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Member Since: May 18, 2006
Last Login: March 12, 2008
Location: Rochester, NY
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Biography

Diagnosis

Recent Posts by fd411

Posted in: Support & Community Connections + African Americans with breast cancer., Created: Mar 1, 2008 10:00 am

Roll Call November 2007

Hello Ladies,

Ferne here. 

I'm hangin'. Had some progression being off of chemo for 7 weeks while doing the wbr which wiped me out. I started a new chemo (Ixempra) yesterday, so I'm patiently waiting to get back in the groove. I'm still working full time, although some days I don't know how. I just keep praying for the strength to make it through all this. 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Mar 1, 2008 08:08 am

I never wanted to post here, but what do I do now??

Dear Deb,

What a rotten blow it is to get that news. I'm so sorry you have gotten it. But you did a few NED years. I think that's good that you had that time. 

After the inital shock wears down and you have a treatment plan, hopefully things will go smoothly for you. Being on chemo for my mets has been ok. I'm still working full time and doing what I can. The hardest was the brain mets treatment and I'm still bouncing back from that, but the chemo so far has been tolerable.

So I know you can do this and don't even think you're going to die anytime  soon. My nodes had success on the chemos, you just have to find the ones  that work for you. 

Try not to worry yourself to death either. I know it's hard, but please try. 

I'll continue praying for you and sending positive thoughts,

Hugs,

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 28, 2008 06:50 am

Well, here it is............ no more treatment

Joanne and Erin,

I'm so sorry that this time has come for you both. 

Hugs and prayers,

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 27, 2008 06:55 am

For those with Skin Mets

I think bc mets website has pictures, or the IBC website. My skin mets never oozed or bled. Never scabbed over. But some do.

But I also have some skin condition on my hands where the skin has become very hard and cracks and peels and grows fast and gets very thick. This has been going on for years and no medicine I've been given had solved the problem, and it's not cancer.

The skin change near the scar would prompt me to get a skin biopsy. That's how mine was found. 

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 25, 2008 03:30 pm

Decadron or dexamethazone side effects

Luckywife,

When I took it to counteract chemo side effects it wasn't too bad. Just made me hyper for a little bit and I couldn.t sleep for a night. 

But taking it for my brain mets was a horror story. Even after I was done and still had swelling, my rad onc said she wasn't going to keep me on it. I completely weaned off the decadron Jan 31 or so. I still have the moon face, the hump in the back of my neck, and the bloated stomach. My legs still hurt, too. I also gained weight. But my appetite has returned to normal, and I'm not as snappy or short tempered as I was on the decadron. I'm glad to be off of that stuff in that capacity. I had no idea it would make me feel that way in the brain mets doses.

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 24, 2008 05:58 pm

Lung Mets NOW starting pain on chemo?

Hi Watson,

I completely forgot about tumor flares. I remember getting breast pains when I did chemo the first time around. I got pains, and the lumps just about shrank to nothing!  Hopefully it's just the Xeloda kicking some butt after all!

I guess I get a bit tense when I get aches and pains or something out of the ordinary because for me it usually is something.

Be well,

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 24, 2008 12:20 pm

Lung Mets NOW starting pain on chemo?

Hi Watson,

I haven't had chemo since early January, so the pain is pretty constant now, even with pain meds. It's an annoying sharp pain. If I lay on the side where the pain is, it initensifies and if I lay on the other side, the pain lessens. I just started this Fentanyl patch yesterday and have been taking Tylenol with codeine and Oxycodone, but that oxycodone makes me kinda ill.

I agree Watson. I think the only exact science is mathematics, and you know how we are with those and statistics. They don't work on us! 

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 24, 2008 10:49 am

O/T Dolphin birth

I think dolpnins and cats are some of the coolest creations.

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 24, 2008 10:39 am

Lung Mets NOW starting pain on chemo?

Hi Watson,

I progressed alot and fairly quickly on Xeloda. I was on it for about 2 months,  but it just didn't work for me. My lung mets related pain that was in my back was up by my shoulder blades. If you lay or apply pressure on the side where the pains are does it get worse? Hopefully this is not the case with you and Xeloda is working.

Hugs,

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 20, 2008 07:02 pm

CY - She has her wings

That just sucks.

My condolences and prayers go to Cy's family and may they take comfort in the fact that she is no longer suffering from this dreadful disease. 

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Stage III Cancer, Created: Feb 19, 2008 08:51 pm

Things do not look good....

Deb,

I'm so sorry you scan showed areas of concern. Hopefully the nodes will have benign results. 

You're in my prayers,

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Stage III Cancer, Created: Feb 16, 2008 08:49 pm

Im I the only one who really doesn't want to know?

Hi Deb,

I'm glad you were able to get your scan today. I hope everything is b9.

You are in my prayers.

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 15, 2008 07:11 am

Setbacks.Please keep me in your prayers..

Luckywife,

You are in my prayers.

Ferne

Posted in: Connecting With Others Who Have a Similar Diagnosis + Stage III Cancer, Created: Feb 14, 2008 07:53 am

Im I the only one who really doesn't want to know?

Deb,

I'm at the I don't want to know point myself. Althought I know Ihave to know...

I'm thinking of you today sending positive thoughts and saying prayers for benign results. 

Hugs,

Ferne 

Posted in: Tests, Treatments & Side Effects + Just Diagnosed, Created: Feb 14, 2008 06:52 am

Please help Jadipops

Hello Everyone.

I found this post in the "not diagnosed but worried forum" and mentioned to Jadipops that I would move it here for her.

This is the post: 

"in need of support

just found out i have breast cancer so worried confused"

Thank you all so much. 

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Feb 14, 2008 06:49 am

help

Hi Jadipops,

I'm sorry to hear about your diagnosis. It's like you're caught up in a tornado. It's so overwhelming when y0ou first hear those words. 

I'll move this over to the just diagnosed forum for you. You'll get lots of words of wisdom and support.

Hugs,

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 12, 2008 07:25 am

skin mets

Oz,

 Chemo might work for your mets. The treatment in itself had few side effects. It did a good job for me, but I'm triple neg. It knocked it down relatively quickly and is/was all over my entire right (bc) breast, started going to the left side, went under my arm on the bc side and up to my collar bone on the bc side. Ironically I received rads to all of these places on the right side. My rads after lumpectomy plugged up my lymphatic channels in the breast. I find it interesting that rads can also treat skin mets.

I hope you can get successful treatment soon; you've been battling this for a long time.

hugs,

Ferne 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Triple Negative, Created: Feb 11, 2008 08:17 pm

uh,oh....already?

Yes, I have. I finished treatment in Jan 07 and got lung mets in early May 07. Those were my words exactly...Already???

Hopefully it's nothing, or if it is something, it's caught early enough that you still have a shot at NED! 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 11, 2008 08:09 pm

Brain Mets Symptoms

I would push for a brain mri as well.

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 11, 2008 06:48 am

my friend has brain mets

Hi Joanne,

It's so nice to see you posting again. I'm glad the wbr wasn't as harsh on you.

Ferne 

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