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1,356 thoughts on “GUESTBOOK”
hey guys love you so much take care of yourselves. harini from india
Hello, I came across your page after reading some fact on Progeria. I knew it existed but I didn’t know much about it. After reading everything on this site, I felt the need to reach out and say hello. I wanted to offer words of sympathy however I never once had the feeling of sadness while reading your information. Instead I wanted to tell you that not only have you opened my eyes to this but you have also opened my heart. It makes you feel obligated to live each day as if it were your very last. I’m so grateful I’ve come across this and witness the smiles on your beautiful children faces. God bless you for sharing your life with the world.
Hi im McKenzie and im 11 almost 12 years old! I Have been trying to find more facts about progeria. I would love to meet you guys some day!:)
Godelieve en Wim, ik heb dit weekend jullie boek gelezen. Het heeft me zo aangegrepen. Respect voor wat jullie doen! Ik heb er alleen maar bewondering voor. Het zijn ook 2 superkinderen. Ik blijf Michiel en Amber volgen, dat is zeker. Ik wens jullie nog heel veel geluk samen.
/Dear Godelieve,WimMichiel& Amber, In about february 2010 I was staying at the Holiday Inn in Brookline, Massachusets with my little dog Joulee. I heard the most wonderful giggles and laughter and turned around to see the precious faces of Michiel,Amber& Haley behind me. You all were in Boston for treatment and it was my blessing and privilege to meet your family along with Haley and her mom. It was a life changing experience for me and I have never forgotten you all and have dedicated my facebook page to all progeria children,any research and funding causes i can post or link so all will be aware of Progeria and the need for a cure.I even applied to work for the PROGERIA FOUNDATION in Boston after meeting you all because I wanted to do something to help! But they are small and I have found the best way at the moment to make sure the world knows a cure must happen. What I must tell you is this, Though your family is dealing with two diagnosis of Progeria, I was and still am in awe of the amazing job you two parents did in raising such beautifully behaved and impressive children. The four of you made an impression on me not because of progeria but because of the love and respect you four had together as a family.With Michiel being older I was able to speak with him as he was allowed to take my little Joulee when ever we ran in to each other in the Hotel. He spoke of his activities in soccer and tennis and school.He was the most polite well mannered young man I had ever had the opportunity to meet for his age.I pray for you all and think of you often.Though unfortunately I have no news of you on my facebook There was a picture of Michiel and Haley on Progeria Research Foundation page for an event coming up on June the 30th called ‘We Want The Airwaves: A WFNX Tribute at The Paradise Rock Club, 967 ‘ in Boston for a fundraiser today. I was delighted to see news of Michiel and Haley! I hope you will send some news to the foundation so I may include you all in the campaign for progeria awareness here. I have a picture of Michiel and Joulee that I want you all to have too. I am not quite sure how to send it to you. I will try to send it in email through Michiels contact email address on this site. Though you are a grown up young man I wanted to make your parents aware that I would be sending it out of respect and care.I want you to see it, it will make you all smile for it is a wonderful picture of you Michiel and my beloved Joulee! You posed for this picture with her the day you all were leaving to return to Belgium.My thoughts and prayers are with your beautiful family and I will continue to do what ever I can to make sure your cause is known and a cure WILL be found! God bless. Cheryl Bahcall(McKowen)
Joyeux anniversaire Michiel ! On esp_re que toi et ta soeur vous allez bien et que vous profitez bien de cette journ_e. Donne-nous de tes nouvelles.
Wauw, wat een verhaal! Ik ben erg onder de indruk! Het eerste wat bij mij opkwam was respect! Ik hoorde de eerste keer van progeria toen ik in het 6de leerjaar zat, nu ondertussen 5jaar geleden, en sindsdien heb ik daar al enorm veel aan gedacht! Ik ben blij dat ik op deze website er veel over kan bijleren. Ik hoop dat jou kindjes nog veel gezonde jaren tegemoet gaan en dat ze volop genieten van het leven! Vele groetjes!
Ik heb ook jullie boek gelezen en heb veel respect voor jullie allemaal,blijf geloven in elkaar,en steun vinden in elk moment
Michiel and Amber God bless you little angels,my heart goes out to you, and you will be in my prayers. To the parents-God bless you, I dont know how you do it, but you do, thank god you do. I am a mother with a son who has a birth defect and I can understand how it could be. ( not trying to compare the situation at all )God does not give you more than you can handle, he has a plan, as crazy as it may seem. I truly believe he chose you guys to have these kids because he knew you will love them and give them everything they need,will you keep you in my prayers..NEVER GIVE UP
i just wanted to say everyone is a gift from god and he has a plan for all of us and I’am so thankful to have found your page and im glad that your helping people to understand what Progeria is and to live life to the fullest im so thankfull to all of you i love learning new things and your story has touched my heart.so keep up all the good work 🙂 god bless you and take care
hey guys love you so much take care of yourselves. harini from india
Hello, I came across your page after reading some fact on Progeria. I knew it existed but I didn’t know much about it. After reading everything on this site, I felt the need to reach out and say hello. I wanted to offer words of sympathy however I never once had the feeling of sadness while reading your information. Instead I wanted to tell you that not only have you opened my eyes to this but you have also opened my heart. It makes you feel obligated to live each day as if it were your very last. I’m so grateful I’ve come across this and witness the smiles on your beautiful children faces. God bless you for sharing your life with the world.
Hi im McKenzie and im 11 almost 12 years old! I Have been trying to find more facts about progeria. I would love to meet you guys some day!:)
Godelieve en Wim, ik heb dit weekend jullie boek gelezen. Het heeft me zo aangegrepen. Respect voor wat jullie doen! Ik heb er alleen maar bewondering voor. Het zijn ook 2 superkinderen. Ik blijf Michiel en Amber volgen, dat is zeker. Ik wens jullie nog heel veel geluk samen.
/Dear Godelieve,WimMichiel& Amber, In about february 2010 I was staying at the Holiday Inn in Brookline, Massachusets with my little dog Joulee. I heard the most wonderful giggles and laughter and turned around to see the precious faces of Michiel,Amber& Haley behind me. You all were in Boston for treatment and it was my blessing and privilege to meet your family along with Haley and her mom. It was a life changing experience for me and I have never forgotten you all and have dedicated my facebook page to all progeria children,any research and funding causes i can post or link so all will be aware of Progeria and the need for a cure.I even applied to work for the PROGERIA FOUNDATION in Boston after meeting you all because I wanted to do something to help! But they are small and I have found the best way at the moment to make sure the world knows a cure must happen. What I must tell you is this, Though your family is dealing with two diagnosis of Progeria, I was and still am in awe of the amazing job you two parents did in raising such beautifully behaved and impressive children. The four of you made an impression on me not because of progeria but because of the love and respect you four had together as a family.With Michiel being older I was able to speak with him as he was allowed to take my little Joulee when ever we ran in to each other in the Hotel. He spoke of his activities in soccer and tennis and school.He was the most polite well mannered young man I had ever had the opportunity to meet for his age.I pray for you all and think of you often.Though unfortunately I have no news of you on my facebook There was a picture of Michiel and Haley on Progeria Research Foundation page for an event coming up on June the 30th called ‘We Want The Airwaves: A WFNX Tribute at The Paradise Rock Club, 967 ‘ in Boston for a fundraiser today. I was delighted to see news of Michiel and Haley! I hope you will send some news to the foundation so I may include you all in the campaign for progeria awareness here. I have a picture of Michiel and Joulee that I want you all to have too. I am not quite sure how to send it to you. I will try to send it in email through Michiels contact email address on this site. Though you are a grown up young man I wanted to make your parents aware that I would be sending it out of respect and care.I want you to see it, it will make you all smile for it is a wonderful picture of you Michiel and my beloved Joulee! You posed for this picture with her the day you all were leaving to return to Belgium.My thoughts and prayers are with your beautiful family and I will continue to do what ever I can to make sure your cause is known and a cure WILL be found! God bless. Cheryl Bahcall(McKowen)
Joyeux anniversaire Michiel ! On esp_re que toi et ta soeur vous allez bien et que vous profitez bien de cette journ_e. Donne-nous de tes nouvelles.
Wauw, wat een verhaal! Ik ben erg onder de indruk! Het eerste wat bij mij opkwam was respect! Ik hoorde de eerste keer van progeria toen ik in het 6de leerjaar zat, nu ondertussen 5jaar geleden, en sindsdien heb ik daar al enorm veel aan gedacht! Ik ben blij dat ik op deze website er veel over kan bijleren. Ik hoop dat jou kindjes nog veel gezonde jaren tegemoet gaan en dat ze volop genieten van het leven! Vele groetjes!
Ik heb ook jullie boek gelezen en heb veel respect voor jullie allemaal,blijf geloven in elkaar,en steun vinden in elk moment
Michiel and Amber God bless you little angels,my heart goes out to you, and you will be in my prayers. To the parents-God bless you, I dont know how you do it, but you do, thank god you do. I am a mother with a son who has a birth defect and I can understand how it could be. ( not trying to compare the situation at all )God does not give you more than you can handle, he has a plan, as crazy as it may seem. I truly believe he chose you guys to have these kids because he knew you will love them and give them everything they need,will you keep you in my prayers..NEVER GIVE UP
i just wanted to say everyone is a gift from god and he has a plan for all of us and I’am so thankful to have found your page and im glad that your helping people to understand what Progeria is and to live life to the fullest im so thankfull to all of you i love learning new things and your story has touched my heart.so keep up all the good work 🙂 god bless you and take care