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theresac (theresac)


May 26, 2008


Grand Rapids, Ohio


Breast Cancer


12/05 and 2/08recurrence


Stage 4


2.1 - 3.0 cm


Negative


Negative


No


Yes


Mastectomy, Reconstructive Surgery, Lymph Node Removal


Adriamycin (chemical name: doxorubicin), Cyclophosphamide (brand name: Cytoxan), Gemcitabine (brand name: Gemzar)


Cancer Survivor


Live life to the fullest and don't sweat the small stuff


be positive and encouraging


recurrence of breast cancer now mets sm. tumor in liver


5/28 first treatment of clinical trial Gemzar with Avastin




theresac's Cancer Blog

July 25, 2008

Gemzar/Avastin it's workingViews: 263

Finally, today a bit of good news. I had a CT scan on Monday and heard the news today from the onc. that the tumors are shrinking. the mass on the right chest is about 1/2 the size and the lesion on the liver which was 1 cm in diameter is now barely perceptible. This is the first scan since starting the Gemzar/Avastin clinical trail 2 months ago. So- I am so happy and so grateful to all of my family and friends who have been praying for me.
My oncologist is really happy with the progress and is pleased that I continue to tolerate the rather high dose of Gemzar. Blood counts continue to be good and I’m managing the side effects pretty well. So I pray the treatment continues to be effective!

Good new some times come in small packages.

Hug Sherri

It is always a blessing to see good reports. Thanks for sharing.

Hugz
Mac

Dear Theresac,
Great and miraculous news…. I am so happy for you. I am very big supporter of Clincal Trials. When I was dx. 14 years ago, they immediately tested all of my children as possible bm donors though they told me it would be a very small chance of them being a match for they are only half of my DNA.None of my children matched. I was put in the Bone Marror Donor Registry and to this day a match has never been found. But, as scared as I was with this news back then, now I know this wasn’t God’s plans for me. I was put on a nasty drug called Interferon Alpha 2B where I had to give myself sub-q injections @ a dosage of 10 million units daily, and Hydrea. I can’t begin to tell you just how bad the side effects was. I was in the hospital so often and I tried so hard to hold out if I was feeling badly
and if I thought I had a problem I would try to put on a brave face for I had 3 very scared children at home. We were having private sessions with our Pastor to help them deal with this. Then, there was a new drug that was in clincal trials & it was called STI-571. But, unfortunately I wasn’t able to get into the clincal trials at that time.(Thankfully, there has many so many changes and progress with this) I followed the progress for Novartis was waiting for FDA approval. Me and my children actually watched the House of Rep (on C-Span) pass this drug together and we felt as though we had won the lottery. My onc. had me in his office 3 days later and her perfomed a BMB to establish my baseline of the leukemia. He started me on this drug which the drug company, Novartis had named this,” GLEEVEC”. After watching the progress of the leukemia patients that were in the clincal trials, I was so thrilled to now be on this drug and it gets even better, It comes in a Pill that I take daily. My Dear Friend, when I was told to get my “affairs” together for there was no treatment that could put me in remission in 1994 and to now be on this Miracle drug, I had so much hope. So, Doc had me on this drug and waited an entire year to repeat a bone marrow biopsy, though anxious to have it done sooner, of course he knew best. So, exactly 1 year later he did the BMB and the wait was on for the results. This is always tough, but I have learned to deal with it after so long. So, the day came to see my dear Dr. Weiss and when he came into the exam room he was smiling so big and he always greets me with a friendly HUG, and he said, I have some amazing news for you. Patty we are in REMISSION! Can you believe that? What a miracle this is. So, I am sure that you are thinking this is going into a mini-series but I am going to cut to the chase. This new drugs seem to be doing wonderful changes to your body. Clinical Trials are wonderful for they are making such amazing advances so please enjoy the benefits of this and keep me updated on your progress. God Bless you and keep those Positive thoughts going. Hugs and Prayers, Patty

Thanks everyone for the comments and support. Patty you have hit the nail on the head describing all the emotions on waiting for scan results and the determination to raise our children. I really admire you and find a lot of hope in your story- Thank you for sharing!

Hooray! Keep those thoughts POSITIVE!

bo

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June 24, 2008

treatmentViews: 268

Still doing pretty well during treatment. Will go back for treatment 3 in two days and my energy level is pretty good, no real problems. The effects of the second treatment were pretty much like the first treatment. So I know what days my energy and appetite will be low and know which days will be “normal”. So far most days are real good so I feel blessed. I have started back to running a little. It’s slow going but it feels good to be back on the open trail and I enjoy it.

I am with you. I always feel so much better after a run on the trails. Hang in there. ;-)

Hello Theresa,

I found your blog – so proud to know you and so thankful to be in your presence of faith and hopefulness. A

My thoughts and Prayers are with you.
Stay strong. You have a Great Support here.
Hugs, Patty
P.S. I was dx. 14 years ago and I am still going strong. Despite what the DOCS said.

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June 19, 2008

Snail MailViews: 288

Doesn’t it seem like snail mail is just no fun anymore? If you are like me the good ‘ole mail box is usually just filled up with bills (most medical). Well 2 days ago I was blessed to get two cards in the mail. One from a dear cousin who lives out of town and one from a fellow employee at work. So that was really a pleasant surprise, but there was one more element that made it extra super—the two cards were exactly alike- with the passage “If you have faith as small as a mustard seed…nothing will be impossible for you Matthew 17:20. “trust, have faith, be patient, beleive” Well what are the chances of that? So I am grateful for my Cousin Kathy and the “prayer warrior” at LHM, bringing this perspecitve of faith! Thanks to all of my friends and family who have called to check in on me, sent cards and are saying prayers!

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June 10, 2008

Hangin' in thereViews: 356

Brief update- i’m feeling pretty good – blood looks OK so far- went bike riding in the early hours of yesterday morning. For those of you who know me, you know that I had taken up running about 3 years ago. I love to run trail. Roads, not so much. I have not ran in quite a long time, but aerobically I still feel OK so I may put a little jog into my step again, and quit babying myself. Treatment 2 is 2 days away. Praying it goes as well as the first.

Glad you got out on a bike ride. I snuck out for a run today. ;-)

Nothing is better than getting out and seeing what is going on around you. You go gal.

Hug sherri

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June 2, 2008

hidden messagesViews: 403

Very interesting thing happened today at work. I work at a facility for persons with developmental disabilities. A staff member who has a very deep faith and has worked at the facility for years was starting her day with those she cares for. As she was sitting in the dining room looking at the windows, which had recently been painted a festive “beach” scene, she began her usual internal prayer, to the Blessed Virgin Mary for strength for the day.
As she looked at the painted beach ball on the window she discovered it was more than the ususal beach ball. In the middle of the ball, just the way the paint was applied, revealed an image of the Blessed Virgin Mary. As she quietly asked people to look at the beachball to see if they saw anything unusual? One by one, many people saw the same image. It was quite a pleasant focus for the day. Sometimes I guess we just have to stop and look around, and apparently not very far, to get messages of hope.

Teresa thank you for sharing the wonderful story.

Hug Sherri

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June 1, 2008

chemo updateViews: 420

Just an update- It’s day 5 of the first treatment and I really do feel pretty good. Day 2 and 3 a little queasy and tired, but day 4 and 5 were better. Today is a beautiful day in Ohio and I’ve been outside almost all day with the kids. Hope everyone is enjoying the beginning of summer!

Have a great day with the kids!

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May 29, 2008

saddenedViews: 454

5/29/08- Today I am saddened at the news of the loss of a dear comrade suffering from painful cancer for the past 6 months. Discovered late, she endured a lot of chemo and had several complications. We are blessed with the positive memories of her pleasant stay at Northwest Ohio hospice and her beautiful room with a view. I am sure the view is even more beautiful now, May she rest in peace- as I am sure she is with her Savior!

Thank you so much for the CancerCare info, I had not hear of the site. I did sign up for the teleconference, you can never be armed with to much good information. Not only are we triple negative sisters, my first name is also Theresa!

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May 28, 2008

treatment number 1Views: 485

Just to let you know treatment #1 – Gemzar and Avastin went really well and so far I am feeling pretty good. I am at a different clinic than last time, but with the same local oncologist. Everyone was super and it went fine. They gave me a little bag of anti-nausea and a little dexamethasone- steroid-(samller amount than with taxotere the last time) So that is probably why I am feeling really good right now.
Keep you posted!

Blessings, I am sorry you have to do this again. I am also a triple negative just beginnig treatment, was your lymph node involvement the first time round or with the reoccurance?

Yes my lymph node involvement was both first time 3-5positive out of 30 and also recurrence. Note I did not have radiation the first time and I wonder if this would have helped. I am planning on pursuing radiation this time around if I get the liver thing under control and if things remain stable.

To my sister- My thoughts and prayers are always with you. Remain strong and take it one day at a time. You can beat this!
I love you!

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Here we go againViews: 489

For those of you who are just now getting filled in -here we go
late in Nov. 11/07 I’m feeling a lump about 2-3inches below clavical, well above reconstruction area- same side as last time
Doctors think it is nothing but fatty tissue from surgeries. Ultra sound reveals suspicious tumor near implant. I see plastic surgeon who will remove it with local anesthetic (due to close proximity to implant). With the holidays and no particular panic by any Dr. That happens in January.
1/08 Unable to reach it under local, because the surprise is that it is between the pectoralis major and minor, and the procedure was starting to get a little uncomf. for me ( you can’t call me a wimp yet!)
1/08 Go under general anesthesia – they remove a 3cm tumor, we were only feeling the tip of the tumor prior to surgery.
2/08 path report shows IDC- same tumor markers as before. Local oncologist sends me for scans- another area shows up in axilla – probably a luymph node containing same cancerous cells. local oncologist recommends starting chemo again. I contact U of M Cancer Center to get another opinion. takes 2-3 weeks to get an appointment.
3/4/08- Initial consult at U of M. They recommend surgery to remove the two areas, and unfortunatley recommend removing all reconstruction.
3/21/08- I have repeat mastechtomy and rest of axiallry node disection.
4/08 – U of M team recommends trying radiation prior to chemo- I go for first simulation 4 weeks post op. Already they are picking up another tumor and now a spot has shown in my liver. Rest of April is complete restaging process with many scans, some of which I have never had before. So after a liver biopsy it is confirmed the same breast cancer cells have traveled- I am now stage IV metastatic breast cancer. there are several chemotherapy drugs to chose from. I decided to try to get chemo local the two oncologist communicate and I am a candidate for a new clinical trial in phase 2. using Gemzar ( previously approved by FDA for breast cancer and avastin -fairly new for breast cancer- the combo is what is important.

I’ll keep you updated on treatment- which starts 5/28/08

Just wanted to say Hi,

And send a Big Hug,
Sherri

Thanks Sheri- right back at ya’!

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Theresac's Stats

Posts: 9
Photos: 0
Events: 0
My Supporters: 11
I Support: 8
Comments: 18
Views: 3426



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