Oops! You must enter a search term greater than 3 characters.

Invite reviews

Invite friends and colleagues to share their experiences with this nonprofit
24 Reviews
12345
Previous | 1 2 |
Write A Review
July 1, 2010

more

July 1, 2010

MPDCI has provided amazing services to our two children with cystic fibrois, who are now young adults. Summer after summer our family has been the beneficiaries of their generosity in providing tickets to places such as Michigan Adventure and Frankenmuth. For the past couple of summers, my youngest daughter Jamie has been able to attend cross country training camp. We are not a family of means, and thee activities are luxuries we most likely would have forgone otherwise. Casandra, our older daughter, has benefited semester after semester from the educational grant that MPDCI has provided for her. The people at MPDCI have such great hearts. Whenever we apply for a grant or scholarship, they communicate so professionally, and yet so compassionately. They have been patient when we have erred and they helped us to know what we needed to do in order to receive the grant/scholarship we were applying for. I guess, in a nutshell, it is obvious that they are passionate about assisting the CF community in as many ways as possible, and are delighted each time that they do just that. Because of distance, we do not actively engage in social activities they provide, and have participated in very little of their fundraising events. Yet, anyone I have ever talked to in that organization has treated me wonderfully. They are whole hearted, to be sure. It would be wonderful to see this organization recieve this grant, to encourage them for their great heart/efforts, and enable them to do even more. Children and young adults with CF often appear rather "normal" to most people, but to those of us who live with someone with CF, we know their daily challenges. But although we love them and seek to help them in everyway possible, we can never entirely understand what they go through. How grateful we are for an organization like MPDCI who heeps encouragement on these dear invididual.

The Great!

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

I've personally experienced the results of MPDCI in enjoying many one-day holidays with my family that they have provided. My one daughter was able to attend cross country camp. My other daughter received financial aid for college.

More feedback...

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

the spirit and commitment of the volunteers.

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

compassionate and caring.

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

provide in even greater ways for the CF community, epecially in the area of medical expenses.

How frequently have you been involved with the organization?

About every six months

When was your last experience with this nonprofit?

2010

June 29, 2010

more

June 29, 2010

My son has CF and MPDCI has helped him to not feel so isolated. With CF the patients are not to be near each other so often you feel like you are alone. MPDCI just reinforces that this is not something that he is the only one going thru.

The Great!

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

I like to know that there is a group out there that I can contact when I need help for my son

More feedback...

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

The caring they give to CF kids

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

Always very kind and helpful

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

do so much more for the Cf kids and perhaps include activities on the West side of the state or mid state

How frequently have you been involved with the organization?

About every six months

When was your last experience with this nonprofit?

2010

June 28, 2010

more

June 28, 2010

Every summer when I was younger I would receive wonderful care packages from MPDCI. They were always full of fun toys from McDonalds gift certificates to craft kits. They were a great way to start the summer. Another thing about MPDCI I love is the family trips to Frankenmuth or Michigan Adventures Water Park. My family enjoyed taking these trips and having a break for the six of us was always nice. The digital cameras MPDCI provided were great for capturing the days memories. Now that I'm older, I receive grants from MPDCI for college. They come in handy, especially in this economy. I also look forward to joining MPDCI in some of the great opportunities they have for (young) adults with CF. MPDCI has been a great support for me personally and I love to wear my Beaver shirt!

The Great!

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

receiving the Monthly Newsletter, Educational Grants, Summer Care Packages and Family Summer Trips to Frankenmuth/Michigan Adventures.

More feedback...

How frequently have you been involved with the organization?

About every six months

When was your last experience with this nonprofit?

2009

June 26, 2010

more

June 26, 2010

MPDCI has been in our lives since 2004, sending our son, Brian to goalie camp every summer through '07 while he played ice hockey. We have enjoyed summer adventures and next month will be going to Chicago's Shedd's Aquarium, as we are attending orientation at Columbia College where Brian will be a freshman this fall. Over the years, MPDCI has sent care packages with gifts that brighten up the day. Their newsletters and personal connection with Brian has been a huge support for us all. I'm grateful for all their kindness and generosity as they help those families with a child with cystic fibrosis.

The Great!

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

their generousity; sending Brian to goalie (ice hockey) camp which improved his skills, improved his confidence, and made him a better player. Playing hockey helped Brian's fight with C.F. mentally and physically.

More feedback...

How frequently have you been involved with the organization?

About once a year

When was your last experience with this nonprofit?

2010

June 26, 2010

more

June 26, 2010

Michigan Pulmonary Disease Community Inc. is a great organization that brings smiles to faces of children who spend each day facing a life-threatening disease, and often find themselves undergoing proceedures, surgeries, treatments or hospital stays. My grand-daughter spends an average of three hours per day having medical treatments, and another chunk of time trying to eat enough high calorie food to maintain her weight and strength to face the next crisis. MPDCI encourages the kids with gift cards when they comply with their medical regimen, and a few times a year they send out care packages plus tickets to help them enjoy a summer family outing. It means a lot to know that someone understands and cares.

The Great!

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

seeing my granddaughter enjoy receiving packages, or seeing her birthday listed in the news letter. When a child spends a lot of time indoors doing medical routines, a little recognition goes a long way.

More feedback...

How frequently have you been involved with the organization?

One time

When was your last experience with this nonprofit?

2010

June 21, 2010

more

June 21, 2010

OUTSTANDING. This organization was founded by a small group to meet the needs of a few kids with CF to have a summer camp experience. It grew into a camp that met the needs of over 100 campers and as many volunteers. The only funds were those raised by the volunteers until a local group donated golf outing proceeds. When the camp closed, due to CDC policies, this group re-invented itself to meet the needs of kids with CF. Its many activities include Care Packages to younger children, outings for adults with CF, education and a Summer Adeventure for CF families, just to name a few.

The Great!

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

My daughter, Andrea, was diagnosed with CF when she was nearly 5 yrs old. No one we knew had this horrid disease. When she was 13 we met a wonderful nurse named Patty. Andrea fell in love with her. She invited Andrea to Camp Onkoi Benek. Doctor Honicky, a wonderful pulmonolgist and human being encouraged her to go. She had the time of her life! At camp she met others like herself who had special needs but were, otherwise, normal kids. They were able to expereince normal camp activites while also having their medical needs met with professional care from dedicated volunteers. Andrea only attended camp two years. On her second and last visit, she was on oxygen and IVs, but July came and she went to camp! The staff took the BEST care of her so that she could have that wonderful camp expereince. After she died, I became a camp volunteer and later, became a board member. I was the secretary for MPDCI and project leader for a new program called 'Summer Adeventure', somtheing Andrea would loved and been proud of.

More feedback...

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

sharing the joys and sorrows of others

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

OUTSTANDING

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

Conquer Tommorow

How frequently have you been involved with the organization?

About every month

When was your last experience with this nonprofit?

2010

June 18, 2010

more

June 18, 2010

When you hear the words "your child has cystic fibrosis" things seem bleak. You don't know who to relate to what to do...how are you going to explain this to your child as they grow older? When MPDCI came into our lives, it was awesome. They offer a community of people who really know just what you're going through. When my daughter receives a package in the mail from MPDCI it brings the best smile to her face. To receive the newsletter in the mail, is AWESOME! That gives you a glimpse into the lives of the other people living and coping with this devastating illness. The staff here should be commended for the joy and happiness they bring to the cystic fibrosis community.

The Great!

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

the joy and well being of my child. She appreciates the newsletters and packages and help that this group offers. Her step father and I look forward to reading the newsletter and learning all we can from these fantastic people.

Ways to make it better...

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

give them as much money as the world has to offer them. The work they do means the world to a lot of people and they deserve all the help they can get.

More feedback...

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

Watching my daughter's reaction.

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

very friendly and loving.

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

Change the world.

Ways to make it better...

I could do something for them in return.

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

financing the projects.

How frequently have you been involved with the organization?

About every six months

When was your last experience with this nonprofit?

2010

June 16, 2010

more

June 16, 2010

MPDCI has be a great help to me and my family . My family and I have learned so much from be involved with MPDCI how to deal with Cystic Fibrosis on a daily basis. As an adult the retreats and the confernce has beeen a big help

The Great!

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

I got involved with MPDCI when I was 7 years and attented camp. Now as adult I have been a board member and attendet meetings retreats that has been a great help.

More feedback...

How frequently have you been involved with the organization?

About once a year

When was your last experience with this nonprofit?

2010

June 15, 2010

more

June 15, 2010

I have a son with CF and they have sent him to camp and sent care packages to him when he was in the hospital. The staff and board members are very friendly and go out of their way to help.

The Great!

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

sending my son to camp and getting care packages

More feedback...

How frequently have you been involved with the organization?

About every month

When was your last experience with this nonprofit?

2004

June 15, 2010

more

June 15, 2010

Our family loves MPDCI!! Our daughter has Cystic Fibrosis and is part of their CARE packages program. She loves when she gets her special delivery and it lights up her whole world!! They do so many fun and encouraging things for children to help keep spirits up, this helps us parents too!!!

The Great!

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

We are part of the CARE program and are looking forward to taking our summer adventure.

More feedback...

How frequently have you been involved with the organization?

About every month

When was your last experience with this nonprofit?

2010

Previous | 1 2 |
Write A Review

Filter by reviewer role:

Support This Nonprofit

Help this nonprofit get more reviews

5 tips for getting reviews

5 tips for getting reviews...

  1. Sending an email to clients, volunteers, donors, board members, and other partners with a link to your profile page.
  2. Putting a link on your Web site
  3. Including a link in your email newsletter
  4. Putting a link in the signature of your email
    Putting a link on your facebook page and status updates
  5. Tweeting out a link to your twitter followers