MPIP: Melanoma Patients Information Page

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The MPIP is the oldest and largest community of people affected by melanoma hosted through the Melanoma Research Foundation. It is designed to provide support and information to caregivers, patients, family and friends. Once you have been touched by melanoma—either as a patient or as a family member or friend of a patient—you become part of a community. It is not a community anyone joins willingly. But if you must be part of this group, you will find no better place to find the tools you need in your journey with this cancer, and the friends who can make that journey more bearable.

The information on the bulletin board is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.

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Rocklove's picture
Replies 20
Last reply 9/15/2010 - 12:46am

Had scan CT scan results today. There was a 70 to 80% reduction in overall tumor size from 1st Bio-Chemo round started in March 2010.

We finally crossed the main bridge and will start with maintenance protocal Friday August 13th.
Maintenance will be for 2 days per month with IL-2 infusion and will go on for 6 months then switch to every other month for another 12 months. There will be self injections of GMC-SF and IL-2 in between hospital visits.
The doctor said I should have no problem working while on the maintenence protocal.
I feel so blessed and fortunate getting this far with the treatment.
I appreciate all the prayers and positive thoughts from so many of you.
Rocky (Stage IV Liver Mets)

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Jydnew's picture
Replies 4
Last reply 8/10/2010 - 1:35pm


Wanting to share the good news with those of you who might be just starting this scary journey with melanoma.  My husband had his semi-annual onco appointment yesterday and got the fantastic news that he remans NED.  Still seeing a little hypodensity on his liver, but it's been stable for at least 2 years now, so not a concern.

He was diagnosed at age 26 at stage iiia, 1.3mm depth on his right tricep.  Surgery to remove the lesion and an SNB revealing micromets, followed by surgery to remove all the nodes in the basin.  He has been NED ever since, with annual scans, semi-annual bloodwork and onc visits.

He is now 34 and has accomplished so much in life since his diagnosis, including the births of our children (one passed away, and the other just turned 1!), buying our dream house, earning a teaching certificate and a master's degree, and finding rewarding employment as a science teacher.  Life has been good to us, even through the toughest times...

Best to you all,


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ipi in DC's picture
Replies 6
Last reply 8/9/2010 - 12:08pm

Hi JIm,

Just checking in on you and how your first days are going, I meet with everybody today and start treatment on the trial tomorrow.


Fully rely on GOD & try not to ruin today by worrying about tomorrow

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sharmon's picture
Replies 8
Last reply 8/9/2010 - 8:17am


Brent has been on the GSK MEK trial at MD Anderson since Feb 2010.  I keep reading about the B raf trials not being durable.  He will be scanned on the 16th of this month. This is month 7 for him.   He is on the highest dosage for the trial at 2.5 mgs .So far we have overall tumor shrinkage of about 30%.   The side effect of the rash is our worse concern.  He is now taking antibiotics for the sores.   It  seems that there is not a lot of info yet on the MEK  trial results from GSK.   I am trying to closely follow this forum but may have missed the information I am looking for.   I do not want to be scrambling to find a combination trial at the last minute, so any information would be helpful.  We have specifically asked our oncologist about a plan B and  he is dismissive or our question wanting us to wait and cross that bridge if we need to.

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I was able to get in chat for a few minutes on the third. (My time and computer availability problems) NOT MRF problem. 

However when i next got to a place i could get connect to the Internet again, and before I started opening a window to the MRF, I started hearing the chat room bonging.  I then had the following occur.


JerryfromFauq: Why was my name on here when I came on line, (not to the MRF board).  I
heard the bonging , but had no windows open to the MRF.  Went to the off-topic BB and it said
I and Laura were in chat.  I had to go to the MRF website and log in then click "

JerryfromFauq: "Click here to chat"  When the chat window finally came up, Laura was gone.

 I have not been  on line anywhere for a couple of days!



PS do  like some of the additions like the spell check and images.

I'm me, not a statistic. Praying to not be one for years yet.

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Knutes Pam's picture
Replies 10
Last reply 8/9/2010 - 12:25am

Knute had gamma knife last wednesday for the two new brain mets.  We have started the weaning process from the steriods and hope to be able to get in an IPI trial in Sept.  He is doing well and is active on Facebook with the smaller screen provided by his I phone his visual problems are lessened.  A complete computer screen has too much visual information at one time.  It is a crazy side effect of his brain mets and their locations. We hope to get after those new lung mets in the near future.


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skysar's picture
Replies 11
Last reply 8/16/2010 - 8:03pm

Spoke with Dr. Hwu at MDA yesterday regarding the IPI/Temodar trial.  If you are enrolled in this trial at MDA,  I would be interested in finding out how you are tolerating side effects and also handling travel if you don't live in Houston?

Thanks for your help.


Stage IV, lung mets

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skysar's picture
Replies 1
Last reply 8/6/2010 - 4:39pm
Replies by: Jim in Denver

Thanks for your input.  In addition to MDA I have an appointment with Jeffrey Weber at Moffitt in Tampa next week and will compare notes.  If MDA is the place, I have a starting date of 9/3.  We will see what Moffitt has to offer.

I would like to continue receiving your input....progress, side effects, etc.

Take care.

Sue (Atlanta)


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ocularmonster's picture
Replies 4
Last reply 8/7/2010 - 7:08pm
Replies by: sselig, jag, LizzM

we may have a good option for my husband's treament of ocular melanoma that metastized to his liver.  SIRT at Emory in Atlanta.  It is readioembolization. Has anyone experienced this treatment?  Ocular melanoma is resistant to systemic chemo treatment, therefore there have been very few options.  He was not a candidate for liver resection so this blast to his tumors may work.  side effects are minimal and it only targets the liver....

feel like a million bucks, look good, thought I was in perfect health until a MRI revealed my liver monster.

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MaryBZ's picture
Replies 1
Last reply 8/6/2010 - 7:11pm
Replies by: KatyWI

Hi Katy,


I noticed you live in Appleton.  I am in Little Chute (we're practically neighborssmiley)  Just wondering if all your follow up appts are in Milwaukee or if you see an oncologist in Appleton?  I did get a second opinion from Dr. Albertini in Madison (loved him-very caring and compassionate) but I didn't want to drive to Madison for all my follow ups so currently I see Dr. Guenther (smart man but our personalities don't "jive") at AMC.  Just curious cool



You don't know what your future holds but you know who holds your future!

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jeanne harvey's picture
Replies 17
Last reply 8/7/2010 - 6:08pm


For 7 years, my sis, Jan Brockelman (JanB) fought a very courageous battle with dignity and persistence.  She lost that battle last night. Jan was an amazing wife, mother, sister, daughter and friend with a smile that could light up a room.   Jan wanted me to thank each and every one of you for your support, knowledge and guidance through this process.  This board was very special to her and to me.


Keep fighting, learning & laughing. Jan wouldn't want it any other way!








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Anonymous's picture
Replies 0



I pray for Jenna is she doing?? I hope that she is responding to IPI.

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KellieSue's picture
Replies 9
Last reply 8/7/2010 - 2:15pm

After finishing the ALT-801 trial on July 2nd I continue to have positive results.

CT scan today showed stable disease! I would have liked to have seen more shrinkage but

the Dr. said I could continue to have an immune response months down the road! I'm hoping for that! :)

Haven't been around in a bit but glad to come back and keep in touch with everyone.

Kellie(from Iowa)

Cancer Sucks. I'm so not done kicking cancers ass! I have a lot of life left to live

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My oncologist advises me that I can have injection, which I believe is done under the skin in the patient's stomach, to boost my white blood cells, presumably to help fight any infections with chemotherapy. He did warn me that such an injection sometimes give people bone pain which does not respond to normal painkillers. Further he said sometimes patients have to go into hospital for treatment to cope with the pain. I don't know the name of the drug used for the injection and was wondering if anyone has had such an injection -- if so what side-effects did they suffer, and for how long? Any information would be appreciated


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Anonymous's picture
Replies 3
Last reply 8/8/2010 - 5:07pm

My wife is getting ready to start WBR and I am curious if anyone on this board has been through this treatment before.   Looking for any positive notes if possible as well as side effects and expectations after treatment both immediate and long term.  Thanks for the help

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