LungLoveLink

Linking you to resources and support in the lung cancer community!

All Blog Posts (173)

Tammy Simon HDL Levels

Went to see my Onogolist plus did my treatment for Avastin. Every time you see the doctor now they give you a patient report. I check it to see what my levels are. I saw my PLT were low compare my normal. Plus I saw my HDL was high on last January treatment. So I called the drs office and the nurse stated that all cancer patients have this enzyme? I went back and checked all my blood work my was normal all the way up until now.

The question is Should I worry because it's high??? Has anyone… Continue

Added by Tammy Simon on February 11, 2012 at 5:18pm — 6 Comments

Nancy to answer your question

my husband 1st had a brain tumor which was an adenocarsinoma with characteristic of spread from lung, but no primary was found. After surgery they radiated the spot. then another brain tumor showed up and that was successfully radiated. Finally in Dec. a small nodule in the lung showed PET active. It was radiated. Now they do chemo with Alimpta and Carboplatinum, 2-4 treatments 3 weeks apart.  Nancy

Added by Nancy on January 26, 2012 at 9:50pm — 1 Comment

Nancy starting chemo

my husband starts chemo next and was looking for a forum where others were in the same boat. I see posts where spouses are stressed because their affected person is too careful of infection. I have the opposite problem where mine finds it annoying to wash hands, not touch doorknobs, use disinfecting gel etc. and I am the one worried about the consequences. It is very stressful for me, no so much for him.

Added by Nancy on January 22, 2012 at 2:32pm — 5 Comments

Deva Facial Swelling

Does anyone have any help for facial swelling?  I am in month 6 of Avastin, Alimpta, Carbo.  Take Dexamethasone for 3 days every 3 weeks (day before, day of and day after treatment). Each month it is getting worse, along with abdominal swelling - any suggestions would be appreciated.  Already cut out salt and drink lots of fluid (which I don't seem to be shedding).  Hope to hear from fellow survivors.

Added by Deva on January 22, 2012 at 11:41am — 1 Comment

AmyLCA Care you share your thoughts? New Directions Newsletter!

Greetings!

If you are on the Lung Cancer Alliance mailing list, you may have received our New Directions Newsletter a few months ago. This newsletter comes out once a year and highlights lung cancer research so that everyone can stay up to date on what is happening and what advances have been made.

We are currently requesting feedback on what people think of this newsletter as a resource and we are considering making changes to the format and content for…

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Added by AmyLCA on January 11, 2012 at 5:00pm — 5 Comments

nheep Smoking

I stopped  smoking on 7/29/09 on the way to the hospital to have my upper left lobe taken out.  It was a very small tumor so I figured I would smoke up until then.  I have not smoked since.  When I get really stressed I think about it but I know I won't be able to stop at one so I don't start.3 months later the cancer came back so I had 3 rounds of chemo and 36 radiation treatments.  December 28th will be 3 years that I started treatment.  I ended up with post thoracic pain syndrome from…

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Added by nheep on December 23, 2011 at 6:30pm — 4 Comments

Tammy Simon Telephone Workshops

Can anyone tell me if they have done any of these telephone workshops/conferences I see posted. Cost, how they are done, where to get phone numbers if you want to do it. If anyone can help me with this information that would e great. There's one on the 14th of December that I'm interested in.. I know this is a short notice but hopefully someone will see this before then and have the answer for me.
Thanks and God Bless
Tammy

Added by Tammy Simon on December 12, 2011 at 11:20pm — 1 Comment

DavidatpMOD SSDI

Has anyone on disablility had to do an SSDI review? If so, when did you have to do it and what was involved? Mine will be coming up in less than a year and I would like to know a little bit about what to expect. Thanks for any input. Good luck, God bless and keep the faith...

David

 

Added by DavidatpMOD on December 12, 2011 at 11:06pm — 5 Comments

Carolyn cold and oxygen

 

I drink alot of ice water (it has to be ice water) and love to eat ice cream.  I was wondering today if the cold would make me feel as though I was getting more oxygen.  This probably sounds crazy.  I take a big cup of ice water everywhere I go. If anyone thinks this is crazy or it makes sence please let me know Thank you.

God bless all of you and to all of you Merry Christmas

Carolyn

Added by Carolyn on December 11, 2011 at 10:22pm — 7 Comments

sclcsurvivor Who says you can't survive small cell lung cancer?

I have survived SCLC (caused by agent orange in Vietnam) for 3 years

  •  I survived (though my family was told I only had hours to live) a seizure caused by SCLC in 2008
  • I survived 6 different lines and 88 treatments of chemo
  • I survived 88 sessions of radiation
  • I survived 15 sessions of brain radiation and my last MRI confirmed I still have a brain.
  • I survived (though my family again was told I had hours to live) a recent episode of acute…
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Added by sclcsurvivor on December 8, 2011 at 8:19pm — 8 Comments

LindaF Lung Cancer in the News

Today the Richmond Times Dispatch published an essay I wrote about early detection.  My sister Wendy died in August 2010 and I am determined to make a difference in as many people's lives as I can.  I have had two CT scans and so far the two nodules they found have not changed...we will keep scanning and pray there is never a change. I pray for all of you who are suffering with Lung Cancer.  My time with my sister was so difficult.  Watching her in panic from not being able to catch her…

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Added by LindaF on December 4, 2011 at 2:02pm — 1 Comment

Kathy No appetite

Hi everyone. I am very blessed considering some post I have read so I feel a little like a complainer but I do have questions.

I had surgery almost a month ago and am doing well. I believe they got it all. I will see the dr next week and get an update. Everything has a funny taste to me. Has anyone else experienced this?  I don't have an appetite. What I used to love to eat now makes me queasy. 

And this cough, what's that about?? I didn't have one before 

OK I'm through…

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Added by Kathy on November 2, 2011 at 10:26am — 4 Comments

Mary Martin Radiation burn

Burn has lasted 12 days now and still burns and itches. Applying creams, etc. 3 or more times a day. Could anyone tell me how long these burns takes to heal?

Added by Mary Martin on November 1, 2011 at 11:40am — 5 Comments

DavidatpMOD Lemons and cancer

I'm not at all sure I believe this but anything is worth a try if it isn't harmful...
David
 
 
 
 
Subject: Lemons and…
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Added by DavidatpMOD on October 31, 2011 at 8:56pm — 5 Comments

TeamLCA Spot the Lung Cancer Awareness Month kits - we'll send you a prize!

This year for Lung Cancer Awareness Month, Lung Cancer Alliance sent out over 500 boxes of materials to cancer centers all over the country.  The box contained: a nice bright poster with suggestions on how to get support, get information and get involved! Bracelets with "Shine a Light on Lung Cancer" written on them. LCA temporary Tattoos. Fun bookmarks. 

 

Now here's the challenge: If you see this awareness kit set up in your cancer center, post a picture as a comment. We'll…

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Added by TeamLCA on October 31, 2011 at 3:19pm — No Comments

melanie my hair

after chemotherapy my hair is not taking streating to well .  should i put a perm in my hair or shoould i waite a little bit longer.  it been a year since havintg chemo and the lost of my hair.

Added by melanie on October 27, 2011 at 6:19pm — 2 Comments

ms relief from cough attaks

hi everyone my dad has lung cancer he is going to radiation, but hes cough wont go away he has also loose of air like he cant breath does someone know a good way to reilief his cougfing attaks thank you

Added by ms on October 24, 2011 at 8:58pm — 8 Comments

Mary Martin Treating Radiation Burn

Finished five sessions of radiation treatment last Fri, for malignant nodule in lung. Have radiation burn on back. It started out as itch, then burning. Large red area. Have used just Aquaphor on it so far. Anyone have experience with this?

 

Added by Mary Martin on October 24, 2011 at 10:03am — 7 Comments

TeamLCA Interested in supporting someone by phone? Consider being a Phone Buddy Volunteer with LCA!

LCA has had a very active Phone Buddy program for about 15 years. Through the Phone Buddy program, we match people who are going through lung cancer with a person who has "been there, done that," someone who had had a similar experience and can provide support. We match based on the type of lung cancer, stage, treatments, and sometimes other requests such as age, married, living alone, with kids at home...whatever the specific need. Phone Buddies are available to talk to the person, share…

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Added by TeamLCA on October 13, 2011 at 12:35pm — No Comments

AmyLCA Back and active again - And Lung Cancer Awareness Month right around the corner!!!

Hi everyone,

 

I'm sorry I've been away and not active over the last few weeks. We've had all sorts of activity at LCA headquarters as Maureen, Miguel and I have been hard at work assembling and mailing out 500 boxes of goodies to cancer centers and hospitals all over the US in preparation for Lung Cancer Awareness Month. 500!!! That's a lot of boxes! It has been exciting but exhausting and I've gotten very very behind in other things as a result. But we are almost done sending…

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Added by AmyLCA on October 11, 2011 at 9:30am — 4 Comments

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