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Old 05-05-2009, 01:22 PM   #1
Lani
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the cavalry may be coming over the hill! read first and last sentences!

Kaiser Health News/Philadelphia Inquirer examines proposal that would allow people ages 55 to 64 to buy into Medicare


Tuesday, 5-May-2009




Kaiser Health News/Philadelphia Inquirer on Monday examined a plan being touted by Senate Finance Committee Chair Max Baucus (D-Mont.) that would allow people ages 55 to 64 to buy into Medicare. The plan would target people who purchase insurance on the individual market or have no insurance because of unemployment.

About four million people between ages 55 and 64 are uninsured, according to the U.S. Census Bureau. While people in that age group are less likely to be uninsured than others, they are more likely to have serious medical problems and difficulty finding affordable coverage, according to Kaiser Health News/Inquirer.

Most states allow insurers to reject applicants who have pre-existing medical conditions. A 2006-2007 survey by America's Health Insurance Plans showed that individual insurance plans rejected 17% to 29% of all applicants ages 50 to 64, compared with 10% of those ages 30 to 34. In addition, people in their 60s often pay as much as three to six times more for coverage than people in their 20s, according to Georgetown University Health Policy Institute research professor Karen Pollitz.

The Baucus plan would allow people to buy into the program until comprehensive health reform legislation is approved. Complicating the debate is the "tricky question" of whether federal subsidies would be provided for people enrolling in Medicare early, according to Kaiser Health News/Inquirer. Baucus' current plan would not provide subsidies for younger beneficiaries. His proposal does not include cost estimates, but a similar plan analyzed by the Congressional Budget Office found that premiums would cost $7,600 per year for those ages 62 to 64.

Republicans who oppose the early buy-in plan say that rather than expanding Medicare -- which the federal government estimates will run out of reserve funds by 2019 -- the government should promote private sector ideas. AHIP spokesperson Robert Zirkelbach said the insurance industry opposes expanding Medicare because it "underpays providers," who then charge private insurers more to make up the difference. He cited an industry pledge to accept all applicants if all people are required to obtain coverage.

Baucus also has proposed allowing adults with incomes of up to 100% of the federal poverty level to enroll in Medicaid and eliminating the requirement that disabled people younger than age 65 wait two years before enrolling in Medicare
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Old 05-06-2009, 04:52 PM   #2
Rich66
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Mixed feelings on this one. Knowing that some docs are opting out of Medicare and especially Medicaid arrangements already, what happens when there is no private sector payments to, albeit unfairly, cover the difference? Rationing a la NICE? Even less doctors when there is already a shortage of GPs? Of course, I wonder about the cost of visits. Eg. Requested payment for a 30 minute onc vist: $320?? Medicare knocks that down severely(around half) and pays 80%. Not sure if Medicaid pays less. But I imagine private sector insurance, like mine, pays the full price. I guess I feel conflicted about this because I appreciate the flexibility my folks have but wonder whether it would be sustainable in similar fashion if this was extended to all. Even with them, I have already encountered invisible rationing in the sense that things weren't offered simply because the doc assumed they weren't covered by Medicare. First off, they turned out to be wrong..it was covered. Secondly, they only looked into it after a meeting was held with multiple specialists and I made it clear that if it was medically advantageous, "do it" and it would be paid for out of pocket if need be. I wish doctors would stay out of the finances and just present medical options/opinions. I would like to see a national examination of nationalized health care around the world and see what does and doesn't work...and seriously consider the dynamics of our own country relative to that. Some countries have NH but most folks there have supplemental private insurance. I think Australia is like that. And furthermore...(blah blah blah)
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Old 05-06-2009, 05:08 PM   #3
Nancy L
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I am a retired US benefits manager from a fortune 25 company. $7200 for the 62-64 age group is a bargain. I have been retired for awhile but I believe the real cost for a PPO plan is closer to $1K/mo. Look at your EOBs and add up the payments made by you and insurance. I live in a retirement community and those in the 62-64 age group have other expensive health care so it is not just cancer---heart stents, heart bypass, knee replacements, cataracts, etc. If the government gets involved in more health care, you can count on rationing.
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Old 05-06-2009, 06:37 PM   #4
Lani
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My unusual title for the thread had to do with the fact that until now

those with cancer had to wait two years after they qualified for disability to become eligible for Medicare and when they become disabled they may lose their employer provided health insurance, leaving them in the lurch.

I never understood why that was.
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Old 05-10-2009, 05:12 PM   #5
Joan M
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Lani,

Thanks for this post.

I sent an e-mail last week to my local congressman about the 2-year wait to receive Medicare for advanced cancer.

Currently under the law, kidney disease patients and ALS patients get Medicare automatically without having to wait two years.

Joan
__________________
Diagnosed stage 2b in July 2003 (2.3 cm, HER2+, ER-/PR-, 7+ nodes). Treated with mastectomy (with immediate DIEP flap reconstruction), AC + T/Herceptin (off label). Cancer advanced to lung in Jan. 2007 (1 cm nodule). Started Herceptin every 3 weeks. Lung wedge resection April 2007. Cancer recurred in lung April 2008. RFA of lung in August 2008. 2nd annual brain MRI in Oct. 2008 discovered 2.6 cm cystic tumor in left frontal lobe. Craniotomy Oct. 2008 (ER-/PR-/HER2-) followed by targeted radiation (IMRT). Coughing up blood Feb. 2009. Thoractomy July 2009 to cut out fungal ball of common soil fungus (aspergillus) that grew in the RFA cavity (most likely inhaled while gardening). No cancer, only fungus. Removal of tiny melanoma from upper left arm, plus sentinel lymph node biopsy in Feb. 2016. Guardant Health liquid biopsy in Feb. 2016 showed mutations in 4 subtypes of TP53. Repeat of Guardant Health biopsy in Jana. 2021 showed 3 TP53 mutations, BRCA1 mutation and CHEK2 mutation. Invitae genetic testing showed negative for all of these. Living with MBC since 2007. Stopped Herceptin Hylecta (injection) treatment in March 2020. Recent 2021 annual CT of chest, abdomen and pelvis and annual brain MRI showed NED. Praying for NED forever!!
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Old 05-10-2009, 08:39 PM   #6
hutchibk
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The worrisome part is that advanced breast cancer could well end up a "rationed" condition in the not too distant future, when bureaucrats (like NICE in UK) are tapped to pick winners and losers due to cost vs. statistical benefit. I worry day in and day out about when my treatment plan might be "opted" out of the system in order to equalize the system to pay for the 16% who allegedly don't have access. I am reasonably certain that in the not too distant future, "cutting medicare payments" (as has been touted by the folks running things as a way to cut deficits) means exactly that... picking winners and losers.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
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Old 05-11-2009, 09:25 AM   #7
Rich66
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If one qualifies for disability, isn't that an SSI or medicaid issue for health insurance? (If not Medicare age)
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Old 05-11-2009, 09:40 AM   #8
hutchibk
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No, if you qualify for disability and you are under 65, you currently qualify for Medicare, with a 24 month waiting period. You don't have to take Medicare, but you only have a 6 month window to decided whether you want it or not... after that, you don't get another chance to opt in.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
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Old 05-11-2009, 10:04 AM   #9
Rich66
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Hmmm..."qualify for Medicare, with a 24 month waiting period."

I'm trying to imagine an analogous situation that would make sense:

"You got the job! You start in 2 years."

Nope.

How long does COBRA last?
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Old 05-11-2009, 10:38 AM   #10
hutchibk
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Can't tell you anything about COBRA. I always carried my own individual PPO insurance, as I never liked the employer offered options. And I was self employed much of the time as well. I had 2 very short periods under employer provided ins. - first was an HMO and I got out from under that stranglehold quickly. The other was a PPO with one of the biggest providers, and they were so heinous, questioning almost every claim I submitted, that I fired them and went back to individual coverage. I was always of the mindset that I would rather carry my own chosen plan and work a little harder to pay for it than have my care rationed and dictated by an employer based plan or a sub-par carrier.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
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Old 05-11-2009, 11:00 AM   #11
StephN
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Posts: 4,128
A couple of thoughts on this one.

First, Lani is right to point out that some legislators have decided that the 2- year wait for poverty level people under 65 may should go by the wayside. But what about the REST of us??? I was just able to manage it!

I am trying to decipher the "buy-in" part.
I know that Fauxgypsy has been having a hard time keeping coverage, due to qualification restrictions. This may help those in her situation.

About the cost reaching $1,000/mo for a individual PPO. That sounds much higher than average. I had lunch last week with a college friend who is now 62. She had a stroke and can no longer practice law. BUT, she does not qualify for disability! She has numerous health issues and carries her own individual preferred provider insurance (the same one I had, BTW), which now costs her in the $700/mo range for full coverage.

Like Brenda, many of us budget our lives to have security in our health coverage. Means I did not have a new car, or redo my kitchen, but I had the coverage when it counted.

I now have a Medadvantage Plan using my old carrier's plan as my supplement. So far not a peep from them for any of my care in two years.

I don't want to have to change what I have and I will find a way to keep paying the lower premium.
__________________
"When I hear music, I fear no danger. I am invulnerable. I see no foe. I am related to the earliest times, and to the latest." H.D. Thoreau
Live in the moment.

MY STORY SO FAR ~~~~
Found suspicious lump 9/2000
Lumpectomy, then node dissection and port placement
Stage IIB, 8 pos nodes of 18, Grade 3, ER & PR -
Adriamycin 12 weekly, taxotere 4 rounds
36 rads - very little burning
3 mos after rads liver full of tumors, Stage IV Jan 2002, one spot on sternum
Weekly Taxol, Navelbine, Herceptin for 27 rounds to NED!
2003 & 2004 no active disease - 3 weekly Herceptin + Zometa
Jan 2005 two mets to brain - Gamma Knife on Jan 18
All clear until treated cerebellum spot showing activity on Jan 2006 brain MRI & brain PET
Brain surgery on Feb 9, 2006 - no cancer, 100% radiation necrosis - tumor was still dying
Continue as NED while on Herceptin & quarterly Zometa
Fall-2006 - off Zometa - watching one small brain spot (scar?)
2007 - spot/scar in brain stable - finished anticoagulation therapy for clot along my port-a-catheter - 3 angioplasties to unblock vena cava
2008 - Brain and body still NED! Port removed and scans in Dec.
Dec 2008 - stop Herceptin - Vaccine Trial at U of W begun in Oct. of 2011
STILL NED everywhere in Feb 2014 - on wing & prayer
7/14 - Started twice yearly Zometa for my bones
Jan. 2015 checkup still shows NED
2015 Neuropathy in feet - otherwise all OK - still NED.
Same news for 2016 and all of 2017.
Nov of 2017 - had small skin cancer removed from my face. Will have Zometa end of Jan. 2018.
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Old 05-11-2009, 11:45 AM   #12
hutchibk
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Once I decided to opt in to Medicare, I also researched for a good medigap supplement. Per month I pay $96 for Medicare, $150 for supplement, and $65 for prescription part D, all totaled = $311 per month. When I dropped my private insurance I was paying $400 a month.

The only thing I gained by opting in was protection from rising monthly premiums...

What I gave up was:
1) surgical pre-certification so I would know what would be covered and what might not be covered. With medicare they don't tell you up front, you have to wait for determination and "surprises" after the fact.
2) a somewhat simple appeal process for denied claims with consumer protections under the state board of insurance. With medicare, it is a tedious and arduous process to figure out their rules, restrictions, coverage codes, etc. and even then, you have no consumer support. You have to live with their decisions.
3) restrictive rationing decisions like it is not medically necessary for a woman over 50 to see the GYN yearly for annual checkups, even if she is a breast cancer patient.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."

Last edited by hutchibk; 05-11-2009 at 01:10 PM.. Reason: add
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Old 05-11-2009, 12:48 PM   #13
DanaRT
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Posts: 261
A 24 month waiting period--I would be in serious trouble. This is very interesting. We have had a private policy for several years. My husband never wanted to be tied to a job because of benefits. Our premiums are about $700. a month with a very high deductable. It has worked well for us, especially with now having had breast cancer. I am sure our premiums will continue to rise.
__________________
-Dana-

]
Diagnosed - Nov. 2, 2007 at 45
Lumpectomy - Nov. 13, 2007
Tumor 1.2 cm
Stage 1 Grade 3
ER/PR - Her2 +++ (3.8)
Taxotere/Carboplatin/Herceptin- 6 rounds
Neulasta
Radiation 33 treatments - will be done 6/6/08
Herceptin through 12/08
12/07 MUGA 61%, 4/08 MUGA 60%, 7/08 MUGA 64%
three wonderful daughters, a terrific husband,
Life is Good
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