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	<title>Melanoma Research Foundation | Christinad | Activity</title>
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				<title>Christinad replied to the topic Lung Mets? in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/lung-mets-2/#post-280503</link>
				<pubDate>Tue, 15 Oct 2024 04:11:43 -0400</pubDate>

									<content:encoded><![CDATA[<p>I had a similar report after two years of immunotherapy. A scary time for me! Was told lung progression until 3rd scan (1 CT and 2 pet scans). The radiologist who read the third scan read the findings as infection or inflammation, likely pneumonitis &#8211; a reaction from immunotherapy. My oncologist wasn’t convinced I had progression because each s&hellip;<span class="activity-read-more" id="activity-read-more-126905"><a href="https://forum.melanoma.org/forums/topic/lung-mets-2/#post-280503" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic I urgently need help or advice in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/i-urgently-need-help-or-advice/#post-279880</link>
				<pubDate>Fri, 19 Jan 2024 04:39:00 -0500</pubDate>

									<content:encoded><![CDATA[<p>I am now a type 1 diabetic and on insulin after 2 1/2 years of immunotherapy. I ended up in the ICU with diabetic ketoacidosis. I’m still on immunotherapy but unfortunately will be insulin dependent for the rest of my life. </p>
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				<title>Christinad replied to the topic Simple question or not in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/simple-question-or-not/#post-276352</link>
				<pubDate>Sat, 12 Feb 2022 04:48:07 -0500</pubDate>

									<content:encoded><![CDATA[<p>I too have multiple bone Mets. Fortunately, I don’t have pain other than mild aches here and there. So far I’ve only had one scan that showed an overall improvement in all areas. Next one is end of March. My oncologist said if I reach a complete response, I’d have to do immunotherapy at least another year before having a discussion about stopp&hellip;<span class="activity-read-more" id="activity-read-more-13679"><a href="https://forum.melanoma.org/forums/topic/simple-question-or-not/#post-276352" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Still NED - Almost 5 Years in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/still-ned-almost-5-years/#post-276292</link>
				<pubDate>Mon, 07 Feb 2022 02:14:45 -0500</pubDate>

									<content:encoded><![CDATA[<p>Congratulations &#x1f497;</p>
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				<title>Christinad replied to the topic I rang the bell today, folks! in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/i-rang-the-bell-today-folks/#post-276247</link>
				<pubDate>Sat, 22 Jan 2022 04:26:49 -0500</pubDate>

									<content:encoded><![CDATA[<p>Great news! Congratulations!! 🙂</p>
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				<title>Christinad replied to the topic NED for 2 Years in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/ned-for-2-years-2/#post-276180</link>
				<pubDate>Tue, 04 Jan 2022 01:24:20 -0500</pubDate>

									<content:encoded><![CDATA[<p>Congratulations </p>
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				<title>Christinad replied to the topic Happy New Year - an update and some intel in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/happy-new-year-an-update-and-some-intel/#post-276173</link>
				<pubDate>Mon, 03 Jan 2022 19:28:17 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you for sharing the video, Ed. I watched the whole thing. Interesting stuff! The only negative part for me was the OS predictor tool. I was reminded of my reality as I checked almost every box on the tool. I had to have a pep talk with myself and give myself the same advice I give my patients. We are all different and can beat the odds!&hellip;<span class="activity-read-more" id="activity-read-more-11917"><a href="https://forum.melanoma.org/forums/topic/happy-new-year-an-update-and-some-intel/#post-276173" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Happy New Year - an update and some intel in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/happy-new-year-an-update-and-some-intel/#post-276167</link>
				<pubDate>Mon, 03 Jan 2022 03:10:46 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi! I read your blog….thank you for sharing. I read you still suffer from neuropathy. Just wondering if you’ve ever tried acupuncture? It helped me a great deal. My neuropathy is pretty much gone now and at one point it was excruciating pain to put weight on my feet. It continually improved after each acupuncture session. Coincidence or pla&hellip;<span class="activity-read-more" id="activity-read-more-11838"><a href="https://forum.melanoma.org/forums/topic/happy-new-year-an-update-and-some-intel/#post-276167" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Hair loss/thinning in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/hair-loss-thinning/#post-276155</link>
				<pubDate>Thu, 30 Dec 2021 06:01:10 -0500</pubDate>

									<content:encoded><![CDATA[<p>Grace, I’m happy for you that it is not too noticeable. My new hairs growing back in are white. Has that been your experience as well? You’re a little younger than I am, so maybe not, but I now have white lashes, brows, and lots of white hair changes all over. </p>
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				<title>Christinad replied to the topic Hair loss/thinning in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/hair-loss-thinning/#post-276154</link>
				<pubDate>Thu, 30 Dec 2021 05:57:53 -0500</pubDate>

									<content:encoded><![CDATA[<p>Interesting that your hair came back in curly. I hope you like it 🙂</p>
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				<title>Christinad started the topic Hair loss/thinning in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/hair-loss-thinning/</link>
				<pubDate>Wed, 29 Dec 2021 06:04:01 -0500</pubDate>

									<content:encoded><![CDATA[<p>Happy Holidays, </p>
<p>Curious if anyone has had hair thinning while on ipi/nivo? Luckily, I have a ton of hair but it comes out in handfuls daily, similarly to when I was on interferon. While on interferon I ended losing about 80% of my hair during the course of a year<br />
Been on immunotherapy for 7 months and the hair loss isn’t as bad, but n&hellip;<span class="activity-read-more" id="activity-read-more-11668"><a href="https://forum.melanoma.org/forums/topic/hair-loss-thinning/" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Brain mets have shrunk after Cyberknife radiation and Braf/Mek in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/brain-mets-have-shrunk-after-cyberknife-radiation-and-braf-mek/#post-276148</link>
				<pubDate>Tue, 28 Dec 2021 04:17:18 -0500</pubDate>

									<content:encoded><![CDATA[<p>Great news!! </p>
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				<title>Christinad started the topic Anti-cholesterol drugs to increase efficacy of immunotherapy in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anti-cholesterol-drugs-to-increase-efficacy-of-immunotherapy/</link>
				<pubDate>Sun, 12 Dec 2021 16:16:44 -0500</pubDate>

									<content:encoded><![CDATA[<p><a href="https://apple.news/A49r75icUQOWgGACcO4eSEQ" rel="nofollow ugc">https://apple.news/A49r75icUQOWgGACcO4eSEQ</a></p>
<p>Another interesting read &#8211; of course more research needs do be done, but who knows what the future holds in the melanoma world.</p>
<p>&nbsp;</p>
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				<title>Christinad replied to the topic Covid vaccine and immunotherapy in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/covid-vaccine-and-immunotherapy/#post-276083</link>
				<pubDate>Thu, 09 Dec 2021 00:58:26 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you, Ed!</p>
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				<title>Christinad started the topic Covid vaccine and immunotherapy in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/covid-vaccine-and-immunotherapy/</link>
				<pubDate>Wed, 08 Dec 2021 20:39:28 -0500</pubDate>

									<content:encoded><![CDATA[<p>I’ve been putting off getting my second Covid vaccine since starting immunotherapy May of this year. I’m terrified of the unknown affect the vaccine can have on the immunotherapy medications and/or immune system. I’ve read several articles that say cancer patients should get the vaccine but can’t find anything that says it is 100% safe while o&hellip;<span class="activity-read-more" id="activity-read-more-10873"><a href="https://forum.melanoma.org/forums/topic/covid-vaccine-and-immunotherapy/" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Recurrent after 12 years, stage 4 in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/recurrent-after-12-years-stage-4/#post-276057</link>
				<pubDate>Sun, 05 Dec 2021 22:09:20 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi Mary,</p>
<p>I’m sorry your having to revisit the board. I was diagnosed with stage 3a in 2014, which was a whirlwind for me. As the years passed, I didn’t think about melanoma much and thought I was in the clear until May of this year when I was diagnosed with stage 4. I had symptoms similar to a stomach flu, but I knew something was wrong and it&hellip;<span class="activity-read-more" id="activity-read-more-10709"><a href="https://forum.melanoma.org/forums/topic/recurrent-after-12-years-stage-4/#post-276057" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Recurrent after 12 years, stage 4 in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/recurrent-after-12-years-stage-4/#post-276056</link>
				<pubDate>Sun, 05 Dec 2021 05:02:54 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi Mary,</p>
<p>I’m sorry you’ve had to come back to visit the board under these circumstances. I was diagnosed with stage III in 2014 and that was a whirlwind of emotion. As the years passed I thought I was in the clear and started not to worry about melanoma anymore. Earlier this year I started to not feel good with symptoms similar to a stomach bug&hellip;<span class="activity-read-more" id="activity-read-more-10699"><a href="https://forum.melanoma.org/forums/topic/recurrent-after-12-years-stage-4/#post-276056" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Melanoma Trial ends early due to great results in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/melanoma-trial-ends-early-due-to-great-results/#post-276045</link>
				<pubDate>Thu, 02 Dec 2021 03:23:14 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you both for sharing! My interpretation of both articles is combination ipi/nivo is still most effective based on the results.  Is that your understanding as well? Just want to make sure I’m still on the right track with my current treatment.</p>
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				<title>Christinad replied to the topic Antihistamines can influence immunotherapy response? in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/antihistamines-can-influence-immunotherapy-response/#post-276038</link>
				<pubDate>Sun, 28 Nov 2021 16:42:46 -0500</pubDate>

									<content:encoded><![CDATA[<p>Very true, Celeste. This would br difficult to study since NSAIDS and antihistamines are sold OTC. There’s no way to ensure one group does or does not take these meds. As Ed mentioned it would be interesting to study and I’d also be curious to see how the trial would be set up (if it ever happens). &#x1f914;</p>
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				<title>Christinad started the topic Antihistamines can influence immunotherapy response? in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/antihistamines-can-influence-immunotherapy-response/</link>
				<pubDate>Wed, 24 Nov 2021 19:54:16 -0500</pubDate>

									<content:encoded><![CDATA[<p><a href="https://apple.news/AY_CyXfMDRPqv0XH3RgNKiQ" rel="nofollow ugc">https://apple.news/AY_CyXfMDRPqv0XH3RgNKiQ</a></p>
<p>I saw this on the news today and found it interesting, so I thought I would share and get others thoughts or opinions on this topic.</p>
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				<title>Christinad replied to the topic Anyone have an occasional glass of wine while on treatment? in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anyone-have-an-occasional-glass-of-wine-while-on-treatment/#post-276018</link>
				<pubDate>Tue, 23 Nov 2021 05:55:52 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you both for your responses. I did have one glass of wine (just one) and it was nice. I made sure to get my labs drawn this morning to prepare for my upcoming infusion Saturday and liver function was normal which helped make my decision to go ahead and indulge for this special occasion and it was wonderful.</p>
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				<title>Christinad started the topic Anyone have an occasional glass of wine while on treatment? in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anyone-have-an-occasional-glass-of-wine-while-on-treatment/</link>
				<pubDate>Mon, 22 Nov 2021 18:57:10 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi All,</p>
<p>I have not had any alcohol since starting immunotherapy in May, but am going to dinner tonight with my husband to celebrate our anniversary and am considering having one glass of red wine. My oncologist said a glass of wine is okay but for some reason I’m still hesitant to drink it. Anyone have an occasional glass of wine while on treatment?</p>
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				<title>Christinad replied to the topic More vitiligo….yay!!! in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/more-vitiligo-yay/#post-275990</link>
				<pubDate>Tue, 16 Nov 2021 21:13:04 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you all for your encouragement and support.</p>
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				<title>Christinad replied to the topic More vitiligo….yay!!! in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/more-vitiligo-yay/#post-275989</link>
				<pubDate>Tue, 16 Nov 2021 21:12:29 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you for sharing the research reports. Very encouraging   A lighter shade of pale applies to me too LOL. Pale and proud &#x1f60a;. It is awesome you’re a patient of Dr. Webber. I’ve watched some of his videos. Seems like an incredible man. Thank you for paving the way for the rest of us.</p>
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				<title>Christinad replied to the topic More vitiligo….yay!!! in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/more-vitiligo-yay/#post-275988</link>
				<pubDate>Tue, 16 Nov 2021 21:09:12 -0500</pubDate>

									<content:encoded><![CDATA[<p>Bob Marley is the artist and he died of melanoma. I did not know that until I looked it up.</p>
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				<title>Christinad started the topic More vitiligo….yay!!! in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/more-vitiligo-yay/</link>
				<pubDate>Fri, 12 Nov 2021 21:38:43 -0500</pubDate>

									<content:encoded><![CDATA[<p>I noticed my eye lashes and eyebrows turning white a while back. I now have vitiligo on my hands, arms, chest, abdomen and back….whooohoo! Is it noticeable, yes! Do people point out my lashes and brows, yep!! Does it bother me, absolutely not! I’m wearing it proud and praying in my case it’s a good prognostic sign. My Onc says it is, but we know&hellip;<span class="activity-read-more" id="activity-read-more-9854"><a href="https://forum.melanoma.org/forums/topic/more-vitiligo-yay/" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic 35 Year Old with Stage IV Melanoma in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/35-year-old-with-stage-iv-melanoma/#post-275946</link>
				<pubDate>Mon, 08 Nov 2021 01:02:56 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi Grace,</p>
<p>I was stage 3 for 6 1/2 years and diagnosed with stage 4 the end of May.  I am BRAF negative and started immunotherapy (ipi/nivo) the end of May.  Like you, I have tumors in many locations and was symptomatic when diagnosed. I had significant side effects to the 4 combo doses of immunotherapy but am doing much better now that I’m on the&hellip;<span class="activity-read-more" id="activity-read-more-9672"><a href="https://forum.melanoma.org/forums/topic/35-year-old-with-stage-iv-melanoma/#post-275946" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Update Stage 4 in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/update-stage-4/#post-275932</link>
				<pubDate>Fri, 05 Nov 2021 00:34:20 -0400</pubDate>

									<content:encoded><![CDATA[<p>Great news! I’m happy for you and am glad your side effects are manageable.</p>
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				<title>Christinad replied to the topic Brain met stats are so horrific (&#062;3) in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/brain-met-stats-are-so-horrific-3/#post-275931</link>
				<pubDate>Fri, 05 Nov 2021 00:31:51 -0400</pubDate>

									<content:encoded><![CDATA[<p>Jenn, sending good vibes your way for good news on your upcoming scan. Hang in there.</p>
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				<title>Christinad replied to the topic Brain met stats are so horrific (&#062;3) in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/brain-met-stats-are-so-horrific-3/#post-275930</link>
				<pubDate>Fri, 05 Nov 2021 00:29:37 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi Kathy,<br />
I’m sorry you’re going through a hard time. I don’t have stats to share nor do I have brain mets, but I do have a large tumor burden in multiple places and am currently on the ipi/nivo regimen. This sure is a tough road with hard days which I can relate to. Please don’t give up! Sending you big hugs from CA. Keep fighting a good fight!&hellip;<span class="activity-read-more" id="activity-read-more-9598"><a href="https://forum.melanoma.org/forums/topic/brain-met-stats-are-so-horrific-3/#post-275930" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Stomach Mets in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/stomach-mets-2/#post-275891</link>
				<pubDate>Thu, 28 Oct 2021 03:57:12 -0400</pubDate>

									<content:encoded><![CDATA[<p>I meant to say “I’m” not mom.  Autocorrect gets me every time:)</p>
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				<title>Christinad replied to the topic Stomach Mets in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/stomach-mets-2/#post-275888</link>
				<pubDate>Thu, 28 Oct 2021 01:12:32 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi Amanda,</p>
<p>mom happy to hear your results are looking good! That’s great! Sorry you’re not feeling well with stomach issues. Have you tried eating a soft diet? Things like oatmeal, cream of wheat, mashed potatoes, Mac n cheese, yogurt etc. I don’t have a stomach net but have had a lot of stomach issues since starting immunotherapy and am down&hellip;<span class="activity-read-more" id="activity-read-more-9296"><a href="https://forum.melanoma.org/forums/topic/stomach-mets-2/#post-275888" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Anyone have large tumor burden that is now NED in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anyone-have-large-tumor-burden-that-is-now-ned/#post-275875</link>
				<pubDate>Wed, 27 Oct 2021 03:18:24 -0400</pubDate>

									<content:encoded><![CDATA[<p>Thank you Mark! Like you I normally wouldn’t ask for help but I finally did. My Oncologist is very patient with me. He prescribed a medication to help and also referred me to a psychiatrist who specializes in oncology and only sees oncology patients. Hopefully this helps.<br />
I’m glad you’re able to sit through meetings now. That’s a step in the rig&hellip;<span class="activity-read-more" id="activity-read-more-9230"><a href="https://forum.melanoma.org/forums/topic/anyone-have-large-tumor-burden-that-is-now-ned/#post-275875" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Recurrence after 8 years - treatment options? in the forum Cutaneous Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/recurrence-after-8-years-treatment-options/#post-275871</link>
				<pubDate>Tue, 26 Oct 2021 15:11:22 -0400</pubDate>

									<content:encoded><![CDATA[<p>Arlene, sorry you are dealing with this again! Try to stay positive and string. You got this!</p>
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				<title>Christinad replied to the topic Forum activity has virtually ceased and MRF does not seem to care in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/forum-activity-has-virtually-ceased-and-mrf-does-not-seem-to-care/#post-275869</link>
				<pubDate>Tue, 26 Oct 2021 06:08:16 -0400</pubDate>

									<content:encoded><![CDATA[<p>I found this forum in 2014 when I was diagnosed with stage III. I didn’t post much back then or reply to posts but I read everyone else’s posts or searched for specific things I was personally interested in. I relied on this forum a lot for information related to my diagnosis. At that time it seemed like there were many more people on the sit&hellip;<span class="activity-read-more" id="activity-read-more-9182"><a href="https://forum.melanoma.org/forums/topic/forum-activity-has-virtually-ceased-and-mrf-does-not-seem-to-care/#post-275869" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Anyone have large tumor burden that is now NED in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anyone-have-large-tumor-burden-that-is-now-ned/#post-275868</link>
				<pubDate>Tue, 26 Oct 2021 06:00:28 -0400</pubDate>

									<content:encoded><![CDATA[<p>Thank you all for your responses. I saw my oncologist today and told him I need help with anxiety and depression because I was feeling overwhelmed with all of this. Reading all of the posts gives makes me hopeful.  I have a lot to be thankful for and I need to remind myself of that.</p>
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				<title>Christinad replied to the topic Proton Pump Inhibitors - decrease efficacy of immunotherapy? in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/proton-pump-inhibitors-decrease-efficacy-of-immunotherapy/#post-275846</link>
				<pubDate>Wed, 13 Oct 2021 02:10:57 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi Ed,</p>
<p>Thank you for sharing the articles. I will read them both. I know you’ve suffered quite a bit from reflux. I thought of you when I read my PET scan report and it showed intense FDG activity and wall thickening of the stomach, but the radiologist said favorable for “gastritis”.  I didn’t know gastritis shows on a PET scan. I thought&hellip;<span class="activity-read-more" id="activity-read-more-8838"><a href="https://forum.melanoma.org/forums/topic/proton-pump-inhibitors-decrease-efficacy-of-immunotherapy/#post-275846" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad started the topic Proton Pump Inhibitors - decrease efficacy of immunotherapy? in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/proton-pump-inhibitors-decrease-efficacy-of-immunotherapy/</link>
				<pubDate>Wed, 13 Oct 2021 00:58:25 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi All,</p>
<p>I’m taking 2 Prilosec (PPI) and 2 Pepcid (H2blocker) in the evening to help manage gastritis/reflux. Some studies suggest the use of a PPI can lower the efficacy of immunotherapy. Anyone else have insight on this?</p>
<p>Celeste, have you read any reliable article that supports this theory?</p>
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				<title>Christinad replied to the topic WLE / SLNB - what to expect? in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/wle-slnb-what-to-expect/#post-275834</link>
				<pubDate>Mon, 11 Oct 2021 12:43:56 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi JD_NY,</p>
<p>I’m sorry you and your husband are going down this road. I had a WLE and SNB done about 7 years ago. What I remember most in terms of pain is the injections under the skin to locate the SNB. I feels like a sting or burn but is gone quickly. I think I had 4 injections. Pain associated with the WLE probably depends on the location and s&hellip;<span class="activity-read-more" id="activity-read-more-8797"><a href="https://forum.melanoma.org/forums/topic/wle-slnb-what-to-expect/#post-275834" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Anyone have large tumor burden that is now NED in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anyone-have-large-tumor-burden-that-is-now-ned/#post-275821</link>
				<pubDate>Sun, 10 Oct 2021 04:57:11 -0400</pubDate>

									<content:encoded><![CDATA[<p>What a great feeling it must be to have your last oncology visit and scans. Way to fight the fight! I’m very happy for you! Enjoy your success!</p>
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				<title>Christinad replied to the topic Anyone have large tumor burden that is now NED in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anyone-have-large-tumor-burden-that-is-now-ned/#post-275816</link>
				<pubDate>Fri, 08 Oct 2021 21:48:22 -0400</pubDate>

									<content:encoded><![CDATA[<p>&lt;p style=&#8221;text-align: left;&#8221;&gt;John, Can I ask how long it took before you became NED?  Since you were on the clinical trial quite some time ago I’m assuming your infusion schedule and dosing was different than mine. How long were you on the ipi/nivo? Did you start with the combo and finish with nivo for the rest of your treatment?&lt;/p&gt;</p>
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				<title>Christinad replied to the topic Anyone have large tumor burden that is now NED in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anyone-have-large-tumor-burden-that-is-now-ned/#post-275815</link>
				<pubDate>Fri, 08 Oct 2021 21:36:12 -0400</pubDate>

									<content:encoded><![CDATA[<p>Thank you for sharing! Reading your response has me in tears and has given me hope! Congratulations on 9 years NED.</p>
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				<title>Christinad replied to the topic I got my first scan result today after completing four doses of ipi/nivo in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/i-got-my-first-scan-result-today-after-completing-four-doses-of-ipi-nivo/#post-275813</link>
				<pubDate>Fri, 08 Oct 2021 21:12:50 -0400</pubDate>

									<content:encoded><![CDATA[<p>Thank you everyone 🙂</p>
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				<title>Christinad started the topic Anyone have large tumor burden that is now NED in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/anyone-have-large-tumor-burden-that-is-now-ned/</link>
				<pubDate>Fri, 08 Oct 2021 17:58:48 -0400</pubDate>

									<content:encoded><![CDATA[<p>My Oncologist said I’m responding well to immunotherapy but I look at my PET scan result and get discouraged because I have so many areas of tumor burden. I’m thankful the PET scan showed all areas are shrinking but wonder how realistic is that the immunotherapy will get rid of all of it. My Oncologist said he’s seen worse so I’m trying to stay op&hellip;<span class="activity-read-more" id="activity-read-more-8718"><a href="https://forum.melanoma.org/forums/topic/anyone-have-large-tumor-burden-that-is-now-ned/" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad started the topic I got my first scan result today after completing four doses of ipi/nivo in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/i-got-my-first-scan-result-today-after-completing-four-doses-of-ipi-nivo/</link>
				<pubDate>Tue, 05 Oct 2021 03:41:11 -0400</pubDate>

									<content:encoded><![CDATA[<p>My Oncologist called me this evening and said I’m “responding beautifully” to the immunotherapy. All tumors (I have many) have decreased in size. There’s still a lot of work to be done but at least I know I’m on the right track. Of course I am hopeful and waiting patiently for the words complete response, but for now I’ll keep doing what I’m do&hellip;<span class="activity-read-more" id="activity-read-more-8519"><a href="https://forum.melanoma.org/forums/topic/i-got-my-first-scan-result-today-after-completing-four-doses-of-ipi-nivo/" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Brain mets found after being declared NED 3 months ago in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/brain-mets-found-after-being-declared-ned-3-months-ago/#post-275774</link>
				<pubDate>Sat, 02 Oct 2021 03:37:56 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi Jenn, sorry you’ve encountered this bump in the road. Sending good vibes your way. I hope all goes well with the radiation and you are NED once again. Hang in there! ((Hugs))</p>
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				<title>Christinad replied to the topic Fatigue &#038; lack of appetite with Nivolumab (Opdivo) and Ipilimumab (Yervoy) in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/fatigue-lack-of-appetite-with-nivolumab-opdivo-and-ipilimumab-yervoy/#post-275655</link>
				<pubDate>Thu, 09 Sep 2021 23:46:27 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi Marilyn,</p>
<p>Feel free to reach out anytime. I’m certainly not an expert at this and there are others who are way more knowledgeable than I am but I will do my best to answer any questions you have that relates to my experience. This can be a lonely and scary road at times. Having this forum of people who can relate has been very helpful.</p>
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				<title>Christinad replied to the topic Fatigue &#038; lack of appetite with Nivolumab (Opdivo) and Ipilimumab (Yervoy) in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/fatigue-lack-of-appetite-with-nivolumab-opdivo-and-ipilimumab-yervoy/#post-275653</link>
				<pubDate>Thu, 09 Sep 2021 22:08:00 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi Marilyn,</p>
<p>I hope your first combo dose went well. I pray you’ll have minimal side effects. Keeping my fingers crossed for you. I have a friend who just completed his treatment and didn’t have any side effects the whole time. That’s my wish for you 🙂</p>
<p>It took some trial and error of trying different nausea meds to get my nausea under contr&hellip;<span class="activity-read-more" id="activity-read-more-7697"><a href="https://forum.melanoma.org/forums/topic/fatigue-lack-of-appetite-with-nivolumab-opdivo-and-ipilimumab-yervoy/#post-275653" rel="nofollow ugc">Read more</a></span></p>
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				<title>Christinad replied to the topic Fatigue &#038; lack of appetite with Nivolumab (Opdivo) and Ipilimumab (Yervoy) in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/fatigue-lack-of-appetite-with-nivolumab-opdivo-and-ipilimumab-yervoy/#post-275652</link>
				<pubDate>Thu, 09 Sep 2021 21:53:31 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi Nick,</p>
<p>Since completing the combo doses I’ve only had one dose of the Nivo so far. For me the single dose was much easier and tolerable compared to the combo doses. I’m finally starting to feel better.</p>
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				<title>Christinad replied to the topic Fatigue &#038; lack of appetite with Nivolumab (Opdivo) and Ipilimumab (Yervoy) in the forum General Melanoma Community</title>
				<link>https://forum.melanoma.org/forums/topic/fatigue-lack-of-appetite-with-nivolumab-opdivo-and-ipilimumab-yervoy/#post-275619</link>
				<pubDate>Tue, 07 Sep 2021 13:59:54 -0400</pubDate>

									<content:encoded><![CDATA[<p>Hi Nick,</p>
<p>Sorry to hear about your mom. I completed the four combo doses of ipi/yervoy and am now on the nivo maintenance phase. It was about the first week of the combo dose that I lost my appetite and started to experience fatigue. I also had horrible nausea and indigestion to go along with it. I’ve lost 35 pounds in a little over 2 months. My s&hellip;<span class="activity-read-more" id="activity-read-more-7610"><a href="https://forum.melanoma.org/forums/topic/fatigue-lack-of-appetite-with-nivolumab-opdivo-and-ipilimumab-yervoy/#post-275619" rel="nofollow ugc">Read more</a></span></p>
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