New to site

[rwb200]

Hello I'm new to the site but not new to Lupus. My wife was diagnosed with Lupus 18 Years ago. Today we have experienced many things that we never dreamed of 18 Years ago.
2 Heart Attacks, Raynauds, Vasculitis, Arthritis, Pneumonia, Hair loss, Loss of most all her teeth and a drug sensitivity list that looks more like a perscription med list then an alergy list, Rashes, blisters and many more items that just do not come to mind at this time. :wave:
But we have learned to deal with these things as they come and take each day one day at a time.
At this time I do not have any questions but wanted to introduce myself and maybe some day I will see someone who can benifit from my experiences.

[dollface]

Hi rwb200,

Welcome! I'm also a newbie.
My name is Abi and I was diagnosed over 10 years ago.

Just wanted to say a BIG Thank you on behalf of all wives/partners for being there.
hope I'm not speaking out of tone.

Take care and God be with you both.

Abi
xx

[alobreto]

Welcome! ;)
Most of us TRULY appreciate and admire our life partners who are with us through thick and thin. It's tough to have a chronic illness. It's also tough to care about someone who has a chronic illness.

I wish you and wifey the best!
Regards,
Angela :flowers:

[dmb]

I'm pretty new as well (and late in responding), but I just wanted to thank you for hanging around here to help, and give perspective from you and your wife's ordeals/experiences. :flowers: