Nola's Journey

At the end of November 2017, just before my darling daughter turned three months old she began having  what we know now were seizures. After a trip to A&E, the GP and an urgent referral being made she was admitted to hospital on 3rd December 2017. Investigations began and after several various tests, Doctors are almost certain she has a rare genetic condition, however we are still waiting (February 2018) to have this confirmed by a genetic blood test.
I will be writing posts to share Nola's journey, to document where we came from, where we are and possibly where we're going to. I am doing this to document her journey for us and her but also in the hope it may be helpful in some way for parents that experience something similar.
There have been some dark times, I'm sure there will be more but in between the storms, the sun will shine.
 
If you're interested in keeping up with Nola's journey you can also follow the hashtag #NolasJourney on Instagram.
 
 
Nola's Journey Blog Posts...
 
Coming soon...


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