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Re: Welcome Teneya

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,

You are such an inspiration to all of us! You completely knock my socks

off. I never knew about you tracing your renal history back to being five!

When you have (hah!) a spare moment, I would love to hear that story.

Love,

Cy

Re: Welcome Teneya

> Hi Teneya,

>

> I think it always hits me the hardest when a little one gets diagnosed

with

> IgAN. As a mother myself, I know it has to break your heart to hear your

son

> has a chronic illness.

>

> Walt already gave you a great reply which I trust was very encouraging,

and I

> think you will find a number of parents here who have children with IgAN.

I

> do think it seems like the young ones seem to respond very well to

treatment.

> Just this week Crystal reported that her daughter is a success story. I

> really do pray that is the case with your son.

>

> Have they discussed treatments with you yet? We have some Moms whose

> children are just on Ace inhibitors, and others who have gone the route of

> Prednisone, depending on lab results at the time of diagnosis.

>

> I was first symptomatic as a teen, but I know I had protein in my urine

that

> I can trace back to a severe illness when I was 5 years old. I am now in

my

> 40s, and have been extremely active and had a fulfilling life including

getting

> married, raising two children, having a successful career, being very

active

> in my church and even to this day I run three or four days a week for

three

> miles. I am currently down to 20% kidney function but still am working

full

> time and am not on dialysis. I hope that gives you some encouragement

that your

> son can too have a very full life.

>

> is another of our members, who unfortunately did reach end stage

renal

> failure as a college student, but has had a successful transplant, is back

in

> Nursing school full time and even recently engaged over her spring break.

> So, even if the worst does happen, those with IgAN tend to do very well.

>

> Please know that there are many people here who are just waiting to

encourage

> you and share their experiences with you. Please don't hesitate to jump

in

> and ask any questions you may have.

>

> Welcome again,

>

>

>

>

>

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YOU'VE ONLY GAINED FIVE POUNDS SINCE THE ''70's?????

OK, now that I got that out of my system.... Thank you so much for your IgAN

story, ! You've relayed bits and pieces, but never the whole thing.

Boy, that must have been scary for your parents. I think of how little was

know about renal disease back then. I bet they had their share of sleepless

nights.

Hope all is well in your sector. I really appreciate you're telling this

story.

Cy

Re: Welcome Teneya

> In a message dated 5/23/2004 7:39:07 PM Pacific Daylight Time,

> cyashleywebb@... writes:

>

> > I never knew about you tracing your renal history back to being five!

> > When you have (hah!) a spare moment, I would love to hear that story.

> > Love,

> >

> > Cy

> >

>

> Hi Cy,

>

> OK since you asked, here it is:

>

> When I was 5, I had gross hematuria and was very ill for nearly a month.

At

> that time, I did not get a diagnosis. I never was checked again until a

> routine test as a teenager (around 15??) showed protein in my urine. I

was

> referred to a Nephrologist who said it was nothing to worry about,

probably the

> result of a recent strept infection, and I did not need to be monitored.

>

> I began having high blood pressure in the mid 70's, along with extremely

high

> cholesterol, around 325 despite weighing about 115 (I am 120 now) at the

time

> and being 5 ft 6.5 inches, and eating a very low fat diet. I was treated

for

> the cholesterol, but not for the protein. Then I had two more episodes of

> hematuria in the late 70's, but was not referred for a biopsy until 1987.

That

> one came back with " probable IgAN. " I was followed on an annual basis for

> close to 10 years, and was on just one BP med all that time, which was

> lisinopril. In 1997, I got a new Nephrologist when my old one retired,

and he requested

> a new biopsy which gave a definitive diagnosis of IgAN. I was about 50%

> function in 97.

>

> I have never had any more episodes of gross hematuria since the late 70s,

but

> BP has become harder to manage, with treatment requiring 4 BP meds a day

now,

> plus the Zocor and Cellcept I take. Since 2000, I have been on Procrit

for

> anemia, and fatigue has become harder to manage. I am currently at 20%

renal

> function, but as you know still work full time, manage a house hold, run

three

> miles 3-4 days a week, and participate in a Bible Study group one night a

> week. I have had to drop out of my other ministries over the past year

and a half

> or so though. I was more active but these last 18 months, work takes

about

> all I have. Weekends are mostly spend recovering from the energy I have

> expended during the week. I need 10+ hours of sleep a night now, but

overall I

> think I am doing pretty well for the function I have left.

>

> Good thing both my girls are grown, and now I only have my youngest on

summer

> breaks from college. I don't know how some of you at my level with young

> children do it. Just baby-sitting for friends or family for one evening

wipes me

> out :-)

>

> That is my story, so now you know!

>

>

>

>

>

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YOU'VE ONLY GAINED FIVE POUNDS SINCE THE ''70's?????

OK, now that I got that out of my system.... Thank you so much for your IgAN

story, ! You've relayed bits and pieces, but never the whole thing.

Boy, that must have been scary for your parents. I think of how little was

know about renal disease back then. I bet they had their share of sleepless

nights.

Hope all is well in your sector. I really appreciate you're telling this

story.

Cy

Re: Welcome Teneya

> In a message dated 5/23/2004 7:39:07 PM Pacific Daylight Time,

> cyashleywebb@... writes:

>

> > I never knew about you tracing your renal history back to being five!

> > When you have (hah!) a spare moment, I would love to hear that story.

> > Love,

> >

> > Cy

> >

>

> Hi Cy,

>

> OK since you asked, here it is:

>

> When I was 5, I had gross hematuria and was very ill for nearly a month.

At

> that time, I did not get a diagnosis. I never was checked again until a

> routine test as a teenager (around 15??) showed protein in my urine. I

was

> referred to a Nephrologist who said it was nothing to worry about,

probably the

> result of a recent strept infection, and I did not need to be monitored.

>

> I began having high blood pressure in the mid 70's, along with extremely

high

> cholesterol, around 325 despite weighing about 115 (I am 120 now) at the

time

> and being 5 ft 6.5 inches, and eating a very low fat diet. I was treated

for

> the cholesterol, but not for the protein. Then I had two more episodes of

> hematuria in the late 70's, but was not referred for a biopsy until 1987.

That

> one came back with " probable IgAN. " I was followed on an annual basis for

> close to 10 years, and was on just one BP med all that time, which was

> lisinopril. In 1997, I got a new Nephrologist when my old one retired,

and he requested

> a new biopsy which gave a definitive diagnosis of IgAN. I was about 50%

> function in 97.

>

> I have never had any more episodes of gross hematuria since the late 70s,

but

> BP has become harder to manage, with treatment requiring 4 BP meds a day

now,

> plus the Zocor and Cellcept I take. Since 2000, I have been on Procrit

for

> anemia, and fatigue has become harder to manage. I am currently at 20%

renal

> function, but as you know still work full time, manage a house hold, run

three

> miles 3-4 days a week, and participate in a Bible Study group one night a

> week. I have had to drop out of my other ministries over the past year

and a half

> or so though. I was more active but these last 18 months, work takes

about

> all I have. Weekends are mostly spend recovering from the energy I have

> expended during the week. I need 10+ hours of sleep a night now, but

overall I

> think I am doing pretty well for the function I have left.

>

> Good thing both my girls are grown, and now I only have my youngest on

summer

> breaks from college. I don't know how some of you at my level with young

> children do it. Just baby-sitting for friends or family for one evening

wipes me

> out :-)

>

> That is my story, so now you know!

>

>

>

>

>

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Guest guest

YOU'VE ONLY GAINED FIVE POUNDS SINCE THE ''70's?????

OK, now that I got that out of my system.... Thank you so much for your IgAN

story, ! You've relayed bits and pieces, but never the whole thing.

Boy, that must have been scary for your parents. I think of how little was

know about renal disease back then. I bet they had their share of sleepless

nights.

Hope all is well in your sector. I really appreciate you're telling this

story.

Cy

Re: Welcome Teneya

> In a message dated 5/23/2004 7:39:07 PM Pacific Daylight Time,

> cyashleywebb@... writes:

>

> > I never knew about you tracing your renal history back to being five!

> > When you have (hah!) a spare moment, I would love to hear that story.

> > Love,

> >

> > Cy

> >

>

> Hi Cy,

>

> OK since you asked, here it is:

>

> When I was 5, I had gross hematuria and was very ill for nearly a month.

At

> that time, I did not get a diagnosis. I never was checked again until a

> routine test as a teenager (around 15??) showed protein in my urine. I

was

> referred to a Nephrologist who said it was nothing to worry about,

probably the

> result of a recent strept infection, and I did not need to be monitored.

>

> I began having high blood pressure in the mid 70's, along with extremely

high

> cholesterol, around 325 despite weighing about 115 (I am 120 now) at the

time

> and being 5 ft 6.5 inches, and eating a very low fat diet. I was treated

for

> the cholesterol, but not for the protein. Then I had two more episodes of

> hematuria in the late 70's, but was not referred for a biopsy until 1987.

That

> one came back with " probable IgAN. " I was followed on an annual basis for

> close to 10 years, and was on just one BP med all that time, which was

> lisinopril. In 1997, I got a new Nephrologist when my old one retired,

and he requested

> a new biopsy which gave a definitive diagnosis of IgAN. I was about 50%

> function in 97.

>

> I have never had any more episodes of gross hematuria since the late 70s,

but

> BP has become harder to manage, with treatment requiring 4 BP meds a day

now,

> plus the Zocor and Cellcept I take. Since 2000, I have been on Procrit

for

> anemia, and fatigue has become harder to manage. I am currently at 20%

renal

> function, but as you know still work full time, manage a house hold, run

three

> miles 3-4 days a week, and participate in a Bible Study group one night a

> week. I have had to drop out of my other ministries over the past year

and a half

> or so though. I was more active but these last 18 months, work takes

about

> all I have. Weekends are mostly spend recovering from the energy I have

> expended during the week. I need 10+ hours of sleep a night now, but

overall I

> think I am doing pretty well for the function I have left.

>

> Good thing both my girls are grown, and now I only have my youngest on

summer

> breaks from college. I don't know how some of you at my level with young

> children do it. Just baby-sitting for friends or family for one evening

wipes me

> out :-)

>

> That is my story, so now you know!

>

>

>

>

>

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