tag:blogger.com,1999:blog-9911796.post5445041353153972795..comments2023-08-02T08:48:38.920-07:00Comments on Max Mikulak - neuroblastoma angel: Max Medical UpdateAndy (Dad to Max)http://www.blogger.com/profile/15957283970526429773noreply@blogger.comBlogger5125tag:blogger.com,1999:blog-9911796.post-54261308240751943002008-02-15T19:46:00.000-08:002008-02-15T19:46:00.000-08:00Can Max try the COG antibody therapy?Can Max try the COG antibody therapy?Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-9911796.post-47340510900460499052008-02-08T20:44:00.000-08:002008-02-08T20:44:00.000-08:00Andy and Melis,There are no words to express how t...Andy and Melis,<BR/><BR/>There are no words to express how tremendously strong you two are. Your children are beautiful and I wish I knew them personally! I have 3 step children and unfortunately don’t get the opportunity to see them everyday, but I do have an appreciation of how proud you must be of your 3 children, especially Max for being such a fighter.<BR/><BR/>Your entire family is amazing, the bond and strong will you guys have to pull through this terrible disease is awesome. It serves as a reminder to everyone who hears your<BR/>story to live life every day and appreciate all the small things. Miracles do happen and I pray everyday for your Max and the rest of your family.<BR/><BR/>Take Care and Stay Strong!<BR/>Michele VaughnAnonymousnoreply@blogger.comtag:blogger.com,1999:blog-9911796.post-82316305324550994992008-02-06T21:59:00.000-08:002008-02-06T21:59:00.000-08:00Hey--what a cute pic!!! You all are on my mind e...Hey--what a cute pic!!! You all are on my mind everyday!!! I just wish in some way I could ease the burden you must feel every day. I see the wonderful smiles on the faces of your sweet babies and know in the middle of this burden life has presented you, you have the treasure of a lifetime. Smiles like those are rare and to be held close in your heart. Thank you for sharing. God's warmest blessings--Randee<BR/><BR/>PS Mike just found out he works with a lady whose son had NB when he was 2--now he's 16!!!!!Randeehttps://www.blogger.com/profile/02285418683631417382noreply@blogger.comtag:blogger.com,1999:blog-9911796.post-47554742654679533172008-02-05T22:48:00.000-08:002008-02-05T22:48:00.000-08:00We can never experience the feelings you and Andy ...We can never experience the feelings you and Andy have as Max's parents. We are aware of the trials you go through and the agony you must feel as you fight this disease. We pray for you.. for strength for you and Andy, for health and a cure for Max and for one day soon a normal life for all of you. <BR/>It will happen because we will "never,never,never give up"!<BR/><BR/>Love, MomAnonymousnoreply@blogger.comtag:blogger.com,1999:blog-9911796.post-68454748032077737552008-02-05T08:15:00.000-08:002008-02-05T08:15:00.000-08:00Just wanted to tell you that all of you are on my ...Just wanted to tell you that all of you are on my mind and heart everyday!<BR/><BR/>I will keep Max in prayer that he won't experience any nasty side effects from the new chemo and that he doesn't lose that beautiful head of hair.<BR/><BR/>BreeAnonymousnoreply@blogger.com