This is the English version of the Angela Sergio Cleary interview.
Note: Would you like to translate this page? Try the translator. (There is also a translator located on the Home Page).
Enjoy the interview. Ciao!
Question 1: Hi Angela, thanks for sharing your time with us today. Please introduce yourself to our readers who may not be familiar with you, and use this opportunity to tell us where we can find you on the web as well as any projects you are working on.
My name is Angela Sergio Cleary and I am an Italian woman born and raised in Gorizia, a town that is part of the Friuli Venezia Giulia region in the north east part of Italy.
Since I was a little girl, while loving my country and its natural and artistic beauty, I found myself attracted to anything that was new, different and exciting. I have always had a very special and very unusual dream: I wanted to see America.
While in school and while growing up, this dream of mine took me over completely and I spent years dedicating myself to learning more and more about this country, its people and their world.
At the age of 20, after finishing high school and after working as a kindergarten teacher, I came to America to take part in an amazing journey, a journey that made my dreams become a reality.
After 3 and a half years of making it in the country completely alone, I met a wonderful man who later became my husband. Since the day we met, we have been inseparable and we have been able to truly enjoy life together. That was the year 1996.
In October of 2006, my life took an unexpected turn.
During a very stressful time in my life, while waiting to say goodbye to my husband’s dad who was losing his 4 year battle with colon cancer, I had an unexpected day.
After a month of very mild and unpredictable symptoms (problems with my right leg that lasted a few days, tingling sensations in arms and hands, vision blurriness and much, much more), I started having a very strong headache, something that I never had experienced before. The pain was almost unbearable and it forced me to go to see a primary doctor near home.
After doing an MRI of the brain and after finding few lesions in it, I was told that there was going to be a chance of me to have Multiple Sclerosis. Three days later, I had my first MS attack.
I didn’t even have the time to accept the possibility of having this disease and here it is, making me face the reality of it right away. This was the beginning of my journey with MS.
Since that famous day in October of 2006, I have had 6 relapses (3 of which were pretty serious) I have tried and changed 4 different medications, 2 plasma exchanges, lots of steroids and I have had several rounds of rehabilitation.
While this might be what people might remember about my story, this is not what is the most important part of my life and of my MS journey.
What I was able to create in these past two years, Flowers 4 MS, is what is important. This makes my MS just a tool for me to help others in the fight against the disease.
In August of 2007, while I was going through a serious relapse, I received the inspiration to create something that makes me very proud and that is called Flowers 4 MS.
Thanks to the help of someone that came into my life in a very special way, I created something that, by using the beauty of flowers, can bring hope and happiness to others.
Through the sale of floral greetings cards, I hope to raise awareness and funds to aid research currently underway at The Multiple Sclerosis Center at Johns Hopkins Hospital in Baltimore, MD and the Southwestern Medical Center in Dallas, TX.
While the project was created in September of 2007, my website Flowers 4 MS was created in April of last year.
This site allows everyone to get to know my story, to be a part of my struggles with this disease and to be present to all the amazing and touching things that I am able to see, be a part of and share with others.
I also explain why I chose Johns Hopkins and Southwestern Medical Center to receive the funds that I have been raising.
To date, in almost two years, I have been able to raise over 26,000 dollars for the above institutions and for the National MS Society.
In October 2008, I decided to share my story and raise awareness for the diseases creating a page on YouTube under the id: angelusa73.
Note: Want to see the videos? Click here...then scroll down, (and don't forget to come back and finish the interview).
I make videos in English and in Italian and I try to reach people across the globe in the hope of helping others see that they are not alone in battling this disease and that there are many like us that care and that want to help.
This is my passion and my purpose in life. I feel this is what I was meant to do…
Do you have a comment or feedback about this interview? Did this interview help you in dealing with your MS? Do you know the person who was interviewed? Share your thoughts with them!
Click the links below to read other visitors comments or feedback about this Interview.
I met an angel!
One day I met a special person, her name is Angela, she behave like an angel, she is talking like an angel in her splendid Italian! The persons who …
Catena i fiori
Cara Angelusa, Hai creato una catena di fiori che sbocciano in tutto il mondo!!! Il tuo coraggio e la tua forza sono come la linfa che tiene in vita, …
YOU ARE AN INSPIRATION
Hi Angela, Once again beautiful pictures and inspiring words. Thank you for sharing your journey with me. You have set goals for yourself and strive …
I'm Angela's e-mail friend. I am an Italian and live in Pistoia near Florence (Tuscany,) approximately 20 miles far. I'm sorry, sorry, sorry for my …
What a Beautiful Story!
Oh, Angela and dear husband! I also welcome you to Life in Spite of MS! You have quite a story to tell, and you have said it so beautifully. It is …
Volevo farti un salutino e darti un appoggio , un supporto morale per questa tua nuova opportunità, la ricerca!!!
MS -We have to live with !!!
My name is Primoz and I am from Slovenia, EU and also have MS and I have been privilege to meet Angela in Gorizia last May. Gorizia is about under …
"Angela the angel..."
"...with flowers around her head" Go girl! Thank you Angela for being you and doing all you do to fight M.S with your flower cards. Well done, you …
I love Angela very much.....
Hi! I'm a good friend of Angela. I meet her in the USA in 1999, I was there as an AuPair. We are still in touch and she is a very special person …
Angela - you are a hero
Just wanted to say that your hard work for people who have MS, not just in your local area but across the world, is inspirational. You have an encouraging …
Angela, you are great!
I have corresponded with Angela on YouTube for a couple of months and I believe she may be one of the kindest people I have ever interacted with. This …
"Life in Spite of MS is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com."
We'd also like you to know it doesn't cost one cent more when you click through the links here on our blog. Not one single penny. And we willl make a little extra cash when you do click through. We'll be ever so appreciative. You also have our word that we'll only link to things that we would use ourselves, (or wish we could have or use.
Cir & Akrista
You are reading original content written by Akrista or Cir L'Bert of Life in Spite of MS. If you enjoyed reading this blog, please consider following us on Facebook, Twitter, Pinterest. See you there!