Jump to content
RemedySpot.com

For

Rate this topic


Guest guest

Recommended Posts

Hi there ,

Thanks for your words of support and encouragement,

very important at times like this. Replying to all these kind

thoughts has focused my mind on things other than my immediate

problems and given me more pleasant thoughts.

Derrick

Sydney, Australia

Link to comment
Share on other sites

  • 1 month later...

Well, here in Margate, we don't have computers in the childrens ward yet.

All the children do have individual tv's which pull out from their bed. The

trouble is they entertain the kids but not the parents. On my recent stays

in hospital I have found it very lonely. Whilst my daughter has watched

non-stop Scooby Doo for 8 hours whilst lying on her comfortable bed, I have

been stuck sitting for 3 days on a hard chair playing with the kids toys on

my own through complete boredom as it's been impossible to get any

converstation from her!

Perhaps there should be one tv for the kids and one for the parents!

If I am ever unfortunate enough to go onto dialysis, I hope I don't become

addicted to Scooby Doo. I'll know I really am seriously ill if that is the

case. As my son says, its always the man in the mask who did it, so why do

you need to watch more than one!

As usuall I have completely digressed from the IGAN topic.

Frances

Link to comment
Share on other sites

  • 1 year later...

Hello .

Our son ( now 13 years old ) didn't have any major digestion problems

either, but at age nine or ten was starting to have violent outbursts

against others and himself. After a very short time on SCD he became much

more at ease with himself and more loving. Best thing we ever did.

Best Wishes.

Miles.

New to Diet

My son is 22 months and has been diagnosed ASD at about 18 months

(we suspected it earlier). He has multiple speech and developmental

delays and often has viloent, uncontrollable tantrums. He is

engaged most of the time and eye contact is quite good, but we never

really know what will set him off. His diet is terribble and

limited, consisting of GF Pancakes and Waffles, Chicken Nuggets,

Pear Sauce, and PBJ. We are starting him on the SCD diet. My wife

and I to say least are overwhelmed. A couple questions come to

mind. Is is common for a child to not have any noticeable digestive

problems (i.e. diarhea ect..) and still need this diet? Secondly,

after being on the diet for a period of time, do the children become

more open to different varieties of food? Finally he still breast

feeds and we are unsure when it is would be beneficial to ween him

since it is his main source of comfort during his melt downs. Our

son is so limited on what he will eat, I guess I'm just looking for

some encouraging responses. Any info would be appreciated.

Father of 22 months

----------------------------------------------------------------------------

--

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...