May 2005 Archives

Deep Throat Steps Forward

MSNBC has an article up reporting the identity of the infamous Deep Throat.

>Ex-FBI official says he's 'Deep Throat'

Magazine quotes him as saying he was 'doing his duty'

Updated: 12:01 p.m. ET May 31, 2005

W. Mark Felt, who retired from the FBI after rising to its second most senior position, has identified himself as the "Deep Throat" source quoted by The Washington Post to break the Watergate scandal that led to President Nixon's resignation, Vanity Fair magazine said Tuesday.

"I'm the guy they used to call Deep Throat," he told John D. O'Connor, the author of Vanity Fair's exclusive that appears in its July issue. [MSNBC]

No word yet from Woodward and Bernstein, who have pledged not to reveal the identity until the person has died.

More on the Lung

After my bout with acute rejection I woke up to find myself in the ICU again. This was a kind of weird time for me. The medications they gave me to fight off the rejection/possible infection scrambled my brain a little. Between that and being cooped up in the ICU I was more than a bit confused. For a while I pretty much forgot I'd had the transplant.

For the next week or so everything snapped back into place and I remembered where I was and what I was there for. But it was so strange to look back and and my thinking still makes sense. There is a condition called ICU Psychosis what is experienced by some people, and we think I had a touch of that added in. I remember having lots of really odd dreams, which I guess had me speaking out loud too. My parents and sister have all kinds of stories of me talking about too many countries and leprechauns.

After close to a week I was moved back to step down. At this point I'd barely eaten in weeks and my weight was down 35 pounds. So the next week was gaining strength, starting to walk again (with the help of a walker). Getting used to eating again (which took some time).

After just over a week of that I was ready to head home. I was going pretty crazy with boredom and got to leave just in time.

So far things at home are going well. I get better at going up and down stairs every day. It's amazing how hard even little things like that are still.

The Other Big Thank You

I wanted to have this thank you be on its own. I would like to thank Emily for keeping this blog updated. I'd asked her to do it for me years ago and was glad that she was able to do it. My friends and family have all be so impressed with it. And it really helped keep information flowing.

Thanks again Emily!

The Thank You Post

There's so many people to thank for their support with my ordeal. At the very top of the list is my family. My parents, who were there for me every single day without fail, are the best. Even while I was a bit out of my head with ICU Psychosis. My sister, who came up from Louisiana and also watched over me. It was good to have her nearby.

Next are all the people who sent me cards and presents. I'm not even going to try and name everyone because there are just too many and I'm sure I'd forget. But at the top of the list would be Bree and Ellen.

And finally, a big thanks to all the nurses and doctors at Brigham & Womens. They were all so amazing. Even when I felt like I must be bothering them too much they were always there for me.

A Tale of a Lung

On April 13th at around 2pm-ish I got a call from Brigham and Women's asking me to come in for a transplant. After packing things up my parents and I zoomed up to the hospital. After getting there I learned things were a go and was prepped for surgery. At around 1am on the 14th they were done with my surgery.

Fast forward to the Sunday after that. That's the first day I remember being able to connect events together. Everything has gone well with the surgery and I am recovering nicely. Within two days I'm eating solid foods and being ready to moved to what they call Step Down. Step Down is where you go through the second stage of your recovery. They have you exercise every day to get your new lung working better and start to get you learning about what the rest of your recovery will be like.

Unfortunately, after a day or two in Step Down I had a setback and went into acute rejection. At the time they weren't sure if it was rejection or infection or what, so they were treating me for everything. This also meant going back under sedation as they put me back on the ventilator. I pretty much don't remember anything between then and waking up a week or so later in a fairly confused state.

I'll continue this tale in one of my next posts so that this doesn't get too long.

there's no place like home

spoke with greg earlier today. he's so happy to be home. he is hanging out on the second floor of his house, getting to sleep in a REAL BED, taking the stairs SLOWLY, and resting when he needs to.

he's been reunited with his powerbook and mentioned how tiring typing is... i think he'll ease his way back into it. being in the house will get him strong again though, so all this hard work will pay off -- even if it is exhausting for a while.

keep up the good work greg!

RELEASED!

just got word that greg has gotten the ok to go home today. they're giving him the last minute instructions and then he'll head home with his parents.

after hanging out with greg last night, this is such a relief! he was REALLY ready to go home yesterday and didn't want to think about having to stay in until monday.

he's walking with a cane and has managed to conquer 5 steps at a time, so he'll be able to get around his house.

VERY EXCITING!!!

direct from gregory!

just got a call from greg! he recieved the playstation gear sent by ellen and jules and he's stunned and speechless. the thing 'just so cool!' thank you. thank you. thank you. says greg.

AND they are prepping him to go home! they've been meeting with him and his family to go over what to expect when he transitions from the hospital to home. he could be released this thursday or the following monday!!

on that note: if you're sending cards or letters, now's a good time to change your address book to his parents home:

194 Kenyon
Hartford, CT 06105

he's walking now with the aid of only a cane and even though stairs are still a little tough, he knows he will get stronger with time and they will get easier.

it was pointed out to me that the milky way comment from my last update was left dangling out in the wind... sorry about that, but greg's lost SO much weight (he's officially down to 129 lbs!) that they're feeding him high calorie yummies like milky ways to thicken him back up.

visits, haircuts and milky ways!

saw greg tonight after dinner. he had a big day! renee visited him and gave him a lovely haircut. with the ruddiness back in his cheeks he looks very healthy and he's getting his strength back. chris visited as well as bree & mike! that's a lot of visiting!! he was admittedly a little tired but really enjoyed having all the visitors.

another cool accomplishment today... he walked around the halls with only the nurse's hand for support - no walker! one step closer to the hospital door! yay greg!

he specifically asked for everyone out there to send out the positive energy for his continued healing, he'd love to go home soon. cross your fingers & toes, or better yet, throw on your favorite gregory mixes and dance the energy up!

doing great, walking a lot

greg is continuing to do well and is working hard getting his strength and appetite back up. the food is not causing issues any longer and he's doing laps with the nurses as well as physical therapy to regain his strength. they've given him his cellular phone, so you may hear from him! the computer could be coming back soon...

yay greg! keep up the amazing work!!

lovely visit

hung out with greg for a little bit yesterday evening. he looks much rosier again and now has a firm grasp on reality. no more confusion! yay!

he was overwhelmed and excited by the gifts that i was finally able to bring to him from bree et al. i'm certain he'll be using the far side book for weight training!

he wanted to me to be sure to thank you guys for such thoughtful gifts and to send thanks to all his family and friends who have sent notes, cards, blog comments. they really mean a lot to him.

yay greg! go greg! :)

a good couple of days

greg has had a good couple of days. his mom says he's seeming more and more himself and the confusion is starting to fade away. they've taken out the chest and nose tubes again and are starting him slowly again on "clear" foods. hopefully this time the transition back to food won't be so difficult.

they're working hard to get him stronger, walking laps with the nurses and doing his physical therapy.

when i talked to him on the phone yesterday, he sounded positively exhausted. there was a lot going on with doctors and nurses and treatments and such in his room. i've just spoken to him today and he sounds much brighter. i'm heading in to see him now!

cautiously optimistic

the doctors are trying to figure out why greg is still uncomfortable and having a hard time with solid food. his lung looks good, so now they're testing his pancreas and gallbladder to see if they can figure out what is going on. they're being very cautious with him, but think he can get past whatever this is.

back in step-down

sorry for the quiet. i'm back in boston and got to see greg yesterday AND today!

greg moved from the icu to the step down unit last night. he's back on solid food, but lost a lot of weight through this recent episode. the hospital is trying their best to load him up with calories (the nurse suggested a milkshake while i was there today) to get his weight (and strength) back up.

the anti-rejection meds are still making things a little confusing, but hopefully that will pass soon.

i know he'd love to receive more cards and/or letters! i'll print the comments you've all left recently for him this weekend.

slow going

greg and his family opened a bunch of the cards that have come in over the last week or so today. his mom said that it was really wonderful for greg to get support from family, friends... so many people from all areas of his life. it was really lovely for all of them. he appreciated all of them and is thankful you're all thinking of him. keep the cards coming.

that said, greg's condition is about the same today. this part of the process could be very slow going, maybe a few weeks.

more of the same...

greg is still making slow progress. not much has changed since yesterday and his family is with him all the time. keep them in your thoughts, as well as greg, of course.

what a difference a week makes

I’m traveling for work, but am pleased to be bringing you updates from his mom from beautiful Reno NV.

Greg has continued to do well. Today he came off the ventilator. He’s extremely weak, somewhat scared and a little disoriented – as well as slightly giggly and high. The doctors are not rushing him to progress, as they’re still concerned about bringing him along too quickly. His sister has now joined his mom and dad at the hospital to be with him.

Keep the prayers/light/energy flowing folks!

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This page is an archive of entries from May 2005 listed from newest to oldest.

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