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Is it advisable to do exercise when affected by Goodpasture syndrome? Which activities would you suggest and how intense should they be?

See if it is advisable for people with Goodpasture syndrome to practice sports and which ones are the most recommended if you have Goodpasture syndrome

Goodpasture syndrome sports
3 answers
Definitely low intensity exercise and low impact
Posted Jul 2, 2017 by Jade 700
This would depend on the severity of the GPS as it causes fatigue.

If on Peritoneal Dialysis then expertise should be restricted to a brisk walk.

Otherwise, just listen to your body
Posted Jul 6, 2017 by Paul 2200
I still try to increase activity each day. I just watch my blood pressure
Posted Oct 9, 2017 by Debbie 2000

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Stories of Goodpasture syndrome

GOODPASTURE SYNDROME STORIES
Goodpasture syndrome stories
MY STORY
My names Angela D I've had goodpastures for 10 years, I was 14 almost 15 when my lungs began to bleed, I at first was diagnosed with phamonia and was treated with that but I never got better I actually got worse, I was sent to Minneapolis children's ...
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MY JOURNEY WITH GOOD PASTURE
In 2007, I began to have trouble breathing and I started coughing up blood. This went on for several months and I was d diagnosed with pneumonia. I spent nine days in the hospital on IV antibiotics. I got better and didn't have any other symptoms unt...
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LUCEE'S STORY
I been sick on n off with stomache bugs etc since having my daughter in 2012.. last year 2015)- i was sick for weeks on end in n out of dr clinics having bloods done n spending most days in bed allday. I noticed over a period of about 3months my body...
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16 MONTHS AND COUNTING...
March 2016, things were looking pretty bleak. I'd started a new job in the January but, due to a lack of adequate support or training, it was decided I "wasn't suitable" and my contract was terminated. To make things worse, I'd just got a cold. So I...
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MY HERO
My daughter was 33 with 3 small children when she was diagnosised with GPS.  She spent months in the hospital and has been in and out more times than I can count the past 5 years.   I think the hardest thing about being a parent of a GPS patient is...

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