Wednesday, November 23, 2016


A lot of IC patients have either considered trying instillations or have tried it once and felt it didn't help so they gave up. 
If you’ve been trying Instillations and feel you are not having success, I would urge you to work with your doctor about trying different cocktails. For example, if you’ve been using the same cocktail for a 6 months or even many years and it’s not working, then it’s time to move on! First, there are SO many different cocktail combinations that can be tried you should ask your doctor about trying a different one. It took me about 4-5 different cocktails before we hit the right one that works for me. If your doctor is not open to trying a different cocktail, then you need a new doctor!

The instillation cocktail my doctor uses is a basic one of Heparin, Lidocaine and Sterile Saline. Many doctors use Sodium Bicarb and when I asked my doctor why he didn’t use that, he told me he wasn’t seeing enough successful results with that in the cocktail. He replaced it with Sterile Saline and, in his practice, he saw much better results.

So if your cocktail has Sodium Bicarb, but you feel it’s painful or not helping, talk to your doctor about replacing it with the Sterile Saline and see if that works.

In addition, some patient’s cocktail includes Kenalog. I could not tolerate Kenalog, but some patients love it. So the point is to be willing to try different cocktails if one doesn’t work, another might. That’s how we found what worked for me.

Bottom line, an instillation should NOT be painful. So if it is, then don’t keep doing them. The point is to relieve your pain not make it worse. But I would, again, urge you to try a different one to see if you can find one that does work. 

If you explore several different cocktails and none of them work, you may need a referral to a Qualified Pain Management doctor.

I’ll post a link to the ICA website on the different instillation cocktails that you could consider. Read it! Print out things you want to discuss with your doctor. If he’s not interested talking about other treatments, again, you should look for a new doctor! There are treatments out there that can help and don’t give up until you find better help!

In addition, I below are links to two videos I did a few years ago that talk about catheters and catheterizing (either in the doctor’s office or at home). I think there’s some important and helpful information in the video, so you might want to watch that as well.
Video - Catheters 101

Video - Magic Catheters

Sunday, September 25, 2016


Today was the Respiratory Health Association of Chicago (RHA) Annual Hike for Lung Health; 3 miles through beautiful Lincoln Park in downtown Chicago. I did it last year for the first time only 10 months post transplant. I finished and was thrilled that I could raise money for a great cause and accomplished something that, for me, was a big deal so soon after transplant.

Well, since then I have been having physical challenges with my legs; extreme pain and weakness and it's been very hard to keep up with my walking due to the pain. But I have kept at it while going through an array of tests to try to determine what's going on with my legs.

It hasn't been easy. The pain has kept me up all night on more than a few occasions, but I can't allow myself to go back to the poor condition I was in while waiting for my lung. So I persevere and just do what I can do.

I didn't know if I'd be able to do all 3 miles today but I was going to try. Several wonderful ladies from the RHA walked beside me the entire way and that kept my mind off the pain and helped me push through all the way to the finish line!

Here I am crossing the finish line, arms raised in celebration!

I cannot tell you what it means to me, even with all the side effect challenges I have, to be able to walk 3 miles. After being so sick, having my lungs fail me (a mystery we will never understand) and needing a lung transplant to survive, being able to accomplish an event like this means the world to me.

Many of my friends and family made donations to my fundraising campaign and I was able to raise over $1,000 and I am so grateful to each an every single person who donated. But I am also so grateful for all the pep talks, encouragement and support to keep on trying and see if I could do it. You all got me across that finish line. I needed a good nap by the time I got home, but it was so satisfying to be able to say I DID IT!

Check me out getting to meet Illinois Secretary of State, Jesse White
at the Hike and thank him for his support of organ donation!

Me and some of the hard working and wonderful ladies
of the RHA Staff before the Hike!

Me and Chair Elect of the RHA Board of Directors, David B. Yelin, Esq. 

Today was a great day for me and so many fighting lung issues and working to raise awareness and money for clean air! 

My thanks to everyone from the RHA for making me feel I was part of their team and supporting me and my efforts in today's great Hike for Lung Health!

No matter how hard or challenging, I will Never Surrender to it and keep on walking!

"Never Surrender" - Corey Hart

Wednesday, August 3, 2016


Today, as another month has come and gone, I celebrate the 21st month anniversary of my Lung Transplant! It's hard to believe that much time has gone by and yet I am rapidly approaching my 2 year anniversary. That will surely be a day for celebration!

But every month on the anniversary of my transplant I silently thank the generosity of my Organ Donor who believed in organ donation at a young age and signed up when he got his driver's license at just 16, sure that he would want to be a donor should something ever happen. Sadly, for his family, he passed away at only 22 years old. But the gift he gave and lives he saved - not just mine - is something for which I am grateful every single day I wake up. 

Sure, I have my challenges post transplant. Most transplant patients have some issues they must deal with. The anti-rejection medications, while saving our lives, can cause a multitude of side effects and I am dealing with those. I am lucky to have an amazing transplant team and my Coordinator is just the best. She is patient and answers all my questions, no matter how minute or silly they may be. I have such a good team helping me navigate post transplant life. I couldn't do it without them.

I am so grateful that I felt a strong need to try and give back in some way. So I Blog, Tweet and Instagram about organ donation, transplant and lung health. I have gotten involved with the Respiratory Health Association of Chicago and have been lucky to get to go with them to call on both my Illinois State Representative and my Illinois State Senator to thank them for supporting clean jobs and Tobacco21 legislation. I shared my story and why clean air is so important to me and everyone.

The Respiratory Health Association Staff and I thank Representative Sam Yingling 
at our meeting to thank him for supporting Clean Jobs Legislation 

Thanked yesterday for supporting Clean Jobs legislation.

So as I celebrate each milestone, I am always thinking of the greatest gift I have ever received and work to raise awareness and give back to honor my #organdonor. 

“At times our own light goes out and is rekindled by a spark from another person. Each of us has cause to think with deep gratitude of those who have lighted the flame within us.” — Albert Schweitzer

Sunday, July 24, 2016


We all have our daily struggles, some more than others. While I am happy that my lung is doing well, I am struggling with other issues that are making enjoying my transplant difficult. I look for inspiration where I can to help keep me fighting. Sometimes it's a simple quote, other times something more. Today's quote just spoke to me and I hope it speaks to you. 

I have much for which to be thankful, so even though I have my struggles, I keep on going. 

"I'm Alive" - Celine Dion

Wednesday, July 20, 2016


Today was my 61st Birthday! Most women don't like to brag about their age, but when I got sick with  a rare lung disease, vanity kind of went out the window.

I am here thanks to the ultimate #GiftofLife I received in Nov. 2014 and so today I got to celebrate my Birthday with my family. When I was sick these little things were all I thought about and all I wanted more of. Time with my family.

Today, we did not have a fancy party; I didn't want everyone in the kitchen all night long. We had a simple dinner at my request and we got to spend quality time together. It was so wonderful. The family that couldn't be there called to send their birthday wishes.

I got so many wonderful birthday wishes on Facebook and it meant so much to me, that no matter how long it takes, I'll write a personal thank you to each. These are the important things in life to me. Connecting with family and friends, near and far. 

Thanks to the lung donation I received, I am still here. Something that at one point was not certain. So today was the best day. I relaxed, spent time with those I love the most and it made me so happy.

Throughout the evening, I had moments where I thought of my organ donor and family and gave silent thanks for the gift they have so selflessly given to me and my family. Without their support of organ donation, this celebration would not have taken place. I do not take it for granted. Sunday we will go celebrate one of my nephew's college graduation party. Being there with all my family for celebrations like this or just getting any time together is what means the most to me. I am forever grateful to have gotten my lung and that I am here say that I am proud to be 61!

Blowing Out the Candle on My 61st Birthday Cake!

"Forever Young" - Bob Dylan

Sunday, July 3, 2016


I haven't posted in a while. I've had my challenges and didn't want to put up a post that sounded all negative. But nobody said this (being a transplant patient) would be easy.

The good news is my lung is doing well. I'll be going on July 19th for my quarterly transplant check up. They'll give me a good going over and make sure everything is going as it is supposed to.

But I've been having my struggles. Mainly having to do with exercising and trying to regain my strength. I have been working and exercising 4-5 days a week for 18 months and feel I am not making the progress I should. I've been experiencing significant pain in my legs and I would never recover from a workout as one should. The pain got so excruciating that it was keeping me awake at night until 4am and I could not sleep. Walking around the house even felt wobbly. 

The last straw was a 3 mile walk I went on one day and I have never felt so bad as I did that day. My legs felt like they were going to give out on me and I did almost collapse a few times; I was so short of breath I had to stop 6 times, even going to my brother and sister-in-law's house looking for a ride home. Sadly no one was home (I thought it was Saturday thanks to med-head when it was Friday so everyone was at work). I sat on their porch in the shade for a little bit and started out again for home. 

It was the worst walk of my life, pre or post transplant. I have never had an experience like that. I almost sat down on the grass in one of our parks and would have stayed there until I could find someone to drive me home. But I wobbled my way to our house and made it home. 

I had a good drink of water, took a shower (holding myself up by the grab bar) and then took a nap for several hours. By then I knew it was time to contact my Transplant Nurse Coordinator. We had a long conversation about my situation. Every transplant patient is different. Some recover their strength back quicker than others and others never return to where they were prior to transplant. It appears (and they want me to accept this may be my situation) that I am not ever going to be the way I was prior to getting sick. 

My Coordinator said it's possible having only one lung can have an impact on STRENUOUS activity like exercise. Not all do, but it's possible and it makes sense to me. They can't really say 100%. Also my legs may never be the same. I was told what I've been doing is more than most and they know how hard I've been working, which they feel has been a good thing. But at this point the suggestion was to BACK OFF, SLOW DOWN, and CUT MY DISTANCE. 

So that's what I've been doing. It took almost a week for the pain from that last 3 mile walk to subside. I've cut my distance, going less than 1 mile instead of always shooting for 3 miles. Today I walked .68 miles in 18 minutes. 

I will admit to being very frustrated by these physical challenges. It would be so easy to just say "it's too hard, I can't do it and I give up". I've felt like that several times. But I know what it's like to be completely de-conditioned from a year of being sick while I waited for my lung. You lose your muscle conditioning SO fast and I don't want to ever be like that again. So I pick myself up, lace up my walking shoes and off I go for shorter, slower walks. It's good for me and if it goes as I would like, I MAY be able to make progress and go a bit further and a little faster. I can't push it, but I'm hopeful. 

I am so lucky to have gotten my lung transplant and that things are going well. I am here and will be celebrating my birthday in a few weeks. 

Today is my 20 month Transplant Anniversary; a day worth marking and for giving thanks for the Gift of Life. The least I can do is honor that gift and, even if things get hard and challenging sometimes, always remember the gift I was given and the promise I made to do everything I could to care for that gift.

So if that means, adjusting my mind set and goals, then that's what I'll do. I promised never to give up and so I persevere. 

Sometimes it's hard, but then nobody said it would be would be easy!

"Fight Song" - Rachel Platten

Friday, May 13, 2016


My blog a few weeks ago was about the memorial Candle Lighting Service my hospital holds every year to honor organ donors and their families.

I had a picture of me holding my donor's first name at the ceremony taken and I wrote another letter and sent it through the complex and secret process to the donor family. Just like I had to do when I wrote them the first time. I hoped they would like to see this photo of me honoring their son at this very special service. I want them to know how much his gift means to me and my family.

These communications, due to privacy and the delicate nature of transplant, move slowly. And the family can turn down receipt of the letter. So you never really know if they've received it, but choose not to communicate with you; whether they turned down receiving it; whether it hasn't arrived yet.

I am so hopeful this will be meaningful to my donor's family and that they got it and are deciding whether to get in touch with me.

And so I wait to hear. 

I understand it may be too painful for them to reach out to me. I would very much like to meet them. Their letter to me said they were very interested in meeting the recipients. I filled out the release with my information so they could contact me. But they also have to fill one out and I was told they have not yet done so.

And so I wait.

Maybe they're just not ready. I can understand that. But if they reached out I think they might find someone who is so grateful it would give them some measure of peace. I hope so. I really hope they get this letter and picture and it gets them thinking about connecting with me. I have to respect whatever they decide, but I so want to thank them in person.

And so I wait.

If I do hear back, you can be sure I'll write a Blog post about it! My fingers are crossed and even if I don't hear from them, I pay tribute to their son every single day.

This sits on my dresser in my room so I can remember
every day the gift I was given.

"Forever Young" - Bob Dylan

Sunday, May 8, 2016


It's Mother's Day! I want to wish my wonderful Mother a very Happy Mother's Day! She has done SO very much for me as I struggled first through a chronic illness called IC and then through the scariest time of my life called Lung Transplant! She truly is my "sainted mother" and I am so blessed to have her. So this Blog is a tribute to the very best Mom anyone could have! I am so grateful! HAPPY MOTHER'S DAY, MOM!

To My Mother by Robert Louis Stevenson
You too, my mother, read my rhymes 
For love of unforgotten times, 
And you may chance to hear once more 
The little feet along the floor.

Mom and Me Just Home from the Hospital!
Taking Care of Me While I Waited for My Transplant

One Again Supporting Me;  Both of Us at the Finish of the
Hike for Lung Health Post Transplant

"In My Daughter's Eyes" - Martina McBride

Saturday, April 30, 2016


To honor the final day of #NationalDonateLifeMonth, I wanted to put in writing my gratitude to the donor who saved my life. It makes me sad that someone had to die so that I might live. But, if I could write or talk to him, this is what I would want to say.

Dear Trevor;

You don't know me and I didn't ever get the pleasure of meeting you. But we are forever connected because you were the kind of generous individual that wanted to be an organ donor. Sadly, for your family, you became the organ donor you wanted to be, should something ever happen.

I was blessed to receive one of your lungs on Nov. 3, 2014. I had a single right lung transplant that saved my life thanks to you.  I have exchanged letters with your family and let them know how grateful I am for their support of your decision to be an organ donor. 

They wrote back and that's how I know your name, Trevor. I carry it with me every single day. Every day that I wake up, take a deep breath, I think of you. Every time I go workout, even though it is very challenging, I think of you. Every time I get hugged by a member of my wonderful family, I think of you.  If it weren't for you, none of those things would be possible. My family and I are now, and forever will be, grateful beyond words.

I was so sick, my lungs giving out on me so rapidly that if I didn't get my transplant when I did, my outcome would not have been happy. For that I am forever grateful to you.

I was and am so grateful for the Gift of Life the lung I received has given me. I have recovered very well. I was discharged from the hospital only 8 days post transplant, which is amazing! My Transplant Team tells me that I am, and I quote: “doing GREAT!” I have not needed any oxygen at all since my transplant, so being able to be free of the oxygen machine and the Bipap is a wonderful feeling. When I watched the oxygen machine being taken from the house I cried. Again, tears of joy at not having to be tied to an oxygen machine anymore! I can sleep laying down again. These are not huge things, but they are what I dreamed of when I was sick. My dreams are simple. To be able to regain my strength and go for a walk outside again and enjoy nature. I have done this. Just going up and down the stairs and making my own meals and not having to have my mother wait on me hand and foot is wonderful. To take a real shower, without assistance. Small things that are often taken for granted but that I am beyond grateful to be able to do again.

I promised the Transplant Team that if I got a lung, I would do everything they asked of me and do everything in my power to take care of this most precious gift that you gave to me, and I am an extremely compliant patient. I believe they would tell you that I am. I think since you made the ultimate sacrifice so that I might live, it is my responsibility to do everything I am supposed to in order to care for this precious gift you gave to me.

I wish you could actually read this and know how grateful my family and I are for the Gift of Life you and your family gave to me. Your generosity and willingness to help others in such a profound way will never be forgotten and we will honor your gift on each anniversary of my surgery. We will take time to think of you and your family and the gift you gave to me and what it has meant for my family. 

With deepest gratitude,


"Kind & Generous" - Natalie Merchant

Wednesday, April 27, 2016


This Blog, as many know, started after I was diagnosed with Interstitial Cystitis. If you're new to my blog, you may ask "What Is Interstitial Cystitis (IC)"? 

Well, Interstitial Cystitis, or as we call it, IC, is a bladder condition that usually consists of multiple symptoms. Most IC patients have recurring pelvic pain, pressure, or discomfort in the bladder and pelvic region, and urinary frequency and urgency.

IC may also be referred to as painful bladder syndrome (PBS), bladder pain syndrome (BPS), and chronic pelvic pain. You can read more about these different names for IC on the ICA website:

While everyone with IC is different, some patients, like me, have such severe cases where traditional treatments don't help and we end up on Disability. I can't take pain medication so my options are limited. I usually get bladder instillations at my doctor's office and I have to self-catheterize due to retention. This was challenging enough all alone; I had to sell my home and move in with my parents where I still live.

Then out of the blue in Nov. 2013 I came down with a cough and an illness no one could diagnose. I was in and out of the hospital over the course of 3 months. That's when I was advised to make the trip to the Mayo Clinic to get a diagnosis. My brothers really came through and two of them escorted me and pushed me around in the wheel chair that by then I needed.

By the time all the testing was done and I met with the doctor I was given a diagnosis: Idiopathic Bronchiolitis Obliterans. WHAT the heck is that I wanted to know. What I was told next changed my life forever. The doctor explained the disease and told me I would need a Lung Transplant if I was to survive. We were all very quiet and shocked to say the least. I know I was a "deer in the headlights".

Eventually I was accepted for transplant and listed with UNOS. It took about 5 months from being listed until I got THE CALL that they had a lung for me. I have done well since transplant and my lung has allowed me to breathe and enjoy life.

With that said, being a transplant recipient is a lifelong situation requiring I take about 20 different medications and about 35 pills every day. With that come a lot of side effects that can be very challenging.

Having both IC and being a Lung Transplant Recipient do not exactly go well together. Since transplant I have had to work very hard at physical rehab, which my IC does not like. But if I am to regain my strength post transplant I must work out, which is challenging enough by itself. But then my IC goes into a flare from the exercise and I'm miserable from that.

In addition, being a transplant patient means I will be on anti-rejection medication for the rest of my life which means I am immunocompromised and must be very careful about exposure to germs and follow strict guidelines to avoid catching things. Even doing all I can, I can still get things that I might not otherwise if I were not immunocompromised.

Due to my IC retention problem, I have to self-catheterize which can be challenging for healthy people, exposing them to the possibility of a UTI. Well, now that I am immunocompromised, I have had 5 back to back UTI's, which for an IC patient is making a bad situation even worse. I'm concerned that a trend has started and that I will be battling chronic UTI's. I hope this isn't the case, but it certainly could turn out this way.

Those are just a few examples of how these two diseases don't get along and make life post transplant more challenging. I'm learning to cope with all the side effects and problems that pop up from being on so much strong medication. It isn't easy, but I keep going. I listen to my body and if I need a break, I take it. Other days, I persevere and go do my workout. 

It's a learning curve trying to make sure I am following all the guidelines I've been given, looking out for signs of other medication problems - am I sick? is it just allergies? why do I have that cough? 

Thank heaven we are assigned a Transplant Nurse Coordinator who has the patience of a saint and answers all my questions, no matter how minor. She reassures me when I need it and tells me when something needs changing. Aside from my family, without my amazing medical team, I could not do this!

I'd rather not have to deal with all this; who would want multiple medical conditions? But this is my life and the Challenges of Multiple Illnesses. I will deal with whatever is thrown my way!

"One Dream" - Sarah McLachlan
(This was written for the 2010 Winter Olympics
but I Find It So Inspirational)

Thursday, April 21, 2016


April is National Donate Life Month to bring awareness to the need for more people to sign up to be organ donors. As of today there are 120,969 people waiting for a life saving transplant, so this annual effort at raising awareness and getting more people to become donors is so important.

There are many activities going on all month long across the country and it's wonderful to see so many people involved in different events to help raise awareness.

This week, my hospital (Loyola University Medical Center) has an information table set up where individuals could stop, ask questions, sign up as a donor. I volunteered to work the table for a bit on Tuesday and it was the most rewarding experience I've had in a very long time. The table was staffed with all volunteers but of those, I was the only Lung Transplant recipient. While I was there a man in a wheel chair on oxygen and with his wife and daughter came to the table. He was SO thankful to be able to talk to a lung transplant recipient who has been through it, who also had the same procedure he is going to have. His wife was crying as we hugged and she thanked me for talking to them. Thanking me! I should be thanking them! It was a wonderful moment.

Me Volunteering at the #NationalDonateLife #organdonation sign up table.

Today was our Annual Candle Lighting Ceremony held each year during this month in memory and thanksgiving to those who have given life to others through organ donation. 

This year, I wanted to do something special to honor my donor and donor family at the Candle Lighting.  I have written to my donor family and received a letter in reply from them last year, so I now know the first name of my organ donor. I contacted UNOS and requested someone take a picture of my donor's name from the Wall of Names at the UNOS National Donor Memorial Gardens at their corporate headquarters in Richmond, Virginia. I framed the picture of his name and took it with me to the Candle Lighting Ceremony to honor him and his family for giving me the ultimate Gift of Life.

Photo of my Donor's Name from the National Donor Memorial

This was the 25th Annual Candle Lighting at Loyola and it's always a very moving and emotional event. Tonight's highlight was the first speaker and Special Honoree, Dr. Susan Hou. Dr. Hou is believed to be the only transplant physician in history to be both an organ donor and organ recipient. To hear her speak was very special and moving. And she's still going strong. 

Dr. Susan Hou Speaking

I feel that once you have a transplant, you are part of a very special family. I feel a kinship with other recipients and we share our stories with each other and all of us talks about our donor and donor family. The medical staff treats us all like family, readily giving hugs to all of their patients. It's a special group of people.

Me and my Amazing Nurse Practitioner Erin!

To me, the most moving part of the program is the actual Candle Lighting! The ceremony begins with any transplant recipient, persons waiting for a transplant or family members of donors light a candle in memory for all those that have given life to others through organ donation. As I walked up toward the altar to take my candle, I carried my donor's name with me, lit my candle and added it to the other candles, I touched my donor's name in his memory and to honor him and his family. 

This was a very special evening for me and, I am sure, for everyone in attendance. While I don't need reminding that someone gave me the ultimate Gift of Life, it is appropriate that we take time every year - for 25 years now - to set aside a day where we make sure to honor our donors and donor families who made the ultimate sacrifice so we could live.

Candle Lighting Ceremony Video

The depth of my gratitude to my donor and donor family is immeasurable. I also want to acknowledge the Loyola Medical Team who worked tirelessly to save my life and continue to make sure all goes well. 

This poem was in the Ceremony Program and it touched me, so I want to share it to honor all organ donors and their families.

A limb has fallen from the family tree.
I keep hearing a voice that says, "Grieve not for me.
Remember the best times, the laughter, the song.
The good life I lived while I was strong.
Continue my heritage, I'm counting on you.
Keep smiling and surely the sun will shine through.
My mind is at ease, my soul is at rest.
Remembering all, how I truly was blessed.
Continue traditions, no matter how small.
Go on with your life, don't worry about falls.
I miss you all dearly, so keep up your chin.
Until the day comes we're together again.

Sunday, April 3, 2016


April is National Donate Life Month where those of us in the Transplant Community pay tribute to those who have given the Gift of Life through Organ, Eye and Tissue donation.

This video is to honor my organ donor along with all those who have given the Gift of Life. 

Give the Gift of Hope

Every 10 minutes, someone is added to the National Transplant Waiting List. As of today, there are 121,235 people waiting for a life saving transplant. On average, 22 people die each day while waiting for a transplant. One organ donor can save 8 lives. You can learn more at the Donate Life America website.

"Tears in Heaven" - Eric Clapton

Thursday, March 24, 2016


Dates. We all have dates that are important to us; birthdays, anniversaries. For a transplant patient, there are likely many dates we will never forget. At least that’s the case for me. 

November 11, 2013 - That was the day I woke up coughing and believed I had developed a cold. Over 3 months, there were multiple hospital stays trying to find out what was wrong with me.

December 2-9, 2013 - Spent in Lutheran General Hospital Seeking a Diagnosis.

Feb. 11, 2014 - That was the day I flew to the Mayo Clinic looking for a diagnosis. 
Feb. 12, 2014 - The day that changed my life forever. I finally received a diagnosis. I was told I had Idiopathic Bronchiolitis Obliterans. I was also told I would need a lung transplant to save my life.

Flying to the Mayo Clinic in Rochester, MN

April 1, 2014 -The day I got to meet with the Transplant Doctor here at Loyola to discuss my case. I still contend my referring Pulmonologist just pestered him until he agreed to see me. But I am forever grateful that he did.

Waiting to See the Doctor at Loyola

June 10, 2014 -The day Loyola called me to tell me I had been accepted as a transplant candidate and was now listed with UNOS for a lung transplant! Then the waiting began. 

Nov. 2, 2014 11:30PM - on a Sunday night and my cell phone rings. As all Loyola transplant patients know, you get to know a Loyola phone number and when I looked at my phone I knew it was Loyola. My Mom came running down the hall because she instinctively knew that late on a Sunday who else would be calling. It was THE call; get to Loyola as safely and quickly as possible. We have a lung for you. My family went into overdrive getting everything together and notifying other family members that my turn had come and off we went into the dark night to Loyola. I was anxious, and I’ll admit to being scared and it felt so surreal. 

Nov. 3, 2014 -Is the official day that I received the ultimate Gift of Life and my new lung was transplanted. This date is now my Re-Birthday and my family and I celebrated with a quiet family dinner this new important date in my life. We also took a moment and raised our glasses to honor my donor and donor family who made that day possible.

First Time Out of Bed & Sitting in a Chair Post Transplant!

Nov. 11, 2014 - Only 8 days post transplant (and one year to the day that I woke up with that cough) I was discharged and got to go home. I felt like the luckiest person in the world. Slowly I began my recovery and rehab. 

Going Home Only 8 Days Post Transplant!

September 20, 2015 - 10 Months post transplant I participated in the Respiratory Health Association’s 3 Mile Hike for Lung Health in Lincoln Park. I had asked my younger brother to walk with me and he agreed. At the last minute my wonderful family surprised me and everyone who lives in the area walked with me in a show of support. I was also interviewed by two newspapers who told my story and helped raise awareness about organ donation and transplant.

My Video of the Hike of Lung Health 3 Mile Walk!

This changed my life forever. These are the Dates I Will Never Forget as I got sick and went through the process of getting a diagnosis, Lung Transplant and working on my Recovery. 
Grateful & Happy Post Transplant!