I love to hear from you!
Comments on my blog are always welcome but sometimes you might want to say something and you don’t want it to be public. You can email me at dkadams73@hotmail.com and I will absolutely read it and sometimes respond.
The exception to the sometimes part comes if you have a child who has melanoma. This website is for you and I will get back in touch with you as soon as I receive your email.
Please put something catchy in the “Subject” though so it doesn’t go the way of the rest of my junk mail. You need to differentiate yourself from all the Viagra ads. I suggest putting “Melanoma” somewhere in there. “Your blog is super awesome!” will work too.
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Hi Danielle,
Wishing you and your beautiful family all the best on your wish trip
My son has Cerebral Palsy and we will be on our wish trip Sept. 26 to Oct. 2nd~ Maybe we will get to see you! Your daughter is beautiful and I am glad she is doing well. God Bless you and your family.
Tisha
Thank you so much for sharing Rachael’s and your journey with melanoma. I know it must have been difficult for both of you, but through you courage to share those good and bad moments you have helped others who are walking that journey too.
Your family is in our prayers daily. Grace will be starting her Interferon treatments soon. You have helped to give me some insight on what to expect. Some of my fears were confirmed but at least I can be prepared for them.
Love to you and your family,
Donna Fincher
Gracie Jarrell’s Granny
Donna,
Grace is going to be included in the “Other Little Warriors” page before you know it! Rachael really loved meeting her and talks about her often.
Love the blog Danielle. All the places to go and people to see is cool… and the sun wear site… Reminds me of Indo. I’m sure for many this will be not only resource, but comfort as well. Your humor brings relief when one is tense with worry. Works for me and my worries are totally cancer unrelated…. I love you and think you are WONDERFUL. Ela
I am so glad to have found your blog. I was diagnosed with stage II melanoma a month ago at 30 years of age. Knowing that melanoma could be hereditary, I decided to bring my 7yr old son to the dermatologist for a suspicious mole he’s had ever since he was a baby. The doctor took one look at it and told me, “Oh yes, this needs to come off ASAP.” His mole in the lower back is 6mm. I am so afraid of what the possible outcome may be. My daughter also has a suspicious mole at the bottom of her foot and she is going with me as well tomorrow to get checked, while my son gets his biopsy procedure done. I have been scouring the internet of information about pediatric melanoma as I want to be fully aware for the worst. I’ve experienced this anguish when I first learned of my own diagnosis, but I am more worried for my children.
Thank you for all the information on this blog. My three-year-old daughter was diagnosed with stage III pediatric spitzoid melanoma about a month ago. We were in shock and left speechless. Looking at the pictures of your daughter gave me hope that my own child can beat this terrible illness.