Our Story
Hello Friends and Family! I have Cystic Fibrosis. CF is a hereditary disease that affects the lungs and digestive system. The body produces thick and sticky mucus that can clog the lungs and obstruct the pancreas. It can be life-threatening, and people with the condition tend to have a shorter-than-normal life span. At the age of 32 I gave up my career to focus on my health in January 2019. Luckily, in about 7 months time, I received my life-saving double lung transplant on July 28th, 2019 after having 2 dry runs. I spent 30 days in the hospital recovering, another 3 months going to daily pulmonary rehab, and a long recovery at home.
I’ve chosen to enlist the help of the Children’s Organ Transplant Association (COTA) during my transplant journey (before, during, and recovery for years following). COTA (COTA) helps children and young adults who need a life-saving transplant by providing fundraising assistance and family support. COTA is the nation’s only fundraising organization solely dedicated to raising life-saving dollars in honor of transplant-needy children and young adults. 100% of each contribution made to COTA in honor of our patients helps meet transplant-related expenses. COTA’s services are free to our families, and gifts to COTA are tax deductible to the fullest extent of the law.
Mary Asher
Saint Louis, MO
Transplant Type: Lung
Transplant Status: Transplanted
Goal: $25,000.00
Raised: $20,920 of $25,000 goal
Raised by 67 contributors
Updates
June 2021: 2 year update
Posted
It's been almost 2 years since my transplant, so I had a clinic appt to mark the occasion.First up was bone density scan. Last time I had this... Continue Reading »
March 2021 Update: white blood cell injection
Posted
In early February, my white blood cell counts were dangerously low. We discontinued a medication that suppresses my immune system, but the white blood cell count continued dropping.... Continue Reading »
January 2021 Update: Bronch #30 with Mitomycins
Posted
I have been continuously having bronchoscopies every 3-4 weeks. It’s very rare and unheard of that a lung transplant patient needs constant airway dilations. I sure hope that... Continue Reading »
9/19 update: the stent is out!
Posted
2 weeks ago I had my stent removed! I was able to stop 2 nebulized medications. And then I had another bronch this week... They placed the stent... Continue Reading »
Update 9/4/20: hand pain & bronch #25
Posted
Last September, the week I was given the thumbs up to start driving again after my transplant, I was involved in a car accident. (I had to wait... Continue Reading »
1 Year Anniversary
Posted
"I feel like I'm constantly worrying about the next part of my life without realizing that I'm right in the middle of what I used to look forward... Continue Reading »
Hospitalization 7/12/20: allergic reaction & hemolytic anemia
Posted
Saturday, July 11, 2020 I am a little late in updating everyone with my most recent hospitalization. I started feeling dizzy, with tinnitus in ears, and feeling like... Continue Reading »
Hospitalization 6/10/20: an ambulance ride & pneumonia
Posted
So much had been going on these last few weeks. I want to start by saying that I'm so grateful to my donor for my new lungs. I'd... Continue Reading »
Update 5/15/20: Quarantine
Posted
Life in the time of quarantine has been different, but also, the same. Nick began working from home the first week of March. We haven’t been inside a... Continue Reading »
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Our Story
Hello Friends and Family! I have Cystic Fibrosis. CF is a hereditary disease that affects the lungs and digestive system. The body produces thick and sticky mucus that can clog the lungs and obstruct the pancreas. It can be life-threatening, and people with the condition tend to have a shorter-than-normal life span. At the age of 32 I gave up my career to focus on my health in January 2019....
Continue Reading »Mary Asher
Saint Louis, MO
Transplant Type: Lung
Transplant Status: Transplanted
Goal: $25,000.00
Raised: $20,920 of $25,000 goal
Raised by 67 contributors
Updates
June 2021: 2 year update
Posted
It's been almost 2 years since my transplant, so I had a clinic appt to mark the occasion.First up was bone density scan. Last time I had this... Continue Reading »
March 2021 Update: white blood cell injection
Posted
In early February, my white blood cell counts were dangerously low. We discontinued a medication that suppresses my immune system, but the white blood cell count continued dropping.... Continue Reading »
January 2021 Update: Bronch #30 with Mitomycins
Posted
I have been continuously having bronchoscopies every 3-4 weeks. It’s very rare and unheard of that a lung transplant patient needs constant airway dilations. I sure hope that... Continue Reading »
9/19 update: the stent is out!
Posted
2 weeks ago I had my stent removed! I was able to stop 2 nebulized medications. And then I had another bronch this week... They placed the stent... Continue Reading »
Update 9/4/20: hand pain & bronch #25
Posted
Last September, the week I was given the thumbs up to start driving again after my transplant, I was involved in a car accident. (I had to wait... Continue Reading »
1 Year Anniversary
Posted
"I feel like I'm constantly worrying about the next part of my life without realizing that I'm right in the middle of what I used to look forward... Continue Reading »
Hospitalization 7/12/20: allergic reaction & hemolytic anemia
Posted
Saturday, July 11, 2020 I am a little late in updating everyone with my most recent hospitalization. I started feeling dizzy, with tinnitus in ears, and feeling like... Continue Reading »
Hospitalization 6/10/20: an ambulance ride & pneumonia
Posted
So much had been going on these last few weeks. I want to start by saying that I'm so grateful to my donor for my new lungs. I'd... Continue Reading »
Update 5/15/20: Quarantine
Posted
Life in the time of quarantine has been different, but also, the same. Nick began working from home the first week of March. We haven’t been inside a... Continue Reading »