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Thursday, December 8, 2005 5:54 AM CST

It has been a while since I updated her website. She is doing very well off treatment. She is also doing good in school. We have an appointment on December 21 for blood work. Thanks for taking the time to check up on Dianne to see how she is doing.


Thursday, July 5, 2005 11:56 AM CDT

On June 28 Dianne ended her chemo. A wonderful journey has just begun. It will be filled with a lots of worries and happiness. We will take each steps as it comes. We are so thrilled about not taking any more chemo.

Our next step into this wonderful journey will be on July 13. she will have her port remove. To be honest, I am a worried about this precedure. I will be able to keep the port after it is removed. I believe if I leave it in God's hands things will be fine.

On July 28 she will be making her trip to Disney World With her brothers Michael and Stamati, mom, dad and papou(grandfather). We will return on August 3. On August 13th, we will make another trip to Ocean City for one week. This trip will be with papou, mom, stamati, Michael, Uncle George and family, Aunt Chris and cousin Simone. I do have to say this will be an unforgetable summer.



Wednesday, May 18, 2005 11:31 PM CDT

We Have some good news to report. First the biggie. Dianne's last day of treatment will be on June 25, 2005.
We are all looking forward to this. Second surprise is her Make A Wish trip to Disney. We will leave on July 28th and will return on August 3rd. The people included on this trip is mom and dad, brothers stamati and Michael and papou(grandfather) and of course our special guess star, DIANNE. After returning from Orlando Florida we will be getting ready for the ocean. We will leave on August 20 for one week. What a wonderful summer.


Wednesday, May 18, 2005 11:31 PM CDT

We Have some good news to report. First the biggie. Dianne's last day of treatment will be on June 25, 2005.
We are all looking forward to this. Second surprise is her Make A Wish trip to Disney. We will leave on July 28th and will return on August 3rd. The people included on this trip is mom and dad, brothers stamati and Michael and papou(grandfather) and of course our special guess star, DIANNE. After returning from Orlando Florida we will be getting ready for the ocean. We will leave on August 20 for one week. What a wonderful summer.


Thursday, April 28, 2005 2:36 PM CDT

WBC-3.10
ANC-2.32
RBC-3.88
HGB-11.6
PLT-273

Dianne had her appointment today. She is doing very well. She is schedule for a Lp next month, but the date had not been set.

May 1, 2005 will mark her 2 years since she was diagnosed with Leukemia. We will celebrate her 2 years cancer free with a cake.


Thursday, March 10, 2005 9:18 PM CST

These are Dianne counts from March 1, 2005

WBC-5.98
ANC-4.76
RBC-3.83
HGB-11.6
PLT-341

Dianne is doing very well so far. Just 6 more months left. Also we got a letter from make a wish and they had granted her her wish. I will let you know when we will take the trip.


Wednesday, March 2, 2005 1:16 AM CST

Today Dianne had her LP and her chemo treatments today. So far everything is good. On Dianne's right is Dr. Wiley, her oncologist and on her left is Dr. Aron, her anesthesiologist.


Wednesday, February 23, 2005 6:10 PM CST

Dianne is schedule for a lumbar puncture(LP) and chemo on March 1. The good news is, Dianne has 6 more months of treatments left. Since May 1, 2003, I never thought I would see the light at the end of this long tunnel. I feel very excited about this.




Monday, January 24, 2005 10:38 PM CST

Today I took Dianne to the Doctor. She was having pains below her abdomen. Her urine culture showed a high level of white blood cells. They will send out the urine to see if she has an urinary track infection. I will let you know if something shows up.

Take a look at her photos in the photo section. She loves when people write to her. She feels special.


Monday, January 17, 2005 4:12 AM CST

For the past week Dianne had a fever. We had her at the hospital couple times this week, but everything is coming back negative. I am so worried at this point. They want to see her today again. Dianne does complain of back pains and she has symptoms of having the flu. She did have her flu shot so I am hoping it's viral that is causing her to run this fever all week. I will let you know if there is any changes.


Tuesday, December 21, 2004 10:25 AM CST

Dianne is doing so well now. She is excited about Santa coming. Santa on the other hand is not that excited.


Thursday, December 2, 2004 9:19 AM CST

An update on Dianne. She is doing ok. she had developed an infection in her arm. We went to the oncologist and he had given her antibiotics. She will be going in for her spinal and MTX on December 7. Dianne will also get her vincristine through the IV.

She had gotten her call from Make A Wish Foundation. They will come to our home to ask Dianne about her wish. Dianne whats to go to Disney World. She is so happy about them coming.


Tuesday, November 2, 2004 10:49 AM CST

Dianne is doing so well. Just looking at her you would never know she had cancer. She is so alive and full of energy. Dianne is making progress in school after missing so much last year. The teachers are so wonderful to her. Her next schedule appointment is on November 9. She will be getting her vincristine so it will be a short visit. Also to let you all know, Dianne had her flu shot and she was a brave girl. She did not even cry. I will try to keep up with this journal more often.



Monday, September 20, 2004 12:29 AM CDT

Well, it is late Sunday night. Dianne went to the clinic on Friday and got her LP and her chemo. She also started her five days of steriods. So far she is doing great. This Sunday Dianne was complaining about headaches. It is most likely from the methotrexate she had received in the spine. The past few days, Dianne had gone to bed early. I am hoping that she will go to school this week. Thanks to all who had kept Dianne in their prayers .

I had read from the A.L.L. List of some cancer kids who became angels this week. My prayers are with these families and may they find strength through this terrible ordeal.

Check out her photos. These photos were taken at the hospital where she gets her treatments.


Friday, September 3, 2004 9:45 AM CDT

Dianne had just started school on August 30. She had entered the 2nd grade. So far, she had a good week. She said that she is having a good time and made a lots of friends.

As for her health, she doing very well. She is scheduled for a spinal tap and chemo on September 17. It was scheduled for September 16, but the doctor who puts her to sleep for the spinal will be taking off from work that day due to a Jewish holiday.

I hope everyone had a nice summer. I do hope next year will bring greater and better days. If you get a chance, sign her guestbook. She always feel special when people leaves her messages.


Monday, August 23, 2004 12:46 AM CDT

I am sorry I had not updated lately. Just to let you know Dianne is doing well. We went away August 7, to spend a week at the ocean. She had a good time. In the beginning of the week she cried for her grandmom who past away this past April. Grandmom was always with us on vacation. We were with granddad, Uncle George, Aunt Tina and cousins Marie and Stamati.

Yesterday Dianne and the family, along with friends, went to a Picnic in PA. It was really nice.

She had her Vincristine on August 16 and five days of steriods. She started to munch a little more. She is scheduled for a LP on September 16.

Check her photos in the album.


Saturday, July 10, 2004 0:31 AM CDT

Today is Dianne's birthday. We will have a quiet celebration at home.


Wednesday, June 16, 2004 10:40 PM CDT

Dianne contiues to show great progress. She had her LP done on June 14. She is doing great. Today was her last day of school. She will start second grade in September. This is a busy weekend for her and her brother Michael. They will spend the weekend away from me. They will leave on Friday to stay the weekend over our friends Rita and Spiros. They have two wonderful girls Elefteria and Georgina. Sundays evening Dianne Michael and the rest of the gang will go over Uncle george and Aunt Tina's house for a fathers day Dinner. Also, there will be graduation party for my nephew Stamati on Saturday. I don't think Dianne and Michael will attend the graduation party. It will be held at St. Demetrios Greek Orthodox Church. Thanks for checking up on Dianne.


Sunday, May 16, 2004 10:24 PM CDT

Today was a wonderful day for her. Our church and many organizations in the church had a fundraiser for Dianne.The money they made off the luncheon will help to pay her medical bills.

Dianne is half way through her treatments and I am feeling much better about her out come. she has an appointment for her vincristine on Monday, May 17. She is so full of energy and I love it. She has truly been blessed. If you get a chance please sign her guestbook.


Thursday, April 29, 2004 9:40 AM CDT

Dianne is doing so well on her LTM. She is full of energy and life. I am so bless to have her as my daughter. She was diagnosed on May 1, 2003 with Leukemia and this Saturday will mark her one year anniversary. I will still have a cake for her and she will celebrate it quietly with her mom, dad, sister, brothers and her papou(grandfather). I know Dianne will be in good hands because her Yiayia(grandmother) earned her wings on April 5, 2004. Mom you will be missed so much. You will live forever in us.


Saturday, April 17, 2004 7:17 PM CDT

I am sorry that I did not update Dianne's page sooner. My mom past away on April 5 and it has been a long two weeks. Dianne is doing good. She will go to the clinic for chemo treatments on Monday. I will keep you posted after the appointment.


Saturday, April 3, 2004 0:41 AM CST

It is close to 2 in the morning. I am sorry I have not updated this week about the parade. On Monday my mother had a stroke. She has a long road ahead to recovery but with the love of her five kids and a terrific husband (also a terrific father) she will do just fine. She had already started physical therapy.
I want to say thank you to the people on the ALL Kids List who sent there get wells and prayers for my mom.

Dianne had a wonderful time at the parade. I want to thank all the people who were there and made her feel special. I also want to thank my niece Kelly for being such an angel to Dianne. You have been a really big help to me. Without my niece, she would not have been in the parade.


Saturday, March 27, 2004 10:51 PM CST

Today is Dianne's big day. She will be in a parade to celebrate the Greek Indepenence Day.


Monday, March 22, 2004 5:05 PM CST

It is official. As of today, Dianne started her Long Term Maintenance (LTM). I will keep you posted as we go along. she is scheduled in two weeks for a complete blood count (CBC).
Here is what she will be on for a year and three months

Mercaptopurine (6MP) 1 1/2 tabs x 5 days
1 tab x 2 days

Dexamethasone (steroids) 2.5mg a.m. x 5 days
3 mg p.m. x 5 days
A month

Methotrexate (MTX) 7 tabs on Mondays only

Today in the clinic she got Methotrexate (IMTX) in the spine
and vincristine(VCR) through her port.

Thank you for taking the time to visit Dianne's Page.


Thursday, March 18, 2004 7:44 AM CST

Good morning. It is Thursday morning. Dianne had developed a fever last night. It went to 100.8 and she is complaining a lot about her legs and arms hurting. My main concern is she may have relapse but this is coming from a mother who thinks every pain she is having is due to a relapse. I called the clinic and they told me to wait a few hours to see how high her fever gets. If it gets to 101.0 then I would have to bring her in.
Before she was diagnosed, she always ran low grade fevers. it never went to 101.0 and she complained alot about leg pains. Lets just hope its nothing.


Monday, March 15, 2004 7:27 PM CST

Well we went today to start her Long Term maintenance (LTM).
Dianne did not make counts today so she will not start today.
Dianne will have another week off chemo. She scheduled next monday to try again. Well I hope we have better luck next time.
It makes you worry when there is a delay in her treatments.


Sunday, March 14, 2004 10:40 AM CST

Well tomorrow is a very big day for Dianne. She will begin her Long Term Maintenance (LTM). She will Get her lumbar punture (LP) in her spine at 10:30 in the Morning. If her Bood counts are good, she will begin her last journey of her treatments. This journey will last her 1 year and three months. We are very excited to come to this point. Her one year anniversary is fast approaching, May 1, 2004. I will have a cake on this day to celebrate her beautiful life.

Dianne loves it when people leave her messages. Thank you all very much.


Sunday, March 7, 2004 4:16 PM CST

Dianne broke out in a rash on Thursday evening. I had made a call to her onc and he told me to bring her in Friday morning at 8:00. We thought it might be shingles. It turned out not to be shingles. At the moment we do not know what it is. Also they thought she might need a red blood transfusion because her HGB was 7.9 on Wednesday but Friday morning it was 8.2 so they told us it looks like it is coming up on its own. Her next appt. will be on March 15 for her lumbar puncture(LP). This is the first day of the beginning of long term Maintenance.

If you wish to help in any way then please donate blood. You can save a life. Thank you


Wednesday, March 3, 2004 8:22 PM CST

Today Dianne had her appt at the clinic an Sinai. She had her blood test today. Her counts are still dropping.
RBC-3.09
HGB-7.9
WBC-1.66
ANC-.89
platelets look good 190

She also have this terrible cough that won't go away. She is able to take cough medicine without any fever reducer. She will return to the clinic on Wed. March 10 for more blood test. They think her blood counts will continue to drop and if it does then she will get a blood transfusion.


Saturday, February 28, 2004 8:52 AM CST

Well Dianne finally finished her Delayed Intesification (DI).
She had a pretty rough time on it but she made it. Her last visit at the clinic her blood counts were low but not in the danger zone. I will give you an idea what we are looking at.
I will list normal counts for children which I found in a book written by Nancy Keene called Childhood Leukemia and then Dianne's counts.

White Blood Cells 5-10, Dianne's WBC 1.26
A good ANC which is the ability to fight infection
is 1000 and up.
Dianne's ANC is .69 or 690
Red Blood Cells 3.9-5.3 m/cm, Dianne's RBC 3.31
Hemoglobin which carry oxygen and carbon dioxide
in the blood is 11.5-13.5 g/100ml
Dianne's Hgb is 8.9
Platelets-160,000-500,000 mm3
Dianne's PLT 170,000 mm3

Now the onc said that because they were low at the last visit she needed to come back on wednesday, March 3 for more counts because she was getting another week of ARA-C. He said that would bring her counts down lower. She may need some blood. Other then that we just wait and see. She bruising more on the legs and she is running low grade fevers around 99.4.

The best part about this is she is coming to the end of her treatments. She will start Long Term Maintenance (LTM) when her ANC is 1000 or more. This stage is her last stage of her protocol. Her protocol is CCG 1991. This will last for 1 year and 3 months.

Dianne's was diagonosed on May 1, 2003. Her one year anniversary is coming up and I am having a cake for her because she is a one year cancer survivor. If she remains in remmission for 7 years, she has a good chance of living a long and healthy life. I will continue to celebrate each year. As the year approaches you begin to feel both happy and sad. I dwell on the days following her diagnose. How May 1, 2003 changed my life. One good thing that came out of it is that I spend most of my time with her. She really is a joy to have.






Wednesday, February 18, 2004 7:53 PM CST

Well Dianne started her second half of her Delayed Intesification (DI). Yesterday we arrived at Sinia at 10 in the morning and this is when the long day began. Her port was accessed and blood was drawn. Her counts were good. She was scheduled for an Lumbar Puncture (LP) at 12:30. Dianne got her Methotrexate in the spine. They needed to start her on her IV to make sure she had enough fluids before she got her Cyclophosphamide (CPM). After her LP, she was sent to the clinic to get the rest of her chemo CPM and Cytarabine (ARAC). Before they gave her the CPM they had to check to see if she was dehydrated. It turned out that she was dehydrated and she could not get her chemo at that time. They gave her more fluids through the IV and still dehydrated. The bottom line is, we waited about 5 hours more to get her chemo. We ended up leaving the hospital at 8:15 in the evening. Dianne stayed home from school today because she was very tired.
She also had the nurse come to the house today to give her ARAC today. The nurse will also come Thursday and Friday again to give her her ARAC. She also started her Thioguanine (TG). She will take it crushed up in applesauce. She will remain accessed until Friday. She will repeat this next week on Tuesday.


Thursday, February 12, 2004 1:28 PM CST

Well Dianne did not start her second half of her Delayed Intensification(DI) as planned. She had been complaining about her right arms. She could not use it to well. She was still having problems with her legs. When she got examined by her oncologist, she decided to do an MRI on her in fear that she might have a blood clot. We were told it is quite normal to have a blood clot after getting the Pegaspargases(PEG) shot. The MRI showed no clots. They come to the conclusion that it is from the chemo vincristine.
The next thing they did was xrays of her hip. They needed to see if any tissue between her hip and leg bone is damaged. We went home after the xrays so I don't know what they saw. She is scheduled for Tuesday, Feb 17 to start her second half of the DI.

Cyclophosphamide(CPM) through IV over 20 minutes
Cytarabine(ARAC) IV push times 4 days
IT Methotrexate(IMTX) in the spine
Thioguanine(TG) by mouth for 14 days
She will remain accessed to receive her ARA-C at home by a home care nurse.
Dianne will get another week of this treatment.

I wait for the day she starts Long Term Maintenance.




Tuesday, February 3, 2004 1:44 PM CST

Well Dianne will be starting her second half of her Delayed Intesification. Her appt. is on Feb.11 at 8:30 in the morning at the clinc at Sinai. Her LP is scheduled for 9:30. This is when they put her to sleep and remove fluids from the spine and also give her her chemo. She will get her port accessed and have her blood drawn. They will check her blood counts. If her ANC remains 1000 or more then she will go ahead and start the second half. If her ANC is below 1000 she will not get her chemo. The ANC is what helps fight infections. This is her treatment plan for the second half:
Cyclophosphamide(CPM) through IV over 20
minutes
Cytarabine(ARAC) IV push times 4 days
IT Methotrexate(IMTX) in the spine
Thioguanine(TG) by mouth for 14 days
She will remain accessed to receive her ARAC at home by a home care nurse.
Dianne will get another week of this treatment.

Her hair is starting to fall out. But it is ok. She is a real trooper. When she is done her two weeks of this treatment, she will enter her long term maintenance(LTM). Her LTM will last about 1 year and three months. I DO SEE A RAINBOW AND I AM LOOKING FORWARD TO GIVE DIANNE AN END OF CHEMO PARTY.


Wednesday, January 28, 2004 7:44 PM CST

Today Dianne had her appt. for more chemo . As you all know, Dianne is in her second Delayed Intesification(DI). It has been rough on her. On Friday we had her in the hospital for a few hours due to bad leg pains. Let me tell you what happened that Friday morning. She got out of bed and fell to the floor. She was in a lot of pain. She could not stand on her legs. Well I was told by one doctor that it was cause by the chemo called Vincristine. Today when Dianne had her appt. I was told that steroids can cause these pains. She also suffered from heartburn and stomach cramping. Now today she got Vincristine IV push and Doxorubicin IV. Dianne will also begin another week of steroids. Her blood counts are good except her ANC (her ability to fight infections). A good ANC is 1000 and up. Her ANC today was 730. She is running a fever but it is holding at 99.2. If it goes to 101 she needs to be in the hospital.
She is schedule in two weeks to to start the second half of her DI. Well after her second half she will begin her long term maintance. I do see a rainbow at the end of the tunnel. Sign her guest book if you have the chance. Dianne loves it when I read it to her.


Sunday, January 18, 2004 11:00 AM CST

Since Dianne started her second Delayed Intensification (DI) and its been bad. Her steroids kicked in fast. She is screaming and yelling and very demanding. She is eating everything in sight. Sometimes I just can't keep a handle on it. Her first DI was a breeze.

She is also suffering from leg pains. At night, she does a lot of crying. The only thing I can do is rub her leg and give her pain medicine. The onc still said it is from the chemo called vincristine. Her PEG shot gave her a reaction. She is itching alot. She has red lines on her face starting under her eyes down to her chin.

She is scheduled for another round of chemo on Tuesday. Sign her guess book if you have a chance. She always ask who signed her book.

Also, There is a Mother on the ALL Kids list who just lost her son Marcus. I know he had been having a really tough time since he was diagnosed. He was admitted in the hospital over the weekend for chicken pox and died Tuesday morning. Please keep his mother Teresa in your prayers.


Thursday, January 15, 2004 0:09 AM CST

Well Dianne is really having a bad day. Her legs been hurting all day. I do believe it is coming from the vincristine. Since she came home from her treatments she has been vomiting. She had started her Dexamethasone last night but could not hold it down. I had decided to start it today. I crushed it up and put it in vanilla pudding. She took it ok. The evening was a little more difficult. I was out of pudding so I had to use apple sauce.

I kept her home from school because of her legs hurting and her upset stomach. She is a sweet and strong little girl. Without Dianne I am nothing.

If you get a chance view her photos. She was a flower girl in her cousin Effie's wedding. She was adorable all dressed up in her gown and the bride was just as beautiful. Dianne really had a good time. We all had a good time. Please sign her guess book. She likes it when people leave a message for her




Tuesday, January 13, 2004 6:33 PM CST

Dianne started her second delayed intensification today. We arrived at the hospital at 9:00 this morning. She was scheduled at 12 for her lumbar puncture (LP). I tell you, it was a very rough day. We did not leave until 5:30 this evening. Today she got vincristine and Doxorubicin through IV. She got Methotrexate in her spine (LP). Of course they put her to sleep. I am tired. I just want to go home and rest. She will also start her most famous Dexamethasone ( steriods) today. She will take this for seven days and then seven days off of it. Dianne did vomit a lot today. I feel awful when I see her like that because I can't do nothing for her. I will keep you post how she does for the rest of her DI.

Please sign her guess book. Dianne likes to know who wrote to her.


Saturday, January 3, 2004 8:19 PM CST

Dianne has ended her second Interim Maintenance. She will go to the hospital for blood counts on January 7. If all goes well, she will begin her second Delayed Intensification in a week or two. This should last about 2 months. When this stage is over she will be heading into maintenance. This is the last part of her treatments which will last about 1 1/2 years.

Dianne's hair had just started to grow back. It is lighter and so far straight. She has a lot of energy and she is feeling very well. Dianne has been enjoying her Christmas Holiday. She was very please with Christmas this year.

If you get a chance, please sign her guestbook. She really enjoys it when people leave her messages.


Tuesday, December 2, 2003 9:46 AM CST

I hope everyone had a wonderful Thanksgiving. Now the Christmas season has just began. She is doing very well on her treatments. Dianne is nearing the end of her second Interim Maintenance (#2IM). On November 24, that is a Monday and Thanksgiving week, she broke out in a rash on her left hip in the back. I left it alone because she did not run a fever. It did itch her a lot. She was scheduled for treatment on December 1, which is a Monday, to have Methotrexate by spinal, Methtrexate through her central line and vicristine. The oncologist saw her rash and postponed the treatments. It turned out Dianne had shingles (part of the chicken pox family). She will get her treatments on Monday December 8. I had told the doctor that she had been in school that week but he said because her shingles were covered by her pants and shirts there should be no problems with the other children. She had a mild case of it. If she had treatment it would have made her shingles go out of control and she would have ended up in the hospital.
Her blood counts are very good.Dianne ANC is 3000. Well Dianne is getting her list ready for Santa. Michael had made his list and had already mailed it to the North pole. If you get a chance sign her guess book. She likes it when I read it to her.


Tuesday, November 4, 2003 9:16 AM CST

Dianne had finished her Delayed Intensification #1. She did well on it but had a hard time when the nurse came to our home to give her chemo.She would begin to vomit when she got chemo. I think a lot of it was in her head because she started to get sick before the chemo was given. Dianne hates the taste of saline.It is injected through her port to flush out the port. She said it tastes very salty.
She had just started her Interim Maintenance #2. Her last appointment was on 10/30/03. She had a spinal tap and Methotrexate was give to her in her spine. That same day, she got Vincristine and Methotrexate through the IV. She will remain on Interim Maintenance #2 for 2 months. After the 2 months, she will begin her Delayed Intensification #2.


Monday, September 8, 2003 11:32 PM CDT

Dianne had started her Delayed Intensification stage on August 27. On that day she got a spinal tap which included Methotrexate. After the spinal, She was given through IV Vincristine and Doxorubicin. These are the names of the Chemo she is currently on. For the next seven days she took Dexamethasone which is a form of steroids. On August 29 she received her Pegaspargase which was given to her in her muscles of both legs. That was very painful for Dianne. She said it felt like her leg was burning. On September 3 she received Vincristine and Doxorubicin through IV. For this week she is off steroids. Dianne's next appointment will be on September 10. On that day she will receive the two chemos through the IV and start her one week steroids.

Since the beginning of her Delayed Intensification, Dianne started to have many nose bleeds. She is complaining about stomach pains and she gets tired very easy. On top of this her hamster by the name Booboo died. Dianne took it well but her brother Michael cried alot. We buried Booboo and planted Mums on his grave so they have something to remember Booboo every year.

Since she was Diagnosed on May 1, 2003 Dianne had been through alot. She still is a very happy child who enjoys people very much. She really loves her cousins Kelly, Effie and Phedra. They have been a very big help to me.


Sunday, July 27, 2003 6:45 PM CDT

Dianne is doing just fine. She is enjoying her summer so far. Dianne is on her new protocol and Arm D was chosen for her. That is the most intense arm. She will return to the hospital on Monday for more treatments. She will be put to sleep so they could do a spinal tap and inject methotrexate in her spine. This is chemo to kill the cancer cells around her brain. Her hair had thinned out some.

Dianne is on med for her stomach. She been getting stomach pains everyday. She is also on colace because her stool has gotten hard. Dianne is on two types of chemo Methotrexate and vincristine. All in all she is in good spirit.

This Sunday Dianne went and tried on her dress for her cousin Effie's wedding. She looked adorable. She is thrill about being in this wedding.


Saturday, June 28, 2003 9:56 PM CDT

On Thursday, June 26, 2003 Dianne began her new protocol. The computer had to pick which arm she would be treated with. These would be the the chooses:
Standard treatment(Methotrexate by mouth and one delayed intensification phase)
Experimental treatment 1(Methotrexate by mouth and two delayed intensification phases)
Experimental treatment 2(escalating Methotrexate by vein and one delayed intensification phase)
Experimental treatment 3(Escalating Methotrexate by vein and two delayed intesification phases)

The one thing that bothered me the most about the new protocol was that I was afraid that the computer would pick Experimental 3. That would be the most intense treatment.I thought with 4 chooses what would be the chases of her getting experimental 3. Well guess what. The computer picked Experimental 3 for her. For the next 58 days her schedule would be every 10 days she gets chemo and Methotrexate by vein. Before this is done the doctor will take her blood and check for her counts. They will also check her liver. They will continue to increase the Methotrexate until the liver says no more. If any thing goes wrong they will stop treatment and she will continue with the standard treatment.

These are scarey days for me but Dianne is doing so well. Sometimes I feel ok and other times I feel awful. I had to call her oncologist today because she had a fever of 99.6 and her ears were hurting her. The doctor told me that her blood count were high and just double her bactrim and give her tylonol.


Wednesday, June 18, 2003 1:23 PM CDT

Today was Dianne's last day of school. I took her to school today so she could see her friends and say goodbye to her teacher, Miss Covert. She was able to meet her first grade teacher today. This Friday she will go back to Sinai to have her spinal tap and blood counts. On Monday She started to cry because a girl teased her about her hair falling out. She also asked why she has cancer. I really couldn't give her an answer to that question. I just held her in my arms and told her she will be fine and that mommy loves her.


Friday, June 13, 2003 11:09 PM CDT

Dianne is doing so much better now that she is off steriods. Her energy level is high. We went to the clinic on Thursday and she did very good. She did not cry when they had to activate her port. She is beginning to know her doctors and nurses. Her blood counts are good. Her White cells are a little low but the doctor said they are not worried at this time. I thank all my family members and friends for all their support.


Thursday, June 12, 2003 10:03 PM CDT

Dianne is 5 years old. She will be 6 years old on July 10.
She Has leukemia. She was diagnosed on may 1, 2003 with ALL. Her cancer is in remission. She is doing very well. I know we have a long road ahead of us but we will take one day at a time.


Thursday, June 12, 2003 8:48 PM CDT

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