Friendships/Camaraderie
legaljen1969
Member Posts: 763
I was thinking last night about how much I enjoy chatting with all of you. It's strange that what we have in common is our "disease," but it's really a very positive place here. Sharing ideas, sharing opinions. It's been interesting for me to see how people process their treatments, their waiting news, and everything else.
I look forward to checking in with you all at lunch time and in the evenings. I think we all sort of get invested in the journeys of each other. It's nice to have a place to discuss this where people "expect" you to talk about your cancer, your treatment, your surgery and they aren't like "Oh, you're on about THIS again?" I know for most of my family they are like "Well, you had your mastectomy. Now we will just put this "cancer thing" in the rear view mirror and truck on. You don't have cancer anymore."
Here, it's comforting to discuss victories, fears, curiosity, anger or whatever. And we all "get it." In short, THANK YOU ALL>
I look forward to checking in with you all at lunch time and in the evenings. I think we all sort of get invested in the journeys of each other. It's nice to have a place to discuss this where people "expect" you to talk about your cancer, your treatment, your surgery and they aren't like "Oh, you're on about THIS again?" I know for most of my family they are like "Well, you had your mastectomy. Now we will just put this "cancer thing" in the rear view mirror and truck on. You don't have cancer anymore."
Here, it's comforting to discuss victories, fears, curiosity, anger or whatever. And we all "get it." In short, THANK YOU ALL>
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Comments
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@legaljen1969 - well said and I agree!0
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Indeed, we do get it when others just don’t want to deal with it all. I’m thankful to have this site to vent and help anyone else I can. It’s comforting to me and I hope for you too. Text anytime!0
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With the onset of the quarantine I lost pretty much all of my local support system. No more Group. No more support services offered through cancer center. No more swim therapy. I do still talk to my mental health counselor by phone but it's not the same as in person although I do appreciate her efforts to be there for me. So thank goodness for WhatNext. I can always count on my WhatNext family to be there. Whatever the issue I can always find someone willing to talk, "listen", argue, discuss, laugh, share experience, offer support or a shoulder. And it is so important to be able to talk to folks who "get it". So, thanks, friends.0
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I have always thought that talking about your cancer, treatments, side effects, the ups and downs and everything in between is therapeutic for most of us. And you don't have to pay $120.00 an hour!0
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We share our strengths, our weaknesses, our humanity.0
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Whatnext probably saved my sanity. I was so frustrated. I didn't fit in. Congress said more cancer support for patients, which is really a good thing that we need. Somehow NM Presbyterian can't process these plans very well.
I went to one support group that met that day in an inner room-no windows. They told me that I needed to wear pink and I should wear a hat at all times- my cancer site was upper lip and nose. If any of you can figure that out, tell me. It just kept going that way.
I started wearing a sun lotion on my face, which doctors and everyone said I should do. The 3rd day, the radiation area started stinging. I looked in the mirror and it was all bright red. I went to the ER, and they noticed that blood was seeping out of the pores on the radiation target. More and more doctors came in and they started arguing about what doctor they should refer me to. I wasn't mad at them, because they really wanted to help me.
I should go to a dermatologist because it was a skin problem. NO its from radiation and she needs to see her radiologist. No way, Can't you see the blood? It's a hematology problem.. They argued for it being an ENT problem, an internal medicine problem, a cancer problem, a vascular problem,
I felt hopeless. About that time, I opened my Email-- and there was a letter from WhatNext. It said-We were sent your name, because you can't get cancer support. Please join our Whatnext group. I did, I could say what I wanted without anybody telling to wear pink and see a shrink.
I am very grateful for all of you. Thank you0 -
I read the WhatNext Digest first thing every morning. I look forward to seeing the posts that everyone has made. I have learned so much from all of you. I don't often ask any questions, but the people that do seem to be thinking the same things that i am. I appreciate having so many friends that can help and support each other.0
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Believe me, this site has been a God send for me. I felt all alone in that I had no other cancer patients to talk to when going through active treatment. I couldn't get to any support groups, and my mother found What Next forme. The rest is history! I really find it helps to talk to people who can relate to the unique issues we face. HUGS and God bless.0
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Totally agree. This is a very safe place and a good place to ask questions or talk about one's illness without judgement or concern that "you're talking about cancer again". Especially during treatment it really is a focus and it is our job to work our way through treatment. I have also found it is a good place to give back. Sometimes I can answer a question, offer a word of encouragement or just convey how it was for me. Very grateful I found this place. I may post a little less often - I am 5 years out from treatment now, just had a good check up with my oncologist, but always glad to know I can check in when I need to do so. Stay safe everyone.0
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It is wonderful to connect to others with many different experiences. So helpful to get your support and be able to help others!0
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This site has helped me more than once. I had pretty much made up my mind to refuse to take a follow-up estrogen blocker (arimidex), but I asked about other peoples experiences here (I was pretty new to the site). After reading everyone's honest experiences, advice, and support, I decided to take it. I'm glad I did. Yes, I have some side effects from it, but I also have the peace of mind of knowing I am being pro-active in fighting for my health. And when any of those side effects are getting to me I can come here, rant, and get a bunch of; "I hear ya, sister!" shout outs from all of you - who REALLY know.0
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I too, am so thankful for this group. No one understands what you go through mentally, physically, and emotionally when you are on a cancer journey unless you have been on that journey too. The support here is truly a gift and a gift that keeps giving and giving. Only someone who has been on a cancer journey can understand that the journey never ends. Not a day goes by that I don't think about cancer. For me this has been going on for 10 years. We are in this community together! God bless you!0
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Sheri 56 you are so right. I have tried to have discussions with some of my doctors and realized I was wasting my time because they really don't have a clue what we're dealing with on a personal level. Then last fall one of my doctors, tragically, was diagnosed with cancer. Last time I spoke with him it was like talking with a different person. He even said, "I'm one of you now" . In other words, now he "gets it". It was before Covid19 so we hugged it out. But my point being, are on WhatNext folks definitely "get it".0
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This is a place where we can say what we really feel and know that someone understands.
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I really appreciate being able to express a fear or concern here because no one tells me not to think that way, that I'm being too negative or being ridiculous or looking too far ahead, etc. When I have expressed fear or worry to some family members or friends it felt like they invalidated how I felt. I've actually stopped talking to them about such things. I have not felt invalidated here - just supported.0
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I agree with what everyone said. I saw a WhatNext post on Facebook. Because I’d been ten years out of treatment, I didn’t know if I should join. Greg encouraged me to join. I feel I’ve made some good friends here and have been helped and have helped. It’s a very personal cancer site on which people can get to know one another if they want to. I’m very grateful for WN.0
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@Carool, I was trying to remember how I found WN, and when I read your response ... that's how I found it too! Someone had posted one of the memes that had the WhatNext logo on it. I liked the meme and went to explore what "WhatsNext" was all about. I joined that day and have been fairly active ever since. I've joined lots of cancer sites over the years, mostly lung cancer-specific, but I like WhatNext best.0
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I have no idea who sent my name in to Whatnext--My oncology radiologist-he said-NO. The Oncology chaplain? my ENT-I don't know-some nurse-maybe, My primary care doctor-could be
But thank you Whatnext in contacting me.0 -
I have no idea how I got connected with WhatNext. I don't recall being contacted by anyone or "invited." I think i just stumbled upon it. If I was directed here, I guess I was just in overwhelmed brain fog of the beginnings of trying to figure out what the heck was going on.0
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One of the members of our Cancer Support Group offered the link. I'm usually not much of an internet user but when I got home decided to just check it out. I think I was up until about 3:00 a.m.
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I have learned so much here. A great bunch of people here that have the Big C in common. I often come here with an idea of who can I help today. If we can share our stories, our pictures and our respect, then it's a good place to be. In a crazy world, this is a safe place to hang out.0
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Legaljen--I went to your home page to talk to you for a minute. You ave a different format than the rest of us. If you visit other home pages-the top has what we want to share with others.
Then there is a purple strip like a banner-that says--POST A MESSAGE ON THEIR WALL---that is an open invitation for WhatNexters to comment to you more personally. Right now, your Homepage isn't welcoming to others.
There isn't anything here for privacy, which keeps us from being too snarky or bossy, but we do you to home pages and comment. Anyway-look at other WhatNext Home Pages and look at yours. It looks like you want others to know more about you. Anyway, you'll do what makes you feel comfortable. We all do that anyway.0 -
Hmmmm? Just out of curiosity I clicked on legaljen1969 to see what her home page looked like. Looked completely normal to me including the post a message on the wall space. Very strange. Wazzup?0
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I just checked out legaljen's homepage and it looked fine to me too?0
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Okay-- I don't know- but all of you have the purple banner to leave a message, and on my computer- there isn't any banner. on her home page.
I just ran my pointer- and her purple strip opened up on another page. Apparently my old PC is reading different coding. .
I'm glad that all of you did comment about this. It is so odd, and it makes me sound so dumb--I really appreciate your help. If I see this again, I'll do some hunting to get in.
legaljen, I hope that you aren't mad at me.0 -
@LiveWithCancer - Yes! I check in on some Reddit cancer sites, but I much prefer WhatNext. It’s much more personal. Btw, thank you for mentioning Barryboomer (in another thread). I’d forgotten him. I miss, kind of, arguing with him.0
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@Meyati. If there is something I need to do to "enable" people posting to my page, I can try to do it. I started my page and asking questions and posting updates. I haven't done anything to exclude anyone, but I haven't done anything to make my page exciting either. I don't know what is causing your difficulty on my page.
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Meyati, I am certainly not mad at you. Your comment above says there is nothing here for privacy to keep people from being too bossy or snarky. I am trying not to be bossy or snarky. I am NOT trying to be bossy or snarky. I don't think it's what you want to do, but if you want to post to my page to be bossy or snarky, I would ask that you reconsider. I wouldn't go to someone's page to try to post bossy snarky stuff, and I hope others would not do it to me either.0
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I don't remember how I found WhatNext. I know that no one told me about it. It must have popped up when I was doing some research about my cancer. @Carool, I was just thinking about Barryboomer the other day. It took me awhile, but I finally came up with his name. He definitely faced cancer his way.0
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I agree with all the comments about the community - it's the go to place for people who understand. I've very thankful for the advice, support and camaraderie I've received over the years that I've been on this site and folks like Greg who keep the ship sailing!0
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