll let you know how she is a about a week unless there is something else to report.  Thanks for checking in.

 

January 27, 2005:  Diagnoses information

 

Click on the link below to get an explanation of Mama’s diagnoses.  She is still in extreme pain in the hospital.  Hopefully she will come home soon.  Thanks for your prayers.

 

Osteomyelitis of the Vertebrae 

 

 

January 26, 2005:  Back to the hospital

 

This past Saturday, Mama had all the pain she could take.  Daddy and I took her back to St. Vincent’s to find the source of this pain and try to find SOMETHING to ease the pain.  It has been a long several days, still suffering through the pain, even with medicine and more tests.  Dr. Beck and Dr. Barnes (the infectious disease specialist) got together several days in a row and looked over her test results, scans and talked with her and could not decide if the lymphoma had spread to her vertebrae or if the recent staph infection had not cleared up there.  This morning they have finally come to the conclusion that it is the infection because they ran a culture on her blood and found staph growing.  The good news is isn’t cancer on her spine, but staph.  The bad news is, she will have three MONTHS of antibiotics at home via IV.  We are not sure when she will be released from the hospital, but they have started the antibiotics TODAY.

 

Please pray for her as she still has bone pain that radiates down her spine, hips and legs whenever she tries to walk or sit up.  Please pray for a FAST recovery and for Mama to regain her strength so we can get back to fighting the lymphoma.  Thanks to everyone for their care and concern.  It means a lot to us.    

 

January 12, 2005:  P-A-I-N

 

I am sorry I haven’t been updating very frequently.  Mama hasn’t had regular appointments and the holidays are always crazy, but I will try harder to do better.  The reason for the title of this update (Pain) is that is how her days have been spelled since the staph infection.  She always hurts, every minute of every day, sometimes terribly, and sometimes less, but always pain.  Dr. Beck and his nurse Allen, have said that they think the staph infection has caused bone damage in her hip joint and leg bone.  We do not know at this time what they can do for her.  The usual treatment is surgery and she cannot undergo any surgeries at this point.  She has various pain meds, but they either do not work well, or make her feel and act “goofy” in her opinion.  Please pray that they can find SOME way to help her pain.

  Her next appointment is in early February.  We think they will set up her bone marrow biopsy then so we will know what the next plan of action against her cancer will be.  Thank you all for your concern and remember to pray for the pain.  Bone pain is intense and affects her walking as well.  Thanks.

 

December 13, 2004:  After last visit

 

Mama went to the infectious disease doctor last Friday and he has agreed to take her pic-line out this coming Tuesday.  (The reason I said “agreed” is, Mama used her charm to get it out a little earlier than expected)  She will be put on an oral antibiotic to take for a full month.  She has gotten much better since she was in the hospital!  Daddy and I think she looks great.  She still is having a hard time getting around and keeping the pain under control.  Keep her in your prayers!  Merry Christmas!!

 

 

December 8, 2004:  Still improving + doctor visit

 

Mama has graduated back to her upstairs bedroom!  She is able to walk with a cane more now than the walker.  She still is on the IV, but she has an appointment with the infectious disease doctor Friday to see how the infection is and how much longer she will have to use the IV.  She went to Dr. Beck’s office yesterday and he still seems encouraged by her blood counts!  Now that we have the staph under control we can focus back on getting the cancer in control too.  The chemo is still doing its work, but again, we will know more clearly HOW good it has done this coming March.  The pain has been an issue still, in her back, hip and down her right leg.  They think maybe she has hurt a nerve with the infection and Dr. Beck said she has bone damage in her hip.  The pain is at times excruciating, but yesterday she got a couple of medications prescribed that will help during the day and at night so she can rest.  She always feels much better after a good nights sleep.  Thank you all for your prayers!  I will update Friday after the following Dr. appointment. 

 

November 15, 2004:  Getting better… slowly but surely

 

Mama is gaining ground, an inch at a time, but progress is progress.  She is still very weak, can only get around with a walker and her lungs have not cleared.  The good news is she is better than she was about two weeks ago, there is no doubt about that.  She is recuperating better at home.  Joe (my husband) has gotten her lap top working at great speeds, so she has been able to check in on her kennel website, which, if you don’t know her well, is her passion.  We are encouraged by her progress and look forward to her improvement in weeks to come!  Thank you each for your prayers.

 

 

 

November 9, 2004:  Coming Home!!

 

Daddy is on his way to bring Mama home as I type!  I know she is thrilled and I know Dolly and Chi-Chi will be thrilled as well.  She will still be on pain meds and IV, but she will be able to rest at home.  Thank you all for your prayers and for God in Heaven hearing them!

 

November 8, 2004:  Good news update

 

Seems that Mama has been showing off and walked down the hall today with a walker, so the doctor said she might be able to come home tomorrow or the next day.  Mama is counting on tomorrow I can tell.  She will still need the IV drip and with home health care, but I can assure you, that is FINE with her.  She hasn’t had any fevers for a while and the pain is a bit better, though still quite present.  Keep your prayers going up; she’s got a ways to go!  But, thank God we have finally seen a great improvement!  J

 

November 8, 2004:  STILL in hospital…

 

All the scans and x-rays and tests (and there were plenty) have proven that she has staph in her blood stream and it has attached to her lungs and in her pelvic and hip bones.  The infectious disease doctor told her that this is the worst staph infection he has ever seen, but they think they can control this and overcome it with antibiotics.  They have not given us a date she will come home, but the oncologist who was on call yesterday said she will have to have a week of physical therapy in the hospital BEFORE she can come home, to prove she can walk, and they haven’t started the physical therapy yet.  She has NOT been able to walk since she has been in.  When she MUST get up for any reason, she has to have her cane and another person to shuffle her feet across the floor to her destination.  It has been up and down for her this week.  The main problem has been severe pain in her hips and pelvic area, her breathing has been shallow and wheezy some of the time, and she is just tired and weak.  Her oncologist has already told her when she DOES come home, it will be with an antibiotic drip and they foresee her needing it for at least six more weeks.  Please pray for her nerves, she misses home, and of course for a speedy recovery.  God bless. 

 

November 3, 2004:  Still in hospital…

 

Mama is still in the hospital.  They have found out that the spots on her lungs are a staph infection, which is more in the lining of the lungs than the lungs themselves.  That is good news, we are praying they can clear that up with antibiotics.  She has been on an antibiotic drip since Sunday and she is still spiking high fevers, so, maybe they will change what they have been using.  They are going to do an MRI on her hip and pelvis today.   She has still been in extreme pain since Sunday.  The pain has now extended to her back.  She is very tolerant of pain, so to see her hurting so badly is awful.  She of course is tired from not sleeping much.  Please continue to pray for her pain, and her hip and pelvis scan.  Thanks.

 

October 31, 2004:  In hospital…

 

Mama has been admitted into the hospital today.  She was up last night hurting severely at the top of her right leg.  She is also running a fever that won’t quit.  She had an appointment tomorrow already, because she has had some bad coughing and breathing problems these past couple of weeks.  Last Tuesday the 26th, Dr. Beck ran a CT scan of her chest last Tuesday where some spots showed up on her lungs.  She will still be seen by the lung specialist tomorrow.  They have been giving her antibiotics via IV today.  I was with her and Daddy at the hospital from about 5 – 8 pm tonight and she is still in much pain and she still has not gotten her fever down.  We do not know how long they are planning on keeping Mama, but I will try my best to keep everyone posted on this site.  PLEASE pray, thank you. 

 

October 5, 2004:  GOOD NEWS!!!

 

Mama had a CT scan done last Friday so Dr. Beck could see if the cancer has shrunk back and to see if her spleen was smaller than when she was diagnosed. This means the chemo has been doing its job!  This does not mean she is in remission, and the spleen is still enlarged BUT, Dr. Beck said the chemo will continue to work these next few months while she is not taking treatments and they will do another bone marrow biopsy in about 4-5 months to see how much the cancer is shrunk back then.  He thinks she will be eligible for the drug Bexxar we were hoping for after that biopsy.  Thank you all for every prayer and keep sending them up.  This was great news today, but I am still rooting for complete remission!  Praise be to God!  J

 

 

September 24, 2004:  Not well

 

Over the past two days, Mama has gotten progressively worse with a chest cold/head cold.  I was with her all day Wednesday and she wasn’t feeling great, but she was able to get around and be in good humor.  Yesterday she felt a bit worse, and today I called her and did not even recognize her voice.  It was so bad that I checked the number I dialed because I honestly didn’t think it was her.  She has had hard chills, a constant cough and a terrible headache.  She had an appointment with Dr. Beck last Tuesday and he prescribed her an antibiotic because her chest (they took an x-ray) had the possible beginnings of pneumonia.  Please pray that this clears up very soon.

 

September 8, 2004:  Last round!! 

 

I haven’t done a very good job keeping everyone up to date lately, sorry.  Mama is on round 6/6 this week.  She has been experiencing a lot of bone pain this past week, unbearable at times.  She is checking with Dr. Beck today to see if there is something they can give her to relieve it and to find out why she is having it. 

She went into this week of chemo with lower white blood and platelets than she usually starts the chemo week with, so please be praying that this doesn’t cause a major drop next week.  I believe her white blood was about 2.7 and her platelets were 136, so we really do not need that going too much lower than that.  She has gotten a cold also so she was given a prescription to clear that up asap.  There are decisions to be made after this treatment is complete and test to be ran to see what the cancer is doing now, so keep Mama and us in your prayers.  If anything new develops this week I will post again.  Thanks for checking in.

 

August 10, 2004:

 

Mama has just started month 5 out of 6 for chemo.  She is excited to be this far, and to be almost through.  Dr. Beck told her yesterday that she didn’t have to take the 6th month if she didn’t want to, but that he would if it were him, so, as usual she is going to take his advice on that.  We have been reading into another possible drug she can try called Bexxar which she mentioned to Dr. Beck today.  He said she would have to wait a year (we are not sure if he meant after treatment or after diagnoses) and that she will have to have less than 25% bone marrow involvement to be eligible.  She will have to have another bone marrow biopsy L in a couple of months when she is through with this treatment, and we will see how much bone marrow is involved.  Bexxar is another monoclonal antibody, but may help when Rituxan has failed to get the patient into complete remission. 

Please allow me to take a moment to thank Shalon, Julie, Alan, Natalie and Dr. Beck for being so sweet to Mama.  You have all made this experience hopeful and encouraging.  She doesn’t speak of you like the “medical staff” at the hospital; she speaks of you on a first name bases like friends.  I know ya’ll have meant the world to Mama at this time of her life, but it also means a lot to me and the rest of our family that only wants the best care for her.  Sometimes, the best care isn’t only which medicine or regimen, but, the people behind the needles and IV’s.  Thank you. 

 

August 6, 2004:  Hard week

 

These past few weeks have been rough on Mama with fatigue.  Her platelets are low too, because her color is not real good.  I know the news hasn’t been very uplifting here lately, and trust me, I hope to be posting some great news real soon, but I wanted to share with ya’ll what she is going through so you can say a prayer for her.  Her chemo is supposed to be next week and we need her blood counts up for her to receive treatment.  Her and Daddy’s anniversary is today… 39 years! 

 

 

July 28, 2004:  Whites low

 

Mama’s white blood count is down to 1 (normal low is 4.1), so, she will have to stay out of public places completely for a while.  Her port in her chest became infected week before last during chemo, so she had been on antibiotics for that (plus a threat that she’d have to be admitted into the hospital for 5-6 days if it didn’t clear up).  The port looked better this past Tuesday, but they gave her another round of antibiotics because it hasn’t healed completely.  With her whites blood count low, she must be very careful with any infection or sickness.  She has also had to deal with sores on her tongue and roof of her mouth, caused by the Fludara, they are very painful and take quite a while to heal.  Her spirits are up though and she is still up and trying to do ordinary things.  Her chemo is on regular schedule, although, she must have white blood counts higher than 1.6 to take the chemo.  Pray the counts rise quickly.  Thanks!  (“shug” page has been updated with birthday party info!!!)   

 

July 13, 2004:  No remission

 

I know the last post said Mama would not go into complete remission this round, but Dr. Beck told her today she would not be going into complete remission ever.  I guess the cancer is too far gone… I really don’t understand completely.   He just said she would finish this treatment to get it beat back as far as she can, and they would try to maintain it where it is, but that she will not ever go into remission.  She has felt very bad for weeks, so was already “down”, this news didn’t help.  Please pray for her and us, as we try to be what she needs right now.

 

June 23, 2004:  “Not going to hit a homerun”

 

Mama had an appointment and, although we weren’t expecting to find out today, Dr. Beck was able to tell her how the treatments were going with her cancer.  He told her she would not be “hitting a homerun” with this chemo she has been taking.  In other words, she will not be going into complete remission on the medication she is on.  They will continue the last three rounds with the two meds and see if she will go into partial remission (aka partial response) where the cancer will be less than it was, but not beat back as she needs it to be.  She has so looked forward to feeling good again physically that this has been a huge disappointment to her.  She hates not being able to get around and do even the little things.  Not to mention, it is frightening to not have the cancer go into remission. We are not definite what route Dr. Beck will take after treatments, and we are not sure whether or not she will go into partial remission either.  Just, please pray for her as she deals with this news.   

 

June 17,2004:  Not feeling well

 

Mama has had a hard weekend and week so far.  She has just been more weak than usual for more days in a row than usual.  With the past two treatments, her “bad times” have been at the end of the 2nd week and 2nd weekend after chemo, but this time, it has been both.  She says she feels better today than she has felt for the past 6 days, but she has done nothing at all in all those days.  She just isn’t able.  She did not have an appointment this past Tuesday because one of Dr. Beck’s nurses, Alan, said he didn’t want to bring everyone down with low blood counts from chemo, so they are waiting until the counts are expected to be up and then will check it.  She had to have medicine called in this past week because of mouth sores that have been caused by the chemo.  We have to assume the weakness is also only caused by the chemo, and of course, we pray it is just doing its job.  Praying it is uphill from here until next round of chemo.  Thank you for all your prayers!!

 

June 11,2004: Round two at an end

 

This week hasn’t been easy at chemo.  Mama has nodes swollen everywhere, a very sore throat and sores in her mouth, which, the doctor’s staff says is all caused by the chemo itself.  She has also been quite weak.  Our prayer, of course, is still that this chemo is doing its job and that whatever grief Mama has to endure will be well worth it because she will be remission and feel better than she has in years!  Pray for a good weekend and the next week ahead too, because that time has been rough so far.  I will update early next week to let you all know how she is. 

 

May 25, 2004: Lymph Nodes

 

Mama didn’t have to go to see Dr. Beck today, although the past two days, her lymph nodes have been swollen and tender all over.  She may have contracted a virus like before when they were swollen, we don’t know.  But, please just pray they go down soon, to relieve her discomfort and that her blood levels are still up when she goes for her check up next Tuesday. 

 

May 18, 2004: Blood tests

 

Mama had a regular appointment, checking her blood levels and today they were good!  They didn’t give her Procrit today (the medicine that raises red blood levels) because her red blood has held up this week on its own.  Please pray they continue to hold!!  Her white blood count IS low, which means she doesn’t need to be out and around the general public still, but this is common with the type chemo she is on.  She is still terribly weak and tired often, but since her blood counts are good, it is probably just her body fighting the cancer, which is good news.  More good news… she doesn’t have to go to the doctor next week unless she has trouble.  She may have to go the week after, and she will definitely be going the next week because it will be time for another round of treatments.  Keep her in your prayers!!  The battle is on!!  J

 

 

May 14, 2004:  End of Round two

 

This week of chemo has taken its toll.  Mama is weak and still has pain throughout her lymph system, especially her joints.  Please pray for her for this weekend and upcoming week.  We are excited to see how mush she improves in her blood count after the initial drop!!  Tuesday’s appointment may show lower blood levels because of the chemo, but should rise the following week, even higher than this last round! 

 

May 12, 2004:  Round two – continued

 

Mama’s lymph system is still causing her pain and she is fatigued.  This weekend and next week is when she really gets zapped.  Keep her in your prayers, please.

 

May 10, 2004:  Round two of chemo begins

 

We had a WONDERFUL Mother’s Day weekend.  Paul, Kim, Joe, me and all the kids spent Saturday with Mama, giving her gifts and filling the house with laughter and fun  memories. 

Her blood counts are really good today.  The only one low is her white blood count, which was expected with Fludara.  She stays out of stores to keep from contacting germs and is even very careful in the waiting room at the cancer center. 

Her arms, joints and legs have been hurting pretty badly, the nurse staff said it is the lymph system doing attacking those cancer cells.  She had no complications from the Rituxan with this infusion and everything went a little more quickly than before.  She still has four days of Fludara left for this week, so pray her white blood count doesn’t drop too low and that her other counts will remain up.  She needs her strength to continue the treatments. 

Her brother, Buddy and his wife, Nikki came today and stayed a good long while to check on her and lift her spirits…. I think it worked! 

I will continue posting this week.

 

 

 

April 20, 2004: Doctor's check-up

Dr. Beck thinks the swelling was due to a viral infection her body must have been fighting. Her blood counts are down again. To see a table of normal low and normal high blood test values, you can view it at patientcenters.com
Mama's White Blood Count is 1.3 (normal low is 4.1), her Red Blood count is 3.15 (Normal low is 4.2), her Hemoglobin is 9.7 (normal low is 12), her Hemocrit count is 28.1 (normal low is 37) and her platelets are at 100 (normal low is 140). The doctor wants her back in next Tuesday to do another CBC (complete Blood Count). He started her on Procrit today, which she will take weekly, to hopefully boost her red count level and help her feel better. We pray her blood levels rise quickly!!



April 18-19, 2004: Not feeling well

Mama's lymph nodes in her neck are swollen pretty bad, it hurts to turn her neck. She also has a large node under one of her arms and her spleen area seems very swollen and tender. She is in much pain and hope the doctor can clarify the problem at Tuesday's appointment.


April 13-16, 2004: Fludara

Mama had her Fludara infused each day this week. She has had problems with nausea, but, Dr. Beck gave her anti-nausea medication, which we hope will help her out. She never got violently ill, but she has felt tired and had many strange symptoms.


April 12, 2004: Chemo begins

Today, Mama and I went to Birmingham to get her first treatment with Rituxan and Fludara. The Rituxan can cause severe reactions at the first infusion, so, we were a little worried about this. (especially Daddy) We were very disappointed to learn that I couldn't stay back with her during it all, but I understand the need for room for all the other patients.
The Rituxan had to be stopped three times. The first time she had sudden chest pains, and I do mean pains. The started it back slowly and then she had a hard chill. The last time she got very sick to her stomach. After about 6-7 hours the Rituxan was finished and they started the Fludara, which didn't take too long at all. She said the whole thing was just weird and that she still feels weird. I guess anyone would after having so much put into their body and considering the cancer cell killing that should be taking place in her body!! She will rest tonight, I hope.


April 6, 2004: CT Scan results

Besides her marrow and lymph nodes, the cancer may have spread to her spleen, although, they aren’t sure. The great news is, it hasn't spread anywhere else! We were afraid of liver involvement because of her yellow eyes, but her liver is clear!
We also found out that she will start treatments next Monday. She will take a monoclonal antibody called Rituxan and a chemo called Fludara. Monday she will take both drugs, but Tuesday, Wednesday, Thursday and Friday, she will take the Fludara alone. She will do this once a month for six months.
The great thing about these drugs is they aren’t very toxic. Her hair will not fall out and many people do not get sick to their stomach with the chemo! I was so glad for this because she despises being nauseous. She is still looking better from transfusion.




April 3, 2004: Feeling Better!

Gloria is feeling the effects of the transfusion and has a bit more energy. She finally has some color to her skin and lips. Hopefully the bruises will be fading soon. We are anxiously awaiting the test results from the CT scan this upcoming Tuesday.


April 1, 2004: CT scan, port, transfusion

Mama and Daddy spent all day at the Hospital today. I got to visit for a while, but they had a full run of the day. First, she had minor surgery to place a port in her chest, so that they can use that source to get blood and administer chemo.
Then they started the blood transfusion, giving her two pints of blood.
Then they gave her the CT scan. The doctor thinks the cancer may have spread outside of the lymph nodes and marrow and this test will show where. We are afraid of where it will be and to what extent it has spread.


March 30, 2004: Day of diagnoses


Mama had been feeling very weak and went to a clinic who ran blood test after blood test. She was very pale, very weak, the whites of her eyes were yellow, and she was very bruised all over. They found her to be severely anemic, but knew it wasn't from vitamin deficiency, so they sent her to a hematologist, which in this case, is also an oncologist, for a bone marrow biopsy. This day, we got the results of that biopsy.
Mama, Daddy and I went to the Hematologist/Oncologist, Dr. Stephen Beck, telling each other It's going to be nothing major over and over and waiting those agonizing moments until we found out for sure.
Dr. Beck came in and told us was Non-Hodgkin’s Lymphoma, indolent Small Lymphocytic, Stage IV. She has had it for many years and it has progressed into her marrow (explaining the anemia symptoms), lymph nodes and possibly elsewhere. Dr. Beck ordered her a blood transfusion, CT scan and port, all to be done the upcoming Thursday.
We were all shocked and scared.

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