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wahine Joined: Apr 2008 Posts: 409 |
May 14, 2008 12:26 am
wahine wrote:
Hi Stephanie, I am so sorry you will be needing surgery, and have to wait so long for it. It sucks, and it is okay to freak out, as it is a lot to take in. I am sorry but I do not know about duct removal, but just wanted to say hi, and give you some support. As for me, my surgery was much earlier than I had wanted, as I wanted to get a lot done at home beforehand knowing it would be awhile till I could do normal things. Would it help if you just kept busy doing things maybe you never had time to do? Or a new project? Or maybe set out some flowers for summer? One weekend I built our deck steps and railing, and called it my "cancer steps"--it was very theraputic. I decided we would have a toast with champagne once I was cancer free..on the steps! Well, today (6 days postop) I got the news that my nodes were clear, and they got it all, but of course still being on pain meds, the toast will have to wait awhile. I had a bilat mast with alloderm and expanders on the 7th. I wish you the best, and be sure to let us know when your surgery will be. We have a May Surgery thread, and I am sure there is a June Surgery thread also, where you will get a lot of sharing and information from so many caring ladies! The best to you for successful surgery and recovery......(((((HUGS))))) Kathy |
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jalydiju Joined: May 2008 Posts: 141 |
May 14, 2008 02:19 am
jalydiju wrote:
Hi ya Stephanie, I to like Wahine do not know anything about duct removal but do understand the anxiety of waiting. Just wanted to add my support and thoughts that everything goes well and send you a little Down Under Sunshine. |
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Nichola Joined: Nov 2007 Posts: 194 |
May 14, 2008 07:32 am, edited May 14, 2008 07:32 AM
by Nichola
Nichola wrote:
Hi stephanie The good news is that they are on the case, so at least you will know one way or another! I'm not sure about the surgery you are having, but pray all will be ok. ...But the waiting....there really is nothing worst! I can honestly say that the waiting was far worst that my diagnosis! I found that actually talking to friends and family about how I was feeling helped and of course coming on to this fab website is truly cathartic. Sending you love and luck... Dx 11/28/2007, 1cm, Stage IIIb, Grade 1, 0/10 nodes, ER+/PR+, HER2- |
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stephanieb Joined: Apr 2008 Posts: 27 |
May 14, 2008 09:34 pm
stephanieb wrote:
Thanks so much for your replies. It just helps SO MUCH knowing that someone is listening, that has been through this waiting situation. My husband, my mother and some of my friends seem to be trivializing the whole thing. Like they just say Oh I'm not worried about it, you are going to be fine. I wish they understood what it was like to be the one headed for the surgery. They want me to say Yeah I'll be just fine and then drop the subject. I guess that is just their coping mechanism because they just don't want to deal with the reality that there could be something there. I catch myself snapping at people or just not being able to sleep, I hate being so crabby, I never dreamed I would react this way. I wish I could handle the whole thing with a little more grace. Anyway it really means ALOT that you guys took the time to answer and offer support. When I see the surgeon for scheduling on May 22 I will know which thread to join, probably June.....again thanks so much for listening to me vent...God Bless you, Stephanie Courage doesn't always roar, Sometimes courage is the little voice that whispers I'll try again tomorrow.
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jalydiju Joined: May 2008 Posts: 141 |
May 14, 2008 11:50 pm
jalydiju wrote:
Stephanie, Back again to check on how you are doing. Read your reply and it is making me feel choked and teary. So feel the same way as you. I also am snappy, cant sleep, nauseas and just tear up out of the blue. Keep telling myself to pull my head in and just get on with it. I can only deal with what is now. Sometimes works, sometimes doesnt. Understand effects of familys helpful comments and your right, it is their coping mechanism. Yesterday I was looking through this site when my sister#1 rang and asked me what I was doing. Told her and her reply was what are you doing that for, you dont need to do that, you are alright. I have to remember to be gentle with my sisters responses as we have been through the cancer thing with sister#2 who passed away in 2003. It was 11 weeks from the time that she was dx till she passed. It was so quick and intensely emotional and it caused some the family to pull away from each other. It is only recently that things are kinda normal between us. I have come to the conclusion that they each had to deal with their greif in their own way and I think to, that a certain amount of personal guilt was felt with some of them. It is this that makes me a very concerned about support from them if the outcome isnt for the best. I worry about my mother as it doesnt seem fair to put her through the trauma and stress that she went through with one daughter all over again with another. I agree with you, it does help that even though we dont know each other on this site, we do benifit from knowing that we are facing similar things and understand the consuming, crushing anxiety that puts us on that emotional rollercoaster until we have some kind of answer. It makes me feel better that someone is there to talk to who knows. Sorry this is so long. Just want you to know someone knows and cares with and how you feel. Vent anytime.....We are listening......Jalydiju |
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drcrisc Joined: Apr 2008 Posts: 524 |
May 15, 2008 12:07 am
drcrisc wrote:
Hi girls, I was just sort of "lurking" around the active conversations and saw this thread. I am a little bit ahead of you in this, but fully understand the "waiting" issue. Mine seems to be always around my pathology reports after surgery, the first one after the core needle biopsy took several days more than they told me it would. And now, I have been waiting almost two weeks for a second opinion on the post-lumpectomy pathology. Waiting sucks!! At least when you know what you've got, you can begin to deal with it. I am waiting for the second opinion before I start chemo. Stephanie - try to keep as busy as possible and do something with your family that you enjoy. Jalydiju - You keep coming here regardless of how your sister feels - this is one of the best supports I have! Cristine ~ Blessed are the flexible, for they shall not get bent out of shape!
Dx 3/24/2008, IDC, 1cm, Stage I, Grade 2, 0/3 nodes, ER-/PR-, HER2- |
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Nichola Joined: Nov 2007 Posts: 194 |
May 15, 2008 09:12 am, edited May 15, 2008 09:14 AM
by Nichola
Nichola wrote:
Steph and Jaly Oh my God how I feel for you - I have been there more than twice now and have come to accept that people have majorly different ways with dealing with this. I too had my friends and family both times either trivialising or even telling me off for "not being able to switch off" (Ha!...if only)! It's like having a whale in your living room: It is in your face constantly. I literally "snapped" a couple of times and that is how I chose to explain to friends and family just how it made/ makes me feel. This is your/our reality and it is/ might be happening... Perhaps I was lucky and managed to get through to people: Now so many have told me how good it is to be able to to talk with me and ask me questions without feeling the whole subject is or should be taboo! It's hard for them too. Dx 11/28/2007, 1cm, Stage IIIb, Grade 1, 0/10 nodes, ER+/PR+, HER2- |
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jalydiju Joined: May 2008 Posts: 141 |
May 15, 2008 11:53 am
jalydiju wrote:
Hi Stephanie, Nichola you sumed it up well, "It,s like having a whale in your lounge room ". You are not wrong. I think I am really becoming obsessive about it, knowing that I have these foreign somethings in me and that they may not be of a very friendly nature is driving me a bit nuts. I find myself continually feeling myself to see if they are still there. Just wish that they would fall out of my breast and introduce themselves so that I know whom and what I am dealing with. "Hello! Im BC1 and this is my friend BC2 and we are here to let you know just what the BC stands for, so now you can start to work on what your plan of action is" Now you probably think I am completely mad. Maybe I am. thank goodness I see my GP this monday and can start the process to enlightenment and the begining of a action plan. (Is a what do we do now appointment. To FNA or to not FNA and just see what happens) Thanks for your support drcrisc. Will be with you in spirit Stephanie on May 22...Holding your hand.......Jalydiju |
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rbcrhodes Joined: May 2008 Posts: 20 |
May 15, 2008 02:26 pm
rbcrhodes wrote:
Hey Girls: I'm having surgery tomorrow morning. I have two areas in my left breast which could not be seen well enought for the stero biopsy. I'm having the wire deal and then two open biopsys. The doc. said I could wait and watch or get them out -- "GET THEM OUT" I yelled! The hospital called and said it will be a long day tomorrow because of having to do two separate sections. I'll be glad when it's over - I'm with you guys - the waiting is the worse |
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Nichola Joined: Nov 2007 Posts: 194 |
May 15, 2008 05:07 pm
Nichola wrote:
Wishing and sending everyone, love, luck and courage... Dx 11/28/2007, 1cm, Stage IIIb, Grade 1, 0/10 nodes, ER+/PR+, HER2- |
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Shirlann Joined: Feb 2002 Posts: 6707 |
May 15, 2008 05:34 pm
Shirlann wrote:
Hi honey, I am so sorry you are on this roller-coaster. And the family is just trying to make you think THEY are not worried, in hopes that this will help YOU not to worry. People truly just do not know what to do or say, and truly, there is nothing they can do or say that doesn't make you want to scream. Only us. And I will tell you that everyone of us has been on this dizzy awful trip. NO FUN! It is horrible. I would ask your onc/doc/surgeon for a little chemical help. You can ask for Ativan, Valium or something to take at night when the squirrels run around the room and to take on the day of the test or surgery. I was jostled around for 2 years, then, they took 3 months to figure out I had an odd type of breast cancer. I was a total wreck. But try not to get too far ahead of yourself. You have not been diagnosed with anything yet. Hang onto that. It is important, and if, you are diagnosed with BC please understand that 90% of us will be just fine. I am 9 & 1/2 years out of treatment and still okay. There are tons of us, but most of the "older" gals have stopped posting and check in only once in a while. So it looks like this thing is a complete disaster. It isn't. I don't mean to make light of this journey, but you can do it if you need to. And here's hoping you don't need to come back with anything but a big fat B9!!! Gentle hugs, Shirlann |
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stephanieb Joined: Apr 2008 Posts: 27 |
May 17, 2008 01:34 pm
stephanieb wrote:
Oh wow, you guys are so awesome!! I really just didn't have any idea that so many people could understand. I especially like that part about the whale in the living room Nichola, that is great. And so true. You want to scream "How can you ignore this !!!" But you guys have helped me so much just by validating my feelings, and letting me know it's ok to feel this way. Jaly, I'm so sorry about your sister. I too lost a sister in law 6 years ago to BC. She was 30 and she fought so hard for 4 years. Now my husband and I sometimes get to look after her son on the weekends. He is 11 now. And no, you are definately not mad~~Everyday I examine this breast discharge like it is my job to see if the color has changed or if it's coming from any additional ducts. It's hard NOT to become obsessive. Drchris I think I will take your advice for the weekend and get some projects done around the house to keep my mind off things. <>Shirlann, you actually made me laugh out loud for real with that image of the squirrels running up and down my curtains in the dark. That is something I'm going to hang on to when my wheels start turning in the middle of the night. Can you guys believe that two of my coworkers donated a week each for me to take off after surgery!! I have not been on this job greater than a year and didn't have the PDO hours built up. But my boss said not to worry (I work in a nursing home as an occupational therapist) and have to lift very heavy patients daily, she wants me back whole and healthy. Sometimes these situations bring out the best in people. That took an enormous amount of $ worries and stress off my mind. Jaly please let me know what your doc advises on Mon and same for Drchris, I want to know the status of the 2nd opinion. Rbcrhodes, when you feel well enough to type I want to know all about how your surgery went. Thank you to every one of you who is helping me to keep my head on my shoulders. Each one of you is priceless with your experience from walking this road before me, please stay close....Love to all, stephanie Courage doesn't always roar, Sometimes courage is the little voice that whispers I'll try again tomorrow.
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rbcrhodes Joined: May 2008 Posts: 20 |
May 17, 2008 07:50 pm
rbcrhodes wrote:
I had surgery yesterday. It was a LONG day! I had to be at the hospital at 6:30AM. I had to have 2 wires put in which took 3 hours! The radiologist wanted to make sure he was right on - which I appreciate- but having your breast squished in that mammo machine for 3 hours was not a treat. The surgeon even came down to see what was taking so long. Anyway, I went straight up to surgery and he ended up taking out a golf ball size section. We won't know results until Tues or Wed. I feel like I'm sitting on a hot potatoe waiting...... the girls in the women's center were wonderful! Lots of hugs and sincere words - I could never thank them enough. The surgeon was great too. Now hopefully, the results will be too! Thanks for your positive thoughts sent my direction.... I'll let you know when I get results |
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stephanieb Joined: Apr 2008 Posts: 27 |
May 17, 2008 11:37 pm
stephanieb wrote:
Please let us know when you hear from the doc. I'm glad at least the surgery part is over. Hope you are not too sore afterward! Courage doesn't always roar, Sometimes courage is the little voice that whispers I'll try again tomorrow.
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Teaches Joined: May 2008 Posts: 22 |
May 18, 2008 01:40 am
Teaches wrote:
Hugs and prayers and best wishes to you all. I'm scheduled for an MRI on Tuesday and will be waiting anxiously for the next step... waiting is the pitts. It's interesting to note family reactions. My husband says do what they say, think positive and "there is so much that is being done today". I think he's right. His reaction to stress is to do lawn work. Our lawn is now beautiful. He just bought a new mailbox and post. It I don't know something soon, I wonder what he'll do next? |
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jalydiju Joined: May 2008 Posts: 141 |
May 18, 2008 07:33 am
jalydiju wrote:
G'Day Stephanie, Shirlann's comment re the squirrels made me chuckle to. Will let you know about what is decided, will know tomorrow. Due to really crappy day lost it with lots of people, some deserved it, some didn't but to sinfully say, it did lessen some of the stress. Teaches best of luck for Tuesday and until then hope your lounge is squirrel and whale free, or sized down to a goldfish and a few moths at least. Jalydiju |
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rbcrhodes Joined: May 2008 Posts: 20 |
May 18, 2008 08:26 am
rbcrhodes wrote:
I can't even begin to tell you how supportive my family has been. My husband has been a real trouper. He has waited on me hand and foot since my surgery - and my 6 year old daughter has been right by my side. I do find my husband getting edgy and I wonder if he's concerned about the results. (I'm sure that's what it is) --- The nurses at the Women's Center were just the greatest. It made me want to work there. They were so gentle and understanding. This whole ordeal has given me a totally new outlook on life. |
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Stickerlady
Joined: May 2008 Posts: 18 |
May 18, 2008 10:26 am
Stickerlady wrote:
I found out just after Easter this year I have Intrusive Ductal Carsanoma. It is cancer in a milk duct (it was actually in the tube that carries the milk to the nipple). I had surgery on April 21. I had a Lumpectomy. I too never felt a lump and none of the Dr. could either. I had a Mamo 10 months ago and nothing was there but I found a bloody discharge on my nightgown and went to the Dr. I live in Alaska and only have 2 MD's here in town and have to fly to Anchorage for any Specialists appointments. I went and a Radioligist studied my Mamo and found a very small tumor. I went the next morning to see a surgeon and within a week I had a Lumpectomy. The surgery was not bad. I only took pain meds for 3 days but was still sore I just took it easy. I now am waiting for results from my Hormone test to see what treatments I will have to go through. I know I have to do 4-6 weeks of Radiation in which time my husband and I will have to live in Anchorage because they are everyday. I know how scared you feel but just think it is caught early if they can't feel a lump yet. I will Pray you get the comfort I did from all my friends and family. Good luck and think Positive!!!! |
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jalydiju Joined: May 2008 Posts: 141 |
May 19, 2008 06:46 am
jalydiju wrote:
Hi Stepanie, Have seen my GP. FNA tomorrow and also going to US L/ breast as well. Will report back on results. I think all you Girls are the best. Just angles as far as I am concerned. I love it most when you make me smile. Jalydiju |
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Ked1019 Joined: Apr 2008 Posts: 101 |
May 19, 2008 10:38 am
Ked1019 wrote:
Hi, I have been lurking on this thread reading up and my heart aches for you all that have less than needed support from your family. I think Steph said her family trivializes it and Jaly your sister said you didn't need to be on these boards checking all this out. Jaly you are in the right place and Steph there is nothing trivial about a cancer scare. Stephanie, I also went through the nipple discharge problems. I did not have atypical cells found in the ducts but did have bright red and at times dark red bleeding always spontaneous and of course on direct expression (didn't do that too much bc when I did it came out more spontenous). I opted out of the same surgery you are having as they did an u/s and mam and could not find a papilloma in the ducts although the duct where the discharge was coming from was slightly enlarged. The decision to cancel my surgery was made in part bc I am having to undergo another surgery for atypical cells in the breast tissue outside of the ducts. She didn't want to do one and then another. However, I did just have an MRI so maybe they will see something else that needs to come out in the ducts. I know had I had atypical cells in the discharge I would have had the surgery immediately like you. I wish you the best. I was told by my dr. when we were discussing the surgery that the side effects could be possibly inverted nipple from scar tissue, lessen sensation of the nipple and I think that was it. I wish you the best on 5/22. Jaly, good luck tomorrow with the FNA. I will be sending b9 vibes to both of you. I wanted to share some thoughts to let you know you are not alone. I began this journey in April of last year with an abnormal mam. We decided to watch and wait and in Oct on f/u mam there was some change in the tumor but not enough to warrant biopsy. I requsted it and my family thought I was nuts wanting to have this done. Was I looking to have breast cancer was the response I got from them. NO I wanted peace of mind. Well the biopsy was b9 and only a fibroadenoma. The discharge started in Feb of this year and I went in for another mam. Well now they find an area of tiny cluster microcalcifications and a stereotactic biopsy came back b9 but there were atypical cells in the tissue samples. Now here I am having a 2nd opinion, an MRI and now awaiting surgery for excision of that area and oh another mass was found on u/s in April. It didn't appear supiscious so they felt we could wait and take it out during excision surgery. My family responded this way. My results were b9 and that is all that matters. Yes we understand you have unresolved issues but you don't have cancer. I am sure there are alot of women walking around with atypical cells and they don't even know it. Oh and lets not forget my mom asking if my dog has been sniffing at my boob because dogs can smell out cancer. Well I don't recall if she has or not so my mom told me I have nothing to worry about. Well we could save a lot of money in this world if we just put a bunch of women with masses in a room with dogs and let them go sniffen. NO copays or deductibles. We only need to clean up doggy mess! :) Hang in there girlfriends. What you are going through is truly stressful. It does not need to be trivialized or pushed aside. Stay on these boards and get support and cyber hugs. I find I can open up more on these boards than I can to my mom or husband. They just don't understand the fears. Don't get me wrong I am truly greatful I don't have a diagnosis of cancer but I still have these other issues and the increased risk of getting breat cancer. I am stressing waiting for my MRI results and my mom told me I was being "dramatic" because I am nervous about them finding something else. Love and Hugs to all of you. We are all scared and that is okay! Peace, Karen |
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Ked1019 Joined: Apr 2008 Posts: 101 |
May 19, 2008 10:49 am
Ked1019 wrote:
Wow I didn't realize how long that post was. Sorry. I left out a few names on my list here that I want to acknowledge. RB - I pray for b9 results for you on TUES and not Wed. No need to wait an additional day. Teaches - Good luck on your MRI. I had a rough time with mine but didn't have any relaxing drugs to help me through. If you can have them please take them. I laughed about your husband doing lawn work when he gets stressed. My husband plays PS3 to tune out the stresses in his life. Nothing like the lawn gets done. Me on the other hand.. I act like I am in my last few weeks of pregnancy cleaning everything in sight. Sticker my friend, I am so sorry about your diagnosis after Easter. At least now you are on the path to survivorship. You go Girl. You are a survivor! Alaska... how nice. Take a mental picture and send it to me. I hope you do well during your treatment and good luck traveling to Anchorage. I get so jealous when I read that you gals are from Alaska, Austraila and the UK. I have never left the US and would love to move far far away. I told my husband I had a dream that we moved to New Zealand and he said, lets go I will try to get a job transfer there.. .we have an office. If only we really could. Not sure why I had that dream but God only knows. Hugs, lots of hugs to you all. |
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Dukemom2 Joined: Mar 2008 Posts: 301 |
May 19, 2008 06:43 pm
Dukemom2 wrote:
Karen, I laughed out loud (literally) when I read your mom's comment about your dog sniffing at your boob. I waited as long as possible before I told my mother (almost 84 years old) about my excisional biospsies. A few days after I told her, it was a Sunday. She gave up driving a couple of years ago (praise the Lord!), so my husband and I take her everywhere she needs and wants to go. That Sunday, as the service was finishing up, a guest minister said that he would be having some "hands on healing" after the service. As we stood to leave, my mother turned to me and said, "do you want to go get healed"? I whispered that since I had only shared my upcoming surgery with a handful of people, I thought I would pass on going up in front of a bunch of people and having a stranger put his hands on my boob to heal me. I was very happy having the surgeon take whatever was questionable out of my boob for me. However, we do love our moms, no matter what they say or do - and sometimes they can say and do some very interesting things!! Dukemom "You have to accept whatever comes, and the only important thing is that you meet it with the best you have to give." ~ Eleanor Roosevelt
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stephanieb Joined: Apr 2008 Posts: 27 |
May 19, 2008 10:08 pm
stephanieb wrote:
Hi Jaly! How long after the FNA until you hear something? My doc says the pathology should come back maybe the same day after she removes my ducts or 2-3 days at the most. I'm saying prayers for you tonight. <> Rbcrhodes, I'm praying for you as well while you are waiting this week. Please let us know as soon as you get news! Stickerlady I am most worried about having DCIS, not even ready to think about if it could be invasive. How long did it take for you to get your path report back? I'm sorry you have to do the radiation, when will you start? Karen, thanks so much for replying. It makes me feel better to know that I'm not the only one with the weird nipple discharge, mine is not bright red blood, but more of an amber rust color and lots of it..I wish our families could understand that being proactive is not the same as "looking" for breast cancer. We desperately need peace of mind one way or the other. I wish all it took was a boob sniffing dog and we could be done with the whole ordeal alot quicker! Dukemom that was too funny~~I can just imagine him laying hands on your boobs in front of the whole church~~I don't think so!! God Bless each and every one of you. NO SQUIRRELS and NO WHALES in our home tonight...Love, Stephanie Courage doesn't always roar, Sometimes courage is the little voice that whispers I'll try again tomorrow.
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jalydiju Joined: May 2008 Posts: 141 |
May 21, 2008 07:57 am
jalydiju wrote:
Hi Stephanie, Have had FNA. Was pretty simple to have had done. Do not know results as they said 48hrs before path results are complete so will have to wait (again) until GP rings me. May not be until Monday next week. Thats OK as there is not much else I can do is there. Know that it took multiple goes to be able to aspirate anything to test. Surgeon said that he wasn't going to have another go if last pass didn't gather anything, must of worked. Cysts didnt collapse after any of the aspiration. Were still same shape and size. Good news is that Left Breast is clear of any drama. Karen, What a crack up. The thought of your mum thinking that the family dog was much more switched on than the rest of the medical communitiy just had me in tears. The funny thing is that my family and I had been out for dinner that night of your post and when we got home, we were greeted by this strange odour. When I turned on the lights I found about six large piles of dog vommit on the lounge carpet and at the back door. Everyone that was with me quickly deserted me and I was left to clean it all up. I then got on this site and thread and read your post. Just could not stop laughing, my sides hurt, tears poured down my cheeks and my cheeks hurt. Thankyou! rdcrhodes, So pleased you have such a supportive family. We do have to remind ourselves time to time that it does have a effect on the people that we love as well. Yes he is concerned re results and probably is edgy for it. Mine to is worried but instead of being able to express it emotionally he tries to drown how he feels with alcohol. jalydiju |
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Ked1019 Joined: Apr 2008 Posts: 101 |
May 21, 2008 09:54 am
Ked1019 wrote:
I am so happy I could add laughter to your day girls. I haven't looked it up yet but I will... I have to see this article about animals sniffing out cancer. I was talking to someone else and they recalled the same sort of thing so there must be something out there. When I find it I will post it. Well I am off to call again to see if my MRI results are available. Talk soon |
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jalydiju Joined: May 2008 Posts: 141 |
May 21, 2008 09:12 pm
jalydiju wrote:
Stephanie, Is 22 May here. Will be constantly thinking of you over next 48hrs. With you in spirit and hopeing for the best possible news for you. I am sure we will be all there holding you hand and helping you through it. Sending comforting hugs, Jaly |
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