Re: EDS and Urology issues

[Guest guest]

In a message dated 5/1/03 6:26:34 PM Eastern Daylight Time, pghand@...

writes:

..

>

> I have an article for you , I'll end it along now....

>

>

Thanks, Jill. You always have something. Now I just found out that my female

urol. is gone!! BoO HHOOO.

[Guest guest]

In a message dated 5/1/2003 5:26:39 PM Central Daylight Time,

pghand@... writes:

> I have an article for you , I'll end it along now....

>

>

I'd be interested too Jill. I'm having bladder surgery June 23rd ...

Pk

[Guest guest]

In a message dated 5/1/2003 6:31:28 PM Central Daylight Time,

Mdmssmile@... writes:

> Thanks, Jill. You always have something. Now I just found out that my female

>

> urol. is gone!! BoO HHOOO.

>

>

>

Aww bummer. My urologist is about 35, tall, dark hair, dark eyes, lean

...extremely good looking ...that's just wrong! Urologists should be middle

aged or old or female. Good looking men should not be allowed LOL

Pk

[Guest guest]

I have an article for you , I'll end it along now....

Jill

I was just wondering as I go down yet another new path, what kinds of

urological issues are associated with EDS....either , written up in the

literature, or antedotially that everyone is aware of.

[Guest guest]

In a message dated 5/1/2003 9:17:49 PM Central Daylight Time,

bheint@... writes:

> When I had my bladder suspension surgery in Jan 03 they used both mesh AND

> cadaver tissue.

>

> I also had a suprapubic catheter after surgery because of the EDS. I

> didn't

> start to feel better until after it was removed which was no big

> thing...didn't hurt to have it taken out at all like I thought it would.

>

> The urologist used glue for the laproscopic sites which took weeks and

> weeks

> to wear off the skin.

>

> Bonnie

>

Bonnie do you have type 3 or 4?

Did they do a sling? I'm having the kind where they tack the bladder up

against the abdominal wall. Not the sling. They didn't think the sling would

be good with my Myasthenia Gravis (neuromuscular disease). It is going to be

an incision rather than laproscopic.

Pk

[Guest guest]

When I had my bladder suspension surgery in Jan 03 they used both mesh AND

cadaver tissue.

I also had a suprapubic catheter after surgery because of the EDS. I didn't

start to feel better until after it was removed which was no big

thing...didn't hurt to have it taken out at all like I thought it would.

The urologist used glue for the laproscopic sites which took weeks and weeks

to wear off the skin.

Bonnie

Re: EDS and Urology issues

In a message dated 5/1/2003 5:26:39 PM Central Daylight Time,

pghand@... writes:

> I have an article for you , I'll end it along now....

>

>

I'd be interested too Jill. I'm having bladder surgery June 23rd ...

Pk

[Guest guest]

Hang in there , when one door closes, another opens.....

Jill

Thanks, Jill. You always have something. Now I just found out that my female

urol. is gone!! BoO HHOOO.

[Guest guest]

how well did the glue work on lapariscopis sites? i am having a lapariscopic

tubal ligation after i have my son.

Thanks

Autumn

-- Re: EDS and Urology issues

In a message dated 5/1/2003 9:17:49 PM Central Daylight Time,

bheint@... writes:

> When I had my bladder suspension surgery in Jan 03 they used both mesh AND

> cadaver tissue.

>

> I also had a suprapubic catheter after surgery because of the EDS. I

> didn't

> start to feel better until after it was removed which was no big

> thing...didn't hurt to have it taken out at all like I thought it would.

>

> The urologist used glue for the laproscopic sites which took weeks and

> weeks

> to wear off the skin.

>

> Bonnie

>

Bonnie do you have type 3 or 4?

Did they do a sling? I'm having the kind where they tack the bladder up

against the abdominal wall. Not the sling. They didn't think the sling would

be good with my Myasthenia Gravis (neuromuscular disease). It is going to be

an incision rather than laproscopic.

Pk