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Hi Becky,

Welcome. You have come to the right place to understand Igan. There

are many knowledgable people in this group who are willing to answer

any questions you have...support is just a click away.

:o)

> HI. My name is Becky and I am new to the group. I was diagnosed

with

> IgaN in March. I am still trying to understand what the disease is

> and what this means to my life. I have had blood and protein in my

> urine since I was 25 and am now 29. I thought joining this group

> might be a comfort to me. My friends and family are there for me of

> course, but they can't identify with my emotions right now.

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Welcome Becky,

I know you¹ll get lots of support and information here. My son who is 13 was

diagnosed 4 weeks ago so I¹m figuring out what this means too.

All the Best, Suzanne

>

> *

>

>

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Welcome to the group, Becky. I'm glad you found us.

Pierre

I'm new

> HI. My name is Becky and I am new to the group. I was diagnosed with

> IgaN in March. I am still trying to understand what the disease is

> and what this means to my life. I have had blood and protein in my

> urine since I was 25 and am now 29. I thought joining this group

> might be a comfort to me. My friends and family are there for me of

> course, but they can't identify with my emotions right now.

>

>

>

>

>

>

>

> To edit your settings for the group, go to our Yahoo Group

> home page:

> http://groups.yahoo.com/group/iga-nephropathy/

>

> To unsubcribe via email,

> iga-nephropathy-unsubscribe

> Visit our companion website at www.igan.ca. The site is entirely supported

> by donations. If you would like to help, go to:

> http://www.igan.ca/id62.htm

>

> Thank you

>

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In a message dated 7/28/2005 8:45:18 A.M. Pacific Daylight Time,

racorbett@... writes:

HI. My name is Becky and I am new to the group. I was diagnosed with

IgaN in March.

Hi Becky,

A very warm welcome to the group! I am sorry you have a reason to find your

way here but I do hope you can find much support and information on our two

sister sites. If you have not already checked out our sister site at

_www.igan.ca_ (http://www.igan.ca) , that would be a great starting place.

The emotions can feel overwhelming at first. My only advice there is to be

patient with yourself and give yourself time to work through all the stages

until you get to acceptance. It does take time but honestly, it all becomes

second nature after a while.

In the meantime, we are here to support you each step of the way.

Welcome again,

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  • 2 years later...
Guest guest

Dear ladies, thanks so much for this sight. I've done some looking

around and this is the best by far. I need help and just to vent. I've

had my share of both vulvar and vaginal problems lately. Started out as

severe vulvar pain-felt like the nerve endings were fried. With that

came bacterial vaginosis, which is treated with antibiotics- Flagyl And

metrogel, which in turn caused yeast infections. The last had to be

caused by a strain of resistent yeast because it wouldn't respond to

monistat or Diflucan. Boric acid did work well. My dr. told me I had

Lichen Sclerosis as well, though the symtoms wasn't much as described,

especially in appearance. To try and make a long story short this has

been a nightmare. I was prescribed a strong steroid cream and Estrace

as well as tablets. What with the creams the pain has gone. That's

why I'm wondering if it's possible to have a mild case of LS, one that

caused pain and itching but doesn't change the appearance. I still

have minor irritation and itching. It itches down the inside of my

thighs and way up front where the hair is but there's nothing to see.

Oh, Ladies, I just want to feel normal againand it seems so close but

not quite. I'm thankful to having improved so much but at this point

any of it is too much. I was told low hormones was the culprit. I'm

50. Norm

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