Team Addison USA

Team Addison USA Team Addison USA promotes awareness for Addison's Disease. Administrator - Colleen McMahon

For better knowledge & care for those affected by Addison's Disease..We hope for updated treatment protocols & sublime medical care within the USA & Global.

Hey there, just an update regarding my knee surgery for horn root repair which was scheduled at the end of the month… Po...
08/20/2025

Hey there, just an update regarding my knee surgery for horn root repair which was scheduled at the end of the month… Postponed at this point for at least 6weeks or more, due to several injuries sustained from a bad fall… Originally was told no fractures from the ER , they missed it on the catscan! Fractured 10th lateral left rib… Plus going to a spine Orthopedist tomorrow to make sure my acute coccyx pain isn’t involving an additional fracture… We know long term steroid usage for replacement in Primary ADRENAL Insufficiency can & does cause Osteoporosis & Osteopenia which results in fractures… The recent traumas on top of would be knee surgery is too much pulmonary wise & for having Addisons Disease to do the surgery yet.. Although the Orthopedic medical people for the knee were encouraging me to proceed with preop and that I might feel better in a few days or the following week.. I kept saying this is not a good idea now & my pulmonologist backed me up with not approving surgery.. Plus she listened to me and sent me for further X-RAYS scan of the ribs which in turn discovered the rib fracture which emergency didn’t through a catscan… Always advocate for yourself & trust how you feel & don’t be pushed into something that could turn disastrous if you listen to Doctors or their staff when your body is already overtaxed!!To have a surgery which is a long & complicated recovery … When you are NOT up to it!!Team Addison USA promotes Awareness for Addisons Disease for all affected by it… 🩵

Please vote for Team Addison Global for a media raising award.. They are the foundation of Team Addison throughout the w...
08/19/2025

Please vote for Team Addison Global for a media raising award.. They are the foundation of Team Addison throughout the world.. Team Addison USA is very proud to be a part of this amazing Team in promoting Awareness for those affected by Addison’s Disease for knowledge & better understanding and expeditious treatment… 🩵

Taking place in February, which also marks the occasion of Rare Disease Day, our annual EURORDIS Black Pearl Awards celebrate the outstanding achievements of people living with a rare disease, along with those who go that extra mile to make a difference to their lives. The awards celebrate hard work...

08/11/2025
I have been dealing with a posterior horn root tear to the medial meniscus since late April, which has now progressed to...
06/28/2025

I have been dealing with a posterior horn root tear to the medial meniscus since late April, which has now progressed to a complete/complex non-displaced tear. Surgery is necessary, as conservative treatment is ineffective in healing or repairing the tear. The recovery process will be extensive, requiring six weeks of non-weight-bearing, utilizing crutches or a walker, followed by a lengthy rehabilitation process and challenging recovery. Daily pain and mobility issues have been persistent problems. My orthopedic specialist recommends undergoing surgery within three months; however, sooner is preferable to prevent irreversible cartilage loss, which may lead to advanced arthritis and knee replacement if left untreated. As someone with Addison's disease, surgery poses additional risks, including pain management and anesthesia aftereffects. Living upstairs with a staircase further complicates my recovery. I must schedule the surgery soon. The phrase 'get on with it already!' resonates with me. I would rather forget the ordeal and enjoy my long-awaited summer. Life is full of challenges, and overcoming them is crucial. Team Addison USA promotes awareness for Addison's disease. I will provide updates on my progress. Wish me luck. 🍀 🙏🫶🏻🩵

Bravo, Martin Norrman founder of Team Addison Global !! We are so thankful for all of Martin's Global dedication & exten...
05/31/2025

Bravo, Martin Norrman founder of Team Addison Global !! We are so thankful for all of Martin's Global dedication & extensive work to bring Awareness of Addison's Disease & bring hope to all those affected by Addison's Disease. This film is a true example of courage and not allowing fear or a diagnosis to prevent you from pursuing your dreams..Team Addison USA promotes Awareness & provides their experience & knowledge and life-long journey to the forefront to bring hope to those affected by Addison's Disease within the USA...So you have the tools & courage to live you absolute best life and enjoy it regardless of an Addison's Disease diagnosis...🫶🩵

How do you live fully with a chronic illness?This short documentary shares the personal journey of Martin Norrman with Addison’s disease — a rare but life-th...

In Honor of the very first ADRENAL DISEASE DAY which was on April 7th 2025! In addition it's Adrenal  Disease Month! 🩵
04/09/2025

In Honor of the very first ADRENAL DISEASE DAY which was on April 7th 2025! In addition it's Adrenal Disease Month! 🩵

02/28/2025

Team Addison USA celebrates Rare Disease Day! 🩵

02/28/2025

Team Addison USA We have been spreading Awareness for Addison's Disease (Primary Adrenal Insufficiency) since 1/20/20..We would like to continue to build our followers to so many more...🩵 This is RARE DISEASE DAY!! .. Addison's Disease is one of the many Rare Diseases in which there is no cure..Someone with Addison's Disease is life dependent on steriods..Help us to spread Awareness for this rare population in which lives with Addison's Disease daily.. By following and sharing, knowledge is then spread and lives are saved or helped...Thank you with ❤️...

01/28/2025

Team Addison USA recognizes & honors this truly amazing man, Martin Norrman my friend who founded Team Addison Global & gave myself the opportunity to start & build & organize & run Team Addison USA !! He inspires many worldwide 🌐 those living with Addison's Disease/Primary Adrenal Insufficiency. His travels & journey help people worldwide within this rare community and shows them you can live your best life living with Addison's Disease. An not allow illness to prevent you from following your dreams....Martin's phenomenal & brave adventures, give specifics on how to avoid & prepare and handle & treat a setback while traveling with Addison's Disease.. Team Addison USA is so proud of you Martin, feeling blessed to be a friend and fellow Addisonian and part of this great Team - Team Addison Global ....🩵🌐💙

01/20/2025

Team Addison USA spreads Awareness for Addison's Disease - Primary Adrenal Insufficiency..People with Addison's are life dependent daily on steriods for survival..We need more exposure for knowledge & better & more expeditious life saving treatment for this rare population in all communities & countries and within all medical facilities wihin the USA & Global...Help us build Awareness throughout by following and sharing our knowledge & experience throughout the USA and Globe...So knowledge and awareness grows and saves lives and helps people with Addison's Disease live their absolute best life! Help us connect with more people within the USA and world..Thank you so much for supporting Team Addison USA...💙

Team Addison USA is sending my love & prayers to our very dear friend & fellow warrior Martin Norrman founder of Team Ad...
01/05/2025

Team Addison USA is sending my love & prayers to our very dear friend & fellow warrior Martin Norrman founder of Team Addison Global who survived a Adrenal Crisis while traveling abroad in Thailand..THANK GOD, he was well prepared for his trip medically with Solucortef injections & oral medications & Addison's Disease & Adrenal Insufficiency Crisis literature, for this life threatening event.. The medical care team in Thailand had to be advised & explained by Martin how to treat his Adrenal Crisis! Thank God he was prepared & alert to get the emergent treatment protocol..Martin happens to be normally very physically active and in supreme shape while living with Addison's Disease and other Comorbidities ..Although when you have Addison's Disease a Adrenal Insufficiency Crisis can occur when you body is stressed.
This is exactly why among other reasons, we spread Awareness of Addison's Disease & Adrenal Insufficiency Crisis...An Adrenal Crisis can be brought on anytime or anywhere due to - trauma or fever or infection or vomiting & diarrhea & surgery & stress induced...Always be prepared on the daily carry your oral medications (steriods) & injectable Solucortef and literature explaining Addison's Disease & Adrenal Insufficiency Crisis treatment protocol..Especially while traveling, not all medical care abroad or domestic is sufficiently experienced or knowledgeable on treatment of Addison's Disease & Adrenal Insufficiency Crisis .. You would not want to be caught in a situation that requires immediate emergency care & treatment that the medical team is not experienced enough or does not have the medication to save your life in a Adrenal Crisis.... God bless & May you have a fast and full recovery and return home safely Martin.. 🫶❤️🫂 🙏🏻... Team Addison USA spreads Awareness for Addison's Disease...

Team Addison USA We grieve for you Michael, and are so very deeply sorry you lost your fight to Addison's Disease due to...
10/11/2024

Team Addison USA We grieve for you Michael, and are so very deeply sorry you lost your fight to Addison's Disease due to lack of proper treatment...Thank you for all you did for your team in Germany...May you find infinite love and peace with the Angel's in Paradise..Sending love to your family and Nadine....🫶❤️ We will continue to spread Awareness and fight for proper treatment in honor of all the soul's we have lost too soon and unfortunately, including you dear Michael Scharf....🙏🩵🙏

PLEASE SHARE and follow us so we can spread awareness of Addison's disease.
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Hey,

My Name is Nadine. I myself don't have Addison' disease. But my boyfriend Michael had it.

12 years ago we had a hard time figuring out whats wrong with him. We went to multiple doctors but no one could help him. At some point he suffered a collapse and was admitted to the intensive care unit. They didnt know whats going on so they just gave him everything and hoped for the best. Luckily they also gave him cortisone. He nearly died that day. A urologist who was interested in rare diseases found out a few days later that he had Addison's disease. We finally had a diagnosis after 6 months of running from one doctor to another.

He started learning all about Addison's Disease, read multiple studies and then found out about Team Addison's Global. Because of Team Addison's Global he started with running and weight lifting and was always so proud of what he can do despite the illness. And i was too. You guys helped him to be a better version of himself. And to give something back he started helping others that struggle with Addison's and give them advice on multiple discussion boards and FB Groups in Germany, cause he sadly learned himself how hard it is to be heard with such a rare disease.

It was always a fight when he needed to go to the hospital because of an Addisonian crisis and not being taken seriously. He was sometimes so angy about the ignorance of the doctors not willing to learn something about it and that people need to beg for help and need to explain themselves in such a struggling situation instead of just helping them.

On 11th September 2024, just 2 days after my birthday, he woke up at night with really bad back pain. He went to our doctors office early in the morning, because he thought it might be a crisis. She was alarmed cause his blood preasure was really high which is unusal for a crisis. She called an ambulance and let him brought to the ER. They just run a blood test and an ECG and send im home.

No treatment,nothing. Still in pain and with high blood preasure. He collapsed some hours later and had a seizure so i called the ambulance again and they took him to the hospital again. But without even examine him they told him that he can go home or into the psychiatry. So we went back home, where he collapsed again a few hours later after hours of pain and not understanding why they dont helped him at the hospital even though he was there 2 times that day. I called the ambulance again and they took him back to the hospital and I wasnt allowed to come with him. I called after an hour as they told me and at this point they where already reanimating him. They tried it for nearly 2 hours.

He passed away on 12th September because of an aortic dissection which could have been found and fixed if they just had examined him properly.

He always tried his best helping others and encouraging them to make themselves been heard and seen and to outgrow themselves even with a medical condition like Addison's disease.

Sadly at the end he wasnt been heard and seen by the doctors which makes it so much worse to know that he could still be here and so much more important that you keep on spreading awareness and raise your voices.

He was so proud of all of you ❤️

Www.teamaddison.se

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