I've Named My "Wigglys" - (Hickman Line)

[elise]

My First One is Named Sunny Jim
My Second One Is Named Craig Because Dad Means The World To Me.

I Know, It's A Crazy Thing To Do . Haha

Take Care,

Elise xx

[missy1306]

I don't think it is crazy I think it is cute! 

[dbab]

Elise,  It shows that you are taking it all in stride.  I have a friend with colitis and she named her colon, he is called Larry 

It makes things easier to deal with is what she tells me.  Keeps the sense of humor also through everything.

Thanks for the smile today Elise 

[Poochie]

Hi there Little One, I think it's wonderful that you are coping with this like you are.  I think those names are quite appropriate and loving. 

As you know I named my neuropathy "Fred".  It's so much easier to put a name to these things and fight with "them" as a person instead of a thing.   "Fred" (as in Fred Astaire) is always trying to teach me new dance steps.  His newest one is stopping suddenly on the left foot and pitching forward.  I don't really like this step, unless he intends to catch me up in mid flight.    But I always remember, "it could be worse".

Take care dear and say HI to your Dad,

Hugs, Love and God Bless,
Pooh 

[lynnmarie219]

Elise,

I don't think its a crazy thing to do at all.....and what an honor for your dad...to have your wiggly named after him because you love him so! 

You are certainly a special young lady!

[Crabcakes]

That is SO cute! If I had a line, I'd name it Piggly Wiggly! I love the idea of naming "symptoms". I'll have to think up something for mine! Good for you all on this positive and humorous aspect of this crazy disease!

[irish]

Elise, That is a great idea. Since you 2 are so close you might as well be on a first name basis. Take care now. Irish

[elise]

thanks for all the replys in so little time!
nice one, piggly wiggly!! Today i am just having a relaxing day.

BUT tomorrow i have to go to school for a meeting about my wigglys and how they work. Mrs Carter, Liz me and mum and dad will be there. i will just need to show her the end and she will know more then. thats at 12:30AM.

Then we will go home and have some lunch.
THEN  we will go to Kingsmill Hospital To see Dr Helen Venning And Jane Ellis About My JDM - Juviniele Dermato Myositis.
And THEN we will go on holiday for the weekend. im going to skegness but i will be taking my laptop so i'll contact you iif i get internet connection.