I'm writing sitting next to mom in the recovery room, gotta love technologies like Blackberries!
We both worked the last several night shifts, so when the hospital called this morning to ask us to come in earlier due to a cancellation we didn't quite get the message since we were asleep! After an hour nap mom got up though and we headed over to North Memorial.
Preop went very smoothly this time, IV on the first try and all the doctors and nurses we ready for her, so she rolled on back to the OR with versed warming her veins a half hour ahead of schedule.
The half hour was wasted though when mom, in her sedated state, reached up to scratch her nose and contaminated the surgery site- Oops!
Dr. Mestitz did an excellent job once again and placed the port just under her right collar bone without any complications. She has no subcutaneous fat in the area, so you can see the lump under her skin and it will be a little sore for awhile with nothing to pad around it. It's about the size of a quarter and already has worked efficiently (good blood return).
Well mom's already feeling great and ready to get home for some much deserved couch time... I better help get her dressed and go get the car!
I'll update again tomorrow night and let you know how chemo goes. Please pray that mom tolerates chemo well with little side effects.
As always, thanks for being with us on this journey, we couldn't do it without you!
Love mom and Lins
Wednesday, September 30, 2009
Wednesday, September 23, 2009
Chaos before Chemo...
Hi guys~
It's official, chemotherapy is in our plan. Our meeting with Dr. Londer and nurse Jean went well this morning. It was a bit overwhelming the wealth of information we received, but after reviewing our notes I think we have a good handle on what we're signing up for.
Monday mom will have another general checkup and surgery preop appointment with her primary doctor. Then next Wednesday she will have a 'metaport' placed. As Andrea already explained, it's a type of IV, but more permanent and sits right under the skin under her collar bone. The port will be accessed with a needle whenever it needs to be used and that way medications can be given and blood can be drawn through it.
The protocol we will follow is the 'TC Regimen'. Mom will be administered two different chemotherapy medications, Taxotere and Cytoxan. She will also take a steroid, Dexamethasone, for a few days around chemo to help prevent fluid overload and nausea.
Next Thursday, October 1st, will be our first of four rounds of chemotherapy. She'll have it once every three weeks. The treatments, including lab draws, doctor visits, etc. last between 4-5 hours. The day following chemo she will have to go back to clinic to have a small injection called Neulasta, that helps stimulate white blood cells to grow.
Other side effects from treatment are weight gain, bone pain, insomnia, fatigue and hair loss. We won't know how severe mom's side effects will be, we'll just have to wait and see and then tackle them as we go. Hair loss is inevitable however, so today after the doctor appointment we went and got a really cute wig! It looks great, actually very natural!
Mom will also have to take extra precaution not to get sick during chemotherapy. This means all of us around her have to be careful too. She got a flu shot today and I picked up some extra hand sanitizer! We'll have to be very diligent with keeping the house as germ free as possible, avoid crowds and especially anyone who's ill or not feeling well.
We've got lots to do these next several days to get as prepared as possible for what's to come. Mom will mostly be pretty fatigued and not feeling well for the first week after chemo. Then she'll hopefully feel ok during week #2 and 'good' week #3 before the cycle starts over again. If all things go as planned our last chemo treatment will be December 3rd and we'll be done and feeling good by Christmas! Then after the first of the year we'll move along to radiation.
That's the scoop for now- we're happy we can get the ball rolling soon and be closer to putting this cancer thing behind us. Like Grandma Marie said, this is our journey- and we are ready to go!
It's official, chemotherapy is in our plan. Our meeting with Dr. Londer and nurse Jean went well this morning. It was a bit overwhelming the wealth of information we received, but after reviewing our notes I think we have a good handle on what we're signing up for.
Monday mom will have another general checkup and surgery preop appointment with her primary doctor. Then next Wednesday she will have a 'metaport' placed. As Andrea already explained, it's a type of IV, but more permanent and sits right under the skin under her collar bone. The port will be accessed with a needle whenever it needs to be used and that way medications can be given and blood can be drawn through it.
The protocol we will follow is the 'TC Regimen'. Mom will be administered two different chemotherapy medications, Taxotere and Cytoxan. She will also take a steroid, Dexamethasone, for a few days around chemo to help prevent fluid overload and nausea.
Next Thursday, October 1st, will be our first of four rounds of chemotherapy. She'll have it once every three weeks. The treatments, including lab draws, doctor visits, etc. last between 4-5 hours. The day following chemo she will have to go back to clinic to have a small injection called Neulasta, that helps stimulate white blood cells to grow.
Other side effects from treatment are weight gain, bone pain, insomnia, fatigue and hair loss. We won't know how severe mom's side effects will be, we'll just have to wait and see and then tackle them as we go. Hair loss is inevitable however, so today after the doctor appointment we went and got a really cute wig! It looks great, actually very natural!
Mom will also have to take extra precaution not to get sick during chemotherapy. This means all of us around her have to be careful too. She got a flu shot today and I picked up some extra hand sanitizer! We'll have to be very diligent with keeping the house as germ free as possible, avoid crowds and especially anyone who's ill or not feeling well.
We've got lots to do these next several days to get as prepared as possible for what's to come. Mom will mostly be pretty fatigued and not feeling well for the first week after chemo. Then she'll hopefully feel ok during week #2 and 'good' week #3 before the cycle starts over again. If all things go as planned our last chemo treatment will be December 3rd and we'll be done and feeling good by Christmas! Then after the first of the year we'll move along to radiation.
That's the scoop for now- we're happy we can get the ball rolling soon and be closer to putting this cancer thing behind us. Like Grandma Marie said, this is our journey- and we are ready to go!
Saturday, September 19, 2009
A bump in the road, but we will get over it
Hi guys, Andrea here. Lins is on vacation in Colorado and Mom and Dad are busy cheering on the Badgers in Wisconsin this weekend (GO BIG RED!) so I'm updating the blog today! I'm not as well versed in this stuff as Lins is, but I'll try to explain things to the best of my knowledge, so here it goes. Last Thursday, Mom received a phone call from Dr. Londer regarding her Oncotype DX results, the one we have been desperately waiting for. Basically we needed this test before determining Mom's final treatment plan. Specifically, this test yields a recurrance score of 0 through 100, which correlates with the likelihood Mom's cancer would return in addition to indicating whether or not Mom would benefit from chemotherapy. 0 through 18 suggests a low chance of recurrance and that chemotherapy would not be beneficial. 19 through 30 indicates a moderate chance of recurrance and that chemo may be beneficial and over 30 states that chemotherapy would most likely be beneficial. With that said, Mom's results were unfortunately not what we were hoping and praying for. Her score was 28 with a 19% chance of recurrance. We assume this higher score is due to the fact that Mom's cancer cells are grade 3, the most aggressive type possible. This news was quite shocking to us all, including our doctors and practioners. There have been tears and feelings of anger and great disappointment. Mom really really really didn't want to have to go through chemo. So what does this mean? Well, basically we need to meet with Dr. Londer, our oncologist, next week, but he will probably leave the decision up to us whether Mom does chemo or not. With the results we got and a score of 28 being very close to 30 with a 19% chance of recurrance, how could we not decide to go with the big guns and kill this son of a bitch all the way. We probably will go ahead with chemo. We have talked a lot about it and feel that we don't want to have any regrets throughout this and want to give Mom every percentage we can possibly get towards a better out come. We will meet with the doctor next Wednesday to discuss our finalized treatment plan from here on out. It will most likely go something like this: Mom will have a port surgically placed in her chest, which is a large catheter that will be used for blood draws and chemo administration. It will stay in until her treatment is completed. She will most likely have 4 rounds of chemo, 3 weeks apart, totaling 12 weeks. Then will do radiation after that. Its going to be a long journey, especially through the holidays, but Mom will be fine. She is so strong and such a trooper. Please pray for us that we are making the right decision, for Mom's strength throughout this, for her health overall, and that the side affects of the chemo are minimal. We want to thank everyone again for their continued support. We need you guys to help us get through this. Have a great weekend and we will be in touch soon.
love,
the peterson's
love,
the peterson's
Thursday, September 17, 2009
So sorry it's been so long :(
Hello everyone!
I know what you’re thinking, ‘they’ve abandoned the blog!’ Nope, just haven’t had much to update and not a lot of time to do so! That being said, yesterday was a busy one in the cancer department…
We had our follow up appointment with Dr. Londer the oncologist at 11:30am- tough getting up to go since mom and I had both worked 12hr night shifts! Unfortunately he was running late, very late and almost wasn’t going to be able to see us before our next appointment with the radiologist oncologist scheduled for 1pm. But since this appointment was for us to find out the oncotype dx results, it was imperative for us to talk to Londer first (this test result would determine whether or not mom would need to have chemotherapy, which would have to be done first before radiation). Eventually he was able to get us back into a room, when it was unfortunately discovered that the oncotype results were not back yet- such a bummer. They tried to call the company in California, but still they weren’t going to be available for at least another day. We’ve all been a little uptight about getting these results since it could significantly impact the course of treatment; we just want to know what the plan is! So after a few wasted hours, Dr. Londer still advised us to go see Dr. Nisi, the radiologist oncologist, because he’s 90%sure that the results will come back with good news, meaning mom won’t have to do chemo (Dr. Nisi also thinks this will be the case).
Trying not to be too disappointed, we walked down the hall to Dr. Nisi’s office. We first met with a nurse who educated us about radiation, told us tons and tons of information and gave us paperwork that reinforces everything. Then Dr. Nisi came in and we talked more about what to expect, side effects, etc. It was all very informative and great to meet another member of our cancer butt kicking team!
Mom is scheduled next week to have her Radiology Mapping done- it’s a series of XRays, Catscans, etc. to determine a 3D image of her chest and chest wall so they know exactly where to administer the radiation. We did learn that they irradiate the entire breast for 28 treatments and then the last 5 they give a ‘boost’ to the tumor site.
So pending no surprises from the oncotype dx results, mom will begin her 6 weeks of radiation on September 28th (she’ll have treatment every Monday through Friday for a total of 6 weeks) and finish a little before Thanksgiving. She even got the 9am spot she was hoping for!
Thanks everyone for checking in- shout out a few big prayers for a low recurrence score on the oncotype results! I’ll update when we have the them.
Love you all, we can never thank you enough for the continued support you all bless us with!
The Petersons
I know what you’re thinking, ‘they’ve abandoned the blog!’ Nope, just haven’t had much to update and not a lot of time to do so! That being said, yesterday was a busy one in the cancer department…
We had our follow up appointment with Dr. Londer the oncologist at 11:30am- tough getting up to go since mom and I had both worked 12hr night shifts! Unfortunately he was running late, very late and almost wasn’t going to be able to see us before our next appointment with the radiologist oncologist scheduled for 1pm. But since this appointment was for us to find out the oncotype dx results, it was imperative for us to talk to Londer first (this test result would determine whether or not mom would need to have chemotherapy, which would have to be done first before radiation). Eventually he was able to get us back into a room, when it was unfortunately discovered that the oncotype results were not back yet- such a bummer. They tried to call the company in California, but still they weren’t going to be available for at least another day. We’ve all been a little uptight about getting these results since it could significantly impact the course of treatment; we just want to know what the plan is! So after a few wasted hours, Dr. Londer still advised us to go see Dr. Nisi, the radiologist oncologist, because he’s 90%sure that the results will come back with good news, meaning mom won’t have to do chemo (Dr. Nisi also thinks this will be the case).
Trying not to be too disappointed, we walked down the hall to Dr. Nisi’s office. We first met with a nurse who educated us about radiation, told us tons and tons of information and gave us paperwork that reinforces everything. Then Dr. Nisi came in and we talked more about what to expect, side effects, etc. It was all very informative and great to meet another member of our cancer butt kicking team!
Mom is scheduled next week to have her Radiology Mapping done- it’s a series of XRays, Catscans, etc. to determine a 3D image of her chest and chest wall so they know exactly where to administer the radiation. We did learn that they irradiate the entire breast for 28 treatments and then the last 5 they give a ‘boost’ to the tumor site.
So pending no surprises from the oncotype dx results, mom will begin her 6 weeks of radiation on September 28th (she’ll have treatment every Monday through Friday for a total of 6 weeks) and finish a little before Thanksgiving. She even got the 9am spot she was hoping for!
Thanks everyone for checking in- shout out a few big prayers for a low recurrence score on the oncotype results! I’ll update when we have the them.
Love you all, we can never thank you enough for the continued support you all bless us with!
The Petersons
Tuesday, September 8, 2009
Happy belated Labor Day!
Hi everyone-
hopefully you all had wonderful long weekends and enjoyed the beautiful weather! I apologize for not 'blogging' for so long- I've been back at work and on a long stretch (4 down of 6 nights in a row- all you nurses out there know what that's like!).
There really isn't much to update- things are actually feeling semi-normal around the house. It's still tough to mention the 'C' word, but we're getting a bit more comfortable dropping it here and there. Mom is doing fabulous- she even fit in a couple nights of work too. I know she was anxious to get back and see her work crew and get some much needed adult interaction aside from Dad and I!
Her incisions are healing up well (she's been showing off her scars!)- we go for a follow up appointment with our surgeon Dr. Mestitz on Thursday. Tomorrow mom will have her bone density scan done to establish a baseline before hormone therapy begins. We learned that the Arimidex medication won't actually start until after radiation. Hopefully today we'll schedule our next meetings with Dr. Londer and also a Radiologist oncologist- the MD appointments are never ending!
Lets see, what else? Oh yeah a couple quick things to mention...
1) Part of our oncology team includes a wonderful woman named Jean Pupkes- she is an oncology clinical nurse specialist (CNS) who has practiced for over 30 years. She spent time with us last week going over all the information Dr. Londer had presented and also talked with us about a support group and an a program called 'Pay It Forward Fund.' This non-profit organization was started by a breast cancer survivor and helps women around the Metro area with living expenses while they undergo breast cancer treatment. I want to encourage everyone to visit their website: www.payitforwardfund.net. It is a really cool organization!
-Sidebar: Another great organization out there for women only, is the 'Avon Army of Women'. You can learn more about it at: https://www.armyofwomen.org
Please join!
2) I wanted to mention too that we are very thankful for all the great phone calls and messages! We are so very lucky to know so many amazing people and have everyone checking in on and supporting us. Just want to say that if you called and we have not called you back, SORRY! All 3 of us could spend hours visiting on the phone, but we're trying to catch up on the rest of our To-Do lists too! So we apologize for our untimely return calls, we are kinda backed up, but we won't forget you!
Have a good short work week! I know we're looking forward to this weekend and celebrating at 2 weddings! Lots of friends and family coming into town the next few days- prayers for safe travels and great MN weather! Until next time...
Love Lins
hopefully you all had wonderful long weekends and enjoyed the beautiful weather! I apologize for not 'blogging' for so long- I've been back at work and on a long stretch (4 down of 6 nights in a row- all you nurses out there know what that's like!).
There really isn't much to update- things are actually feeling semi-normal around the house. It's still tough to mention the 'C' word, but we're getting a bit more comfortable dropping it here and there. Mom is doing fabulous- she even fit in a couple nights of work too. I know she was anxious to get back and see her work crew and get some much needed adult interaction aside from Dad and I!
Her incisions are healing up well (she's been showing off her scars!)- we go for a follow up appointment with our surgeon Dr. Mestitz on Thursday. Tomorrow mom will have her bone density scan done to establish a baseline before hormone therapy begins. We learned that the Arimidex medication won't actually start until after radiation. Hopefully today we'll schedule our next meetings with Dr. Londer and also a Radiologist oncologist- the MD appointments are never ending!
Lets see, what else? Oh yeah a couple quick things to mention...
1) Part of our oncology team includes a wonderful woman named Jean Pupkes- she is an oncology clinical nurse specialist (CNS) who has practiced for over 30 years. She spent time with us last week going over all the information Dr. Londer had presented and also talked with us about a support group and an a program called 'Pay It Forward Fund.' This non-profit organization was started by a breast cancer survivor and helps women around the Metro area with living expenses while they undergo breast cancer treatment. I want to encourage everyone to visit their website: www.payitforwardfund.net. It is a really cool organization!
-Sidebar: Another great organization out there for women only, is the 'Avon Army of Women'. You can learn more about it at: https://www.armyofwomen.org
Please join!
2) I wanted to mention too that we are very thankful for all the great phone calls and messages! We are so very lucky to know so many amazing people and have everyone checking in on and supporting us. Just want to say that if you called and we have not called you back, SORRY! All 3 of us could spend hours visiting on the phone, but we're trying to catch up on the rest of our To-Do lists too! So we apologize for our untimely return calls, we are kinda backed up, but we won't forget you!
Have a good short work week! I know we're looking forward to this weekend and celebrating at 2 weddings! Lots of friends and family coming into town the next few days- prayers for safe travels and great MN weather! Until next time...
Love Lins
Thursday, September 3, 2009
Good news!
Sorry to anyone who has anxiously awaited this post... we've been going non-stop since before 8am!
I'm going to try and sum up as best I can the wealth of information that was imputed into our brains today- most everything was fairly technical too, so I'll do my best to explain it in a way that makes sense. Here we go!
We received the final surgical pathology report from our oncologist Dr. Londer (he's great by the way:), and reviewed it in detail with him. Our prayers were answered again and final results confirmed the lymph nodes are cancer free and negative margins were achieved during the lumpectomy last Friday (this means the tissue removed from mom's breast has no cancer cells in the outer edges of the sample, so there should not be any remaining cancer cells left in her breast). To quantify things, mom has Stage 1A breast cancer: it's a small tumor (<0.5cm) and there is no metastasis (hasn't spread beyond the breast).
Other results: her tumor is estrogen and progesterone positive- meaning the hormones estrogen(ER) and progesterone(PR) are necessary for this type of cancer cell to grow and divide. This is a good thing! With ER/PR + cancers, hormone therapy is recommended (this type of therapy is considered 'systemic', which like chemotherapy would kill any straggling cancer cells anywhere in her body; where as radiation is a 'localized' treatment that only kills cancer cells in a specific area on the body). Since mom is post-menopausal, the medication Arimidex is our drug of choice- mom will be prescribed Arimidex and will take it once a day starting now, and continue to take it for 5 years (at least this is the recommendation based on current research). There are some potential minor side effects, for example hot flashes, fatigue, nausea and osteoporosis; so she is going in to have a baseline bone density scan next week; but if the side effects end up effecting her too much, there are other drugs on the market to try- this one just happens to be the most researched and has shown to prevent recurrence the best.
Other good news: the tumor cells are HER2 negative- HER2 is a protein and if the tumor cells have this it tends to be a more aggressive type of cancer, and harder to treat. Don't have to worry about that!
With all this information so far, Dr. Londer says that chemotherapy would not be necessary. This conclusion was reached using the 'Adjuvant Treatment plan' for breast cancer- it's a standard tool doctors use to determine how different treatments will benefit you- it's really complicated, so in general it shows that chemotherapy would not benefit mom. The only minor hesitancy here is that the cancer cells are 'grade III' (graded I-III). This means these cells are very different looking from healthy milk duct cells and tend to multiply at the fastest rate; the only negative so far in this journey. We learned there is one other test that can be done, called 'oncotype DX'. The really smart scientists of this company created a test that assesses 10 year breast cancer recurrence risk; it also sheds light into the benefit of certain types of chemotherapy. Mom, Dad & I decided we want to have this test done in order to better quantify the grade III cells and be more confident with the current treatment plan- we'll hear from our insurance company tomorrow if the test will be covered (it costs $3,500) and if it is we'll get results in a few weeks.
I'm sure by now I've thoroughly confused everyone! I'm going to stop here and recap: for now the plan is to 1) do radiation therapy that will start in about a month and last 4-7 weeks; and 2) start hormone therapy with Arimidex now. Potentially the oncotype DX test results could change this, but for now this is what our treatment plan is. We will meet with a Radiologist Oncologist in 2 weeks to discussed the details of radiation.
I'm beat, and heading to bed! Thanks again everyone, we'll be in touch soon!
I'm going to try and sum up as best I can the wealth of information that was imputed into our brains today- most everything was fairly technical too, so I'll do my best to explain it in a way that makes sense. Here we go!
We received the final surgical pathology report from our oncologist Dr. Londer (he's great by the way:), and reviewed it in detail with him. Our prayers were answered again and final results confirmed the lymph nodes are cancer free and negative margins were achieved during the lumpectomy last Friday (this means the tissue removed from mom's breast has no cancer cells in the outer edges of the sample, so there should not be any remaining cancer cells left in her breast). To quantify things, mom has Stage 1A breast cancer: it's a small tumor (<0.5cm) and there is no metastasis (hasn't spread beyond the breast).
Other results: her tumor is estrogen and progesterone positive- meaning the hormones estrogen(ER) and progesterone(PR) are necessary for this type of cancer cell to grow and divide. This is a good thing! With ER/PR + cancers, hormone therapy is recommended (this type of therapy is considered 'systemic', which like chemotherapy would kill any straggling cancer cells anywhere in her body; where as radiation is a 'localized' treatment that only kills cancer cells in a specific area on the body). Since mom is post-menopausal, the medication Arimidex is our drug of choice- mom will be prescribed Arimidex and will take it once a day starting now, and continue to take it for 5 years (at least this is the recommendation based on current research). There are some potential minor side effects, for example hot flashes, fatigue, nausea and osteoporosis; so she is going in to have a baseline bone density scan next week; but if the side effects end up effecting her too much, there are other drugs on the market to try- this one just happens to be the most researched and has shown to prevent recurrence the best.
Other good news: the tumor cells are HER2 negative- HER2 is a protein and if the tumor cells have this it tends to be a more aggressive type of cancer, and harder to treat. Don't have to worry about that!
With all this information so far, Dr. Londer says that chemotherapy would not be necessary. This conclusion was reached using the 'Adjuvant Treatment plan' for breast cancer- it's a standard tool doctors use to determine how different treatments will benefit you- it's really complicated, so in general it shows that chemotherapy would not benefit mom. The only minor hesitancy here is that the cancer cells are 'grade III' (graded I-III). This means these cells are very different looking from healthy milk duct cells and tend to multiply at the fastest rate; the only negative so far in this journey. We learned there is one other test that can be done, called 'oncotype DX'. The really smart scientists of this company created a test that assesses 10 year breast cancer recurrence risk; it also sheds light into the benefit of certain types of chemotherapy. Mom, Dad & I decided we want to have this test done in order to better quantify the grade III cells and be more confident with the current treatment plan- we'll hear from our insurance company tomorrow if the test will be covered (it costs $3,500) and if it is we'll get results in a few weeks.
I'm sure by now I've thoroughly confused everyone! I'm going to stop here and recap: for now the plan is to 1) do radiation therapy that will start in about a month and last 4-7 weeks; and 2) start hormone therapy with Arimidex now. Potentially the oncotype DX test results could change this, but for now this is what our treatment plan is. We will meet with a Radiologist Oncologist in 2 weeks to discussed the details of radiation.
I'm beat, and heading to bed! Thanks again everyone, we'll be in touch soon!
Wednesday, September 2, 2009
Big Day Tomorrow...
It's late, sorry this might be short :)
Tomorrow will bring our first appointment with our oncologist, Dr. Londer. We have anxiously awaited this day for awhile now. We will receive the final pathology results from the tissue and nodes removed during the surgery and will hopefully begin to develop our treatment plan. We know things won't get started for at least another 3 weeks (the skin/tissue has to heal around the incision sites before mom can be submitted to more invasive therapy such as radiation), so this time should bring some normalcy back into our lives; we're really looking forward to the 2 weddings we have 9/12 because mom will be feeling great and we'll get to celebrate with many of you in person!
Tomorrow holds alot of anxiety too because at this point we don't know what the future will hold, so it will be somewhat of a relief to have a bit of a plan to look forward too (that doesn't quite sound right 'look forward to', but this waiting for the unknown is so tough). We don't expect these next steps to be easy, but we are ready to face them, one day at a time, and beat breast cancer!
We'll update later tomorrow with the things we learn from Dr. Londer. Thanks for checking in, talk to you soon!
The P's
PS- thanks for the cards, etc that keep flowing in! And we've had great dinners this week thanks to some special chefs! THANKYOUTHANKYOUTHANKYOU!!!
Tomorrow will bring our first appointment with our oncologist, Dr. Londer. We have anxiously awaited this day for awhile now. We will receive the final pathology results from the tissue and nodes removed during the surgery and will hopefully begin to develop our treatment plan. We know things won't get started for at least another 3 weeks (the skin/tissue has to heal around the incision sites before mom can be submitted to more invasive therapy such as radiation), so this time should bring some normalcy back into our lives; we're really looking forward to the 2 weddings we have 9/12 because mom will be feeling great and we'll get to celebrate with many of you in person!
Tomorrow holds alot of anxiety too because at this point we don't know what the future will hold, so it will be somewhat of a relief to have a bit of a plan to look forward too (that doesn't quite sound right 'look forward to', but this waiting for the unknown is so tough). We don't expect these next steps to be easy, but we are ready to face them, one day at a time, and beat breast cancer!
We'll update later tomorrow with the things we learn from Dr. Londer. Thanks for checking in, talk to you soon!
The P's
PS- thanks for the cards, etc that keep flowing in! And we've had great dinners this week thanks to some special chefs! THANKYOUTHANKYOUTHANKYOU!!!
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