TK2 CURES
Estopinan Blessing:
We would like to provide hope and opportunities for parents who have discovered, or need help discovering, rare diseases like TK2 Mitochondrial DNA Depletion Syndrome.
Our son Arturito is living testimony that these experimental medications are significantly boosting his motor skills and communication skills. Arturito is getting stronger each day and we would like for you to learn about his progress and the available limited resources we have found. Help us research the treatments and further conduct studies to continue improving the outcome of our trials.
Our Goal is the find solutions and help save the Lives of TK2 patients!
Latest Updates
Valentin, Argentina
Valentin's mother provides before and after photos of her sons progress after the trial.
Experimental medication has improved and saved this families disappear without resources for solutions.
They contact us during the COVID pandemic and we were fortunate enough to facilitate the necessary treatment to improve his conditions.
Our hearts are filled knowing we've impacted his life.
Melinda, Mexico
Melinda's family found our foundation in desperate need of helping their four-year-old daughter.
She has TK2 and the debilitation was not allowing her to eat. This rare disease limits the necessary nutrients for energy to proceed with treatments.
We successfully provided Melinda with various gastro intestinal tubes . With the essential nutrition, we can continue seeking medical help.
This family has hope and believes in miracles too.
Sofia, Costa Rica
Meet Sofia from Costa Rica, she's only 42 pounds at the age of 9. We're proud of fund her experimental medications to help improve the TK2 DNA Depletion of her muscles.
- November 2022: Sofia is improving remarkably to the medications for her degenerative condition
- October 2022: Began treatment with medication to improve mitochondrial disease
- September 2022: Sofia received our package with the treatment for doctors to administer
- August 2022: Sofia's family solidified our teamwork to help her recover
Earlier this year, Sofia's mother had send us this video to show us the trouble to stand and walk.
This video shows us how she manages to get up from the floor and walks so carefully.
We need your help advocating for children like Sofia who need support outside of the traditional medicine.
To help click here
Helping Parents Save Lives
This is Jared from Honduras, we happily funded his genetic testing for accurate diagnosis. Our Foundation has funded equipment for his legs recommended by his physician.
This newest video shows that Jared has begun to struggle more to maintain posture and his muscles are weaking. We must remedy the treatment and proceed to help this family save their child.
Our goal is to advocate to educate health ministers, their staff and other policy makers regarding Mitochondrial Disease treatments. It is our pleasure to give families HOPE is a Blessing.
Together we can help children around the world and find a cure.
The research and progress from the experimental medications and therapy are working and Arturito is living proof!
Video July 2022
We Appreciate You
My wife Olguita and I are extremely grateful for the medical advances which continuously improve our sons’ living conditions. We whole heartedly believe in the science lead by Dr. Michio Hirano with the help of Columbia University Medical Center and The Johns Hopkins Hospital. The time and efforts generated by multiple teams of doctors, specialists and researchers are reflected in our sons’ eyes today. His advancement is the fuel that ignites our energy to find a cure. Our goal is to further help families in need of funds for diagnostic exams, equipment and the necessary experimental medications and treatments. Thank you for joining our journey in watching Arturito's growth and development.
There is HOPE and Research is the Key!
Follow us @tk2cures for live updates.
TK2 Cures Newsletter
TK2 CURES MISSION
The mission of TK2 Cures is to advocate for scientific research of studies to improve experimental medications and treatments to sustain health of patients with Mitochondrial DNA Deletion syndrome and their families around the world.
Email us:
contact@tk2cures.com
101 Hillsmere Court
Annapolis, MD 21403
You can also find us here:
