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Review for Muscular Dystrophy Association, Tucson, AZ, USA

Rating: 5 stars  

Thank You MDA! What About The MDA Sometimes to understand the functions, Of an organization like MDA... We need to hear from people they've helped. I have a poem with something to say. Six months after I married my bride, I was diagnosed with Muscular Dystrophy. I turned to the MDA for help. This is what they did for me. They gave me the information I needed... To make choices concerning my health. The helped me pay for needed equipment. I'm not a man of wealth. They gave me the peace of knowing I'm helping. I'm allowed to take part & volunteer. I share my ideas as well as my poems. In my heart they are very dear. The MDA does so much more. They offer people peace and hope. Without the help of MDA. It'd be much tougher to try and cope. Thank You for serving your community with integrity and for your time. . Trust GOD and Never lose your dreams. Perfect Peace! Thank You Very Much! Robert. A. Mingo (Humanitarian Poet) I was born Robert. A. Mingo in Minneapolis Minnesota to my parents Donald and Barbara in October of 1961. I don’t know much about my father as he left when I was four and never saw him again until I was 19 at a family reunion. My mother was raising six children by herself Three sisters and two older brothers, I was the fifth of six. It seems I was born to struggle, My earliest medical history is pages and pages of heart related medical issues. I don’t remember any of it but spent a couple days reading through page after page of medical documents. Sometimes I would stay awake for days at a time and the doctors would give me injections to make me sleep. They never knew why I struggled to breathe and passed out so many times between the ages of 1-3 years old. I was told my heart stopped so long once that I had to learn how to walk and talk all over again at two and a half years old. My mother said no to open heart surgery or message should they not be able to get me breathing again. I started kindergarten a month before my fifth birthday and struggled for C’s And D’s all through school except my senior I got a few A’s every quarter which was due to the difference between public and private school back then. When I was growing up I could run, jump, ski, swim into my late twenties despite my severe scoliosis. I always had to do things a little differently to perform the same tasks. I could not throw a frisbee more than a couple feet like normal people no matter how hard I tried so I learned to use my wrist to throw and was an excellent thrower. At thirteen I started having trouble combing my hair. And brushing my teeth, my knees, back, arms and shoulders started aching a lot. The doctors always had an answer as to why I had these issues and mother did not have a lot of patience for dealing with me so I pretty much kept my mouth shut and went with the program. I grew up a troubled youth struggling physically and mentally to fit in any where I could find acceptance. Some how I managed to graduate from High School in 1980 after spending three of those years at De LA Salle High School and working afterwards cleaning the building to pay my way. This really helped to set my spiritual compass for the life Journey ahead of me. At age nineteen I sustained a severe knee injury while playing football which required multiple surgeries and it did not respond well to physical therapy though I worked extremely hard at it for a year. I was never the same after that. I started working in the animal field and it quickly became a passion but a sustained another debilitating knee injury so I went to veterinary technician school. It seemed I was really at peace when helping people and their pets. I started working at a Hospital in Brooklyn Center Minnesota and was very proud to be there. I began to feed my hunger for knowledge by reading all the medical books in Dr Dudley’s office as well as ever encyclopedia I could find. I also discovered my gift of poetry while working There. I learned a lot while there both of the heart and mind. Soon I could not lift the animals on the tables anymore but blamed myself. I thought I was lazy and sluggish and that because of that I was weak. It was actually the other way around, because I was so weak I became lazy and sluggish. Man did those ten years fly by! The pains got worse and my ankles swelled often but I ignored all this in the midst of my new 4 day work weeks and three day northern Minnesota fishing adventures. I stayed busy by studying the Bible for 5 years as I worked my way into a managers position by working the over nights shifts. I was during that time I met my Bride and Joy in the year 2000, What a beautiful way to start a millennium! We married in September of 2001 and had six beautiful months and then I seemed to just fall apart concerning my health. I was diagnosed with FSH Muscular Dystrophy in March of 2002, lost my job and went bankrupt and wanted to die, but that is not the end of the story. After a year of depression I attended an MDA informational workshop and after hearing a man speak about his situation I was inspirired and enrolled in Acts International Bible Collage and went back to school for my degree in ministry. In 2003 I wound up in the ICU fighting for my life and came very close to having a respirator and trachea put in but in but by a miracle of GOD I’m still very active and breathing free. I now use a power wheelchair full time. I’m a writer and author of Poetry For The Soul Volume one. I’m very active with the local MDA and volunteer at many lock ups as well as attend the balls and fund-raisers. My Goal in life is to leave this world a better place than when I entered. A special thanks To Amy my Bride, My Siblings and My MDA Family for loving me even when I didn’t want to be loved.

I've personally experienced the results of this organization in...

A MAN CALLED JERRY LEWIS I’ve never met the man in person, Yet he’s truly changed my life. The MDA is where I turned. When torn with pain and strife. I was just a six month newlywed, When I had to tell my bride. I had this strange neuromuscular disease. The task just tore me up inside. Now I sit here in a wheelchair. That MDA has helped to pay. If we had to buy it all ourselves. We could’ve never found a way. But Jerry’s done more than just help buy chairs, Throughout my life he’s given me laughter. He also helps raise needed funds for research. So kids with MD have a happily ever after. Without the MDA and Jerry Lewis, I shudder to imagine. Were we’d be concerning research. Would there be a place that kids can camp in? This simple poetic letter for Jerry. Can truly never measure up. This man called Jerry devoted his life. So Muscular Dystrophy can’t tear us up. (Thank You Jerry Lewis!) Robert. A. Mingo (Humanitarian Poet)

What I've enjoyed the most about my experience with this nonprofit is...

The love and acceptance.

The kinds of staff and volunteers that I met were...

The nicest people in the world!

If this organization had 10 million bucks, it could...

Do alot more research.

When was your last experience with this nonprofit?


Role:  Client Served & Was stricken with Muscular Dystrophy.

Review for Mobility For Independence, Minneapolis, MN, USA

Rating: 5 stars  

Thank You Mobility For Independence! When I think of Mobility for independece... I think of the freedom & hope they are giving others. If not for Mobility for independence... Living life would be much tougher. If not for my van I'd be stuck at home. MFI helped us raise the money. After years of being stuck inside. I now travel with my Bride whom I call honey. This poem may seem kinda corney. Though the message is pain stakenly serious. Thank you so much dear MFI friends. To feel imprisoned made me somewhat furious. I cannot thank you enough Marrianne. You work quite hard & persevere. Thanks for all those vans being raised. I hope my appeciation is clear. I want to do better at giving back. This includes giving some time to you. If given the honor I'll do my best, Just let me know what I can do. Thank You for helping those in need. With our van we're giving back. We help others with the van we've been given. Because our freedom we no longer lack. Robert. A. Mingo (Humanitarian Poet)

I've personally experienced the results of this organization in...

I've personally experienced the results of this organization in the gift of freedom.

If I had to make changes to this organization, I would...

I would Give them more volunteers, more money & more people to help.

What I've enjoyed the most about my experience with this nonprofit is...

They have helped me & others live our lives to the fullest.

The kinds of staff and volunteers that I met were...

Too few I think Marrianne works to hard. The volunteers were very humble yet had a glow in their smile.

If this organization had 10 million bucks, it could...

I know beyond a doubt MFI would imediately start finding mo people to help. So many others who have so much to offer thwe world need a van to get out into the real world and make a positive difference.

Ways to make it better...

I was very happy with my experience

In my opinion, the biggest challenges facing this organization are...

Not enough money or publicity.

One thing I'd also say is that...

Thank You MFI. I love what you do & would be honored to help you if given the honor.

When was your last experience with this nonprofit?


Role:  Client Served & Recieved help in obtaining my freedom through the gift of a handicap accessible van.