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- Newsgroups: misc.kids
- Path: sparky!uunet!destroyer!gatech!darwin.sura.net!tulane!js
- From: js@cs.tulane.edu (Jan Silbermann)
- Subject: Eliana
- Message-ID: <1992Dec29.163543.29685@cs.tulane.edu>
- Sender: news@cs.tulane.edu
- Organization: Computer Science Dept., Tulane Univ., New Orleans, LA
- Date: Tue, 29 Dec 1992 16:35:43 GMT
- Nntp-Posting-Host-[nntpd-29611]: caesar
- Lines: 47
-
-
- Thank you to everyone who sent words of love and prayer to us. The
- response has been overwhelming. I am sorry that I did not reply in
- person to everyone, but the last couple of weeks have been hectic.
-
- Ellie spent a week in the hospital having test after test. We survived
- them all more or less intact (except that I almost passed out when
- the doctor drew blood from her head.)
-
- Ellie is now on ACTH. The drug lowers her immunity. I cannot go back to
- work untill she is off the drug (2 months) as I am a teacher and
- am around kids all day. Also it would be impossible to put Ellie
- in daycare now . The drug also makes her gain weight. She looks cute!
-
- Ellie is responding to the medecine. The seizures have reduced .
- considerably, but they haven't stopped. She now gets about 2-6
- a day. Previously she was having approx. 30. She mainly gets seizures
- when she is upset, so ironically she gets them in the morning when I give
- her her shot of ACTH!
-
-
- Her father and I oscillate between great hope and great despair.
- We have seen some amazing changes in Ellie since she started the medecine.
- Her head control is better, she rolls to the side, she pulls my hair,
- she smiles all the time, she vocalizes more. Ellie is receiving
- intense physical therapy. I try to stimulate her every way I can think of.
- We are trying to teach her how to use her body and brain. We had
- some encouraging news, she is not that far behind developmentally, I hope
- it keeps up.
-
- My older daughter, Tovah, is acting very strangely. She insists that her
- name is Ellie and that Ellie is Tovah. Tovah also acts like her sister.
- I think I give Tovah enough attention, but maybe I'm wrong. Now comes
- the difficult job of helping the normal child to feel as important as the
- "special" child.
-
- I am glad to be home. Spending a week in the pediatric ward really
- changes your perspective on life. When Ellie was first diagnosed and they
- told us how bad it could be, I actually found myself envying the
- parents of terminally ill children. At least they could see an end
- to their pain and could get the grieving over with. Now, I feel that
- there is hope. Ellie is so beautiful and wonderful.
-
- Now to my questions...
- Does anyone have any toy recommendations for stimulating play?
- Does anyone know of a good Physical therapy text?
- Any suggestions on how to stimulate Ellie when we are in the car?
-