› Forums › General Melanoma Community › Stage 3 for now. So scared
- This topic has 22 replies, 7 voices, and was last updated 5 years, 10 months ago by
Suzana65.
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- July 15, 2019 at 2:51 pm
I was diagnosed in June of this year with invasive melanoma on my back . After WLD and sentinel lymph node biopsy one of the lymph nodes out of 6 was positive with approximately 0.35 mm burden. I am now scheduled for PET scan and to see an oncologist. I am paralyze with anxiety. It makes it worse that I already have an autoimmune issue. Sojgren ‘s syndrome and psoriasis. Can anyone with autoimmune issue in the forum help me understand if I’ll be eligible for any kind of therapy. Thank you.
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- July 15, 2019 at 4:06 pm
Hi there Suzana65, if you go to the 40:30min mark of the following link Dr. Mario Sznol a melanoma experts talks about treating melanoma patients with immunotherapy drugs with previous history of autoimmune issues. The link is from Research to Practice and might ask you to join, don’t worry they don’t spam you afterwards. Best Wishes!!! Ed http://www.researchtopractice.com/DOU119/Video/1?playlistIndex=2#t=43m58s-
- July 15, 2019 at 4:08 pm
I copied the link a little farther into the talk so here is the beginning part, and if you look down below it if written out as well. http://www.researchtopractice.com/DOU119/Video/1?playlistIndex=2#t=40m38s
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- July 15, 2019 at 4:19 pm
Suzana65, im Mike, i had to write just to say BREATH! try and slow your anxiety in a way you know how, iv been there we ALL have been there gettin the frightful news, if this can be helpful and not scare you more, i was stage 3b for 10 years! Surgerys alone kept me there! I mean, our situations are different but bottom line one can be stage 3 for 5, 10, 15, 25 years or MORE! I cant be of any help with your autoimmune disease, im sure theres a way around that, and thru immunal therapy, maybe that alone can be addressed! ( kill 2 birds with one stone!) Always know that 2019 is a great year to have Melanoma, so many weapons at our disposal!!! Take it easy sis, and keep us posted!
Im sure someone will chime in with your similiar situation…breath! Breath!-
- July 15, 2019 at 6:27 pm
Ha! I dont even know the answer to that wonderful question, i do know this, because my “pain” level is manageable, its easier to tolerate and be positive, so far the only tumor thats causing me pain is my stomach one, (the one that was suppose to be taken out!!) Naproxins help big time, id imagine if pain worsened, i dont know if my Positiveness would change, for now, today, im feelin ok…stay strong Suzana!
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- July 15, 2019 at 7:17 pm
So sorry to hear you had to join this little club. Two positive things to remember are that you had only one node affected and that there are a LOT of Stage III survivors out there. I am one and am nearing the 10 year mark.Not sure who your doctor is, but what’s very important when you are diagnosed with Stage III melanoma is that you are seeing an oncologist with experience in melanoma at a medical facility with a department devoted to melanoma. And yes, there are places like that: Johns Hopkins, Sloan Kettering, Dana Farber, University of PA, MD Anderson, etc. In your case, it would be crucial since you also are dealing with autoimmune issues at the same time. The emphasis on a melanoma specialist is because these folks will be the most up to speed on available treatments because they deal with this disease on a daily basis. We are light years ahead of where we were as little as 10 years ago when I was diagnosed. And, the only ones who will be able to keep up with that rapid of a pace are these specialists.
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- July 15, 2019 at 7:34 pm
Thank you Linny. I’m in New York area. Have been seen by oncological surgeon on Long Island for now. Having PET Scan on Wednesday and oncologist on Friday. Meanwhile gathering all my results to send to Sloan Kettering. Have already been in touch with them. Thank you for the encouragement and advice .
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- July 15, 2019 at 8:24 pm
Just got an appointment with dr. Paul Chapman at Sloan Kettering. Anybody has the sam dr.?-
- July 16, 2019 at 12:24 am
Hello,I fully understand the balancing act of having psoriasis and melanoma. At first, I thought I was going to have to stop treating the psoriasis, but that was not the case.
I can’t stress enough, find a doctor you really trust, and who understands and treats both diseases.
I suffered without help, as in medical for about two years after my melanoma diagnosis, and then I found a doctor who backed up my own conclusions about the diseases and my treatment.
I use an abbreviated schedule of narrow band UVB and methotrexate, which is working fo me. Current medical literature seems to indicate no increased risk with these treatments.
I was diagnosed as !a and I think you are more concerned with immunotherapy.
I’m not qualified to answer those questions, but you have given some links to follow, I hope they help, I had some similar questions about balancing the two diseases, and I was helpfully provided a link in my last post, ANGRY Second Opinion! You may find that link helpful.I truly understand the additional burden of having an auto-immune disease along with melanoma. Reach out if I can help.
Sue
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- July 16, 2019 at 3:38 am
Hi Suzana65, I also live on Long Island and go to SLoan in the city and same group of doctors who are wonderful. I’m sure they will come up with a great plan for you. I have been stage IV since Feb 2016. It’s totally normal to have this kind of fear so your not alone. Do you live in Nassau or Suffolk County? Heidi -
- July 16, 2019 at 3:39 am
Hi Suzana65, I also live on Long Island and go to SLoan in the city and same group of doctors who are wonderful. I’m sure they will come up with a great plan for you. I have been stage IV since Feb 2016. It’s totally normal to have this kind of fear so your not alone. Do you live in Nassau or Suffolk County? Heidi -
- July 16, 2019 at 2:49 pm
That was a good move to head to Sloan. There are other patients on this board who have gone to him. You may want to do a search on his name in the forum to see what they’ve said about him.The great thing about being so close to NYC is that not only is Sloan Kettering available to you, but so is Langone at NYU and they also have a world class melanoma team. It would not hurt you to give them a call to see of you can get an appointment with either Jeffrey Weber or Anna Pavlick. They’re located on 34th Street, so probably reachable by taking a train to Penn Station..
You’re going to be with the oncologist you choose for a while, so you want to make sure your personalities click. Getting a second or even a third opinion never hurts.
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- July 16, 2019 at 8:20 pm
Sorry you are dealing with all this Suzana. However, Chapman has a great rep in melanoma world. Weber and Pavlick are amazing as well. You can’t go wrong with either of those three and they are all excellently equipped to help you deal with melanoma as well as your pre-existing autoimmune disease.Yes at Stage III are likely to be eligible for the FDA adjuvant treatments of either anti-PD-1 product (Opdivo or Keytruda) or a BRAF/MEK combo if your tumor is BRAF positive. It will need to be tested for that. There are some current trials ongoing with the ipi/nivo combo for Stage III peeps, but we know that ipi is the bad boy of side effects in the immunotherapy realm, so that may not be your best choice given Sojgren’s and psoriasis.
Here is a primer regarding standard melanoma care that I put together that might help you understand various treatments better and be more prepared for a talk with your onc about your options. If you are interested: https://chaoticallypreciselifeloveandmelanoma.blogspot.com/2017/08/melanoma-intel-primer-for-current.html
I shared the link Sue referenced – folks with immune related diseases will need careful monitoring, but they can tolerate and have responses to immunotherapy! Here is a link to articles, with more links within: https://chaoticallypreciselifeloveandmelanoma.blogspot.com/2017/09/immunotherapy-for-melanoma-with-pre.html
So – as I always say…no matter who you are….no matter the stage…..melanoma sucks great big hairy stinky green wizard balls! But – there is hope. I am still here after being diagnosed with Stage IIIb melanoma in 2003 (no legit treatments then, unlike the world we have today!!!!) with progression to stage IV with lung and brain mets in 2010 – treated by Dr. Weber in a nivo only trial from Dec 2010 to June of 2013. I remain NED for melanoma today. AND – I had the pre-existing diagnosis of asthma. Yes, immunotherapy can cause pneumonitis – in anyone – and it did in me. But, I wheezed my way through it and am still here today. It won’t be easy, but you can do this, too!!! I wish you my best. celeste
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