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Gail Csizmar
  • Female
  • Salemburg, NC
  • United States
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Latest Activity

Chronic rejection is the pits!!
on Thursday
Gail Csizmar updated their profile
on Thursday
Are you a fan of CBS's new transplant drama TV series 'Three Rivers?' Then this is the group for you to meet other fans and discuss your favorite episodes!
October 12
Gail Csizmar joined Holdol's group
Cooking tips, recipes, games, nutrition and more!
September 29
September 25
September 24
Gail Csizmar added 2 photos
May 28
Congratulations Tara !
May 27
Mine stays between 1.6 and 1.9 been like that for 15 years. When it starts going 1.9 the doctors usually lower my Sandimmune (cyclopsorin) dosage.
May 26
Hi,I would like to know if anyone crentinine is raising like mine after 7 years.it is between 1.4-1.5.The prograf which I take 6 and the cellcept i take 750 twicw a day is ok,but I get bad neuropathy from prograf the docs are going to start me on th…
May 26
Congrats on your 15 year transplant anniversary! Only 2 days before my 10 year post double lung transplant anniversary...i hope you had a wonderful day today. im thinking of the person's & the family's that gave unselfishly for us to be here today &…
May 26
Gail Csizmar added a blog post
Such a very special day for me. First Thank You to all of our Soldiers who gave their Life for our Freedom. Also for those who are serving in the armed forces...Thank You. A very special Thank You to my Donor and her Family. I received a second c…
May 25
Gail Csizmar updated their profile photo
May 22
I talked to my transplant coordinator today and was told I would be allowed to take tamiflu if it was needed. And gave the same advice that Glenda's coordinator gave her. Don't forget to clean off the supermarket carts before putting anything in the…
April 28
Does anyone know if we are able to take the tamiflu if we do happen to get sick?
April 27
Does anyone know if we are able to take the tamiflu if we do happen to get sick?
April 27
Gail Csizmar added a discussion
Just want to let everyone know that LEVAQUIN antibiotic can cause tendons to rupture and also tendon problems. I was on it for 7 days and after 3 days of being off it I wound up with edema in my ankles and feet. Also a burning sensation up the back…
April 25
April 1
Gail Csizmar added a song
 play gift for life - Debby Boone
Holiday Collection, Vol. 1 [Universal]
04:21
March 27
Hello Maria, I am glad you joined the TC. I also had Primary Pulmonary Hypertension. I had a double lung transplant in May 1994. I was diagnosed at the end of 1992 and was listed in May of 1993 for a double lung tx. . It is hereditary in my family.…
March 27

Profile Information

What is your city / state and country of residence?
Salemburg, North Carolina,USA
How are you touched by transplantation?
I am a Recipient
If you are a recipient, what type of transplant did you receive?
Double Lung
Recipients: In this space, feel free to list those you are grateful to for receiving the Gift of LIfe:
Aloha Koll Rindy who was my donor.
Dr. Dwayne Davis my transplant surgeon.
My family for encouraging me throughout my illness and transplant journey.
If you are a recipient, what type of donor did you receive your Gift of Life from?
Deceased Donor
If you are a recipient, when did you have your transplant(s)?
May 25,1994
What is your principal transplant med(s)?
Sandimmune
Prednisone
Rapamune
What is your hospital and, or doctor's name, city / state and country?
Duke University
Durham NC
USA
About Me: Please use this space to tell the community about yourself and your unique experience with transplantation:
I had Primary Pulmonary Hypertension and received a double lung tx May 25,1994.
I was 35 when I was diagnosed with PPH. It unfortunately is hereditary in my family. There is no cure for it. At that time there were no medicines for it but there was a study being done for an experimental drug called flolan. I was lucky enough to be put into the study program for it. It worked for a few months but my health started to deteriorate very quickly. In May of 1993 I was put on the transplant list for a double lung. The following May I got my call that a donor had been found. I was just a month shy of turning 37 when I received my lungs. I am proud to say I have turned 52. When I was diagnosed I never thought that I would even be alive at 40 never the less 52. Needless to say when asked my age I proudly will admit I am 52 and hope to be around many more years.
Well I just found out October 2, 2008 that I am experiencing my very first time with rejection in my airways. I guess they are right when they say it can happen at any time. I am grateful that I have gone so many years without it.
What is your relationship status?
Married
Entertainment: What is Your Favorite Type of Music, Bands, Movies, Art, Books, etc.?
I like old movies. My favorite is "A Wonderful Life"
Favorite animated movie "Annabell's Wish".
I like all kinds of crafts. Enjoy making jewelry for family and friends.
I enjoy country music.
What is Your Favorite Quote(s)?
I'm walking , talking and breathing so I am fine.
My "MySpace" Page:
http://www.myspace.com/windsong1

Gail Csizmar's Photos

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Gail Csizmar's Blog

Gail Csizmar

Memorial Day..... May 25,2009

Such a very special day for me.

First Thank You to all of our Soldiers who gave their Life for our Freedom. Also for those who are serving in the armed forces...Thank You.

A very special Thank You to my Donor and her Family.

I received a second chance at life 15 years ago today. A family was going through great sadness and heartache but still found it in their hearts to give "THE GIFT OF LIFE". It is a day of great sadness for me because a life was lost to give me life. It is hard to be happy… Continue

Posted on May 25, 2009 at 3:28pm — 3 Comments

Gail Csizmar

No Rejection

I am finally out of rejection. My bronch showed that I am rejection free. Hope I will continue to stay that way.

Posted on February 6, 2009 at 10:52pm — 2 Comments

Gail Csizmar

Why I joined TransplantCafe

I finally found a support group that I could identify with so many people. We as transplant patients know to some extent what others are going through. I need to know that there are people who understand what I am going through. I have found a lot of support from this group.
I hate it when you get people that have no idea what transplant means.
I hear people say I know what you must be going through. NO they DON'T know. Until they have walked in a transplant patients shoes they have no clue as w… Continue

Posted on October 8, 2008 at 8:33pm — 1 Comment

Gail Csizmar

rejection :(

I now know what it feels like to be told you are in rejection. It is scary. I am really pissed off because I have gone 14 years without rejection. The only thing that changed this year for me is that the *#@*# insurance company changed and I had to go on the generic sandimmune. I believe if they would have let me stay on the brand name that I had been on since first transplanted I would not be in rejection now. Now my meds are all going to change and the insurance won't cover the 3 days of solu-… Continue

Posted on October 2, 2008 at 7:30pm — 3 Comments

Gail Csizmar

Bronch is over yipee!!

Well there was no mucus plug and the scare tissue from the tx is not causing my pft's to drop. I should hear back from the bronch tests by tomorrow or Friday.

Posted on October 1, 2008 at 2:04pm — 1 Comment

Comment Wall (19 comments)

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At 3:41pm on April 1, 2009, Maria Fuller said…
I am very thankful that you responded to my blog. How did you feel after your tx? I think it will be crazy to be able to breath without oxygen machine hanging of my shoulders. I will just be glad to finally play with my children. That is what keeps me motivated. I am also nervous about being kicked off my medical card after the surgery. They said that most people go back to work after about a year and then you have to figure out what you are going to do about paying for the meds. Are working? And what kind of insurance do you have? Sorry i am asking so many questionswhenever you feel like you can comment back thanks for your time.
At 4:38pm on March 21, 2009, Kathryn Flynn said…
You are so welcome and I am so proud of you for getting this altogether on your own.
At 2:48pm on October 20, 2008, Nulungs95 said…
Been busy with my trip to NYC and my daughter coming to see us last week. She had a few days off (more days than Thanksgiving) from NYU and came to visit. We had a great long weekend.

Thanks for asking.
At 7:32pm on September 23, 2008, Carmalita Shafer said…
Hi Gail, I enjoyed reading your profile. It gives me hope knowing you are a 15 year survivor! Hope to talk to you again soon.
At 11:20pm on September 16, 2008, KidneyKorner.com said…
Ya we are working on it (other designs) .. but .. umm.. should I delete my last comment before this since we are no longer allowed to add links?? I don't want to upset anyone..

- Angie
At 5:51pm on September 15, 2008, Kathryn Flynn said…
Hi!
I think it is about a 3 mile walk.
At 12:11pm on September 14, 2008, Justine said…
hey lovely..hows u? Thanks for your last message. All has been going good for me..just been keeping busy with life. What have u been up to too..and hope u r well too. x x
At 8:37am on September 7, 2008, Kathryn Flynn said…
Hi Gail-
Sorry to hear about your sister-in-law. I think I have seen you in clinic as your face looks very, very familiar. See you at the walk!
At 7:14pm on September 3, 2008, Meghann M. said…
Thanks Gail! :) I think it's quite beautiful, thanks for noticing. Mark sure isn't too happy about it though. HEHEHE.
At 12:53pm on August 21, 2008, Susan Friesen said…
Wow, that's awesome you received a double lung transplant!
Susan, mom of 2 daughters with heart transplants, would be glad to be your friend
 
 

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