Jump to content
RemedySpot.com

IVIg - Belinda, Dayna

Rate this topic


Guest guest

Recommended Posts

Hi from a long time lurker. Dayna, my daughter also has a

low IgA level (17) and doesn't produce antibodies to polysaccarhide

coated antigens. I can tell you that her life has improved

dramatically since beginning regular IVIg infusions 5 years ago.

Although life is still not normal - for example she was so sick that

she missed the whole last couple of weeks of eight grade last year;

the dance, graduation, everything - the quality is amazing compared

to pre-IVIg. I will warn you that because of her low IgA level she

does have some trouble receiving her infusions...but we have worked

so that she can receive them over a reasonable amount of time with a

reasonable amount of discomfort. It is scarey and overwhelming in

the beginning, but this group can make it a lot less so.

Belinda, just a quick thought. I noticed that Cassie receives her

infusions every 28 days. I know that we can't keep Jess healthy with

anything more than every 21 days. Sometimes even that is too long.

Have you ever considered having the infusions closer together? Jess

is 14 and receives 20g every 21 days.

Kim, mom to -selective antibody deficiency

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...