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Member Since: August 23, 2007
Last Login: October 10, 2008
Location: Cocoa Beach, FL
Occupation:

Biography

Diagnosis

Recent Posts by sandeefeet

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 30, 2008 10:14 am

Need Prayers for Our LuAnn

Hi LuAnn,

 Just checking to see how you're feeling. I hope a lot better!!!!

 Have a blast in Vegas!!!

Laurie

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 26, 2008 10:47 am

Alaska Deb Update

Dear Deb,

Praying that everything goes smooth as silk for you this morning!!!
Laurie

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 26, 2008 10:41 am

Need Prayers for Our LuAnn

LuAnn,

 My heartfelt prayers are with you!!!!

(((Gentle Hugs)))

Laurie

Posted in: Connecting With Others Who Have a Similar Diagnosis + Palliative Therapy/Hospice Care, Created: Sep 26, 2008 08:39 am

I am losing my mom and having a hard time.

Enjohnson,

My Mom was diagnosed Dec '05. Mastectomy Jan '06. Diagnosed with bone mets Aug '07 which progressed to lungs, liver, spine, and brain. Jesus took her home with him last Thursday Sept. 18th. Four days before my 40th bday and 5 days before my son's 20th bday. My Mom had moved to WV to be near my Grandmother who is now a 20year BC survivor. We brought my Mom home to FL 3 months ago to live with us.

I can't tell you how to accept that your Mom may not be here with you physically. I'm still trying to grasp that myself. I can tell you, like the other ladies here have said, tell her you Love her every chance you get, hug her, hold her hand, talk to her about special memories.

It's a very very difficult time but I really do believe now that God doesn't give us more than we can handle.

My heartfelt prayers are with you, your Mom and your family!!!

Laurie

Posted in: Connecting With Others Who Have a Similar Diagnosis + Palliative Therapy/Hospice Care, Created: Sep 26, 2008 08:28 am

My Mom's got her wings

Thank you all for your kindness!!!

Rhonda, my Mom lived in S. Charleston. She moved there from here in FL to be near my Grandmother. My Grandmother is now a 20 year BC survivor now at the young age of 84. I feel so bad for her speaking with her on the phone. She misses my Mom terribly.

Posted in: Connecting With Others Who Have a Similar Diagnosis + Palliative Therapy/Hospice Care, Created: Sep 25, 2008 02:52 pm

My Mom's got her wings

My Mom's always been an Angel but she has her wings now. After a tough two years...left mastectomy then bone, lung, liver, brain and spine mets she was blessed with her wings last Thursday, Sept 18th. We had to have her taken to the hospital the Sun before by ambulance and the Dr. released her on Wed. so we could bring her home where she was comfortable. We had not signed up for Hospice at that point but they came to our house that afternoon that we brought her home and stayed with us over night. 

She made me promise to take her down to the beach in her wheel chair and big floppy hat, like on the movie beaches, when the time had come. We only live a few houses down to the board walk but it was physically impossible to move her at that point. I took the Aaron Chang picture we had in our bedroom and hung it in her bedroom right in front of her. It's a beautiful scene of the beach and palm trees with the rays of a sunset. When she woke for a few moments I showed her that she was at the beach, she smiled and said she was so happy.

My husband lost his father to mesothelioma 17 years ago tomorrow. I asked him how do you got over the pain. He said you never get over it, you listen to music different, the sky looks different, you react to things in life differently, everything changes. He's so right. I miss my Mom terribly. I turned 40 on the 22nd, my son 20 on the 23rd. Our bdays just won't be the same anymore.

I just wanted to thank everyone here for all your support, kind words and advise during this time.

I pray for each and everyone you and your families.

God Bless,

Laurie

Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Sep 3, 2008 10:43 am

Decadron and WBR

Hi Lauralynne,

 Thank you for chiming in!!! It's comforting knowing other people are going through the same side effects as my mom.  I keep telling her to have faith this won't last for much longer.

 She will also go back to chemo (Xeloda) once the rads is complete for bone, liver and and lung mets.

Good idea on the Kleenex stock!!!!

Laurie

Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Sep 3, 2008 08:48 am

Decadron and WBR

Hi Annie,

My mom fell twice yesterday. Limp legs being one of the SE's of the Decadron. The radiologist said she has to take the Decadron during the radiation to help reduce the swelling on the brain. They did tell her no more driving while she's doing this treatment.

We meet with the Onc today after radiation. We'll talk to her about it as well and see what she says.

 Are you scheduled to start rads soon?

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 2, 2008 11:18 am

Problematic Puking

Deb, this may sound weird but have you tried Dramamine? It's for motion sickness I know and that's what I usually use it for but I've used it for other nausea situations and suggested it to others with success.

Active ingredient:  Dimenhydrinate 50 mg

Inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, lactose, magnesium stearate, and microcrystalline cellulose

 They sell a non-drowzy form. Who knows, maybe it would help.

Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Sep 2, 2008 10:38 am

Decadron and WBR

Is anyone taking Decadron during their WBR? My mom is. They raised the dosage then reduced it. She's had SE's since starting it and they worsened with the increase, hence the decrease. She's on an emotional roller coaster anyway ( completely understandable) but seems like things are worse for her now. RO says it's too early for SE's from the actual rads, has to be the Decadron. Lot's of crying, lots of short term memory loss, unstable balance, sometimes can't get legs to work, SOB increased at times, sleepless nights, just overall feeling like sh&t. I asked the RO about giving her Ambien to help her sleep. The Xanax doesn't seem to be doing the trick. That was brushed off but they did reduce the Decadron. I'm going to ask her regular Onc tomorrow when we see her.

 Can anyone give me their experience. I don't want my Mom to feel like it's going to stay this way.

Posted in: Support & Community Connections + For Family & Friends of Those Who Have Breast Cancer, Created: Aug 14, 2008 03:59 pm

i hate the word!!!!

Hi Ladies,

My mom was diagnosed Dec. 05 and had her mastectomy in Jan. '06. Then last year she was diagnosed with mets.

She was in WV but when my family and I went to visit her this past June she was hospitalized for 10days. At first her Dr's told us we couldn't bring her home to FL with us but then one of them finally caved and gave the go ahead. So here we are and taking one day at time. She's really happy to be here with us and I think she's actually a bit stronger now that she's here.

This disease is awful but there are a whole lot of very strong and wonderfully supportive people in this community that can help answer your questons. As I'm reminded somtimes, don't forget to go through the other sections of the forums and post any questions you have there also.  This website has helped me a lot. I'm finding lately it's hard for me to talk to some of my friends anymore about this anymore. They'll ask how things are going and once you tell them you can just see the look in there face, "damn why did I ask". It got really frustrating for me the other day talking with a really close friend of mine who now seems a bit disinterested but I suppose it's kinda hard to be interested in something that doesn't directly affect you. My husband on the other hand is awesome has really been there for me. I can talk to him about anything and he listens to me and is so supportive.

You can always PM me also if any of you need to vent!!!

God Bless!!!

Posted in: Support & Community Connections + For Family & Friends of Those Who Have Breast Cancer, Created: Aug 14, 2008 03:35 pm

WBRT

Happy Thursday!!!

 I posted a question about this in radiation as well.

Is there anyone here or anyone who has a family member who has had or having the whole brain radiation?

 My mom will be starting soon and just wondering what we can expect.

I will be taking her to the sessions everyday and she lives with us now. I just want to know how to best help her through this.

Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Aug 14, 2008 03:32 pm

Whole Brain Radiation

Hi Barbara, thank you this information. I'm really glad to hear your friend did well with this treatment.

God Bless!!

Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Aug 14, 2008 10:08 am

Whole Brain Radiation

Hi everyone, we met with my Mom's Oncologist yesterday. Between my mom's recent PET Scan and MRI there is now a 1" tumor on the left side of her Cerebelum and smaller ones surrounding it. Her Oncologist has recommended stopping the Xeloda for now and starting whole brain radiation for 3-6 weeks to take care of those mets.

 Is there anyone here who's gone through this experience that can give us some insight on what we can expect through this process?

This is the first radiation she's had through all of this.

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 14, 2008 09:14 am

Pet Scan results

Hi Ladies,

Thank you for your support. Met with the Oncologist yesterday. She advised the one tumor on the brain is about 1" in size then there are smaller ones surrounding it. My mom is going to start full brain radiation soon. She's only got a few days of this round of Xeloda to finish so they will start the radiation after that.

I'm not real clear on how radiation works. If any of you have done this and can give me some insight that would be wonderful. I'm going to look through the radiation forum also.

Her Oncologist is very positive and believes my Mom will do well.

LuAnn, My Mom said she's suffering from CRS too :).  she has been on this site a couple times but not recently. I mostly just share with her the different things I've read along the way.

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 12, 2008 08:45 am

Pet Scan results

We received my mom's PET Scan results Friday. The Mets that have been in her ribs and hip, 1 lung and 1 lobe of her liver have spread. They are now through the spine, ribs, both hips, left arm, right femur, both lungs and both lobes of her liver. The original nodules on the lung and liver have increased in size from the last PET Scan. There is also a suspicious spot on the back left side of her brain. They are presuming this is a met as well. I take her today for an MRI for a better look. I guess this explains the recent unsteadiness she's been feeling. She's not having headaches but feels a bit of a burning sensation and like waves in her vision.

She's on her second round of Xeloda right now and the onc wants to start on Zometa. She thinks this is futile. We meet with the onc tomorrow to get the MRI results and I'm assuming get direction for what is next.

I'm not sure if my mom will do the gamma knife if this is an option.

Can anyone who is going through this same thing please let me know how you're coping?

Posted in: Support & Community Connections + For Family & Friends of Those Who Have Breast Cancer, Created: Aug 12, 2008 08:33 am

SSI & LTD Question

Hi LuAnn, talked to my mom's LTD carrier. My mom is getting widows benefits from SSI so LTD had me call SSI to see if my mom had more benefit continuing with the widows benefits or filing on her own. Widows benefits is better so LTD said there is no reason for my mom to file on her own. She was so relieved!!!

 Thank you again for your support and advise!!!

God Bless!!!

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 11, 2008 04:29 pm

Counts Low No Chemo - What can I do?

Hi Stephanie, I don't have the answer for you but you've got my whole hearted prayers!!!

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 8, 2008 09:13 am

I'm in the hospital

Hi Deb, many, many, many, many prayers for you and your family!!!!!

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 6, 2008 09:18 am

Genetic Testing

Thank you Jill, do you mind telling me how they do this testing?

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