Member Since: October 21, 2006
Last Login: October 10, 2008
Location: Chestermere, AB Canada
Occupation: IT Manager
| Diagnosis: | Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
| Diagnosed: | September 25, 2006 |
| Type: | Invasive or Infiltrating Ductal Carcinoma |
| Recurrent? | No recurrence |
| Metastatic? | Yes |
| Stage: | |
| Lymph Nodes Removed: | 15 |
| Positive Lymph Nodes: | 1 |
| Tumor Size: | 4cm-4.9cm |
| Tumor Grade: | Grade 3 or high grade |
| Hormone Receptor Status: | Tumor has both estrogen and progesterone receptors |
| HER2/neu Status: | Tumor does not have an excess of HER2/neu receptors or genes |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 30, 2008 06:00 pm
Joni could use our prayersHello all, I have a couple of days pass out of the hospital, so just thought I would write and say thank you for all your kind words. It's been a scarey last couple of weeks. Thanks for all your prayers...I really think they are working. Hugs....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 30, 2008 05:57 pm
Starting Chemo in JAN 2007Hello Tatas, Well they gave me a few days out of the hospital. I came home yesterday, and depending how I do will determine when I go back. I have home care care nurse and a a pallatiative nurse, and of course Dan. Feeling very weak, but very little pain, so that is good. I'm starting to eat things like ice cream and boost and orange juice...yogurt. Anything fattening. I'm sorry to get everyone is such a dither. They may be giving me chemo next week if I keep improving. Love you all......hugs all around....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 27, 2008 08:52 am
Starting Chemo in JAN 2007Hello Not well my liver is in failure. Still in hospital..if I get out it will be hospice or or pallative...will watch over you all. Hugs Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 14, 2008 09:07 pm
Starting Chemo in JAN 2007Hello TaTas, Well we made it to Alaska. I slept quite a bit of the trip. I did make it on my Dog Sled Run....it was a blast. They had 16 dog pulling our sled, and it was so much fun, and so fast. Afterwards they let you hold the puppies...I was in heaven. Sharon, sorry about the BRCA genes testing positive. At least you can do few things ab out it. Skye, that wedding looked beautiful. This week are all my scans and meeting with my oncologist. Melia....congrats on the great news on your daughter. hugs to alll......Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 3, 2008 12:14 pm
Starting Chemo in JAN 2007Hello all, Well I have more bad news. They stopped all chemos on me yesterday, my liver is not able to take any more. I've been really sick for about 10 days now, and after they did my blood tests yesterday, my onc said no more. He says I can go on the Alaska cruise, but I can't even get from my bedroom upstairs to the main floor, so Dan & I are going to wait until Friday to make a decision whether to go or not. They are doing an MRI, CT/Pet scan on Monday Sept 15, and I'll see my onc on Sept 16, or if we don't go on our trip he said he would see me any day next week. Just so scared right now, saw my priest yesterday and Father Reg helped to calm me down a bit. I hate this disease. Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 31, 2008 03:34 pm
Starting Chemo in JAN 2007Also wanted to say my prayers are with all the people on the Gulf Coast. That hurricane looks very dangerous. Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 31, 2008 03:32 pm
Starting Chemo in JAN 2007Hello Tatas, It has been very cold here the last few days, we already have had frost so lots of my flowers are gone. It's snowing today in Banff & Canmore, and it may snow here in Calgary tonite. The high today is only 5 C.....42 F....but it feels colder than that. With each chemo I seem to get weaker, and this week was no exception. I'm so glad after Tuesday I don't have chemo for 2 weeks. I only have 6 more sleeps til our cruise, starting to pack already. Hugs to all....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 31, 2008 02:30 pm
TAXOL, pre-meds, & NEULASTA questionHello, I am on weekly Taxol. I get Benedryll and Zantac in IV, then I get Dexamethasone in IV, then I get 130 mg of Taxol each week. I do not get anything else, however, my doctor did give me a prescription for Stemetil (anti-nausea), but I rarely take it. If I get an upset tummy I find that gravol helps most, and it also makes me sleepy. I do crash on Day 3/4 after chemo. I get the floppy legs and arms. The Benedryll does make me sleepy, and if you can manage it, it might be a good idea to have a ride home. The Dexamethosone kind of counteracts the sleepiness, but it still would be advisable to have a ride. I will be having 6 sessions of this (6 * 3 = 18 infusions). One session is 3 weeks on, one week off. I'm just finishin off Session 3 on Tuesday so half way done. I get my scans in September. As it gets further down the line, I find now I'm down 2 days, I used to only be down 1 day. I think that is common with any chemo. I have never taken a neulasta shot, my WBC come back each week. If you can avoid them, I think you'll be better off. If you need anything or need to know of any s/e's feel free to email me, and I'll try to help you thru the tough ones. Hugs to you....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 29, 2008 05:00 pm
I want to share my good news!Kasey hugs to you....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 28, 2008 07:21 pm
Wonder if fertility treatment brought on my b.c.I too took fertility drugs, tried the Invitro, Danazol for 8 months one time and 6 months another time (to get rid of endometriosis)...all to no avail. I too have wondered if this was part of my problem. I was 8/8 positive for ER and 6/8 positive for PR. Also, way back in my younger days my doctor asked me if I knew whether my Mom took a drug called DES. She said she didn't take that but the doctor had given her something to help with her iron counts. Never will know for sure. I did have cervical cancer at 26, couldn't have kids, and then dxd with BC at 51. It's almost out of the DES textbook. hugs to all.......Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 27, 2008 12:18 pm
Starting Chemo in JAN 2007Hi TaTa's, Sorry I have not been feeling all that great. I was down just about all last week, and then on Monday I had all kinds of problems. They could not get my port to work properly, so I was sent to get xrays. I think the nurse just put the needle in too close to the edge. Anyways hopefully next week will go better. I also had to have another bone scan last week, and they took lots of extra pics of my hip (walking with a cane always now). On a brighter note I only have 10 more sleeps til our Alaskan cruise. Dan says he'll carry me on if necessary. When I get back I have an MRI and CT scan scheduled, and then I'll meet with my onc on Sep 19th...should have all the results by then. He said he could give me the bone scan results, but I said NO not until I get back from my trip. We are going on a "dog sled run" in Juneau & on the White Pass Railway in Skagway. Dan is also going on a fishing trip in Icy Point, I'll stay back that day and enjoy the scenery. Caya, your shoe stories sounds like nightmares. Lynn, I loved your pics!! Skye, have you written about "Water Horses"? Mel, I can relate on the thinning hair...no wait a minute, I don't even have any hair. I have a bit of peach fuzz but thats it. RobbinJaye, glad to hear your surgery went well. Mary, Viddie, Cindy, Nancy, Amera, Jan, Shorti, Debbie, Melia, Rebecca, hope everyone is well. Hugs to all....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 24, 2008 09:03 pm
Where in the World Are You? Pin Your Location on our Map!I'm in Chestermere, Alberta about 20 KM out of the city of Calgary, Albera, CANADA. Joni xxxoooxxx Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 24, 2008 09:01 pm
I miss my old lifeI can really relate to this conversation..and especially the comment "I Miss Me". I was only married for 6 months when dx with this blasphemous disease. I have some bad pitty parties, especially when I'm in a lot of pain. It's bad enough going thru all the chemo on a regular basis, my the loss of dignity with no hair, no eyebrows, no eyelashes, and the no nose hairs, just makes me cry more. Thanks for reminding me you guys are all here, and even when I'm really down I always have someone to listen to me whining. Hugs to all my fellow BC sisters.....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 18, 2008 11:15 am
Starting Chemo in JAN 2007Hello Tatas, I lost our google account....can someone sent it to me privately. I had a great weekend with the girls in Canmore. I didn't get out to look at condos, but Dan says we'll go in a couple of weeks. We got a quote on our back deck, $5,000. I think that is a bit to much, but I don't know how much these things cost. We want it built with that Trex stuff and it is pricey. I shot a 52 for 9 holes in Canmore, so that was pretty good for me. That's my first golf game since we were out last year, and my first since I got my port. I was a bit nervous with the port, but eveything was okay. I was just pooped after the game. I went and laid down and the girls did the annual shopping of main street in Canmore and stopped at a nice patio pub for a cool drink. It has been very hot here all weekend. Friday 29, Saturday 30, Sunday 30, and today is suppose to be 33. I'm just heading out to chemo at 11:00...yuck. Had my blood work on Friday and my onco has a few concerns about the elevation of some of my liver enzymes again. I never seem to catch a break. I have all my scans set for the week of Sept 15, so we'll know more then. Only 19 more sleeps until our Alaskan cruise. When we fly into Vancouver we are taking two of Dan's elderly aunts out for lunch prior to boarding our ship at 3:00. Those pics are beautiful Lynn. Mel Happy Birthday and Happy Anniversary. Cindy sorry you had such soggy weather, but it sounds like you had fun anyways. Mary, I watched a bit of that golf from Detroit, but I think you were only there for the preliminaries or something. Shorti, how are you? RobbinJaye, are you enjoying your summer? Amera are you back yet? My niece is due to have her baby on Oct 12th, and she is getting quite large. That must be very tough when it is so hot out. Hugs to all....Thor sends his love too....he's been running through the hose already this mornig. Cheers...Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 14, 2008 04:30 pm
i am scaredTracy, I'm doing weekly Taxol, and you may not lose all your hair. You will lose your eyebrows & lashes, but I have a fair amount of hair still on my head. Here's hoping this turns things around....hugs to you....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 14, 2008 01:34 am
Taking Care of OurselvesHi Sandy, I find I eat a healthier diet now, take 1000mg of Vit D daily, 200mg of Vit B, plus my clondronate (oral for bones...1600mg), plus I get chemo Weeks #1, 2, & 3, with Week #4 off. I live a pretty good life....try to get out for a walk each day, some days during chemo that walk might just be around the outside of the house, but I like to get out. I love the summer as I'm an avid gardener, and I hope to live a long time even if I have to stay on chemo. Hugs to you. Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 14, 2008 01:26 am
INSURANCE COVERAGE DICTATING OUR OPTIONS?Hello everyone, I have to step in and say, I'm fortunate to live in Canada. Yes we are TAXED to death, yes we do have shortages of health care professionals which sometimes gives us a wait time to see specialists, and yes lots of Canadians run across to the USA for quick medical attention. BUT since I have been dxd with BC, I have only 1 time had to wait on results of a Bone & MRI scan. This delay was my onc's nurse's fault, as she did not book me an appt in a timely fashion (this has been corrected with a letter to the Cancer Advocate), and as my onc does not give results over the phone I was made to wait. If my onc wanted me to have an MRI, Bone Scan, Pet Scan, or CT scan, the longest I would have to wait is 2 weeks, as I am a cancer patient and therefore given priority over people with minor ailments. I also do not wait in any ER room, as the cancer card is always given a bump up. Is Canada perfekt? Far from it, we have lots of problems in the medicare system. Long lineups at ER's, shortages of GP's, wait times for minor operations of up to 2 years, a huge country with limited access in some areas to MRI's, Radiation Therapy and the generally accepted cancer treatments. I feel for all my American friends on here that not only have to worry about their lives and their futures, but also whether they will have enough money to cover the next treatment that they will receive, or whether their insurance will cover it. It is a crazy world we all live in, where the drug companies and politics determines whether we live or die. There is a drug in research here at the University of Alberta, (DCA) that has shown immense potential as a cure, but the drug companies don't want to support it, because it is cheap to make and it won't make them any money. Someone earlier mentioned that in NC in the early years they paid a doctor on a horse to do his rounds, and I believe sometimes his pay wasn't money, but chickens, produce, etc. I think we were maybe better off then, where everybody cared about everybody else, and not about the Darn Holy Dollar. There is no right answer, even Medicare has it's lows and highs. Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 14, 2008 12:51 am
BC and spinal cord injuryHello MOC, I don't know of anyone in this particular situation, but my brother was a quadrapalegic and I have BC. If I can help your friend in any way, I'd be more than willing. Hugs....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 14, 2008 12:49 am
Advise and hope needed : Bone metastasisThere are many girls on this list that have lived a long time with Bone Mets. Please keep up the faith. There is another site too that you can review different aspects of bones mets.....www(dot)bcmets(dot)org. May God Bless you and your family, and keep you all well. Hugs Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 14, 2008 12:42 am
Delay Treatment for a Vacation? How Long?CalGal, I was facing the same dilemma, but what my onc did was move my MRI & Bone Scans up to my Week #1 of Chemo, and now I won't miss anything. I have Chemo Week 1, 2,3, and then usually aa break on Week #4....We leave on our Alaskan cruise 4 days after my Chemo #3, and then we return on a Sunday. My Monday would be my normal chemo Week #1, but that day is now my Scans, and then Tuesday I will be getting my chemo. My onc always tries to work something out. Watson is correct, lots of times people have to go 2 or 3 weeks with no chemos because of bad blood counts. Have a GREAT TRIP, and kiss the Blarney Stone for me. Hugs....Joni Joni, Chestermere, AB, Canada, Today is the BEST day of my life EVER!! Dx 9/25/2006, IDC, 4cm, Grade 3, 1/15 nodes, mets, ER+/PR+, HER2- |
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