Louize Lowe

❤️

[Louize Lowe @LouAL87]

From a seizure on Christmas day 2021 to a diagnosis of a rare genetic disease just 30 days later #NHS75 #ThankYouNHS #apstypeoneawareness

[World Athletics @WorldAthletics]

Another one 👏

@JohnsonThompson wins her second #WorldAthleticsChamps heptathlon gold medal after a scintillating 800m.

6740 points for the win 💪

[HypoPARA Association @HypoPARAassoc]

Today is #ChronicDiseaseDay and we need your help in raising awareness for #hypoPARAthyroidism, a #raredisease that affects ~70K-115K people in the U.S. Consider sharing this resource on your personal pages to help others learn more: https://t.co/OW0wHWUIgX

[APS Type 1 Foundation @APSType1]

#DidYouKnow that APS Type 1 is inherited in an autosomal recessive pattern? That means that the parents of APS Type 1 patients each cary one copy of the mutated gene, but typically do not show signs of signs and symptoms of the condition. #genetics #raredisease #APECED

[APS Type 1 Foundation @APSType1]

Did you know that APS Type 1 is often misdiagnosed or diagnosed late due to its rarity and variable presentation? This can lead to delays in treatment and potentially serious complications.

[APS Type 1 Foundation @APSType1]

Today we celebrate the remarkable achievements of women all over the world. We’d like to take this opportunity to give a shout-out to the incredible female caregivers, nurses, & doctors who provide exceptional care to patients with APS Type 1. #InternationalWomensDay #APS1

[APS Type 1 Foundation @APSType1]

APS Type 1 is rare, but you’re not alone! To help us celebrate #RareDiseaseDay you can #ShowYourStripes by joining the APS Type 1 (APECED) Registry at https://t.co/evQE4g4KKZ

[APS Type 1 Foundation @APSType1]

Chronic adrenocortical insufficiency (Addison’s disease) is a rare disorder characterized by chronic, usually progressive, inadequate production of the steroid hormones cortisol and aldosterone by the outer layer of cells of the adrenal glands (adrenal cortex) Source: NORD

[APS Type 1 Foundation @APSType1]

Hypoparathyroidism in APS-1 has an autoimmune cause, but it can occur as a separate disorder associated with maldevelopment of the thymus, aortic arch and parathyroid glands (DiGeorge syndrome) or may also arise as a separate inherited disorder. Source: NORD

[BBC Sport @BBCSport]

"I was just going for a run for a mate" ❤

#Ultra7in7 #BBCRL #RLWC2021

[World Athletics @WorldAthletics]

Male Athlete of the Year nominee 🇰🇪

Retweet to vote for @EliudKipchoge in the #AthleticsAwards.

[World Athletics @WorldAthletics]

Female Athlete of the Year nominee 🇯🇲

Retweet to vote for @realshellyannfp in the #AthleticsAwards.

[APS Type 1 Foundation @APSType1]

Newly diagnosed or simply looking for a backgrounder on APS Type 1? Check out this recent article by the NIH Study Team: “Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy.” -- Ferré et al., (2021). https://t.co/B3zkpuWPkA

[Bianca Williams @BiancaaWills]

Having a baby shouldn’t stop you from achieving your goals 🫶🏾🫶🏾🫶🏾

#CommonwealthGames2022

[Lionesses @Lionesses]

🏆 OUR ENGLAND. OUR CHAMPIONS. 🏆

[British Athletics @BritAthletics]

BRONZE FOR DINA 🥉

@dinaashersmith clocks a 22.02 in the 200m final...

Proud ❤️

#WorldAthleticsChamps #WhereItStarts #WCHOregon22

[AW @AthleticsWeekly]

BRITISH RECORD

So so close for @dinaashersmith last night as she finished fourth in the 100m final, equalling her British record of 10.83 in the process.

That time was enough to win silver in Doha but the world 200m champion had to settle for fourth in a crazy quick race.

[World Athletics @WorldAthletics]

🥇🥇🥇🥇🥇

FIVE-TIME WORLD 100M CHAMPION

🇯🇲 @realshellyannfp 🇯🇲

10.67 ‼️ CHAMPIONSHIP RECORD ‼️

[APS Type 1 Foundation @APSType1]

#DidYouKnow that APS Type 1 is inherited in an autosomal recessive pattern? That means that the parents of APS Type 1 patients each carry one copy of the mutated gene, but typically do not show signs of signs and symptoms of the condition. #genetics #raredisease #APECED

[APS Type 1 Foundation @APSType1]

#DidYouKnow that APS Type 1 is a rare genetic disorder caused by mutations of the #AIRE gene? To learn more about #APS1 and #AIRE, check out this article entitled “AIRE deficiency, from preclinical models to human APECED disease.” https://t.co/4nQ6p1S8vk