The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

Orange County, CA – Support Groups?

Forums General Melanoma Community Orange County, CA – Support Groups?

  • Post
    holy moly melanomy
    Participant

    Hello lovelys!

    I've been able to hold most of myself together during these last 19 months A.D. (After Diagnosis).  It took me a bit to get back to stable ground and I've been doing just fine for about the last year or so.  However a recent "bump" in the road….or I should say "lump" on my back…threw me back into darkness of Mela-Land.  My husband found a mass on back about an inch or so between my spine and my WE scar the first of this month.  I'm fairly certain it's just a lipoma, but of course there is that evil voice in my head that is telling me the beast is back.

     

    Curious if anyone in Southern CA has a support group that they go to?  I went to one about a year ago after I had an enlarged lymph node pop up on my neck/base of skull.   Although the ladies were super nice – I just didn't fit.  They had all been together for like 10-15+ years and about 95% of them were Breast Cancer survivors as well as they were all 65+ years old.  I'm not discriminating on age or cancer, I'd just personnally rather attend a meeting for Melanoma, or at least a group with a few Melahomies.

    I'm open to all suggestions πŸ™‚  Thank you!

     

    ~Amber~

    holymolymelanomy.blogspot.com

Viewing 8 reply threads
  • Replies
      JC
      Participant

      There should be general cancer support groups in your area.  Check with the American Cancer Society in your area.  There might be melanoma specific support groups as well.  There are a few organizations that can link you up with someone else who has a similar cancer diagnosis.  The organization I connected with is Immerman Angels.  http://www.imermanangels.org/

        holy moly melanomy
        Participant

        Thank you!!  The hospital that I had my surgery at had a therapist available, but I am not longer a patient there as I am now with Kaiser.  It's funny because in my last derm appointment – there was a 'skin cancer' poster and it says on there that if diagnosed that you should start seeing a Melanoma Specialist.  Kaiser doesn't really have that – only one in Riverside and you have to be stage 3+ in order to see them…  So silly. 

         

        But thank you, I really appreciate it πŸ™‚

        holy moly melanomy
        Participant

        Thank you!!  The hospital that I had my surgery at had a therapist available, but I am not longer a patient there as I am now with Kaiser.  It's funny because in my last derm appointment – there was a 'skin cancer' poster and it says on there that if diagnosed that you should start seeing a Melanoma Specialist.  Kaiser doesn't really have that – only one in Riverside and you have to be stage 3+ in order to see them…  So silly. 

         

        But thank you, I really appreciate it πŸ™‚

        holy moly melanomy
        Participant

        Thank you!!  The hospital that I had my surgery at had a therapist available, but I am not longer a patient there as I am now with Kaiser.  It's funny because in my last derm appointment – there was a 'skin cancer' poster and it says on there that if diagnosed that you should start seeing a Melanoma Specialist.  Kaiser doesn't really have that – only one in Riverside and you have to be stage 3+ in order to see them…  So silly. 

         

        But thank you, I really appreciate it πŸ™‚

      JC
      Participant

      There should be general cancer support groups in your area.  Check with the American Cancer Society in your area.  There might be melanoma specific support groups as well.  There are a few organizations that can link you up with someone else who has a similar cancer diagnosis.  The organization I connected with is Immerman Angels.  http://www.imermanangels.org/

      JC
      Participant

      There should be general cancer support groups in your area.  Check with the American Cancer Society in your area.  There might be melanoma specific support groups as well.  There are a few organizations that can link you up with someone else who has a similar cancer diagnosis.  The organization I connected with is Immerman Angels.  http://www.imermanangels.org/

      Julie in SoCal
      Participant

      Hi Amber,

      After my initial diagnosis, I also was looking for a support group, where I would find folk who were dealing with the big fat harry deal of stage 3 cancer treatment. I wanted to talk, listen, cry and laugh with new friends. 

      In looking around in OC,  I did not find a support group specifically for melanoma.  I checked all the local hospitals (Hoag, Memorial…) and did not find a one. When I went to the general "Cancer" support groups at the hospitals, I found that they tended to be education oriented.  That was fine, just not what I was looking for. 

      Eventually I went up to the Cancer Support Center in Pasadena http://www.cscpasadena.org/ (there's also one in Santa Monica).  Yes, it's a long trip (I live in HB) but they were wonderful and I never regretted the trip.  I cannot more highly recommend the folks there.

      Sorry I'm not more help,

      Julie

      Stage 3c, WLE, + SNB + LDN + HD-INF + GM-CSF= NED. Recurrance + IPI = NERD

       

       

        holy moly melanomy
        Participant

        Thank you!  I appreciate any information.  The one I went to was also at a hospital and I picked it because it was meant for early diagnosed people and how to move on from it…..and then as I mentioned, these women had been in the same group for seriously like 10-15+ years.  I just found it odd.  I couldn't wrap my head around it and I ended up just crying my eyes out during the whole damn hour. 

        It just sucks when Melanoma creeps back up and takes up all of my mental time.  It's definitely hard on my husband and he tries to give advice – to which I blow up and tell him that he couldn't possibly understand.  It's not fair to anyone around me and I just wish I knew how to get a handle on this crap! πŸ™‚ 

        Thank you for the input, it's really REALLY appreciated πŸ™‚

         

         

        JC
        Participant

        Sometimes there are tools and techniques to learn as well.  Such as (just examples). . sometimes you can find classes/sessions through support networks that can help. . .

        CHANGING PATTERNS OF NEGATIVE THINKING AND WORRY WITH HYPNOSIS
        This program will focus on how the mind creates negative thinking/self-talk that creates stress and worry. Participants will learn how they can use hypnosis to interrupt those thought patterns, and will be given an opportunity to practice this technique during the class.

        Acceptance and Commitment Therapy (ACT) is a new approach to handling stressful thoughts and feelings. Research shows that ACT is effective for helping people impacted by cancer overcome obstacles and live a fulfilling life.

        holy moly melanomy
        Participant

        I would totally be into the hypnosis deal….  Although, I am completely imagining myself being hypnotized into clucking like a chicken – or acting like a prom queen on a parade float everytime my mind wanders to the dark side.  I'd still take that over crippling fear πŸ™‚

        JC
        Participant

        not quite the kind of hypnosis they portray in the movies. 

        http://connectionscounselinginc.com/hypnosis/

         

         

        JC
        Participant

        not quite the kind of hypnosis they portray in the movies. 

        http://connectionscounselinginc.com/hypnosis/

         

         

        JC
        Participant

        not quite the kind of hypnosis they portray in the movies. 

        http://connectionscounselinginc.com/hypnosis/

         

         

        holy moly melanomy
        Participant

        I would totally be into the hypnosis deal….  Although, I am completely imagining myself being hypnotized into clucking like a chicken – or acting like a prom queen on a parade float everytime my mind wanders to the dark side.  I'd still take that over crippling fear πŸ™‚

        holy moly melanomy
        Participant

        I would totally be into the hypnosis deal….  Although, I am completely imagining myself being hypnotized into clucking like a chicken – or acting like a prom queen on a parade float everytime my mind wanders to the dark side.  I'd still take that over crippling fear πŸ™‚

        JC
        Participant

        Sometimes there are tools and techniques to learn as well.  Such as (just examples). . sometimes you can find classes/sessions through support networks that can help. . .

        CHANGING PATTERNS OF NEGATIVE THINKING AND WORRY WITH HYPNOSIS
        This program will focus on how the mind creates negative thinking/self-talk that creates stress and worry. Participants will learn how they can use hypnosis to interrupt those thought patterns, and will be given an opportunity to practice this technique during the class.

        Acceptance and Commitment Therapy (ACT) is a new approach to handling stressful thoughts and feelings. Research shows that ACT is effective for helping people impacted by cancer overcome obstacles and live a fulfilling life.

        JC
        Participant

        Sometimes there are tools and techniques to learn as well.  Such as (just examples). . sometimes you can find classes/sessions through support networks that can help. . .

        CHANGING PATTERNS OF NEGATIVE THINKING AND WORRY WITH HYPNOSIS
        This program will focus on how the mind creates negative thinking/self-talk that creates stress and worry. Participants will learn how they can use hypnosis to interrupt those thought patterns, and will be given an opportunity to practice this technique during the class.

        Acceptance and Commitment Therapy (ACT) is a new approach to handling stressful thoughts and feelings. Research shows that ACT is effective for helping people impacted by cancer overcome obstacles and live a fulfilling life.

        holy moly melanomy
        Participant

        Thank you!  I appreciate any information.  The one I went to was also at a hospital and I picked it because it was meant for early diagnosed people and how to move on from it…..and then as I mentioned, these women had been in the same group for seriously like 10-15+ years.  I just found it odd.  I couldn't wrap my head around it and I ended up just crying my eyes out during the whole damn hour. 

        It just sucks when Melanoma creeps back up and takes up all of my mental time.  It's definitely hard on my husband and he tries to give advice – to which I blow up and tell him that he couldn't possibly understand.  It's not fair to anyone around me and I just wish I knew how to get a handle on this crap! πŸ™‚ 

        Thank you for the input, it's really REALLY appreciated πŸ™‚

         

         

        holy moly melanomy
        Participant

        Thank you!  I appreciate any information.  The one I went to was also at a hospital and I picked it because it was meant for early diagnosed people and how to move on from it…..and then as I mentioned, these women had been in the same group for seriously like 10-15+ years.  I just found it odd.  I couldn't wrap my head around it and I ended up just crying my eyes out during the whole damn hour. 

        It just sucks when Melanoma creeps back up and takes up all of my mental time.  It's definitely hard on my husband and he tries to give advice – to which I blow up and tell him that he couldn't possibly understand.  It's not fair to anyone around me and I just wish I knew how to get a handle on this crap! πŸ™‚ 

        Thank you for the input, it's really REALLY appreciated πŸ™‚

         

         

      Julie in SoCal
      Participant

      Hi Amber,

      After my initial diagnosis, I also was looking for a support group, where I would find folk who were dealing with the big fat harry deal of stage 3 cancer treatment. I wanted to talk, listen, cry and laugh with new friends. 

      In looking around in OC,  I did not find a support group specifically for melanoma.  I checked all the local hospitals (Hoag, Memorial…) and did not find a one. When I went to the general "Cancer" support groups at the hospitals, I found that they tended to be education oriented.  That was fine, just not what I was looking for. 

      Eventually I went up to the Cancer Support Center in Pasadena http://www.cscpasadena.org/ (there's also one in Santa Monica).  Yes, it's a long trip (I live in HB) but they were wonderful and I never regretted the trip.  I cannot more highly recommend the folks there.

      Sorry I'm not more help,

      Julie

      Stage 3c, WLE, + SNB + LDN + HD-INF + GM-CSF= NED. Recurrance + IPI = NERD

       

       

      Julie in SoCal
      Participant

      Hi Amber,

      After my initial diagnosis, I also was looking for a support group, where I would find folk who were dealing with the big fat harry deal of stage 3 cancer treatment. I wanted to talk, listen, cry and laugh with new friends. 

      In looking around in OC,  I did not find a support group specifically for melanoma.  I checked all the local hospitals (Hoag, Memorial…) and did not find a one. When I went to the general "Cancer" support groups at the hospitals, I found that they tended to be education oriented.  That was fine, just not what I was looking for. 

      Eventually I went up to the Cancer Support Center in Pasadena http://www.cscpasadena.org/ (there's also one in Santa Monica).  Yes, it's a long trip (I live in HB) but they were wonderful and I never regretted the trip.  I cannot more highly recommend the folks there.

      Sorry I'm not more help,

      Julie

      Stage 3c, WLE, + SNB + LDN + HD-INF + GM-CSF= NED. Recurrance + IPI = NERD

       

       

      DZnDef
      Participant

      Hey Amber, I don't know of any myself but if you hear of one or if you want to start one, let me know.  I live in Orange County and am Stage IV.  Was only correctly diagnosed in March of this year but I've been stage IV since at least July of 2012.

      Cheers – Maggie

      DZnDef
      Participant

      Hey Amber, I don't know of any myself but if you hear of one or if you want to start one, let me know.  I live in Orange County and am Stage IV.  Was only correctly diagnosed in March of this year but I've been stage IV since at least July of 2012.

      Cheers – Maggie

        I live in San Diego County and looked for support groups in Southern Cal after I was diagnosed in 2012, but couldn't find any for melanoma. I would be interested in participating if you find a group or want to start one. There are a number of patients in the San Diego/Orange County area and some good "halfway meeting points." With so much happening in the field, sharing information would be a great. idea…

        I live in San Diego County and looked for support groups in Southern Cal after I was diagnosed in 2012, but couldn't find any for melanoma. I would be interested in participating if you find a group or want to start one. There are a number of patients in the San Diego/Orange County area and some good "halfway meeting points." With so much happening in the field, sharing information would be a great. idea…

        I live in San Diego County and looked for support groups in Southern Cal after I was diagnosed in 2012, but couldn't find any for melanoma. I would be interested in participating if you find a group or want to start one. There are a number of patients in the San Diego/Orange County area and some good "halfway meeting points." With so much happening in the field, sharing information would be a great. idea…

      DZnDef
      Participant

      Hey Amber, I don't know of any myself but if you hear of one or if you want to start one, let me know.  I live in Orange County and am Stage IV.  Was only correctly diagnosed in March of this year but I've been stage IV since at least July of 2012.

      Cheers – Maggie

Viewing 8 reply threads
  • You must be logged in to reply to this topic.
About the MRF Patient Forum

The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

The information on the forum 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 byΒ MRF posting policies.