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.

Husband’s new treatment starts today -feeling terrified!

Forums General Melanoma Community Husband’s new treatment starts today -feeling terrified!

  • Post
    Maureen038
    Participant

      Hi All,

         Bill is in his sixth year of this disease. After being stable for almost 3 years he has lung nodules again. He is starting the Cleopatra regimen for breast cancer since he has the her-2 mutation (Sloan Kettering testing) and immunotherapy stopped working. 

         I greatly admire people on this board who remain positive despite difficult circumstances. I’m having trouble getting my fighting spirit back so I can help bill. Please help.

       

      Maureen 

    Viewing 4 reply threads
    • Replies
        BrianP
        Participant

          Hey Maureen,

          I was hoping you would update us on Bill's next treatment plan.  Hang in there Maureen.  The toughest time is always the grind of trying to find a treatment path and then the anxiety of not knowing if it's going to work.  Once you get into the treatment routine I'm confident you'll get that fightning spirit back.  How is Bill holding up?  You guys have been an amazing team through this journey.

          Brian

            Maureen038
            Participant

              Thanks so much Brian for your kindness. Bill is feeling great ! He’s in great physical shape but his blood levels are lower because of the previous chemo drug. Of course, he is optimistic as usual. I think you’re right that I will slowly get it back. I just hate seeing him go through all of this!!! Thanks for boosting my spirit. Love to you and your family !!

              Maureen

            Bubbles
            Participant

              Dear Maureen,

              I have always felt that my struggles have been harder on my dear B than they have been on me!!!  (He would tell you differently, but….)   I think having to watch and wait and hope, while feeling as though you have no way to intervene in your loved one's trajectory must be maddening.  But!  That's where you are right…and wrong.  When our loved ones are there beside us…with uplifting courage as well as when they acknowledge they are down and worried….it is a gift greater than any that medicine can provide.  Not all relationships survive such stressors.  But when they do, those are peeps that we KNOW have our backs and guard our souls…no matter the fluctuations of their spirit.  So, in whatever state you find yourself in – know that Bill is thankful for your love, your touch, your smile, and yes….even your tears.  It is the teamwork, the feeling that there is in fact someone in the fight WITH you ~ that matters.

              You can do this.  I hope this treatment with be just the thing that Bill needs and is not too difficult to manage.  Much love, celeste

                Maureen038
                Participant

                  Here goes my tenth time in trying to post this!

                  Celeste, you are such an amazing person! Thanks from the bottom of my heart for lifting my spirits. For you to take the time to write to me and so many on this board since you have been through so much lately speaks volumes of your kind spirit. I hope you are feeling better! Much love to you and your b!

                  Maureen

                lkb
                Participant

                  Maureen, my husband went to a couple of support group meetings specifically for spouses of cancer patients and he says they helped him. I noticed the change, more calm, more stable. The uncertainty can surely be excruciatng, but the treatment routine will help. Sending you and Bill all good wishes.

                  Lisa 

                    Maureen038
                    Participant

                      Thanks Lisa. I appreciate your advice. It’s been awhile since I’ve been to a support group but I think I should do it again. It does help knowing you are not the only one going through things.

                      Maureen

                    MelanomaMike
                    Participant
                      Hi Maureen, im Mike nice to meet you (under our shared circumstances anyways!) Like brother BrianP & others have said, your inner Fight Mode will reappear cuz it NEVER left Maureen! We are built to survive & to support our loved ones, it aint no thang, it aint no thang…Bill & you got this!
                        Maureen038
                        Participant

                          Hey Mike,

                              Thanks Mike! You are in fact one of the people I admire on this board because of your uplifting, funny, caring personality. I truly hope your surgery goes well ! Take care.

                          Maureen

                        bjeans
                        Participant

                          Hi Maureen – I’m so sorry you and your husband have to go through this mess. One step at a time, you’ll get through it.

                          Are you in the MD-DC-VA area? If so, read on. If not, ignore the rest of my babbling. Inova’s “Life with Cancer” program is quite good, free (!), and you do not have to be an Inova patient to attend anything. There’s Individual counseling, groups, nutritional counseling, a gym, lounge to just hang out. I attended an art therapy workshop for patients/family/friends that’s held monthly, and my husband and I met with a dietician after he had gut side effects from nivo and/or ipi. Most activities are in a serene lodge-like “house” with free parking/easy access, and area hospitals have some programs. 

                          (Reading your profile, Dr. Venna left WHC to start up/direct the Melanoma Center at Inova, and my husband squeaked into a trial through them a day or two before it closed worldwide.)

                          Hang in there –

                          Beth

                            Maureen038
                            Participant

                              Thanks so much for the information Beth! We miss Dr. Vienna! We live in Gaithersburg Maryland and his doctor is at Aquillino Cancer Center which provides the same wonderful support systems. Also, I volunteer at Hope Connections for Cancer Support which provides many free support systems too. I stopped going to the caregiver support groups because Bill was doing great but I need to go back. If you and your husband ever want to get together with us let us know. Take care and we wish you the best!

                              Maureen

                        Viewing 4 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 by MRF posting policies.

                        Popular Topics