Heart to Heart - a linky for sharing posts about congenital heart defects and life as a heart family

Heart to Heart – June

Heart to Heart linky was set up to help other heart families share their stories and experiences in order to help support each other as a community.  It opens on the 15th of each month and stays open for a week so there is plenty of time to share your CHD-related posts. You can share as many posts as you like – old posts or new posts, updates on how your heart child is progressing, poems, advice – whatever you like as long as it is related to life as a heart family. If you would like to add the code below to your post that would be great and please do visit other posts in the link too!  I’ll also try and share posts on Twitter – and will try and retweet those with the hashtag #hearttoheartlinky


We’ve been back in hospital this month with a planned cardiac catheter admission to help Jessica’s cardiac team plan when her next stage operation might take place.  I’m linking up the update from Jessica’s blog on this as well as my reflections on it.


Thank you to everyone who linked up last monthSwallow, My Sunshine shared a very informative post on the practicalities of the chylothorax diet with some great ideas for meal and treat options and Heart Mammi shared an update on Martha Grace after her latest cardiac check-up.


I have added posts previously linked up to Heart to Heart on my Pinterest board as well as sharing other CHD-related posts.  If you would like an invite to pin to it, please do let me know.   Looking forward to reading your heart-related posts this month.

Follow Little Hearts, Big Love’s board CHD stories – Heart to Heart linky on Pinterest.

Little Hearts Big Love
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