Why Wobbly Wife?
So I figure before I get too far into this thing, I should explain why I decided to share my life and experiences being married with Cerebral Palsy (CP). Why Wobbly Wife?
I have dabbled in blogging sporadically before, but I had come up with the name and idea for this blog even before I got married. Being married with CP, or any other physical disability for that matter, was a mystery to me. Obviously because I have never been married before but also because I have never really seen, or remembered seeing, a "CP marriage" up close and personal.
I had so many questions in the months leading up to our wedding, in regards to how it would work with me having this extra set of challenges. I even went so far as to Google certain topics related to marriage and CP, but I found no answers to my questions and there weren't many resources readily available to me. My fiancé had questions too, and I felt bad that I couldn't answer them, even though his questions were about such an integral part of myself.
I was a little nervous in deciding to go through with this, because I knew that I wanted to be real and straightforward with my readers. It helped that my husband was, and is, super supportive. But I still had my reservations.
However, I realized that if I had unanswered questions, maybe others did too. And I could use this blog as a resource for people who had some of these same questions, to provide a real look into how a marriage with CP works and to provide hope.
You may be one of those people. Maybe you have CP yourself, or some other disability which makes you question a future that you are dreaming of. Or maybe you are just curious and want to know more. Whatever the case, I'm glad you've happened upon my little corner of the internet.
Feel free to ask me any questions you may have, either through Facebook messenger or my profile through the blog site.
Thanks again for joining me on this journey!
I have dabbled in blogging sporadically before, but I had come up with the name and idea for this blog even before I got married. Being married with CP, or any other physical disability for that matter, was a mystery to me. Obviously because I have never been married before but also because I have never really seen, or remembered seeing, a "CP marriage" up close and personal.
I had so many questions in the months leading up to our wedding, in regards to how it would work with me having this extra set of challenges. I even went so far as to Google certain topics related to marriage and CP, but I found no answers to my questions and there weren't many resources readily available to me. My fiancé had questions too, and I felt bad that I couldn't answer them, even though his questions were about such an integral part of myself.
I was a little nervous in deciding to go through with this, because I knew that I wanted to be real and straightforward with my readers. It helped that my husband was, and is, super supportive. But I still had my reservations.
However, I realized that if I had unanswered questions, maybe others did too. And I could use this blog as a resource for people who had some of these same questions, to provide a real look into how a marriage with CP works and to provide hope.
You may be one of those people. Maybe you have CP yourself, or some other disability which makes you question a future that you are dreaming of. Or maybe you are just curious and want to know more. Whatever the case, I'm glad you've happened upon my little corner of the internet.
Feel free to ask me any questions you may have, either through Facebook messenger or my profile through the blog site.
Thanks again for joining me on this journey!
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