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Michael Strane
  • 35, Male
  • Pasadena, CA
  • United States
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It's a new day, hold on with all your might

Latest Activity

Cynthia, as you can see from others responses. Prograf dosage varies wildly. I'm 1/2 years out and on 1.5 mg twice a day. It's a delicate balance that the transplant doctor has to find with Prograf, between keeping a transplantee sufficiently suppre…
on Thursday
Michael Strane and Jenny Romanova are now friends
on Thursday
Nice job, my friend. Keep up the good work and the positive attitude.
on Wednesday
Here is a test to find whether your mission on earth is finished: If you're alive, it isn't.
March 5
Honestly, I'm very happy to see you post. I've struggled with contacting my donor family for the exact same reasons as Peggy. Seeing you note, has encourage me to get past my hesitation and contact them. Thank you
March 4
February 27
February 25
February 20

Profile Information

What is your city / state and country of residence?
Pasadena, CA
How are you touched by transplantation?
I am a Recipient
If you are a recipient, what type of transplant did you receive?
Heart
If you are a recipient, what type of donor did you receive your Gift of Life from?
Deceased Donor
What is your principal transplant med(s)?
Prograf, Prednisone, Imuran
What is your hospital and, or doctor's name, city / state and country?
Dr. Barr, Los Angeles, CA
What do you do for a living?
Geologist
About Me: Please use this space to tell the community about yourself and your unique experience with transplantation:
I had a massive heart attack on 7/30/08, my heart was so damaged that a bypass failed and I was put on a heart assist device called a BiVAD. I was sedated and/or comtosed for nearly 6 weeks and woke up in mid September. Miraculously I recovered quickly and was listed on 9/24/08, even more miraculously I received my heart the same day, only 7 hours later.
Please help us reach other members by telling us how you found Transplant Cafe:
Helpful friend
What is your relationship status?
Engaged
My Facebook Page (copy and paste your profile page URL):
http://www.facebook.com/profile.php?id=788778971&ref=profile

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Michael Strane's Blog

Michael Strane

Too Much Info

Warning: A lot has been going on with me over the past couple months, some of it good, some of it bad, all of it going seems to continue to on and on

It is a time of good news and bad news for me. First the good news, my one year anniversary was on September 24, 2009. Outside of car accident that left Wendy without her car for a month, it was a good day. Wendy and I visited the hospital, delivered a cake and some thank you cards, and went out to a great dinner at Providence . Actually one of th… Continue

Posted on October 25, 2009 at 8:16pm — 4 Comments

Michael Strane

Platelets up, migraine gone

Well, I can easily say that the last 4 days have been the roughest for me since leaving first leaving the hospital after my transplant, just about a year ago. Over the past few weeks my platelet count had slowly been decreasing. Last tuesday, my platelets had dropped to 11,000, prompting my post-transplant doc to refer me to a hematologist. She ordered a platelet transfusion, which bumped the count up to 32,000, which was about half the response they were hoping for. Back on Friday to see if I'd… Continue

Posted on October 7, 2009 at 11:49am — 5 Comments

Michael Strane

Almost a year - down to 2 medications and 8 pills a day

On Monday, I had some extra blood because some previous blood work had shown that I had very low platelets. Well, the platelet count is continuing to go down. As result, I was taken off my last non anti-rejection med, Lipitor, and one of my anti-rejection meds, Arava (which was a replacement for Cellcept). I'm not even 1 year out from my heart transplant. Even before these reduction, my post-transplant Dr., said I was on next to nothing. Now I 'm down to 2 mg of Prograf twice a day, and 5mg Pred… Continue

Posted on September 17, 2009 at 4:56pm — 5 Comments

Michael Strane

New discovery may end transplant rejection

A new development in transplant rejection research

http://www.examiner.com/x-1242-Science-News-Examiner~y2009m4d7-New-discovery-may-end-transplant-rejection

I take it all with a grain of salt. If they come up with something great, either way, just keep living your life.

Posted on April 8, 2009 at 4:26pm — 2 Comments

Michael Strane

Anyone have any experience outside of Arava (Leflunomide)?

I'm now just over 6 months from my heart transplant. While I've not had any issues with rejection, I did manage to come down with the BK virus back in January. The treatment for the BK virus is supposedly pretty toxic, so my doctor has pretty much ruled it out. Anyway, I feel fine. At my last appointment, my blood came up clean, but my urine is still coming up "very" positive for the virus. Long story short, my doctor has taken me off of Cellcept, and put me on Arava (Leflunomide). Does anyone h… Continue

Posted on April 2, 2009 at 5:32pm —

Comment Wall (51 comments)

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At 1:27pm on February 25, 2010, lisa marie gottlieb said…
Yoiu said you work in Valencia, really?? sweet, where at?
At 2:50pm on February 20, 2010, Holly Werlein (Holdol) said…
8 hours is the magical number for us then:) How's everything going with you?
At 11:42am on February 11, 2010, Paula M. Rice said…
Michael, since you live reltively close, could you tell me anything about Caspar ave, off Col. Blvd. in Eagle Rock? We lived in the 3rd house from the top, on the left as you were looking up the street. It was the estate house for the old grove,not at all grand, but, home to me & only the 2nd. one I ever really liked when growing up.That might have had something to do with the pool my dad had put in. My older sis told me not to go back as it had changed & not for the better? I didn't listen to her about Idylwild & cried when saw our old home. Hated every second we tere there! Michael's done aerials, but, it's not the same. Just thought you might know something. Hugs & Blessings. Paula PS. Hope you were spared all the flooding & slides. Can't remember the last time that happened in La Canada!
At 7:56pm on February 7, 2010, Paula M. Rice said…
Boy, do I know what U R going thru! After 30+ yrs. of marriage, it was qustionable whether or not we would make it. The only thing more stressful was when he was in Thailand/Viet Nam! I truely believe he wanted the TX more than I did, but then, I'd been dealing w/hrt. probs since I was very small. Diagnosed myself in 1960; the docs in 1980. Rare type of hrt disease. Ah well. You R both in my Prayers. I strongly suggest seeing a Psychiatrist familiar w/TX patients. Our depression isn't lke others & they know it. Ask your TX docs,if possible. Could be you only need a mild tranq or psyhcotropic. The only dumb question is the 1 U don't ask. Hugs & Blessings, Paula
At 2:57pm on February 3, 2010, Holly Miyagawa said…
No worries...I thought that since you were going to be at the 5K on May 1 it might be something you are interested in. For me, the games were (and continue to be) a great way to meet and interact with other recipients. My transplant was in 2000 and I didn't get involved until 2005. If anything, I can keep you posted on Team So Cal meetings if you'd like. That way you can meet others here in So Cal. We're a fun group!
At 2:06pm on February 1, 2010, Marcelita Cea said…
I am roasting myself here in Chile, and waiting soon the winter hahhaa

34º celsius = 93.2 fahrenheit

At 1:33am on February 1, 2010, Paula M. Rice said…
Reading some of your comments & find it amazing that more people aren't on ati-depessents. W/all we've gone through & go throug, who wouldn't get depressed. A zombie, that's who. TG we'r humans, w/all the pluses & negatives. I've been on psycohotropics for yrs & can't survive w/o them. Hooray for bi-polar + tx! TW, ypor bride is absolutely gorgeous. Congrats to both of you. Hugs & Blessings, Paula PS Just had 37th. anniv. Something to strive for! LOL.
At 4:49pm on January 29, 2010, Paula M. Rice gave Michael Strane a gift
At 10:02pm on January 26, 2010, Paula M. Rice said…
I feel the same way, for the most part. It's only when they get too personal or gruesomely curious (RE: donors' death & history, they're almost salacious. Can't think of another word. Sorry.) that I smile & change the subject. Besides, as I said, I've fought many battles &, so far, won all of them! Talk about tempting fate! Hugs & Blessings, Paula PS. I have way too many to photog.!
At 4:43pm on January 26, 2010, Michael Strane said…
Thank you so much Marcelita. I hope you are doing well too. Surviving the Chilean summer, I hope :-)
 
 

Latest Activity

RichardT updated their profile
9 minutes ago
34 minutes ago
Been on Prograf 1+1 and myfortic 360+360 for 23 months now. I have had somme minor problems with my sugar. I am now hyplogycemic+diabetic. I can deal with that . I just have to eat continuosly. No hair loss at all. In fact,just the opposite. More ha…
1 hour ago
I was 18 when I became ill. What are you hobbies??
3 hours ago
MMmm I would have as much as possible done. lol. Anywhere they can massage without hurting me right now. Get a manicure, hair colored, make up done, and a facial. =D
3 hours ago
-- If you ever feel a little bit stupid, just dig this up and read it again; you'll begin to think you're a genius.. ,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,, (On September 17, 1994, Alabama's Heather Whitestone was selected as Miss…
6 hours ago
Hi Carlos, It is my understanding that in the 1970s Congress passed a resolution to help cover medical costs of people with serious illnesses by putting them on Medicare. They started with kidney failure and began covering transplants. But the cost…
9 hours ago
SO TRUE
9 hours ago
lisa michelle hartley added a discussion
I am a mother of a 20 year old that has.been diagnois as a 12 year old . They said shw could compete in the 11-13 years old group but ahe is not allowed to get any medals. I find this unfair . Who else can help me make them understand this is not fa…
10 hours ago
I Totally agree with you LOL I'm one of the extra special recipient I had Liver (2004) and a Kidney (2009) PKD I have imedicare and a private ins, and the premiums are costing us 860.00 per mo. we are currently in forclosure and all our retirement s…
10 hours ago
Hi everyone. I was implanted with an LVAD 4/30/08.It will be 2 years since i was listed for my heart. No calls yet
11 hours ago
For those on the waiting list. Come find support and encouragement from others who are waiting.
11 hours ago

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