Me and Mary Grace

Me and Mary Grace

Saturday, September 3, 2011

Race for the Cure

Ok Friends and family need everyones support for the Race for the Cure. I would like as many of you as possible to join me on the 5k walk/run. I am a survivor and together we can Race for the Cure!!!!

*************Here's the information**********************
Komen Oklahoma City Race for the Cure
October 15, 2011 - Expo Opens at 7 am
... Event Location - RedHawks Ballpark at Bricktown

All funds from the Komen Race for the Cure go to research, education, screening and treatment programs.

Thursday, August 11, 2011

August 11

Update
Sorry it's been awhile. Had chemo on Monday and Drs appointment. Chemo went well except the nurse accidentally didn't have my port connection closed right and she squirted blood all over. The nurse was so apologetic, it was actually pretty funny looking back. Meet with radiation docs tomorrow for simulation. A little nervous but sure it will go well. Thanks for all the prayers and support!!!

August 11

Update
Sorry it's been awhile. Had chemo on Monday and Drs appointment. Chemo went well except the nurse accidentally didn't have my port connection closed right and she aquifers blood all over. The nurse was so apologetic, it was actually pretty funny looking back. Meet with radiation docs tomorrow for simulation. A little nervous but sure it will go well. Thanks for all the prayers and support!!!

Monday, July 25, 2011

Sunday, July 17, 2011

Thursday, July 14, 2011

Drains

Drains came out today. Yea!!!
Feeling much better! Still brusing but much better!

Saturday, July 9, 2011

After surgery

Surgery went well. Lost a lot of blood and almost
Had to have transfusions.
Chest looks better than thought it would.

Monday, July 4, 2011

July 4th

Only two days till surgery. Getting nervous.
I know it's for the best just a little scary.
Please pray for us we need it!

Wednesday, June 29, 2011

Week 21

Wow made it to week 21 in chemo treatments.
Hair is still holding on a little thin but I'll take that everyday of the week.
Treatment is working and not feeling to bad. How lucky am I!!!
My little girl says I am the best mommy in the whole wide world!!
How blessed am I.
I'm really lucky that my great sister and brother-in-law are letting us stay with them.
It is so nice to have family around every day!!!
Sorry this post is so mushy just am so happy to be a live and kicking this cancers b..!!!!

Well blood work came back and white blood cells are low have to wait for dr to approve chemo.
Got approval for the go to have chemo. Glad don't want any delays :)

Week 21

Wow made it to week 21 in chemo treatments.
Hair is still holding on a little thin but I'll take that everyday of the week.
Treatment is working and not feeling to bad. How lucky am I!!!
My little girl says I am the best mommy in the whole wide world!!
How blessed am I.
I'm really lucky that my great sister and brother-in-law are letting us stay with them.
It is so nice to have family around every day!!!
Sorry this post is so mushy just am so happy to be a live and kicking this cancers b..!!!!

Wednesday, June 22, 2011

Week 20

Week 20

Week 20 chemo done. Counts were good. Yea!
Results of pet scan and bone scan were good. It was scary till I got the results. :)
Glad chemo is doing it's job and kicking this cancers rear!!
All the prayers and support helps so much.
Thanks friends and family!!

Thursday, June 16, 2011

Week 19

Week 19
Counts are good! Blood pressure good just
Higher than normal. Ku is really nice and my nurse is great.
Next week bone scan and pet scan to see
How chemo is working. Please pray for us
That we get great news. As always thanks
For the luv and support!!

Thursday, June 9, 2011

Week 18

Week 18 chemo
Awesome results on my heart scan went up almost 20%. yea
This is great so I can continue taking perception.
Only 2 more rounds before surgery.
Still have my hair :)
Missing all my kc chemo friends.

Thursday, June 2, 2011

Week 17

Week 17 chemo
Counts were good today yea!!! Think that yummy steak I had for dinner really helped!
Only a couple more rounds of chemo this time.
Feeling pretty good today! Thanks for all the prayers and support!!!

Thursday, May 26, 2011

Week 16

Week 16
Counts stayed the same.
Dr scheduled another heart scan in a couple weeks.
Hope it goes well.
Thanks for all prayers and support!

Thursday, May 19, 2011

Week 15

Counts remain same, that's good. Only for 5 more rounds of chemo this round.
My friends at chemo are mostly doing good.
Thanks for all the prayers and support.

Wednesday, May 11, 2011

Week 14

Week 14 chemo going good!!
Counts looked good.
Drs advised will have to have double masectomy once complete chemo treatments.
Drs still very optimistic that chemo is working.
Thanks for all the prayers and support!!

Friday, May 6, 2011

Day after chemo

How lucky am I my sweet little girl Mary Grace came up and gave me a hug and told me I'm her very best friend and the best mommy in the whole wide world. Then she said I love you more than anything and gave me a hug and kiss. How lucky am I !!!!!

Thursday, May 5, 2011

Week 13

Chemo going good. All counts went down a little but still ok. Still have my hair just alittle thinner. Still a miracle that I have it!!
Thanks for all the prayers and support.

Thursday, April 28, 2011

Week 12

Week 12 chemo counts look good yea!!! Results of heart scan are down 10% from initial scan. Going to have to watch it since it has to be over 50%. Next one will be in June. That's a little scary hopefully will remain over. Thanks for all the prayers.

Tuesday, April 26, 2011

April 26

Hair still hanging in there. Yea!! Eyebrows not so much! Spending the day with my little munckin today!! Feel so lucky and blessed that feel good today.
One of my fellow chemo friends is having a very rough time so sending prayers and love her way!!
As always thanks for the prayers,love,and support

Monday, April 25, 2011

April 25

Feeling good today nausea gone today. Yea! Had a great Easter with great friends!! So lucky!!
Eyebrows slowly falling out. Lol
Thanks for all the prayers and support.

Friday, April 22, 2011

After chemo

Today was a little rough. Nausea pills weren't working this evening. Unfortunately Mary Grace saw me throwing up. She was so cute. She rubbed my back and said I was going to be ok! Luckily soon passed and am better now! Just tells me chemo is working! Hanging in there :)

Thursday, April 21, 2011

Week 11

Week 11 chemo going good. My best girlfriend Kristina came with me today. How lucky am I to have such great friends and family. Still have my hair losing my eyebrows which is weird. My fellow cancer friends were both at chemo today! Angela lost her hair but looks beautiful in her new wig. Rhonda finds out to the results of her pet scan pray it's good news!!!
Wish the nasty night sweats would cease. Small price to kick this cancers rear!!!

Wednesday, April 20, 2011

Heart scan

Today have to be poked again. Having a heart scan to make sure chemo is not weakening my heart. My heart feels good so hope the scan reflects that! Makes me a little nervous. Thanks for all the prayers. FYI still have my hair another miracle. :)

Friday, April 15, 2011

Week 10 chemo

Made it through week 10 chemo. Counts down some but still pretty good. Still have short hair just a little thinner. :) nausea is a little bit worse but battling through meds really help. Made some good friends at chemo. Both are also battling breast cancer. Rhonda is ahead of me on treatment and is doing good. Angela just started treatment. Please pray for them also. It helps to talk to friends that know all the emotions that you go through with this crazy cancer. It also helps to stay positive and to hopefully help others with there battle though the big C. Would like to help other cancer fighters beat this disease and stay positive after I win this battle. As always thanks for all of the prayers and support!!!

Monday, April 11, 2011

Monday April 11

Feel great today didn't even have to take nausea medicine today.  GOOD DAY!
Feel lucky to still have my hair can't believe it has been almost 10 weeks of chemo.  I feel so blessed and lucky to have so many wonderful friends and family supporting me through this difficult journey.  It means so much to me and Mary Grace.  We love each of you dearly.
I know I ask for prayers all of the time but I am asking again but not for me today.
 Please pray for my cousin today as he is having major eye surgery today his name is Devon and he is only 13 years old. I know he is going to come through with flying colors but thought added prayers could help.  Thanks
love, Heather

Wednesday, March 30, 2011

Test results 3/30

Received great news from the doctor today. The chemo is working and doing everything they wanted it to do. YEAH!! We are so glad and excited. I am overwhelmed with all the hope this shows. God is great!! I know all the prayers and support helped so much. Thanks everyone please keep praying for continued success. Still have a long treatment plan ahead however we are going to continue to beat this cancer and WIN!!

Tuesday, March 29, 2011

Tests

At MDA getting ready to have petscan that will show if chemo is working. VERY nervous and scared for the results. Hope it goes well! Will get the results tomorrow when I meet with the doctor. My name just got called...

Friday, March 18, 2011

Chemo week 6

Counts were good today was worried since had a bad cold this week, counts weredown from prior week but still good. Yeah. Lucky still have my hair think cutting 8 inchs last week helped. It's taking some getting used to but happy still have it. :)
Tonight was a rough night nauseous and couldn't sleep. FYI tv is not good after 2am. Lol.
Thanks for all the cards, gifts, and donations words can't express how much it means to me and my family. Thank you so much!

Thursday, March 10, 2011

Doctor's appointment today

Today John and I are in OKC with Heather. We met with her doctor this morning and he is still optimistic that her treatment is working. We'll know for sure after her MDA tests later this month. Her doctor is shocked that she still has her hair, but she does! She's doing her 5th chemo right now...and her spirits are still high!

Friday, March 4, 2011

Fundraiser---Heather's Hope Necklace

My cousins (Diane and Debbie) came up with an idea to wear a piece of jewelry to show our support for Heather.  So me and my friend (Maggie) contacted a jewlery designer (Stacy from bellawish) on etsy.com and she custom designed a necklace for Heather.  The necklace is handmade, sterling silver, with 2 charms (a pink crystal and a silver breast cancer ribbon) and a Hope silver disc.  It is absolutely beautiful, I'm so excited to wear it! We decided that it would be a great way for all of her friends and family to show support so we are selling the necklaces as a fundraiser to help raise money for her upcoming trips to Houston and her medical bills that are arriving daily.  I've attached a picture of the necklace.  If you're interested in purchasing one please email me at heidi.birtciel@yahoo.com and I'll give you the details. :)

Optimistic news from the doc

Yesterday Heather was able to see her Oklahoma oncologist before her chemo treatment.  After he examined her he said that he is "cautiously optimistic" that the treatment is working, i.e. he thinks the breast tumor is shrinking!  This is awesome news!  Dr. Alvarez (doctor from MD Anderson) said that shrinking the tumors is the main goal of this first round of treatment.  If these drugs can shrink the tumors then that's the first step to controlling the cancer.  This was the best news that we've heard in months!  The last couple of weeks her attitude has been positive and optimistic so I'm glad that she received this news so it will help her continue to keep the great attitude. She has her MDA appointments scheduled for the last week of March so that's when additional tests will be done and the results will be compared to her original tests.  Keep your fingers crossed that the chemo continues to work!

Heather wants everyone to know how much all of the flowers, cards, messages, comments, donations, etc. have meant to her!!! It makes me feel so good to know that there are so many awesome people out there who care so much about my sister!  Thank you from the bottom of my heart!  You and your thoughts and prayers are helping her everyday!

Monday, February 21, 2011

Update

Heather has completed 2 chemo treatments and this Thursday she'll do her 3rd. She has tolerated it fairly well with only mild side effects...as long as she takes her medicine.  The first time she took her anti-nausea medicine consistently for the first 3 days and didn't get nauseous.  The second time she thought that she didn't need to take it because she wasn't nauseous before, she learned her lesson though...always take her meds! :)  Now she's feeling a lot better.  She hasn't started to lose her hair yet, but she did go and pick out a really cute wig.  It looks super good on her!  I tried it on today and I loved it too. Her spirits are up and she seems to be adjusting to the chemo schedule.  She met a single mom last week that was diagnosed with breast cancer 10 years ago and she's still living a good life today.  I think she helped Heather realize that she can get her cancer under control and live the life she wants to live.  I'm proud of her for being so strong and having a positive attitude!  P.S. We go back to MD Anderson in April.

Saturday, February 12, 2011

Finally home!

After Heather's chemo treatment this past Wed night we were finally able to head home on Thursday morning.  It was a 8 hour trek to Oklahoma City, but dad drove the whole way so Heather was able to rest (thanks dad!).  Luckily Heather didn't experience really bad side effects from the first treatment so she wasn't too uncomfortable in the car. The fatigue did set in, but being in the car gave her plenty of time to rest. From the beginning she took the prescribed medication to keep the nausea from getting too bad.  The nurse said if you don't take it at the first onset of nausea, then it's too late.  We were warned by Dr. Alvarez that the side effects will get worse after each treatment because the chemo is killing all cells, not just bad ones.  The most noticeable side effect will be the hair loss, which will happen around week 3 or 4.  While we were in Houston we checked out some wigs and figured out that there are some really cute ones available. 

Heather is hoping to be able to do her weekly treatments in Springfield or Kansas City, but unfortunately her ex-husband is fighting her about that.  Neither him or his new wife have been compassionate about the situation at all.  They have told Heather that they don't care if it's in her best interests to get treatment somewhere else, they want Mary Grace to stay in Oklahoma City.  While Heather tried to explain the severity of her diagnosis and what it's going to take for her to beat it, they said they didn't care.  If anyone knows the ex, this is typical behavior for him, but we were hoping that his new wife might help him be a little nicer.  The crazy thing is, the ex only gets custody every other weekend so it's not like he would see her any more or any less than he already does.  Heather promised him that she would have Mary Grace back in OKC every other weekend for his pre-determined visitation, but he didn't care. To most people, this sounds completely ridiculous that someone could act like this, but unfortunately we have been dealing with his irrational behavior for years so it doesn't surprise us. We were just hoping that when it really mattered he would come through, but he didn't.  It breaks my heart that Heather is having to worry about him and going back to court when she has a much bigger fight on her hands.  The last thing she needs is additional stress. 

Thank you so much for all of the supportive messages, emails, and cards...they all mean a lot to Heather (and her family)!

Wednesday, February 9, 2011

Another crazy day...

Today Heather was prepared to get her liver biopsy done and then head home. Houston was/is supposed to get freezing rain so we wanted to head back asap. She was in surgery and then post-op until about 1:30. Then dad and MG picked us up and we hit the road. We had already accepted the fact that Heather would not start treatment until next Wednesday so we were just happy to be going home. We were about 45 min from MDA when we received a call from Dr. Alvarez's nurse. She said he wanted to see Heather asap, but she didn't say why. We actually turned around at the same exact exit as we did yesterday...weird.
Anyway, once we got back to MDA Dr. Alvarez told Heather that he had reviewed all of her tests, notes, etc. and had decided on a treatment plan. We were shocked because we weren't expecting this news. But in reality we receive unexpected news everyday so we shouldn't have been shocked. We had left dad and MG in the car so he had no idea what was going on, he was just driving around in circles waiting for us. :(
Dr. Alvarez said that the treatment plan would initially be the same one as her doctor in Oklahoma had suggested. He was much more positive about the outcome though. He said the scary mortality statistics include everyone in the world and people outside of the US don't have access to the drug herceptin because it's not approved there. He said this treatment is the best to use to shrink the tumors. He said if it doesn't work as well as he would like then there are 4-5 more options. He didn't really mention the research trial, he just expressed numerous times that this is the best option for right now. It was a little overwhelming for Heather (and me) to hear that she was going to start chemo in 15 min. They shuttled us upstairs to the chemo department and put us in a room and got started. We barely had time to call our family to tell them what was going on before they had her hooked up and going.
Neither one of us brought anything to do because we weren't expecting 3.5 hours of chemo so it was sad when they made us turn off our cellphones. Now the Ipad is the only source of entertainment. The 'good news' is that she'll be able to do her weekly treatments in Oklahoma or wherever she wants. The doctor here will communicate with her doctor back home and then she'll come back for some follow-up tests in 8 weeks or so. The doctor says the chemo is fairly mild so the side effects hopefully won't be too bad. She has been so strong the last 4 hours! I am so proud of her! My anxiety was out of control when we found all of this out so I can only imagine how she was feeling. We knew this day was coming, we just weren't necessarily prepared. I really think we'll actually be able to go home tomorrow. And at least we finally have a game plan...the chemo is almost done so we are going to head back to the hotel. We'll keep you posted...
-Heidi

Tuesday, February 8, 2011

Crazy day in Houston...

Today was a crazy, but good day! Last night my parents were able to get Mary Grace to Houston so Heather was finally able to see her little girl after more than a week.  I think that helped her morale more than anything. Also, yesterday we accepted the fact that Heather would not be able to get her liver biopsy done until next Wednesday.  We planned on heading back to Oklahoma City (and then Kansas City for me) after her last appointment today.  Bright and early we went to the hospital for her to get another biopsy on her left breast (we were told the slides from her first biopsy never arrived at MDA).  Well, we received what we considered great news once she check in! The radiologist refused to do another biopsy because the slides had arrived.  Heather was actually happy to not have the biopsy done...now, it's the little things that we get excited about it!  Then she was able to get squeezed in for her afternoon appointment 4 hours early. Yay! We were happy that we would be able to get an early start back home.  Once we got back to the hotel we packed up our stuff and jumped in the car and started our 8 hour journey to OKC.  We were only 30 minutes outside of Houston when one of the research nurses called and said that there had been a cancellation so they could get Heather's liver biopsy done tomorrow morning.  The car was turned around and headed back to the hotel before Heather even got off the phone.  It's crazy that we're "excited" for her to be getting the biopsy tomorrow because it's painful, but we know her treatment will start at least a week earlier now.  She's very anxious for her treatment to get started. The doctors have ensured her that her prognosis is no worse if the treatment starts this week, next week, or in two weeks, but she just wants to start killing the cancer. Totally understandable!  Now we'll be down here until at least Thursday because Heather can't travel for at least 24 hours after the biopsy.  We'll continue to keep you update...
-Heidi

Monday, February 7, 2011

Monday 2/7/11

Well today was very frustrating. Mda didn't receive my biopsy slides that were supposedly overnighted. Now have to have them redone tomorrow which sucks. I hate biopsies. Sorry to be so blunt. Now I also have to have a liver biopsy,which of course takes a week to get an apptment. So ready to go home!!!! Also had to have a new petscan because ok technology I guess sucks. I know this seems negative but I just want to start treatment and every time they tell me a new test needs to be done and put it off again. I don't know why they couldn't have made me do these tests earlier as really nothing has changed from last week. I know this is supposed to be the best place, but sometimes they don't seem very organized and it gets frustrating when they tell you that you will start your treatment then they put it off again and again. Please pray for me to have patience and to beat this cancer! Thanks for all of your support and prayers

Thursday, February 3, 2011

2-3-11

Today we spent the day at MD Anderson, hoping to get all of the additional tests out of the way.  We were told that if the tests were completed then the doctor would be able to see Heather today instead of Monday.  Well that proved to be untrue because he wasn't even in the clinic today so we talked to the research nurse instead.  Since monitoring clinical trials is my job I at least know what questions to ask.  I wanted to make sure we had all the tests completed and the documents in place in order for the doctor to verify if she qualifies or not.  Luckily we did this because we discovered that MD Anderson did not have copies of her previous biopsy slides, which they need before they can include her.  We found the slides in Oklahoma and they are now on their way to Houston, but it might add on 3-5 days to our stay because the pathologist at MD Anderson has to read them before the doctor gets them.  It seems like everything is such a long process, I guess we need to get used to that.  In the meantime Heather had another mammogram and ultrasound.  During the ultrasound they decided to do another biopsy, this time on her right breast.  That ended up being positive, which was a big blow...yesterday Dr. Alvarez said that he didn't see any cancer there when looking at her PET scan.  Now there's nothing we can do except wait for our appointment with Dr. Alvarez on Monday and hope that everything is in order.  She's pretty bummed out about the whole day so she didn't feel like writing the update herself, but she really appreciates the messages and comments.
-Heidi

Wednesday, February 2, 2011

Wednesday 2-2-11

Had first appointment with MD Anderson today.  Had a physical and met with the doctor.  The doctor scheduled another mammogram and ultrasound, and blood work.  Once all this is completed over the next couple of days will meet again with the doctor to see if qualify for a study that is having good results.  The doctor was more optimistic about getting the cancer in remission as long as everything goes ok with the treatment. That was better news than we had been hearing. Hopefully will get into the study.
Please continue to pray for us.  I appreciate everyone's support and prayers.  It means more than words can say.  Thanks

Tuesday, February 1, 2011

Tuesday Feb 1

Tomorrow I go to my appointment at MD Anderson at 7:30am.  I am scared and overwhelmed but trying to remain calm and think positive.  I know I am going to beat this.  Just need prayers and support.  Thanks

Heather's Blog

I started this page for my sister, Heather, in order to keep friends and family updated on her journey to fight inflammatory breast cancer.  Heather is a 36 year old single mom of a beautiful 3 year old little girl, Mary Grace. Mary Grace always insists that her mommy is her best friend, it's so cute and definitely true. MG is definitely Heather's inspiration to fight and beat this disease. Heather is also the best sister that a girl could ever ask for. She has always been there for me and I have promised to her that I will be here for her every moment of her journey. We all know she can beat the cancer, but she'll need continuous encouragement and support.

She found out about the diagnosis the day we were all leaving for my wedding in Antigua. Despite the awful news, she still made the trip to be there for me. Heather, her daughter, and my parents left early to return to Oklahoma for further testing. We are so happy that she was there to share in our special day even though she had just received life-changing news. The additional tests showed that the cancer had spread to her liver and bones. Her oncologist verified that it is Stage IV. Last Friday, MD Anderson called and offered her an appointment on Wed, 2/3. We were so excited to finally hear a little good news. Now we know that Heather is going to get the best care in the world.
Many people have asked what they can do to help and show their support.  Obviously, Heather needs all of the support and prayers that she can get. You can send her messages via this website, text, email, snail mail, and/or her voicemail. 

Her address is:
18212 Piedra
Edmond, OK 73012

Also, John and I have set-up a PayPal account to accept donations to help Heather pay her medical bills and support Mary Grace since she will not be able to work during her treatment.  We want her focused on fighting this disease, not worrying about how she's going to pay her bills. We don't want anyone to feel obligated, but just click on the link below if you want to help.




I'll let Heather take over the blog now...

Thanks-
Heidi