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File - Roll Call-Check In   Message List  
Reply | Forward Message #1813 of 2355 |
Re: [cerebralpalsy] File - Roll Call-Check In

HI everyone!

Ethan is doing well. He started preschool this fall
and he is doing awesome! He is in a class with
children who all have speech delays and receives
speech, OT and PT. He also receives private PT and we
are on a waiting list for a permanent speech time
slot but they will begin "co- treating" (speech during
his PT) tomorrow.

He is getting his DAFO's next week. He did so well for
the casting. He just sat there so still smiling and
helped pick out the colors for the velcro.

The school district bus service finally gave up their
fight against me. Originally they did not want to come
to the house to pick up Ethan. SEveral phone calls and
tears and educating them on what CP is and that he
falls often and tires easily finally got them to come
to the house to pick him up and drop him off. THen
began the battle of explaining that I needed
assistance with my other "able bodied children" (as
they put it, because I could not be in 2 places at
once. I think the thing that helped was talking to the
supervisor when I was still upset. My instunct is to
go calm down then make my calls. THe call that I got
the furtest was the one where I let them hear how
upset I truly was (not angry..but upset). Sometimes it
feels like Ethan is the only child to have ever had a
disability in my school district. Thankfully his
teacher is wonderful and supportive and helped steer
me and guide me.

I am also coming to terms with being a parent of a
child with special needs. Ethan has had special needs
all along (he began therapies at 12 months) but the
diagnosis made me face it head on. I think I greived
well, read books about greiving. Don't get me wrong I
still have my days but I don't even see the CP
anymore..I just see Ethan and he's "typical" to me and
I jsut love him to pieces. I think the hardest part
was the guilt I felt for greiving. Even though I knew
it was necessary to greive I felt terrible for feeling
that things were different when I had such a wonderful
child. I still wish Ethan didn't have CP, I just wish
that now for HIM instead of for me. I just feel so
lucky that I get to have him and how he has enriched
my life and my other children's life.


I hope everyone else is doing well.

Sandy,
Mom to Brandon (7) Cameron (5) Ethan (3)& Logan (7mos)

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Fri Nov 2, 2007 3:49 am

suecassy
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Message #1813 of 2355 |
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Jan, I am so sorry you are having such a time with doctors!! Please get a second and 3rd opinion...and not from a doctor that the original docs refer you...
Castle
castletowery
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Nov 4, 2007
4:11 pm

HI everyone! Ethan is doing well. He started preschool this fall and he is doing awesome! He is in a class with children who all have speech delays and...
Cassy Sue
suecassy
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Nov 2, 2007
3:49 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Dec 1, 2007
8:56 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Jan 1, 2008
8:57 am

Hi ALl well I hope 2008 takes a turn for the better as Daire has started this year being really sick, we thought at one stage we were loosing him. GP perplexed...
dairewendy
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Jan 4, 2008
5:55 pm

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Feb 1, 2008
8:59 am

Hi all, We have been very busy these last few months. I finally had a baby last August and i am just now up to speed physically and hormonally. I forgot that...
betsy pajak
pajak4
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Feb 2, 2008
11:41 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Mar 1, 2008
9:00 am

Hello, My name is Lisa and my son Joshua is 4 yrs old and has CP, Hydrocephalus w VP shunt, CVI, and profound cognitive delays. He goes to a special needs...
my_special_son2
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Mar 7, 2008
10:00 pm

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Apr 1, 2008
8:13 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
May 1, 2008
8:01 am

Hi, My name is Lisa and my son Joshua is 4 1/2 yrs old and has CP, Hydrocephalus, CVI, and profound cognitive delays. We have been working on strengthening his...
my_special_son2
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May 1, 2008
6:38 pm

my son is doing alot better he was put on baclafin in march we can see a little bit off changes in his activity he is starting on it very slowly he is getting...
David Havens
davidhavens2007
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May 11, 2008
2:17 pm

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
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Jun 1, 2008
8:05 am

Happy June!!! I have not been very active....winter was hard....my son Jordan was sick all the time and hospitalized for a 5 day stay for pneumonia. Now that...
sandra700mlappy
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Jun 2, 2008
12:14 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Jul 1, 2008
8:02 am

WOW we have been busy!!! Cayden is starting intensive therapy next...she will be getting suit therapy 3 hours a day 5 days a week for the next 3 weeks ...
Castle
castletowery
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Jul 1, 2008
10:59 pm

Castle, Please let me know how IMOT goes for Cayden...I have been wanting to try it with Aubrey but I'm not thrilled with the (only) center in town that offers...
Lindsey Duckworth
lindseyinjapan
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Jul 2, 2008
12:36 am

Hi Castle, yes, my guess is that the irritability is from the diazapam.  it is valium and she may be working through the dependence.  Matt was on it too for...
betsy pajak
pajak4
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Jul 2, 2008
1:08 am

Castle, I remember when my daughter was little and she went off Phenobarbital she wouldn't sleep as much and was cranky to say the least. I also know as they...
Carleen Briney
pinkfuzzycow...
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Jul 2, 2008
6:45 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Aug 1, 2008
7:58 am

Castle and other group members, My son Joshua is now 4 1/2 and has been having a great summer. We live in NC but are spending the entire summer in Las Vegas,...
my_special_son2
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Aug 2, 2008
7:26 pm

Dream Therapies in NC?  My sister lives there and my niece is a horseback riding instructor who is young and very interested in this type of therapy. Debra...
Debra Marasco-McNulty
debraphp
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Aug 5, 2008
1:54 am

We're spending the summer in Las Vegas, NV and Dream Therapies is here. But we do therapeutic riding at Stepping Stone Stables in Pikeville, NC back home. It...
my_special_son2
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Aug 5, 2008
4:36 pm

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Sep 1, 2008
7:44 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Oct 1, 2008
7:51 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Nov 1, 2008
7:44 am

Here's an update on our family.  Wish I could say it's short, but it's not.   I'll go from youngest to oldest. Jacob (dx-spastic quad. CP secondary to shake...
Angela Golembeski
momslove1990
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Nov 6, 2008
11:12 pm

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Dec 1, 2008
8:48 am

How is everyone doing? Please take a second to give us a update. Let us know if there are any new milestones your child has reached. Anything new in your...
cerebralpalsy@yahoogr...
Send Email
Jan 1, 2009
8:38 am
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