Thursday, June 28, 2012

Name came up on the Elective Waiting List

I did add more to the last post in case you missed it.  It wasn't much of a post.

I finally caught up with Jan today and Marina this week too.   It is funny that I have been out in the wettest coldest time of the year but it means I am feeling somewhat better, but I just don't last very long. Half hour stints have been OK.  I tried to go shopping for a TV for the bedroom but I got too peculiar and allergic to standing again so I gave up when I could not get a park right out the front of the second shop I went to.  It has not been scooter weather.  Back to online shopping.


On Wednesday S phoned once he was already on his way here. I am trying to get him to phone well in advance but it takes a while to sink in.  He interrupts my plans. He was really just wanting the facilities and he has been here for two nights.  His mood is not settled by any means.  He was going to check out rentals today but it did not happen. He's changed his mind.  This visit, I feel like my life has revolved around his indecision about what laptop to buy.  Looking things up for him.  Trying to teach him to do a side-by-side comparison of features.  It mostly all revolves around him and his needs but then out of the blue he goes and buys me a top from K-Mart (size 12 yesterday, size 8 today when he took the size 12 back because he didn't like it on me).  It is the thought that counts they say.  But I can see I have to fit in to the ones that are on special.  I wonder what tomorrow will bring - hopefully a size 14?  He will be leaving tomorrow.  I say so.

Potentially Life Changing News:  Ange and family are moving to Brisbane, not for 9 months but that will mean seeing even less of Connor for me - much less - because I suspect S will be much more likely to drive to see him than I will.  He may even have more of  a reason to move there himself.  I really miss not being able to see Cohen.  We missed Christmas so I am now aiming for Christmas in July.  It has never happened like that before and now it is going to happen with Connor too.

Endoscopies:  I had a phone call yesterday lining me up for the pre-admission clinic next week and both procedures are being done on July 18.  I don't know whether it is am or pm but I suppose it will lay the Whipple's Disease hypothesis to rest.  Colonlytely here I come.  Yuk stuff.  Hopefully they will leave me alone for at least another five years after that.  I can't wait until it is over already.

I have been blaming taking Tramadol or codeine for the constipation that seems to have got into a cyclic pattern for well over a year now.  You know the big D has always been my most prominent gut problem until then.  I have discovered by quitting all those pain killers on a daily basis that it makes no difference.  I am still alternating between C and D with more gut cramps than I have had for years and all these pains around my rib cage as well now.  The pain on the right side has been around for about the same time but these left sided ones are this year's addition to the list of symptoms I have.  Is the list ever going to stop getting longer?  I have been having lots of prickles on my skin and a few itchy lumps, nothing major but what is causing it?  I always have something erupting on my face these days too not to mention this strange eczema-like red blotches that can get crusty but also alternate between itching and stinging.



Gut link of the day: http://crohnsandibsbreakthrough.com/blog/natural-antibiotics-for-multi-pronged-attack-on-map/

Wednesday, June 27, 2012

Can't Keep Track

I remember last weekend he was at Dad's but Roger was away camping with Connor for the weekend and S brought him back here on Monday when he called in surprising me.  He stays for a long time.  But he went home again.  I seem to have to talk him out of going to Brisbane all too often lately - at least until he has accomodation arranged.  He uses too much petrol not being decisive.





Thursday, June 21, 2012

Korean Share House Days Are Over

He arrived here...heading to Brisbane after spending night in the car.  He does not know what happened or why he had to leave.  or so he tells me.

This is the day after the Dept sends out a survey about under occupancy and a spare declare who is living with you form and I phone to remind them S is Not HERE.

He won't be staying.

Monday, June 18, 2012

Dr Lewis and Car Doctors

I emailed that guy you suggested Zena to see if he will take new patients in 2013.  I knew about him from others but it all seemed so hard so I missed out and I knew you were coming up this year so maybe next year?  His web site says he is not taking new patients now.   I think I would rather see him than the one in Brisbane simply because I will have your support.  I don't think I can keep on pushing myself to go it alone.

Donvale Specialist Medical Centre
Suite 8, 90 Mitcham Road, Donvale VIC 3111
phone: (03) 9841 4500
dlewis@cfsdiscovery.com.au



 S is still here, trying to find a part for this Rodeo with an Isuzu motor which he finally got but he has called his father anyway because the tools we had here were not long enough or something and Roger just happens to be in Maroochydore.

Connor was taken home yesterday afternoon.  He is now into a computer game called Minecraft at his other Nana's house but he spent quite some time on youtube watching instructional videos on how to play the game, hints and tips.  Things ARE that complicated in the gaming world.  It is way too hard for me!  I'll stick with Dragonvale.  He still likes that too.

I booked my car service for tomorrow but Dwayne turned up this morning early and I was up so I let him take it.  It was back in time for S to use it to run around in.  No comments are necessary at this point in your reading.  I am up for a few significant repairs in 6 months time and a couple of front tyres Now!  Here I was thinking I had a chance to get to stay a day or so in HB to see B and Cohen.  Now it is tyres first and by the time his birthday comes along, he will have his license back and will have to get their car registered but then he can drive down here and install my RAM I've been waiting for since Xmas.  B actually phoned me today but now he has broadband again so I guess it will be easier to keep in touch.  I'd love to Skype or do a Google Hangout with Cohen again like we used to.

Was happy to see my Pale-Headed Rosella pair back this year to pick at the seed heads on the Crepe Myrtle now that it is bare-leafed.



I'm going back to cutting my toe nails and then my toes will be getting plonked on the foot warmer.


Saturday, June 16, 2012

POTs Movie: Changes

Thanks to Amity for pointing me to these


The following information was first published in the May 2000 issue of the Lyndonville Journal - a bi-monthly newsletter from Dr. Bell's medical office that preceded the Lyndonville News (DavidSBell.com). It is reproduced here with kind permission,* and offers basic information on a subject of great current interest, with researchers at various centers(1) working to unravel the link between orthostatic dysfunction and ME/CFS.

Orthostatic Intolerance and Chronic Fatigue Syndrome (ME/CFS)

“In many medical illnesses, the patient will feel ill regardless of whether he or she is lying down or standing up. With CFS, patients will say, ‘"I feel so exhausted I have to lie down.’” 
Orthostatic intolerance (OI) is a term used for illnesses which are characterized by inability to maintain the upright posture. It is a group of illnesses that overlaps with CFS just as fibromyalgia does, and it may give up leads as to the underlying pathology of the illness. The most exciting new leads are happening in the world of orthostatic intolerance.

Because much of the literature on OI may be unfamiliar to the reader, I will try to summarize it. For those interested in more in-depth reading, I would start with “The Epidemic of Orthostatic Tachycardia and Orthostatic Intolerance.” The February 1999 issue of the American Journal of the Medical Sciences. This issue [unfortunately fee based] is devoted to a review of OI, and much of what I will say here is taken from that issue.

Defined simply, OI is the presence of symptoms due to inadequate cerebral perfusion [blood flow to the brain] on assuming the upright posture. The usual symptoms include fatigue, nausea, lightheadedness, heart palpitations, sweating, and sometimes passing out.

Many persons with medically proven OI have been assumed to have emotional problems when they don’t.

Like CFS, there have been many terms in the past to describe this group of disorders, including “asthenia.” Sound familiar? It is not known what is the exact relationship between OI and CFS, and up until recently studies in the two areas have followed separate tracks.

The one very nice advantage OI has over CFS is that it can be proven and there are well defined subgroups.

Over the past year in our office we have been testing patients with CFS for OI by two methods.
• One has been a circulating blood volume study [low blood volume is common in ME/CFS],

• And the second is a test for orthostatic intolerance. This test is easily done in the office and requires only a blood pressure cuff and a good nurse to catch the patient before passing out.
The test is relatively simple.
• The patient lies comfortably for ten minutes and BP and pulse are taken several times.

• Then the patient stands quietly (no moving around) with the blood pressure cuff on, and BP and pulse are taken every few minutes.
This is a poor man’s tilt test [tilt test video], and I would argue that it is more accurate because it reproduces exactly what happens to a patient waiting in the checkout line at the supermarket. [For detail, see sidebar on "Orthostatic Testing Procedure."]

A person with CFS nearly always has orthostatic intolerance.

They describe the symptom of fatigue (which is not fatigue at all), which is characterized by being relatively OK while walking down the aisle of the supermarket, but being unable to stand in the checkout line. The orthostatic testing describes physiologically why this occurs.

There are five separate abnormalities than can occur during quiet standing:
1. Orthostatic Systolic Hypotension

Where the upper number (systolic) blood pressure drops. The normal person will not drop BP more than 20mmHg on standing up.

One patient I follow with CFS had a normal BP lying down (100/60) but it fell to 60/0 on standing. No wonder she was unable to stand up – a blood pressure that low is really unable to circulate blood to the brain. In any ICU they would panic seeing a BP like that. And she was turned down for disability because she probably was a hypochondriac.

2. POTS - Stands for Postural Orthostatic Tachycardia Syndrome

A healthy person will not change their heart rate standing up for an hour.

In a person with POTS, this heart rate increases 26 beats per minute (bpm). Some experts say the heart rate should exceed 120 bpm to have POTS. But either way, this increase occurs frequently in CFS.

I think the increase in heart rate is linked to the decrease in blood volume. Orthostatic intolerance has been called idiopathic hypovolemia [low blood volume] in the past.)

3. Orthostatic Narrowing of the Pulse Pressure

The pulse pressure is the difference between the upper number of the BP and the lower number. For example, a normal person with a BP of 100/60 would have a pulse pressure of 40.

It is actually the difference between the upper (systolic, maximum pressure) and lower number (diastolic, minimum pressure) of the BP that circulates blood.
• If the pulse pressure drops below 18, it is abnormal, and blood would not circulate in the brain well.

• We routinely see in our patients with CFS blood pressures of 90/80, thus a pulse pressure of 10.

• The current record holder is a young woman with CFS whose pulse pressure fell to 6 mmHg before she passed out.
4.  Orthostatic Diastolic Hypertension

The lower number of the BP often reflects the systemic resistance, and while standing, many persons with OI and CFS will raise their lower BP number in [the body's] attempt to push blood up to the brain.

Sometimes this is dramatic. One patient being followed with CFS has a low blood volume, about 60% of normal. While lying down, his BP was 140/80. After standing, his BP rose to 210/140 before we made him lie down. His pulse went up to 140 bpm. He felt rotten but refused to sit down by himself.

As an aside, everyone thought he was a fruitcake – a healthy looking man who said he felt poorly and couldn’t work. He was denied disability as usual. Yet when we did the test, he was so determined to stand up I was afraid… But he was standing with a BP of 210/140 and a pulse of 140 bpm. He is definitely not a wimp.

After the test, we gave him a liter of saline in the office because he didn’t look too good and his blood pressure fell to 90/80 after an hour or so.

It is important to note that we had measured his volume the day before so we knew he was hypovolemic [had low blood volume]. Normally you would never give saline to someone with high blood pressure, it just makes it go higher. In the future, orthostatic testing will require being done in an intensive care unit because these number are so scary.

Now it is ignored, and patients with CFS called fruitcakes!

5. Orthostatic Diastolic Hypotension

This represents a fall in the lower number of the BP, and seems to be the least frequent abnormality in patients with CFS I have tested.

[To learn more, read "Maggie's Panic" - Dr. Bell's intriguing case study of a CFS and fibromyalgia patient whose 'strange symptoms' were finally diagnosed as orthostatic intolerance and low blood volume.]

Below is a listing of these BP abnormalities and normal values, taken from Dr. David Streeten’s book Orthostatic Disorders of the Circulation.... These are important as they will directly measure treatment responses with something other than symptom improvement.

NORMAL systolic blood pressure (sBP) - upper number:
Recumbent: 100-142;
Standing (4 min): 94-141;
Orthostatic change -19 to +11

NORMAL diastolic blood pressure (dBP) - lower number:
Recumbent: 55-90
Standing: 61-97
Orthostatic change: -9 to +22

Orthostatic Systolic Hypotension:
Fall in systolic blood pressure of 20mmHg or more

Orthostatic Diastolic Hypotension:
Fall in diastolic BP of 10 mmHg or more

Orthostatic Diastolic Hypertension:
Rise in diastolic BP to 98 mmHg or higher

Orthostatic Narrowing of Pulse Pressure:
Fall in pulse pressure to 18 mmHg or lower

Orthostatic Postural Tachycardia:
Increase in heart rate of 28 bpm, or to greater than 110 b/min

Jean Pollard, Dr. Bell's office manager, adds:
In our office we see a number of patients for assessment of disability..... [One part of such an evaluation is a Summary of Laboratory Evaluation.] Supportive laboratory evaluation such as orthostatic testing, circulating blood volume or immunologic status should be reported along with negative studies. Supportive laboratory evaluation should be referenced to show that it has been noted to occur in CFS. For example:

Orthostatic testing revealed orthostatic tachycardia with an elevation of pulse on quiet standing of 47 beats per minute.(1,2)
(1) DeLorenzo F, Hargreaves J, Kakkar VV. Possible relationship between Chronic Fatigue Syndrome and postural tachcardia syndromes. Clin Auton Res 1996 6(5);263-4

(2) Jacob G, Biaggioni I. Idiopathic orthostatic intolerance and postural tachycardia syndrome. Am J Med Sci 1999; 317:88-101. 

______________________________________
Orthostatic Testing Procedure
- David S Bell
A number of people have requested the procedure for orthostatic testing that we perform in the office. It takes about 45 minutes and requires a nurse to be constantly present. It is important to note that this test is difficult for some persons with CFS, and an opportunity to rest for an hour after the testing is offered. Intravenous saline is helpful to aid recovery.

1. Patients should be tested late morning or early afternoon with no unusual activity prior to testing. Large meals and large volumes of fluid prior to testing should be avoided.

2. Normal medications should be taken the day of the test. Medications which affect circulating volume should be stopped at least two weeks prior to testing, as they will affect the results. Examples are Florinef, diuretics, blood pressure medications, large salt loads. Tricyclics and SSRI medications are acceptable if not for research studies.

3. Blood pressure should be taken with manual blood pressure cuff every three to five minutes, along with pulse. If available, a dynamap or other accurate BP device can be used.

4. Step 1. Patient lying down comfortably for 10 minutes. Pulse and BP are recorded at onset, 5 minutes and 10 minutes. Pulse and BP are recorded at onset, 5 minutes and 10 minutes, along with recording of observations of spontaneously reported symptoms.

5. Step 2. Patient stands without moving or leaning on any object for 30 minutes or as long as tolerated. If patient pre-syncopal (feeling about to faint), the test is terminated. Right arm is resting on table at mid chest (heart) level with BP cuff in place. Pulse and BP are taken every 5 minutes, and spontaneous symptoms recorded as well as observations (e.g., yawning, feet mottled or bluish, etc). If symptoms become more severe, pulse and BP are taken every 3 minutes.

In recording results, use the listing of normal values and abnormalities per Dr. David Streeten, provided above.

___

Reproduced with kind permission of the author from the paper archives of the Lyndonville Journal, © Bell, Pollard, Robinson, 2000. All rights reserved.

1. Other Resources. For recent research reports, see also:

• "Pulse abnormalities at rest and during tilt test could be highly indicative screen for ME/CFS" - Newcastle University

• "Fibromyalgia-like pain as a cause of autonomic dysregulation," (animal study data "corroborate findings in humans with FM.) - University of Iowa.

• "Postural Orthostatic Tachycardia Syndrome following Lyme Disease" - University of Toledo Medical Center

• "Orthostatic symptoms predict functional capacity in chronic fatigue syndrome: Implications for management," - Newcastle University

• "Orthostatic Stress Impairs Cognitive Function in CFS with POTS," - New York Medical College

• "Blood pressure testing should routinely check for orthostatic hypotension too, researchers advise," - Rosalind Franklin University of Medicine & Science, Chicago

Note: This information has not been evaluated by the FDA. It represents the personal research and opinions of the authors, is for general informational purposes only, and is not meant to prevent, diagnose, treat or cure any condition, illness, or disease. ME/CFS/FM is an extremely complex illness, and advice in a newsletter may not be appropriate for a specific individual. Therefore, should you be interested or wish to pursue any of the ideas presented here, please discuss them with your personal physician.

Mobility Scooter Madness

I went for a long ride yesterday.  To Jan's place down town and back a couple of hours later.  It was a lovely day but I still needed added warmth.

Today, S and Connor arrived after lunch and they are still here.


Friday, June 15, 2012

Registering Mobility Scooters and more slides

To register a mobility scooter in Qld and get CTP insurance for free you have to: Get a letter from your doctor, Fill in a Registration Application Form (F-3518), Fill in a Vehicle Details Form (F-3529), Fill in a Motorised Wheelchair Statement (F-4414) and then write a statement of acquisition letter with seller details, date of purchase and cost. This will keep me busy for a while before I even get to Main Roads. 


I am NOT allowed to ride it in bike lanes!


S is coming down over the weekend which could mean today and we will hopefully be getting Connor so Dragonvale, here I come.  (It's a game Mum - for the ipod, iphone and ipad).


I am feeling much better.  Still have some pain but it is not bad enough to stop me enjoying the lovely weather.


Mt Baw Baw 1965 (but the slide casing says 64 M)


Was trying to be artistic 1964
I'd rather try the Bounceball
1972

Thursday, June 14, 2012

Ambulance Ride and More Slides

Am not enjoying sitting upright at the computer for long so instead of filling you in about what has been happening I am just going to copy and paste.  I have heard from S via email who says he is living with Asians in Noosa but will be moving again soon.  Also a one-liner about his job being "fine".

I wrote this on Monday:

I have just got back from Emergency at the local hospital. Pains in chest, shoulder, arm, boob up to neck started last night. It feels like a stitch, pain moves when I change position but still won't go away. I phoned the doctors after hours number today and because there was going to be a five hour wait, the doctor ordered an ambulance. I really did not suspect my heart but with all the anxiety my HR was so high the ambos took me up there to the hospital. I got the all clear from the heart attack type tests and here I am sitting here with the same pain back at home and pretty darn exhausted. He wondered if it could be muscular when he pressed under my arm and asked if it hurt which I said yes to but anyone with fibro has sore nodules every darn where. Happy Queen's Jubilee Birthday everyone - last place I expected to be celebrating it.


it still hurts more when I breathe - but I guess the chest x-ray being all clear rules out lung problems. It feels a bit like when you get trapped wind (say after a laparascope when they fill you up with C02) pushing on diaphragm and referring pain everywhere but it is on the left side, still up to my shoulders, neck and it has made for a restless night sleep last night. I wonder what it is - aspro clear seemed to help yesterday - gut does not usually like that sort of anti-inflammatory though.

I wrote this on Tuesday:


 Today saw GP as ordered by hospital with discharge letter and he says its inflammed ribcage - anti-inflammatories, will take a few weeks and is just "one of those things".


I wrote this today after someone suggested Chostochondritis:

GP didn't really call it anything except inflammation, did not check for infection except to ask if I had a recent cold (pleurisy) and he listened to my lungs and only felt the under arm side of ribs. But it is sore in many places to touch including the breastbone but I have fibro nodules everywhere even on the non-affected ribs. He also did not say whether it was muscle or cartilage but it seems it just goes away in most cases. It is still very annoying and combined with the gut problems I am having really badly - (cannot wear anything without causing spasms, diarrhea, or eat more than a few of mouthfuls) - I am feeling very miserable. Chest has improved some though but the post-hospital malaise and post-adrenaline crash kicked in yesterday. I am feeling depressed now. I hate having a body that is so sensitive to everything. It really is hard not to believe I am dying sometimes - sorry I am sounding dramatic but like I said negativity has hit hard today....and what I usually keep to myself is spilling out with tears.

I thought to myself, at least I obtained some scripts and a doctors letter so I can register my mobility scooter. But his letter says I am fit enough to operate a mobility scooter and the Main Roads site says it is supposed to say that I am NOT fit - supposed to say that due to a physical or medical condition the person’s mobility is severely impaired and they require the use of it. So his letter is going to be useless and with my fear of doctors and what they really think of me, it will probably be a quite a while before I go back. Perhaps I will get it done before Christmas.

 All Slides processed 1964 -back to front?
Who's that?  Cobram? You can edit this Zena if Mum tells you.
I suppose that is Great Grandad Quick's birthday - Is it Frank and Cinderella?  And Nana of course.



Saturday, June 09, 2012

ME/CFS as atypical Polio

http://cfs-facts.blogspot.com.au/2012/06/chronic-fatigue-syndrome-polio-by.html explains it in a chapter of the book:

Chronic Fatigue Syndrome


A polio by another name

Jane Colby, What Doctors Don't Tell You, 6(9)

Undies, Socks and Noosa

All morning I had been trying to duck out just long enough to grab some undies and socks from K-Mart.  It's too hard online.  I sucked it up (against body's wishes) and went to K-Mart after lunch.  It has been raining a lot and being a weekend it was hard to get a park close enough.  I was just about to leave after circling several times when a car pulled out.  I marched in briskly looking like a fit grandmother in her leggings and long boots.  But I discovered that boots and two pair of socks don't keep my feet warm.  I sat down on the lounge inside the shopping centre getting ready for the next spurt and 10 minutes later I was sitting on the floor at the bottom of a 3 tiered stand of cheap underwear looking for my size/s (one size for bloated, sensitive to touch tum days, one for not).  At the checkout having to queue, had me sitting down again on the empty bottom of a display stand, then squatting when I got further down the queue.  All this because of racing heart and light-headedness and the more general woeful feeling that I get.

I was really jealous of the lady in the queue who was on her mobility scooter.  She was brave to go out and risk the rain.  We struck up a conversation and she let me in front of her in the queue.  All this pantomime of dizziness was followed by a brisk walk back to the lounge chair so that no-one could possibly believe how I felt on the inside.  I desperately wanted to get out of the shopping centre that was incubating the local virus being spread by too many people in too small a space but I really needed to sit for 15 minutes before I strode back to the car also armed with some exotic thick looking socks and leg warmers from a Chinese import stand in front of K-Mart.

I could not get in my driveway when I arrived home just as it was beginning to spit with rain.  There was a car in the drive.  An oldish extended cab 4 wheel-drive ute.  It was "you know who" back from Brisbane already after spending the night in the car.  I wonder how his gear faired in the rain.  He was actually ready to leave but after moving the car so I could get in I was expecting him to come inside but he had already been inside and made a cuppa, used the Net and was heading to Noosa.  He did come in and tell me eventually but it was the short version.  So much for living in the big smoke.

He thinks the hearing went well and he has a good chance but the final decision has not been made yet.  He went to check out at least one hostel but there is a minimum stay of 28 days.  Perhaps that means an up-front payment.  I'm afraid that is all I know.  In the last 24 hours he seems to have found a place to move into tonight at Noosa.  I assumed when I saw his car in the driveway that he would be staying the night so this was a surprise.  He and I spoke only for a few minutes and then he left.  I went with the flow of things as it all unfolded without any involuntary inner adrenaline surges which was a nice change.

He liked my boots. LOL

Thursday, June 07, 2012

Off to Brizzy Again

I got the phonecall driving down the highway again.  I half expected that he would want to stay the night because I knew he had a QCAT meeting tomorrow in Brizzy and I have spoken to his paid support person Sally on the phone twice now.  She'll be doing her best.

What I didn't know was that he is not planning on coming back from there.  Job or no job, he has changed his mind (again) in favour of a city life.  Changed from not wanting to live in a hostel because that is too demeaning to finding whatever he can take tomorrow.  He says he has a couple of things or places in mind.  He just can't seem to sit and pass time in Kin Kin despite the much improved relationship with his father.  I suppose he sees that as a waste of time.  I am not sure what this implies about his Solar job in Noosa.

I slept most of yesterday, hoping that a day in bed would help.  It has but I did not rest enough today despite not doing much of anything.

Wednesday, June 06, 2012

Rifaximin for IBS

Taken from: http://www.newswise.com/articles/cedars-sinai-physician-definitively-links-irritable-bowel-syndrome-ibs-and-bacteria-in-gut

Newswise — LOS ANGELES (May 25, 2012) – An overgrowth of bacteria in the gut has been definitively linked to Irritable Bowel Syndrome in the results of a new Cedars-Sinai study which used cultures from the small intestine. This is the first study to use this “gold standard” method of connecting bacteria to the cause of the disease that affects an estimated 30 million people in the United States.
Previous studies have indicated that bacteria play a role in the disease, including breath tests detecting methane – a byproduct of bacterial fermentation in the gut. This study was the first to make the link using bacterial cultures.
The study, in the current issue of Digestive Diseases and Sciences, examined samples of patients’ small bowel cultures to confirm the presence of small intestinal bacterial overgrowth – or SIBO – in more than 320 subjects. In patients with IBS, more than a third also were diagnosed with small intestine bacterial overgrowth, compared to fewer than 10 percent of those without the disorder. Of those with diarrhea-predominant IBS, 60 percent also had bacterial overgrowth.
“While we found compelling evidence in the past that bacterial overgrowth is a contributing cause of IBS, making this link through bacterial cultures is the gold standard of diagnosis,” said Mark Pimentel, MD, director of the Cedars-Sinai GI Motility Program and an author of the study. “This clear evidence of the role bacteria play in the disease underscores our clinical trial findings, which show that antibiotics are a successful treatment for IBS.”
IBS is the most common gastrointestinal disorder in the U.S., affecting an estimated 30 million people. Patients with this condition suffer symptoms that can include painful bloating, constipation, diarrhea or an alternating pattern of both. Many patients try to avoid social interactions because they are embarrassed by their symptoms. Pimentel has led clinical trials that have shown rifaximin, a targeted antibiotic absorbed only in the gut, is an effective treatment for patients with IBS.

“In the past, treatments for IBS have always focused on trying to alleviate the symptoms,” said Pimentel, who first bucked standard medical thought more than a decade ago when he suggested bacteria played a significant role in the disease. “Patients who take rifaximin experience relief of their symptoms even after they stop taking the medication. This new study confirms what our findings with the antibiotic and our previous studies always led us to believe: Bacteria are key contributors to the cause of IBS.”
The study is a collaboration with researchers at Sismanogleion General Hospital in Athens, Greece, and at the University of Athens. 


Tuesday, June 05, 2012

Sacred Kingfisher and Forgetting Brisbane Living

Yesterday, I went for a ride on my scooter and I am still trying to feel comfortable enough with it so that I can call it my second home and so that I can stop thinking about bumps, gradients, debris, and whether I can get through this way without having to go on the road. I saw either a Mangrove or Sacred Kingfisher on the Mangrove Boardwalk and I just sat there for a while in a sunny sheltered spot. I putted along slowly to visit a fisherman on the grassy bank on the edge of the Pumicestone Passage. It was somewhat gusty at times (worse today) and I started to get really cold when the sun went back behind the clouds but I didn't want to come home straight away so I wrapped myself up in an ugly rain coat just around my legs. I was happy that I got my vitamin D for the day and that I didn't use up much energy doing it so that my new toy is serving a purpose. Actually I did use too much energy. I spent the heat that was in my body so next time I must take more warm clothes even if it is fine and warm when I leave. I think it was getting chilled that made me feel so horrible and achey today including my neck glands. Had more gut pains too.

 

I also had a phonecall from guess who last night saying that he was going to be on his way to Brisbane today and that he would call in and pick up his mail. I reminded him to check that the accomodation he had planned was still available BEFORE he went.   However, I did not see him all day.  I got another call at about 6 pm tonight asking me for a pair of headphones because he was actually on his way and would call in to pick them up.  So you've heard from your new boss then, I asked.

By the time he got here he had phoned (while driving) the lady who was in charge of the hostel only to find out that there was no longer a room - he hadn't checked before he left after all.  He was then either going to sleep in the car tonight in Brisbane or stay here the night and find another place tomorrow when he got there.

He made some phonecalls and jumped on the Net and then realised that he was heading to Brisbane for no good reason because his new boss was not going to be his new boss after all.  No room left on the roster.  He had his chance when he had it and missed it it seems with both the job and the accommodation so now the tune has changed again.

He does not want to live in a "shelter" as he called it and he has set his sights back on being an independent solar sales person in Noosa where he would like to live but in the meantime he would go back to Kin Kin with his Dad (he had already suggested he live here permanently during the evening but once again I said "no").

Jan says that she couldn't be so forceful about it with her son but she is glad he is not with her now.  I think she was surprised last time she was here when she heard me say "Go home" at how easy it seemed for me to say.  It has not been easy really but I know I cannot deal with the stress and I actually live in fear of him coming here.

His next QCAT (blue card) hearing is on Friday so he will be heading to Brisbane probably via here at some time.

Bad news:  The company pruning around the sewerage pumping station completely cut down my Lilly Pilly, the one that was struggling to come back to its former glory after I found holes and dead leaves on one of its twin trunks.  I was blaming the Council but after a phone call to them they told me it would have been Unity Water.  I assume it is my land but even the council could not tell me that and neither could Unity Water who said they would put in a report and phone me back..........one day.

Friday, June 01, 2012

Everyone has Gone

It is quite common for this 4wd ute of Roger's to blow fuses.  It is still a work in progress.  There was a fuse here that got S going this morning but he was not in a hurry to leave.  He went to the shops and then locked the keys in the car.  I did not know this was happening until Roger appeared on the doorstep looking for a wire coat hanger.  It just so happened that he had a job at the local caravan park and S phoned him for a rescue before he had even got to the job.

S came back here and R went to work after the break-in.  S was still troubled and he could not handle the fast pace when my friend Jan came over to visit me and get away from her life.  He said that we (referring to Jan and myself) made him scared.  I just told him it was time to leave because he had just been postponing it.  While he was packing up his gear and I was talking to Jan in the garage where I allow the tobacco smokers, Roger pulled up having finished his job.  We were all out there and S even bummed a cigarette from Jan.  He says he has 6 or 8 a year but usually cigars.  Roger was smoking too and yet he had to have a dig at me for "still" vaping in his joking kinda way that always meant that he was getting laughs at my expense.  I remember that.  I don't miss it.  An ex is an ex.

S explained to his father what his plans were and Dad did not approve.  He wants him to stay with him and he told me earlier in private that if he goes to Brisbane, that's the last time I'll be helping him.  Heard that one before too.  I told him to chill because he's more likely to be back than not.  S told him that he was going to Brisbane to live in a hostel.  He has found one but has decided not to go until he finds out about the job for sure.  We all agreed that would be best.  Jan was privvy to all of this.

S left three times.  First he came back and was speaking to Roger about the car.  Next he came back for a protein shake that he told me he doesn't want to use.  It has been sitting around untouched for a couple of months and it seemed to be a huge decision for him whether to take it or not.  I half suspect he came back to hear the rest of the conversation going on here because Roger was still here.  By three o'clock I had decided that he had really gone this last time.  Once the ceiling fan inspector turned up and I was otherwise engaged, Roger left after being stuck talking with Jan in my absence and then Jan went home.

Finally I could have a shower.

Ocean Grove 1964
Where is this?  Did we have a picnic at hanging rock? 1963
1963