Friday, February 20, 2009


Welcome to Safe Haven.

A place for you to find comfort, help, encouragement, resources, and most of all a connection to intercessors who want to pray for YOU.

If you are dealing with infertility, miscarriage, stillbirth or infant loss, or waiting for a child through adoption, this blog is for you.

Here, you will find links to websites that offer advice, and place where you can share you story and have others intercede on your behalf, ministries who are there to meet all of your different needs, and many other helpful resources.

Most of all, we want to connect with you to lift you and your families up in prayer. This is our hearts desire!

This blog is still very much under construction and will probably change frequently. So please come back and visit often for new posts and updates. If you have a prayer request for yourself, a friend or family member, please leave a comment, a name, and/or website and we will add it to our prayer link list!

We love to pray for you and your precious, precious children. Thank you for visiting and we hope this page can somehow be a blessing to you.


  1. I just found this site. Although I do not have a child that is ill or have we lost a child. I do have prayer in me and believe in the power of prayer. My best friend had TTS in her identical twins. One didnt survive and died while still in her mama's womb. Abigail is doing amazing. Please visit there site. I made a button for her when she was pregnant and just lost madison.

    I will be adding this button to my blog as I think it is worth sharing. I too also pray for stellan and have been for months.

    Thanks for making a commitment to prayer through your site for so many.

  2. What a beautiful website and I love the name "Safe Haven". Thank you for putting it together. I was hoping you would include my friend Natalie on your prayer list.

    I've started a blog in attempts to help my friend Natalie who lost a baby full term due to a cord accident who is now pregnant again, to raise money so she can see a specialist doctor that specializes in cord accidents and does a monitoring service to prevent it from happening again. I was hoping you would consider posting about it and putting our button on your attempts to get the word out. You can visit the blog here: , you can get the code for the button on the blog too.

  3. I would be grateful if you could add us to your list.

    Thank you,


  4. It would be wonderful if you could share my son's journey with hydranencephaly ( through your site and also my Hydranencephaly Information & Inspiration Blog (

    Both are great reminders to never give up on hope & faith, and believe in miracles and the wonderful power in prayer!


  5. My Friend told me about this site,she lost a child.My daughter is 4yrs old and has luekemia i just made a blog for her and am looking for other moms that are going through this.she was just diagnosed on June 24,2009.I feel so alone cuase i really dont know others that are going through this.


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