Happy_girl
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This is great. It does make me wonder- i did choose to get a CLND 4 years ago ( even though Dr Coit was very comfortable with me not getting one.). I do get very nervous abou not having done any extra therapy – Is it a question I should ask after i have my daughter in January- if I need anything, or since it is several years removed- it is not necessary unless (hopefully not) something would arise. I often wonder this when I see new things approved for 3A. I hope this makes sense! Thanks!
Thank you! One reason I’m a little nervous right now is that I had a friend who was just diagnosed with melanoma. I’ve been helping her get to OHIO STATE for what she needs- but I think just seeing her live this for the first time is bringing back the fear and uncertainty that first comes. I did tell her about this site as well, so she may join soon.
Thanks for all you do,Catherine! It is much appreciated!
Thanks for asking! I have been doing well. I actually am currently 10 weeks pregnant again!im excited and nervous again all at the same time. We did find out from a test last time we lost a little girl (we named her Ruthie Lucille). She had severe heart defects and had Down syndrome. It made the loss easier because her life would have been so hard for her! She is still loved ( and would have been loved had she beenborn), but im thankful she didn’t have to hurt and struggle in ways that I wouldn’t have been able to fix for her.
We are praying this little babe is healthy!
Thank you! It was a shock and has been a challenge. My brain goes a million different ways- did I do something? Was the baby not healthy? Was this a divine intervention so melanoma wouldn’t return….. it’s been a challenge. Thank you for always listening and being so supportive!
I talked with the nurse- apparently it is a sub cm spot on my liver. I feel like this is even worse. They did a ct scan of chest, abdomen, and pelvis. I guess a tiny spot showed up- but too small to even do anything with. I am being seen at the james cancer center- OSU- by dr Kendra. The plan is to rescan in 3 months …. To compare I am guessing? I’m just really struggling with this because I was finally feeling good- but then this caught me off guard. It doesn’t help that I haven’t gotten to talk with my onc abt it either. That was the one scan that wasn’t back for my appointment with her. The chest was and was clear. I’m just scared. Thanks for your reply. I’m at my 2 year mark- but will be waiting a little longer. I did some research that showed 32 months was close to when most metastasis would have occured for stage 3a. It was from mskcc- so I know it’s reputable. You are very right, Catherine. He is amazing and one of the best! I think I was just having a moment of panic. I do trust his judgement and advise. I know I am truly blessed that I was able to see him. I’m doing better with my anxiety, but just hearing about castle brought it back to surface again. Thanks for your advice. It is much appreciated!!
I’m so sorry about the roller coaster ride of emotions! I understand! Who are you seeing at OSU? I go to the james cancer center and see dr Kendra. I’ve really appreciated her. Hi Dave! I’m just visiting the board after not having been on here for a while. I don’t have advice on your actual question, but I did want to share with you a piece of my story. I was diagnosed at 30 (last April) 6 weeks after having my daughter. I’m now 31… And stage 3a also. I understand what your daughter is feeling. I pray that she is able to stay positive and k ow that she has hope! Never forget that! From my experience, I needed to know my family and friends were with me 100%. They are and that means the world to me. It sounds like you are there 100% for your daughter too. Even if she doesn’t mention it, she is thankful!
Stay positive and have hope!
Thanks so much for sharing your story. I know this is a terrifying experience. It is so hard to keep emotions under control. The hardest times for me were feeding my baby in the middle of the night ( gotta love those crazy feeding times 
I’m glad you’re being seen at a great melanima center. You are right that the pet isn’t bad at all- nerve racking- but not bazar. Try to just relax.
I am curious what genetic testing your getting done?
Let’s keep in touch. As much as I hate that this is happening to you- I’m thankful for someone that shares practically identical thoughts, fear, and dreams.
Also- at 3a…. Is interferon the only option? I’ve been trying to look around pretty hard and haven’t come up with any other treatment besides the watch and wait.
