Dad, Husband, Aerospace Engineer, Computer Geek, and ALS Advocate. These are my thoughts!
Thursday, July 26, 2012
ALS-stricken NFL player and coach, the first patient to undergo new procedure for reprogramming adult stem cells, shows auspicious results
GULF SHORES, Ala., July 26, 2012 /PRNewswire/ -- Eight years ago, Frank Orgel, a former NFL football player and college coach, was diagnosed with amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. Orgel's quality of life declined to the point that he could not move his left arm or leg, walk or even stand on his own. But, within a few days of undergoing a new stem cell reprogramming technique performed by Dr. Jason R. Williams at Precision StemCell (http://www.precisionstemcell.com), Orgel's constant muscle fasciculation (muscle twitching) lessened significantly. Within weeks, he was able to walk in a pool of water and stand unassisted.
The technique performed on Orgel is InVivo reprogramming, which reprograms adult stem cells into neural stem cells. The procedure involves harvesting adult stem cells from the patient's own fat, which Dr. Williams obtains via minimally invasive liposuction, and then using image-guided therapy to insert the stem cells into the patient's spine. For three to five days after the procedure, Dr. Williams places the patient on an oral medication that, as laboratory research has shown, causes stem cells to reprogram, converting them into neural stem cells.
"We are the only facility in the United States performing the InVivo reprogramming procedure," said Dr. Williams. "Frank was the first patient in the world, that we are aware of, to have the procedure done."
Orgel attests to the efficacy of the new procedure. "My leg normally drags and would have to be moved for me, but now I'm able to move it myself," he stated. "I feel that this is definite improvement."
Dr. Williams, a radiologist who specializes in image-guided procedures, had already been performing magnetic resonance imaging (MRI), computed tomography (CT), ultrasound and fluoroscopy-guided stem cell injections for joint and orthopedic conditions. "This new technique of InVivo reprogramming shows great promise for possibly repairing or regenerating nerve cells," he stated. "That means it may open up opportunities for treating several neural conditions such as spinal cord injury, stroke, Parkinson's and Alzheimer's disease."
"We are really excited that this technique can help increase the number of neural stem cells that are transferred back into the patient," continued Dr. Williams. "We are hopeful that this will indeed help us heal or regrow nerve cells; however, it is still too soon to really know."
About Precision StemCell
Located in Gulf Shores, Alabama, Precision StemCell conducts stem cell procedures using advanced imaging techniques, which include an Open 3T MRI, a low-dose 64-Slice CT scanner, ultrasound, and real time x-ray (fluoroscopy). Headed byJason Williams, MD, a board certified radiologist with extensive training in image guided procedures, the facility performs advanced stem cell harvesting and processing with image guided stem cell injections.
Contact:
Bob Hubbard
Precision StemCell
251-948-3420
hubbard@precisionstemcell.com
http://www.precisionstemcell.com
Monday, June 04, 2012
The 2012 Transit of Venus
The transit or passage of a planet across the face of the Sun is a relatively rare occurrence. As seen from Earth, only transits of Mercury and Venus are possible. On average, there are 13 transits of Mercury each century. In contrast, transits of Venus occur in pairs with more than a century separating each pair.
The last Venus transit was in 2004 so the second event of the pair will occur on Wednesday, June 6 (Tuesday, June 5 from the Western Hemisphere). The entire event will be widely visible from the western Pacific, eastern Asia and eastern Australia as shown in Figure 1. Most of North and Central America, and northern South America will witness the beginning of the transit (on June 5) but the Sun will set before the event ends. Similarly, observers in Europe, western and central Asia, eastern Africa and western Australia will see the end of the event since the transit will already be in progress at sunrise from those locations.
Tomorrow I will bring in my telescope and have it set up in the RA-11 parking lot for anyone that wants to witness the event.
Stop on by and experience the last Venus transit for 105 years (I think it’s safe to say the last one in our lifetime (2117)).
For Northern Hemisphere locations above latitude ~67° north, all of the transit is visible regardless of the longitude. Northern Canada and all of Alaska will also see the entire event. Residents of Iceland are in a unique wedge-shaped part of the path (Region X in Figure 1). They will see both the start and end of the transit but the Sun will set for a short period around greatest transit. A similarly shaped region exists south of Australia (Region Y in Figure 1), but here, the Sun rises after the transit begins and sets before the event ends.
The principal events occurring during a transit are conveniently characterized by contacts, analogous to the contacts of an annular solar eclipse. The transit begins with contact I, the instant the planet's disk is externally tangent to the Sun. Shortly after contact I, the planet can be seen as a small notch along the solar limb. The entire disk of the planet is first seen at contact II when the planet is internally tangent to the Sun. Over the course of several hours, the silhouetted planet slowly traverses the solar disk. At contact III, the planet reaches the opposite limb and once again is internally tangent to the Sun. Finally, the transit ends at contact IV when the planet's limb is externally tangent to the Sun. Contacts I and II define the phase called ingress while contacts III and IV are known as egress. Position angles for Venus at each contact are measured counterclockwise from the north point on the Sun's disk.
Table 1
Geocentric Phases of the 2012 Transit of Venus
Event Universal Mountain Position
Time Time Angle
Contact I 22:09:38 4:09:38 41°
Contact II 22:27:34 4:27:34 38°
Greatest 01:29:36 7:29:36 345°
Contact III 04:31:39 10:31:39 293°
Contact IV 04:49:35 10:49:35 290°
Table 1 gives the geocentric times of major events during the transit. Greatest transit is the instant when Venus passes closest to the Sun's center (i.e. - minimum separation).
I added the Mountain Time Zone to Table 1. First Contact begins at 4:09:38 p.m. and because the sun sets at 8:24 p.m. (a bit earlier because of the mountains) the total transit is not visible.
During the 2012 transit, Venus's minimum separation from the Sun is 554 arc-seconds (During the 2004 transit, the minimum separation was 627 arc-seconds). The position angle is defined as the direction of Venus with respect to the center of the Sun's disk, measured counterclockwise from the celestial north point on the Sun. Figure 2 shows the path of Venus across the Sun's disk and the scale gives the Universal Time of Venus's position at any point during the transit. The celestial coordinates of the Sun and Venus are provided at greatest transit as well as the times of the major contacts.
Note that these times are for an observer at Earth's center. The actual contact times for any given observer may differ by up to ±7 minutes. This is due to effects of parallax since Venus's 58 arc-second diameter disk may be shifted up to 30 arc-seconds from its geocentric coordinates depending on the observer's exact position on Earth. Table 2 and Table 3 list predicted contact times and corresponding altitudes of the Sun for locations throughout Canada and the United States, respectively. Table 4 provides similar predictions for a number of cities around the world.
Friday, April 06, 2012
Can Stem Cells help ALS Patients?
Article Highlights:
To learn more, read the full ALS News Online article. als.mda.org
Scott Wiebe
National Director — Outreach Services & ALS Division
Thursday, March 08, 2012
Help Save the ALS Research Program
U.S. Representatives Elton Gallegly (R-CA) and Chellie Pingree (D-ME) are circulating a letter requesting the House Appropriations Committee provide $10 million in funding for the ALSRP next year. We urge you to contact your Representatives today to request that they sign onto this critical letter and help us find a treatment for ALS.
The text of the Gallegly-Pingree "Dear Colleague" letter is available by clicking here.
Representatives Gallegly and Pingree have set a deadline of March 15, 2012 for signing onto the letter. So please contact your Representative TODAY and urge Congress to continue funding for the ALSRP -- tell them that they need to stop ALS, not the funding that is so urgently needed to find a treatment.
A sample letter you can email to your Representative is available in the Advocacy Action Center of our website here: http://capwiz.com/alsa/home/.
Congress needs to understand how critically important the ALSRP is to the search for a treatment. They need to know how important this program is to their constituents, the people with ALS they were elected to represent. Contact Congress TODAY!
If you have any questions or would like assistance reaching out to your Representative, please contact us at advocacy@alsa-national.org or toll-free at 1-877-444-ALSA.
Tuesday, February 28, 2012
Acclaimed physicist Hawking 'a regular' at Calif. strip joint
By PHIL HELSEL
Stephen Hawking certainly has discovered some new heavenly bodies — at a California jiggle joint.
The apparently sex-crazed 70-year-old genius astrophysicist, who is confined to a wheelchair by Lou Gehrig’s disease and uses a computer to speak, has been spotted several times getting lap dances at California sex club Devore, RadarOnline reported today.
Hawking, whose work on black holes earned him international acclaim, arrives at the club with an entourage of nurses and assistants and has "naked women grind on him," RadarOnline reported.
"I have seen Steven Hawking at the club more than a handful of times," the source told the online celebrity gossip site. "Last time I saw him he was in the back 'play area' laying on a bed fully clothed with two naked women gyrating all over him."
AP
Acclaimed physicist Stephen Hawking.
Although debilitated by the disease, which is also known as motor neurone disease, Hawking has been a member of the Freedom Acres swingers club for more than a decade, according to the report.
Hawking and his second wife, Elaine, divorced in 2006. His first marriage, to Jane Hawking, ended in 1990.
Diagnosed at the age of 21, Hawking was given only a few years to live but has defied medical opinion by reaching his eighth decade.
"I'm sure my disability has a bearing on why I'm well known," he once said. "People are fascinated by the contrast between my very limited physical powers, and the vast nature of the universe I deal with."
Much of his work has centered on bringing together relativity (the nature of space and time) and quantum theory (how the smallest particles in the universe behave) to explain the creation of the universe and how it is governed.
Hawking is a good sport, according to RadarOnline, and will even pose for photos with fans as long as the pics are taken in "a neutral area."
"But Stephen is by far the last person I ever expected to see in this club," the source told the site.
-- with NewsCore
Saturday, January 14, 2012
Update on Roger and Our Family: By Julie
Dear Family and Friends,
I thought it would be helpful for me to give you an update on Roger. It has been over 6 years since his diagnosis.
He continues to have a slow progression and we are very grateful for that. However, slow does not mean NO progression unfortunately. The biggest change lately has been his speech. We have for several months been adjusting to this change. We can still understand him, but it is just getting more and more difficult. It is extremely difficult to have to say "what" over and over again in a day to a man you just don't want to make repeat what he said because it is so difficult to talk in the first place. His legs continue to be pretty strong but they are progressing as well. He recently was fitted for leg braces (AFO's) to help give him some lift in his step which will help with any slight drooping he has in his feet. We think this will make him feel more confident when walking any distances. He did just have a check up in November to see how things are going. He had a routine FVC (forced vital capacity) test. This is the total volume of air expired after a full inspiration. A healthy person's measures at 100% or more. Back in July, 2010 it was at 84% and now it is at 70%. This is actually pretty good 15 months later, but is still tough to see it go down. The doctors say that usually when a patient's FVC gets down to 50%, it is usually time for a feeding tube because the swallowing is usually effected by then as well. Needless to say, he is not looking forward to not eating.....neither am I for him.
We are doing our best to all just take this disease one day at a time, but that is not so easy to do. We're told to be proactive which means thinking ahead.
We want to thank all of you who have supported us one way or another over the past 6 years. I know that Mary has been our sort of spokesperson without being asked to be. She has gone above and beyond what I ever imagined or expected. I cannot thank her enough for driving to see us 3 times now. Her and Carli are like Thelma and Louise I call them.....always up for a road trip. I also want to thank Roger's parents again for coming out to take care of the boys while I went to Premier's National Rally back in July. That was huge and I am very grateful for them coming out here to help. I definitely know where Roger gets his do do do personality. His dad was quite busy around here, as was his mom. My Auntie Pat and Gary were also out here to visit. Gary was a huge help to Roger with several projects he was hoping to see done. I also want to thank everyone who have been able to contribute to our Childs' Supplemental Care fund over these years. I hesitate bringing this up because I never want ANYONE to feel badly if they cannot contribute. We are just as grateful if not more grateful for simply keeping in touch with us and praying for us. THANK YOU SO MUCH!
I want to address the fact that I would love to talk with all of you but can't always do so. We really do appreciate hearing from you though and even emailing us and/or leaving us messages is nice. I will do my best to call back or email back, but appreciate your understanding if I don't right away. I really hope no one is upset with me in regards to this. I want to hear about your lives too!
This journey has been and continues to be a daily struggle mostly for Roger of course, but all of our lives have changed drastically and we really are trying to do our best with all that is happening to our family. Being diabetic is also an aspect of our lives that I am trying not to neglect.
I truly hope people don't stay away from us because they think we have enough on our plate or maybe because it is just too painful to hear about what is going on with us. Trust me.....it is much more painful on Roger's end. But here is what is most amazing.....ROGER HAS THE GREATEST ATTITUDE 99% OF THE TIME!!!!!!! He absolutely puts me to shame! I am learning how to be a caregiver...not just a caregiver, but a good one. There are times I basically go through the motions. This wonderful man can't help that he needs so much help (not at all his fault he has this) and care......care being the most important word here. Trying so hard to give care with care is something I didn't think would be difficult but actually can be at times. Roger does need me to feed him, shower him, dress him, undress him, brush his teeth, shave him, clip nails and get him what he needs/wants. We love each other and will continue to be here for each other. The boys are strong, but it does break both Roger's and my hearts to see them live through this. It really is so unfair and we can't change it so we do try and see the good that does come from it. They are compassionate boys who certainly know how to persevere through rough times in life. As their mother and father, we just never imagined they would have to persevere through anything like this. None of us did. Please pray for patience on my part and for each of our parts in our family. Connor is 15 now, a freshman in high school and is such a good kid who loves his dad so much, but can get agitated once in awhile. After all he sees his mom get that way sometimes too. Brandon is 11 now, a 5th grader and is also such a good boy who thinks the world of his daddy. He too helps him so much. He needs prayer for his worrying about daddy falling. He has seen this happen several times. It is just part of what happens to people who have ALS.....another aspect we need to keep an eye on and make changes when necessary. They both help me help Roger and I don't know what I would do without their help. I am so grateful to God for their strength. He gave us 2 amazing young men!
I continue to work my business with Premier and am super grateful for all it has done for me and our family. Because of Premier, I do get to stay home and take care of Roger during the day and not try and figure out how to do that while going to a regular day job. The boys do help here when I go to my shows. Again, looking ahead, there will need to be help to come in at some point as the care for Roger increases....but back to one day at a time.
We are looking forward to all going on a cruise I earned with Premier this coming March. We are excited to bring the boys this time. What a total blessing!
I once told Roger that I really didn't think he would be able to handle this disease very well (who could honestly?.....not many) because of how he is such a doer and likes to keep busy and moving. I then said that he has just been so strong through it all. His reply to me was that it wasn't him at all, but it must be because of God. That was huge to hear! Thank you God! He certainly does work miracles. We all just have to open our eyes and our hearts to recognize them when they happen. Who knows.......maybe we will get a miracle and Roger will be cured (along with the thousands of others living with this heinous disease). If that does happen, get ready for the biggest celebration on a sunny beach that you have ever been to!!!!!!
If you could please forward this out to others you think might want to get an update on Roger and our family, I would very much appreciate it.
Love,
Julie
Friday, January 06, 2012
Stephen Hawking Turns 70 This Month, Baffles Lou Gehrig Researchers
Diagnosed with Lou Gehrig’s disease when he was only 21-years-old and a student at Cambridge it was believed he would only live several years before succumbing to the disease that quickly cripples and then kills those who suffer from it.
Realizing he only had a few years left to live Hawking quickly began examining the universe and all it has to offer, become one of the most well known and respected astrophysicists the world has ever known.
The director of the Motor Neurone Disease Care and Research Centre in London recent told the Associated Press:
“I don’t know of anyone who’s survived this long.” while calling his progression ”extraordinary.”With his disease in tow Hawking has never really slowed down, his book A Brief History Of Time was released in 1988 and has went on to sell more than 10 million copies worldwide. Despite being paralyzed in a wheelchair Hawking used a computer and twitching with his right cheek to communicate, he even went on to become the Lucasian Professor of Mathematics at Cambridge University, a position he just recently retired from.
One thing Hawking has never been able to master in our universe? Women, the one entity he still calls a complete mystery.
As a personal hero of mine I have to say that it’s quite fitting that a man who has fought with parts of the universe that baffle most people have himself baffled the very people studying him and his debilitating disease.
Are you a fan of Stephen Hawking? Share your favorite subject matter he has covered.
In the meantime enjoy the full screening of Hawking’s “Curiosity” video:‘
http://www.youtube.com/watch?v=fpb7NMR-XOo
Rog