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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MelanomaMike's picture
Replies 23
Last reply 7/26/2020 - 11:08pm

Hello fellow Warriors, i hope this finds you all in good health whether it be NED, remission or stable, either or is a victory, and if your still struggling with your team to fight these bastards, keep up the strength that got you this far, i didnt realize the strength i had to endure this whole last 4 or 5 months back when my Sigmoid tumor pain had hours & hours of breaks between them & ESPECIALLY this last 30 days when my tumor pain became a 24 hour torture device, i held on to faith that something good is gunna happen very soon & it did, surgery...
Well folks, where do i began, to start, i made it through what i would call Hell On Earth. Having a tumor, a 4 inch Demonic Mass in your Sigmoid section of our intestine is no joke, especially when my team & i decided to let it be to see if just one more infusion will have shrunk it by a few Centimeters (at the VERY least) but no, story of my life, my OX40 & ICOS combo that im doing in my trial is doing a good job on all my other tumors but not on the big A-hole, same situation with the other 6cm blob on my left side under my ribs remember? Gave us the middle finger, then back in my Pembro, Ipi & Nivo days at Kaiser, my 3inch Demon Ball in my right lower lung lobe defied & gave its middle finger as well while other tumors shrank, disappeared or stayed humble and submissive. Once again i took one for the team cuz, maybe to have the meds take care of it is a hell of a lot nicer then having intestinal surgery which wasnt half bad like i thought, i woke up without a poop bag on my side AND! no staples or stitches! Very small incision to! And he did an "Open" type, not the Laparoscopic type, my surgeon Dr. Mark B. Faires (look him up he's great! he has a write up in the New England Journal of Medicine! He deals mainly with Melanoma) anyways, he said its at a size that he needs to pull out my Sigmoid & cut the section out & solder me back up, he could see why my pain was SOOO Severe, the Demon was wrapping its "tentacles" around the nerves in my lower spine, pushing & shoving its way anywhere it wanted to grow in me, huh, explains the Horrific, constant deep, excruciating, up all night, up all day, crying out in pain i was in! I'll never forget those last 3, 4 weeks after deciding to wait one more infusion (3weeks) the day of the scan the report comes in (they have scanners & readers on premises) that its getting larger, (grew from 7.0cm to 9.1cm in 2 months) surgery is eminent & Dr. Hamid orders it ASAP on June12th at Cedars Sinai, the Mel Demon was extracted & instantly "Relief" was there, well, once i woke anyway, even in my doped up stupor i found relief and cried because of the nightmare it caused me & my wife. Up at night messaging my lower back, heating pad, Naproxins, and the not eating, FEAR of eating, wheres it gunna go? I went from 189 to 140 in a month or so, thats to fast, much to fast, I never used opiates out of fear of even more constipation, at 3 weeks before my surgery, that would be the last bowel movement i would have or could have til "after" my surgery, the mass was blocking 98% a lil' gas could get thru once in a while thank goodness! can you believe that? A lot of the pain to was the feces "pushing" against the 9.1cm mass, trying to move along & out the door, picture a 1inch minimally "flexible" pipe with a 4 inch dia. ball stuck inside of it, yep, that was me in a nutshell guys....
Im so glad its overwith, dont take one for the team like that if yer not willing to put up with the possible pain that could occur afterwards, once it became an every day "constant" pain towards the end, then it got worse, health declined dramaticly..not fun...
But Anyways, ive wrote a novel already, i know i have some fans so, you guys will love a good read haha..iv been healing nicely, ill get back on soon ok? Oh!!!! A quick shout out to sister Chuco! I just met her at our mutual place The Angeles Clinic last Thursday, She heard my name being called out then said "Mike? Melanoma Mike? I was blown away! I wish we could have talked longer, off she went to do her thing & i went to start back on my treatment downstairs, small ya all, and ill be back, you can take that to the bank...

What doesn't kill you only makes you wanna Go After It And Kill It!

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Gene_S's picture
Replies 5
Last reply 7/13/2020 - 2:54pm

July is the mark of my husbands 8th NED Anniversary!

He was in a Clinical Trial that started in March 2011 and became NED in July 2012. When he became Stage IV with an
unresectable lesion pushing on the C1 C2 Cervical spine, a few subcutaneous lesions, lesions in the lungs and lesions in the liver.
His trial was Ipi (Yervoy) 10 mg/kg IV for every 3 weeks and GMCSF (self injected every day for 14 days and then 7 days off).
He remained on this regiment until Dec. 2013.

He does have vitiligo of the eyebrows, parts of the beard and face down to the collar bone. He also has a few white blotches
on his arms. His adrenal gland does not work properly and has to take 5 mg of prednisone daily.

If you would like to read more about his journey, which started in Jan. 2008 with Stage III and 4 surgeries later he became
Stage IV, check out his profile page.

Judy (loving wife of Gene - Stage !V and NED for 8 years)

Live 4 today. Thank God for all he has done for us. Looking forward to enjoying tomorrow.

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caman's picture
Replies 5
Last reply 7/3/2020 - 1:40am

Has anyone here with stage 3 melanoma, started neoadjuvant therapy and had such rapid and great response from the immunotherapy that you decided to skip the surgery and the removal of nodes?

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THMoore's picture
Replies 2
Last reply 7/21/2020 - 5:15pm
Replies by: Bubbles

I’m am BRAF - for the V600 but positive for the K601E BRAF gene. I am researching and am wondering if anyone in this Forum has the K601E gene? If so, what treatments have you and how are you doing?

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AmyM's picture
Replies 9
Last reply 7/15/2020 - 4:16am

I had posted in April about my dad who was recently diagnosed with brain mets. I wanted to give an update and also ask further advice.
Dad is on targeted therapy enco binni combo & an MRI after 5 weeks of treatment showed shrinkage. It was a satisfactory response but not enough to enable sterotactic radiosurgery. They said they wouldn’t have usually scanned again that early but because I chased it they did which was helpful to see things were moving in the right direction.

Dad was on a high dose of steroids to start and now has been off steroids completely for a week. In addition to the 3 intracranial lesions dad has a Sigatal sinus region lesion and 1 liver lesion. Today we had a review and the doctor said the liver lesion has also shrunk which is great news. An MRI brain is now scheduled for mid July which means he will be 13 weeks on this targeted therapy combo. I am so thankful things are going well and I’m hoping we get further shrinkage to allow sterotactic radiotherapy.

When dad was initially started on the targeted therapy the consultant had said it usually only works for 3 months or so and things would then progress. Immunotherapy wasn’t an option due to high dose of steroids but I’m wondering now as steroids are off should we be thinking about switching to immunotherapy or staying with targeted therapy?
I had expressed my concerns regarding a window of opportunity for immunotherapy and she said we would be continuing on targeted therapy until it no longer worked. Is there people on this forum who are on targeted therapy longer term? I’m not sure if I should be pushing consultant on thinking about switching to immunotherapy as it stands we won’t speak to anyone until end of July. Stereotactic radiosurgery is still on the table if things continue to shrink however when I asked today she said they would usually only use it for people who have max two brain lesions. So I’m concerned he’s already ruled out even if we get all lesions to shrink below 2.5cm. From memory I think lesions are 1.9, 2.3 and, with the Sagital sinus lesion being 4cm.

Dad is feeling great, he’s 56 tomorrow, still working, strong and active so I just want the best treatment and care for him.
Sorry I have wrote an essay! We are being treated in the NHS in the UK.

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Replies by: MelMel, Bubbles

I have been taking the meds for 13 weeks and due to the fever and chills after taking the medication I had to stop twice.. But currently back on the meds I continue to have fever and chills for one to two hours 4 to 5 hrs after taking the medication.
I came to this group to see what specific procedures have helped to address fever and chills
I and currently taking 650 mg of Tylenol 1 hr before each of the two daily doses of medication. I have also been advised that 5 mg of prednisone is also available to curb the fever
I have stage 4 lung cancer with braf 600 e and without the medication the disease will progress. For the first two months the tumor reduced 30%. But with continuation of fever and chills I am struggling
Given that Melanoma has a much longer history, research backing it and clinical knowledge compared to the Veterans administration in San Diego where I am the only patient with Braf 600e lung cancer and research is limited. The excellent medical staff have reached out to the melanoma staff for feedback but I am also requesting your help because you are and have been in the trenches for long time and may have pertinent information to address this critical concern.

Michael mcdermott

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sj's picture
Replies 3
Last reply 7/4/2020 - 3:50pm
Replies by: sj, caman

Looks like the pain in my hip is related to arthritis I have in my back. That's a relief!

NED after 6 months, scan results are unremarkable. Hopefully I remain unremarkable for the foreseeable future!

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sing123's picture
Replies 2
Last reply 7/6/2020 - 9:56pm
Replies by: sing123, Bubbles

Hi I recall that someone recently posted his email address. Was it you Edwin? Will someone please post it here?

Thanks and Best to all of you!


Diagnosed April 2018; Stage IIIc; 1 excision on head, started immuno (Opdivo) May 2018; new spots Oct. 2018; second surgery; continuing on Opdivo, finished Opdivo in March 2019

I'm Still Here!!!

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DT1985's picture
Replies 3
Last reply 7/10/2020 - 4:01pm
Replies by: ed williams, DT1985, tkoss

Happy 4th folks. Hope you all are enjoying the weekend.

So quick recap of me. Diagnosed with Stage 3A back in February. Mole was on the back of my calf, 1.5mm breslow, cancer cells on one lymph node in my groin at less than .5mm. Surgery to remove mole & lymph node went well. Saw Dr. Postow after and a few others, all recommended no treatments since the lymph node was removed and had very few cells. Now I’m getting routine Derm/CT/MRI/PETs (all clean so far)

What’s changed is my genetic test has come back as CDKN2A+. So now aside from melanoma I have pancreatic cancer to worry about. However I’m a fairly healthy and young guy (35, 6’2, 210lbs) and probably won’t have to worry about the pancreatic stuff until later in life.
But with this new genetic discovery, will I constantly develop melanomas now? Should I avoid the sun like a vampire? Should I completely remove every mole on my body? (I have maybe 20 or so besides freckles, not many)

With CDKN2A+, did the road to living a cancer free life just get impossible?

Thank you for help and advice.

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Jubes's picture
Replies 11
Last reply 7/15/2020 - 8:19pm

Hi All

I haven’t posted for a while., but I think of you all
often, especially Les, and wonder if she ever made it to Italy...

I am still NED since my lower lung lobe resection in Nov 2016

I am taking Humira every three weeks for arthritic side effects and it is working just fine

I hope you are all hanging in there. We live in amazing times with fabulous health professionals.... at least those of us lucky enough to live in first world countries

I hope the Covid virus has not set anyone back. Time has stood still here in Australia while we try to get on top of it. And in many ways I love that! No traffic no pollution. No traffic accidents! I’ve been playing golf and practising my instrument. No one can travel so there’s no FoMo.

All the best


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BRR's picture
Replies 13
Last reply 7/8/2020 - 6:50pm


My dear father had VAT surgery in March ( 3 melanoma mets) and no other treatment, only CT for 3 m( his history is on my profile- from stage 2c to 4).
CT 11.06 confirmed new 5 new metastasis in the hilar part of his left lung. Next week he starts OPDIVO therapy.
How this therapy received? What are side efect?
He is 71 years old and in good health.
What are the experiences with this therapy?

I am so sorry for my bad english.
Thanks a lot to everybody.

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MarkR's picture
Replies 13
Last reply 7/26/2020 - 10:18pm

Hi All
Is anyone aware of any Us facilities that can offer TILS therapy either through trial or privately funded. The option in the UK has stopped private paying TILS as they gear up for trials so looking outside the UK at Israel and maybe US. If anyone has paid for TILS in the US I would be grateful for an idea of costs please.

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Mismich76's picture
Replies 4
Last reply 7/16/2020 - 4:21pm
Replies by: lbd, AmyM, sandyd77, Bubbles

Anyone on or has been on Mektovi / Braftovi? How did it work and any side effects you can share with me. I will start both on Monday, June 13, 2020. Thanks

misty crocker

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Shelby - MRF's picture
Replies 2
Last reply 7/20/2020 - 10:55am

Dear MPIP Community,

Our partners at OncoSec are looking for a cutaneous melanoma patient or caregiver to share their story as part of a virtual media tour. At this time, they are looking for a patient and caregiver who:

  1. lives in the Northeast area of the U.S.
  2. has participated in a clinical trial

If this opportunity is of interest to you, please contact me at so that I may share your contact information with the OncoSec team. Thank you!

All the best,

Shelby - MRF

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maryb-z's picture
Replies 7
Last reply 7/28/2020 - 6:28pm

My district is returning to face-to-face instruction in September. I asked my nurse practitioner if there were additional precautions I should take as I am currently on Opdivo as well as low dose prednisone daily. She advised the same precautions as our health department suggests. I'm a bit anxious to say the least. I'm 52 years old and will be in contact with many students daily as I am a specialist teacher. Any thoughts? TIA

No One Fights Alone

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