There is always hope!

[ Follow Ups ] [ Post Followup ] [ Cluster Headaches Messages ]

Posted by Karen ( on June 12, 2000 at 11:55:58:

In Reply to: Is there any hope? posted by R Holden on June 12, 2000 at 10:11:38:

I am very sorry to hear about your wife. I am do not have CH either but have recently discovered my 9yr old son is suffering from them. I know how you feel and it is VERY difficult to see our loved ones suffer so horribly.

The Neurologist just put Steve on Prednisone yesterday and so far today he has had no attacks. We see the Doc tomorrow and are anxious to do so. I have a larg list of questions for our doc thanks to the people on this board, they are truely wonderful and very supportive. I do have some advice though. Try to get your wife to come and post? If anything she will get not only lots of information but a chance to meet a group of fantastic people who will always be there for her.

Even though I am not a sufferer of CH I quickly learned to call this board my home.

Love and prayers to you and your wife and a big congratulations on the birth of your child!

Follow Ups:

Post a Followup




Optional Link URL:
Link Title:
Optional Image URL:

[ Follow Ups ] [ Post Followup ] [ Cluster Headaches Messages ]