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Member Since: May 1, 2008
Last Login: December 1, 2008
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Biography

Diagnosis

Diagnosis: Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Diagnosed: May 8, 2008
Type: Invasive or Infiltrating Ductal Carcinoma
Recurrent? No recurrence
Metastatic? No
Stage: Stage Ia
Lymph Nodes Removed: 7
Positive Lymph Nodes: 0
Tumor Size: 1cm-1.9cm
Tumor Grade: Grade 2 or medium 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

Recent Posts by kwoodson

Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Dec 1, 2008 04:51 pm

November 2008 Rads Group

Hello fellow travelers:

Haven't been on the boards for quite some time but now have a few questions. I've been reading everyone's posts regarding hot flashes and effexor. I've been on effexor since I was diagnosed, and it has helped me maintain an even keel throughout all this but has absolutely destroyed my libido. Is there anything else out there to help the hot flashes? Mine are managable right now. I also can't take soy. Also, I just returned from my radiologist and she suggested something for my "sunburn". For the life of me, I can't remember what it's called. Something like Don Pabo?  Dom something? Anyone here of this? And if so, where can I find it? Thanks for all the good information.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Oct 30, 2008 05:06 pm

November 2008 Rads Group

Hello Everyone,

It's so nice to be moving on to another topic. Had my first tx this morning. I'm the first patient of the day which is kind of nice. I have to admit I think I'm even less informed about radiation than I was about chemo before I started. I'm covered with sharpie marks and my chest looks like a road map. The only SE's I was told to expect was increasing fatigue after about the 3rd week and topical burning.Should I be prepared for anything else? I was prescribed Biafine for the skin. I just can't imagine anything making me feel as awful as chemo did so I'm going to be optimistic.  Thank goodness the weather has cooled. Because August heat and hot flashes don't work with a wig! Hope everyone tolerates tx well.

 Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 12, 2008 06:31 pm

Anyone out there taking anti-anxiety meds?

Hi Wink,

The first person I called after my suspicious mammogram and ultra-sound was my internist. I asked for and promptly received a prescription for effexor.Cancer diagnosis and a needle phobia! I was a mess! I had been on lexapro in the past and it just didn't work well for me. I can honestly say I don't think I could have made it through the past 8 months of surgery, chemo and soon-to-receive radiation without it. I also think that the sudden menopause I've been thrown into has been a little easier to handle because of the medication. I found a valium the night before tx was helpful too. My sleep still suffers but that's from some of SE's of chemo ( and of course menopause! ) but I find Tyleno PM usually helps. Do whatever YOU have to do to help you get through this. Just remember, if you do get some anti-anxiety meds they take at least 2 weeks to kick in. And if the first one doesn't work, try another.  Best of luck.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 12, 2008 09:38 pm

The Road to Hell . . . (or "Laughter is the Best Medicine")

A Fecku? I love it! I work in a school library and I think the teachers would get a huge kick out of that one. I think I'll try one;

Chemo bites the big one.

The wig really sucks with hot flashes.

Thank god for good wine.

Now I'm off to try and find the counted cross-stitch pattern I've misplaced. I've been working on this piece for 5 years as a surprise for my girlfriend who is visiting soon. I'm 90% finished and have no freaking idea where I put the pattern. I just want to know what I can blame for my brain farts when this ordeal is over.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 12, 2008 08:33 am

The Road to Hell . . . (or "Laughter is the Best Medicine")

I love this contest.

I have to admit my house is a clutter magnet when I'm at my absolute healthiest and energized, so I guess I have to lower my handicap (all you golfers or golf widows will get the reference. ) Since my surgery in early June we hosted a graduation party for about 80, added a new deck which required 3 weeks of builders tearing up the yard, hosted ( my kids actually ) another party and packed up and sent  said kids to college. I think the only time the house was cleaned was before the graduation party. I have ca-ca in every room of my house, a pug that sheds endlessly who hasn't been bathed in 6 weeks and now has some nasty ear fungus. My sock basket is overflowing and I seriously can't remember the last time I cleaned my room. The only reason the bathrooms are hygenic is because my dh has taken on that task ( about time after 25 years of marriage! ) I do manage to wash the clothes but they've ( all  clean ) taken up residence on my laundry room floor. I just pick through the mass to find what I need for that day. The good news is my daughter is bringing her roommates home tomorrow and I don't want to be embarassed so the downstairs is actually going to get cleaned before I leave for my Neulasta shot.

I figure we're stuck in this house for at least 10 more years. One, we want to enjoy the deck ( especially if I can talk him into a hot tub ) and two, it will take me that long to get it presentable to sell,

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 12, 2008 07:40 am

Anybody starting Chemo in July 08

Hi All,

Had tx 3 yesterday. They gave me Emend for the first time and it was the first time I came home from tx and had to sleep. Then the steroids kicked in and I was up most of the night. The fact that the air conditioning was off probably didn't help. I'm taking the 2 lower doses of Emend today and tomorrow. Will I be as groggy? I hope not because this is usually the day I feel well enough to get things accomplished.

Laura, I have had a very flushed face and breast ( just the one! ) after each tx. I was told it was a SE of the steroids. If it gets itchy I would call your doctor.

Now, on to a menopause question. I'm 49 and having 4 treatments, followed by radiation and then 5 years of whatever they decide to give me. I haven't had a period since I started treatment and was definitely in perimenopause before I started this journey. Has anyone who stopped having periods started having them again? I would be fine if that whole part of my physical life was over because I really don't want to go on Tamoxifen (sp?) when this is all over. I guess I should also post this question on the hormone treatment board. Thanks for any info.

Hope everyone has a SE-free weekend!

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 2, 2008 11:41 am

What treatment can I expect?

Lynette,

I'm 49 and had 0/7 nodes. Also ER/PR+ and Her2-.

Originally, I was told, if there was no spread to anticipate 6 weeks of radiation. Imagine my surprise when they recommended 4tx of chemo. Apparently it has more to do with my premenopausal state and the rate of recurrence. Get more opinions so you're comfortable with your decision. The chemo is a pain in the ass, but it isn't the end of the world. Even the hair loss hasn't bothered me too much. It might be the anti-anxiety meds I went on as soon as I got a preliminary diagnosis. Use what works for you. Let us know what you decide.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 29, 2008 10:49 am

Hair Hair Hair - Another question

I know this issue has been covered before, but I'm too lazy to go back and find it. Shaved my head 2 weeks ago and got a fabulous wig. However, now I'm sprouting itchy, red splotches across my bald dome. I don't care how it looks, but trying to scratch through the wig or scarf is frustrating. Can you put hydrocortisone cream on your head? Has anyone found anything soothing with no medicine in it? Thanks for any info.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 29, 2008 10:46 am

Anybody starting Chemo in July 08

Emily,

Sorry to hear about your family problems. I'm not a particularly spiritual person, so I probably come across as rather unfeeling to many people. I have always had a hard time with people who stay with abusive spouses and then expect their children to fall in line and support the situation. May I suggest you contact hospice or any other potential support organizations to see if someone can provide some assistance? If there was ever a time for you to be selfish in all ways, this is it. Take care of yourself first, let family and friends help and don't feel guilty.

I'll raise a glass on the 14th. Or should it be the 13th here in the States? Since it will be 3 days after tx, it will probably be my chemo drink of choice: Kool-Aid!

Hope everyone has a very relaxing Labor Day Weekend.

 Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 26, 2008 07:16 am

Chemo and Work

Hi Ladies!

Well, I did about the dumbest thing you could do. I went back for the entire day. Stopped at the grocery store ( had to buy an emergency bottle of pop to deal with the nausea ) and then just came home and collapsed! My husband was none to happy with me. Lorena, I too, am finding the weekend after and the first days of the week awful. Nothing tastes or sounds good to eat and my energy level is crap! I think I learned my lesson and will take it very slow from now on. The only problem is we're being trained the next 4 days for an entire new system. Oh well, my co-workers are just going to have to become my teachers! I have to admit it was great seeing everyone but I've learned my limits. I think that may be one of the hardest things to accept during this journey. Thanks for the encouragement.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 24, 2008 12:41 pm

Chemo and Work

Hello All,

I've been rather lucky in regards to my timing with this disease. I was diagnosed in May and was able to put off sugery and treatment until June when my school job was over for the summer. I'm supposed to start back tomorrow and I'm just wondering how other people cope with work and the fatigue I'm feeling? I just had my 2nd tx last Thursday, Neulasta on Friday and here it is 12:30 p.m. and I'm ready for a nap! And when I'm healthy I never take naps. My first tx had me laid low  for a week-and-a-half ( including three days in the hospital). I'm not anticipating that this time with the Neulasta, but I want to give my boss a heads' up about what she can expect from me this week. There's no pressure coming from her but I don't want to wimp out if I can stick it out for my normal work hours. I'm actually looking forward to getting back to a routine and seeing co-workers. Too much alone time isn't good for the psyche. Thanks for any advice!

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 22, 2008 10:21 am

Anybody starting Chemo in July 08

Hi All,

Had tx 2 yesterday. I'm keeping my fingers crossed that it goes better than the first one.I went from TC to AC. I get my Neulasta today, so I'm hopeful that will prevent the decrease in blood count. Glad to see so many wine lovers on this thread! My stepmother ( who has successfully battled both breast and endometrieal cancer ) promoted " wine therapy " at the beginning of my diagnosis. I've certainly cut back and actually don't have a taste for it ( or anything else ) for about 1 1/2 weeks after treatment. I think it's also helping with the weight. I find wine to be a great appetitie stimulant. My bio... I'm 49, married almost 25 years to a wonderful guy, 2 kids ( 21 and 18 ) and I'm about to become an empty nester. :(  My son is having such anxiety about leaving and is so disorganized it provides a great distraction for me. Actually, we have 3 children. It's just that the 3rd has 4 legs and is a Pug. I work in a high school library and I dearly love my job. I get to be around 7th-12th graders, help with research and surround myself with books. Nothing could be better. Our favorite vacation involves warm weather, a beach and lots of golf ( for my dh ). Oh, and no cooking dinners for me. I'm already thinking about next summer and planning a special get-a-way. Hope everybody had a stress-free, discomfort-free weekend.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 20, 2008 10:27 am

Anybody starting Chemo in July 08

Laura-

About the mouth sores. You might want to ask your doctor for a prescription for Miles Mixture. I'm not really sure what it is, but I use it about 3x daily. Swish, gargle and swallow. So far no mouth sores. I'm also using the Biotene toothpaste and mouth wash. Hope the sores improve. You certainly don't want anything to affect your appetite any more than the usual chemo influence.Heck, I find even a fever blister painful.

kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 19, 2008 10:46 pm

Hair Hair Hair - Another question

O.K. so I'm absolutely a virgin at all this. Only one treatment and my very thick, very course hair was coming out in clumps. Got my wig today and had them shave my head. All I can say is I can understand why men get that whole shaved thing. THAT feels great. The wig feels like shit! It's light and all, but I have the overwhelming sensation that it's slipping off my head. Anyway, I'm finally realizing why some women just go for the ball cap look. I have this sinking feeling it's going to grow back grey. So I'll have to wear the wig until my hair is long enough to color. At some point tonight I just looked at my dog and finally said " you know what, know matter what spin you try to use, this whole situation really sucks ". Fortunately, he's a very understanding pooch and just jumped in my lap and kissed me. God love animals.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 17, 2008 11:55 am

Anybody starting Chemo in July 08

Thank God for this board!

I had read earlier about the shots in the stomach. I have quite the needle phobia so when I was in the hospital I asked the nurse to give me my injections in my ample belly. Probably the only time in my life I'm glad I've got the extra poundage. Anyhoooo....it's very true. You barely feel it, so if anyone is worried about the needle pain ask for your injection in the gut.


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 17, 2008 11:16 am

Anybody starting Chemo in July 08

Good Morning All,

Technically I'm a July Chemo Girl. Had my first tx on the 30th or 31st. Taxotere and Cytoxan. First few days just fatigued. Then diarrhea hit with lots of pain. Ended up in the hospital for 3 days. My hair started falling out on Tuesday and will probably be all gone by the time I get my wig on Tuesday. The itching is driving me mad. I told my neighbor that the scalp tingling reminded me of the 'let-down" reflex when I was breast-feeding 18 years ago! My next tx is on Thursday and I'm keeping my fingers crossed that this one will go better. I had a MUGA scan last week that I assume will allow me a new regimen. I'm not sure what I'll be on yet. I have a question about Neulasta and other injections. Does the Neulasta have to be given during a specific time frame. Like between 24 and 48 hours after tx? They were giving me injections in the hospital to improve my blood count but it wasn't Neulasta. And how bad does the bone pain get? Are there other drugs they can give to keep the RBC and WBC levels up? Thnks for any info.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 15, 2008 08:31 am

I just don't understand!!!

Gosh, priz, maybe we were twins separated at birth. My husband was sending me all sorts of mixed messages. He's also a very black/white, advantage/disadvantage type of person. My advice is to include him in everything possible. All visits, etc... I find that my husband often asks the questions I forget to ask. But ultimately, it is YOUR decision and he needs to understand and support that. We all know that men think we want them to " fix " our problems, when often we're just venting. That's why they invented girlfriends! Good Luck!


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 15, 2008 07:23 am

I just don't understand!!!

Hi priz47,

I could ( and probably did ) write this exact same question about a month ago. I'm also getting 4 tx of chemo. Started with taxotere and cytoxan but will be changing with the next treatment. Initially I was told, small tumor, no nodes, yada, yada, yada, I would just need radiation. When I saw the radiologist she recommended chemo as did the Onc. Kind of an upleasant surprise. This is the information I was able to process....If you haven't gone through menopause ( and I haven't ) the rate of recurrence will go down if you also have chemo. It's not a huge percentage, but as my onc put it, do everything to improve your chances of not getting it again. She said they've advocating this type of tx for about 10 years. Both my radiologist and oncologist said if it was them, they would do it. Now, to put your mind at ease, I would certainly recommend you get a 2nd, 3rd or 4th opinion. If you do decide to go with the tx, just keep in mind it's only 4 tx. Not fun, but managable. Hope that helps.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 12, 2008 06:47 pm

Share the details of your wig with me?

I went to one of the many places recommended by my Onc. It's a hair restoration specialty group and they're very attuned to men and women with health/hair issues.And not just cancer. They even have a great supply of hats, scarves, pillowcases, etc.... Now I'll admit one of the few areas of vanity that remain in my life is my hair and I didn't care how much I spent to get the look I wanted. I figure we'll deduct it from our taxes. The synthetics were hot and unmanagable and made me want to cry but I found a cyberhair wig that looks so much like my natural hair. I go next week to get my head shaved and have my wig styled. I'm not looking forward to it, but it's the one area where I have all the control. Good luck with your search.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Aug 11, 2008 09:29 pm

Anyone on just Taxotere and Cytoxan?

MissNelson- My Onc. also told me to stay away from fresh fruits and vegetables. It's too easy to pick up an infection through them. This is really hard because the one food I've been craving is fresh fruit.  And I was also told specifically that I would not lose weight. I think that's the cruelest joke of all since I could use a 20-25 lb. reduction in my girth. I didn't even lose any after a week of diarrhea and 3 days in the hospital!  I also found the only thing I could drink was cherry kool-aid so I was obviously getting my carbs and calories. As far as avoiding people, it probably can't hurt, and I would definitely do it if your levels are low. I'm supposed to start back at my school job soon but I'm beginning to rethink that plan. It's nearly impossible to not get sick when you work in a school. Best of luck with your treatments.

Kathy


Dx 5/8/2008, IDC, 1cm, Stage Ia, Grade 2, 0/7 nodes, ER+/PR+, HER2-

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