Showing posts with label Illness. Show all posts
Showing posts with label Illness. Show all posts

Thursday, March 19, 2009

Why go postal? Go Karma!

It has it's own sweet revenge!

From Wikipedia: Going postal is an American English slang term, used as a verb meaning to suddenly become extremely and uncontrollably angry, possibly to the point of violence. The term derives from a series of incidents from 1983 onward in which United States Postal Service (USPS) workers shot and killed managers, fellow workers, and members of the police or general public.

I had lost count many years ago the number of times the term ‘Going postal’ was topic of conversation during breaks, lunch, during and after work at social events amongst co-workers and myself.

At one job in the late 1990s a coworker of mine offhandedly asked me, “If going postal means shooting up the workplace at a post office, what would shooting and killing co-workers at a printing company be called?”

My answer, “Graphic violence!”

Although neither I or my friends and former associates in printdom know of any incident of a mass murder rampage (slash) suicide ever happening in a commercial printing company, many of us can fully understand why these things happen in the workplace.

Working in advertising and commercial printing is stressful and highly competitive. There are deadlines that must be met, every facet of production has to run on schedule and there is absolutely no margin of error. Clients pay big bucks for us to produce a product that represents their image favorably. Press time is a valuable commodity that must be started up for each job on schedule.

In newspaper or magazine production, a space is held waiting for the ad to come in by a deadline date. The same is true in commercial printing where press time is reserved. Miss the deadline and the client risks paying an additional charge of $800.00 or more an hour for staging, prepress and press idle time. And God forbid if a press breaks down and the job has to be moved to another press or farmed out to another company. We barely had enough time to get the job ready for press the first time, even if the job came in on schedule. Now we have to make time to rework the darn thing.

Talk about stress!

The fast paced demands of the commercial printing industry could be exciting and physically draining but not to the extreme point of pushing someone past the brink. We had other means of shaking off a bad night at work - the bar - from 8 a.m. till 3 p.m. and we pounded down a lot too; while shooting pool, playing darts. Friday morning bowling league was great for working off the tension of a bad night - while drinking, of course!

It’s not the work itself - it’s the (mis)management; the blame maker; the incompetent bullying taskmaster at the job!

Quite frankly, my friends and former associates can relate to the incidents committed by postal workers pushed beyond the emotional breaking point, however we do question why they (the postal worker), or for that matter, any disgrundled worker has to take out so many people on the way to Mr. Bossman’s office. After all, chances are that some times; many times they had to deal with his crap too.

Yeah we’ve all discussed it; we’ve all figured who might get theirs eventually. We’ve even tried to pinpoint who in the department might become unhinged enough to do the deed and we all pledged to come to that person’s defense in court, if need be. We even had an agreement that, should it be any one of us, remember who the target is and keep our co-workers out of it-we’ve all suffered enough.

So where is this all leading to?

It leads to that one incompetent, cowardly bastard (along with his accomplices) whose actions may have been the catalyst; the finger on the trigger that set my endocrine system awry; the beginning of my decline in good health that I enjoyed for so many years - the one who nearly caused me to have a nervous breakdown; keeping me in a chronic state of adult anxiety.

It was 1994 when I heard about a job opening at the Berea, Ohio printing facility of a large, well-known downtown Cleveland, Ohio publishing company. I was working for a commercial printer in Twinsburg, Ohio at the time and was very unhappy working the day shift. I felt that the midnight shift job in Berea provided, not only the opportunity to leave but, (naturally being a night owl) working the shift of my preference.

About two weeks after applying, I was called to come in for a skills test after work. I was told to meet with John, the second shift prepress supervisor. He would be the one to test me.

Without going into detail regarding the technical aspects of the skills test, John checked my work and told me that the quality of my work was the best of all the people he submitted the test to and that he was going to recommend me for the position. After giving a two-week notice, I started the job in Berea; eventually moving there in 1995.

The job was going great for me and I really liked working there. Several of my friends applied for and got jobs there. I would never suggest to friends to apply at a known hell hole.

Just short of being there a year the problems started.

John accused me of making mistakes that required re-doing my work. I asked him to show me what it was that I did wrong but he couldn’t produce proof.

Soon the mistakes became a weekly occurance, then a nightly occurance yet John could not produce evidence.

My anxiety overwhelmed me; I started having problems sleeping. I couldn’t figure out how I could be making so many mistakes; I did not have a reputation for making mistakes. I had a letter of recommendation from a former department supervisor that clearly stated that I was “meticulous” and had “a keen eye for detail”, so why was I making so many mistakes and WHY wasn’t John able to produce the evidence so that I could correct whatever I was doing wrong?

And there were those constant threats that I better straighten up regarding the errors or face displinary action such as a two-week suspension without pay or being fired.

My doctor wrote a letter on my behalf requesting that my shift start time be changed to 1 a.m. so that I didn’t have to deal with John (he usually left work at that time). Still, he would stay over until I came in so he could tell me about the mistakes that I was making; that too much of my work had to be torn down and restripped. He said that some of the jobs went up on the press wrong and the company was losing valuable press running time, thus costing money.

Finally, John produced the evidence that I had been asking for. He showed me a photocopy of the film ( I ) stripped before it was torn down and restripped. The photocopies weren’t clear because negatives could not be photocopied clearly. He also had the corrected negative taped to the mylar carrier. I checked the label on the mylar carrier that the film was secured to. It was initialed by the original stripper who worked on that particular page. It was initialed CM.

But wait a minute...CM? I don’t initial anything CM and none of the writing on the label was mine.

I told John that was not my writing or my initials. He was insistant that I initialed the job and he would not accept that.

We argued for several minutes over this. I initial everything CDM - for my first, middle and last name-period; and I circle my initials too! Always have; always will.

At the end of my shift, I had to meet with Department Manager Vince V. who told me that he had no choice but to suspend me for two weeks without pay for costly mistakes.

Although going without two weeks of pay would be a financial hardship, I had hoped that I could get my nerves calmed down in that time.

One Sunday night I went into work and began to have problems with lightheadedness; I couldn’t think.

The floors were being stripped and waxed; my department had been finished several hours earlier but the chemical smell lingered. It was disorienting me. (I am still sensitive to chemical smells and MCS is often a componite of fibromyalgia and CFIDS).

The lead person on my shift was Tim M.; a part-time fireman and EMT in Amherst. I went to him and told him I was having problems; or tried to. I was conscious of my surroundings, somewhat coherent but spaced. I felt like I was coming out of a drug induced sleep; feeling much like I was under the influence of sodium-pentethol. I was trying to get help from Tim; I couldn’t think on my own. I needed to go to the hospital but could not convey that to him. I don’t understand why, being an EMT, he did not recognize this.

I tried to work. I started to make mistakes; I corrected them. I made more mistakes; I corrected them. I remember struggling to think and not feeling confident in what I was working on. I was exposed to toxic chemicals at work again and once again I lost my ability to function.

(I've had several exposures to toxic chemicals in my 25 year career).

Now some (still not all) of the mistakes were mine.

My doctor took me out of work for three months. I had to leave work often due to the continuous outgasing from the chemicals; even weeks later.

Meanwhile my best friend Debby, who had started at the company upon my recommendation, had suggested that I make an appointment with a rheumetologist that her sister was going to. Debby was quite aware of the problems I was having with anxiety, sleep and the beginning of depression symptoms and felt that I might have what her sister was diagnosed with; fibromyalgia.
(I will write more about how my diagnosis for fibromyalgia was made in a future posting).

I received a letter from the company asking me when I could return to work. In the letter, they stated that they would have to fill my position if I did not return soon.

Although I didn't feel ready mentally and physically ready to return, I convinced my doctor to release me from sick leave despite his objections. He signed the release papers.

I telephoned the HR Director and told her that my doctor was releasing me to come back to work. The next day, I took the release to the HR Director and was asked to wait in the lobby. About ten minutes passed and then I heard various names announced over the intercom - the company president Bob M., the plant manager, the department manager Vince V., second-shift supervisor and my immediate boss John H. - all called to the conference room.

I knew immediately, I was set up.

Then I was escorted in. The HR Director, her assistant and a secretary (to document the meeting) were also present.

Needless to say; I was let go. The president of the company said that I wasn’t fired - I was being laid off. He said that the company would not dispute unemployment compensation and that I was welcome to apply for any future openings that I was qualified for within the company.

I did apply for an advertised opening in my former pre-press department and was not granted an interview.

I filed with the EEOC a discrimination complaint against the company. During the EEOC investigation, they could not find evidence to support my claim.

After my dismissal, two subsequent charges of sexual harassment were filed with the EEOC against the company. One of the charges, filed January 22, 1997 in U.S. District Court in Cleveland was settled out of court, in favor of the victim, for an undisclosed amount in damages The other victim, in a separate incident of sexual harassment, was awarded a settlement (by jury) in excess of $800,000. The company appealed but, unfortunately, the victim financially could not pursue the case. Both cases were high profile; publicized by Cleveland print and television media!

Years later - after my symptoms worsened, I could no longer work and had filed for Social Security Disability - I ran into a former employee of this company at the library in Berea.

Debbie S., a department manager who had been fired by the company after the sexual harassment jury trial, had been instructed to falsify testimonial documents regarding that particular lawsuit against the company.

Debbie S. told me that she had come to my defense regarding the mistakes that I was accused of making. She showed my shift-supervisor, the department manager and the plant manager writing comparisons between the labels initialed MC and mine which were initialed CDM.

She also told them who MC was. His name was Mike C. and he initialed all of his work with his last name initial first (the C) and his first name initial last (the M).


Mike C. had been at the company for nearly 20 years; was well liked - one of the boys.

Debbie S. said that a comment was made that, since they (the spine-less bastards!) had made the mistake of accusing me, they felt they should continue the charade rather than risk being sued. All of this was on the advice of Russ H., the head of HR at the downtown Cleveland corporate office, and corporate attorneys. The reason why I was laid off rather than fired; the reason why my unemployment claim was not going to be disputed.

However, I believe in Karma.

You see, John H., my shift-supervisor - my immediate boss, had gone on sick leave for anxiety and was very close to a breakdown. After several months on sick leave he was advised to return to work or his position would be filled. He returned and was dismissed!

Here’s is an interesting note about John H. - he was given his supervisory position because - he made too many mistakes when he was a four-color stripper!

In 2006, the company was sold to a Chicago-based printing and publishing company (the largest in the United States) and the Berea facility was closed.

It is believed (in all faiths: all cultures) that, when close to death (NDE) or at the actual time of death, each and every one of us will experience a panoramic life review. I wonder what it will be like for my accusers who were at this particular printing/publishing company?

There is no need to resort to violence - just be patient. What goes around, comes around.

Karma is a good thing. Wait for it. Enjoy the gratification of it!

End

By the way, I DO NOT endorse violence in the workplace!


Please feel free to comment. I would love to hear what you have to say about TOXIC BOSSES!


Oh, Yes! Here are some links you may enjoy:

How to protest at work the French way - take your boss hostage

Boss Bitching: Tyrant Boss Types

AND WE MUST NOT FORGET THE QUEEN OF MEAN. She has had her panoramic life review & she won't be back.





Monday, March 16, 2009

Clinical trials: all in the name of science pays BIG BUCKS!

Seeking evidence of disability

I had some other topics I was planning to write about today but I caught something on the news tonight regarding another drug receiving FDA approval for the treatment of fibromyalgia so I thought I would concentrate on a timely subject by writing about my participation in two clinical trials.

Participating in clinical trials for new or existing drugs vying for FDA approval as a claimed treatment for a medical condition is most definitely a unique experience - but not necessarily easy to qualify for.

During the pre-qualification telephone interview, some participating clinics will reject you on the simple fact (and don't tell them) that you have filed for Social Security Disability for the illness that the trial is doing testing to treat. Their logic is, what if you get the active drug in the double-blind placebo study and you, not only show miraculous improvement (which might destroy your disability case), but leave knowing how to play the violin as well? Okay, that may be a stretch.

Besides
what business is it of theirs anyway? When I heard on the TV or the radio that a clinical research study was taking place to test a new drug for the treatment of fibromyalgia, the first thought in my mind was that hopefully it would work and maybe I could fully function again. There was also no guarantee that I would be getting the actual drug - I might get the placebo.

I have participated in two clinical trials for drugs seeking FDA approval for the treatment of fibromyalgia. Both drugs were already on the market as treatment for other medical conditions but were not "officially" FDA approved as a proven fibro-treatment drug. The doctors may have known it helped their patients and may have prescribed it for pain but they could not say it was a treatment for fibromyalgia . They could say they had fibro patients who were taking it for other conditions and reported it helped with their pain.

It's like this - take Avon's Skin-So-Soft bath oil for instance. Everyone has known (since what seems like Biblical times) that Skin-So-Soft repelled mosquitoes but, without spending millions of dollars in some government approved scientific lab for years of testing thus jacking up the price, Avon legally could not make the claim. Now they can.

Anyway, back to the subject of my clinical trial participation...

My first clinical trial was for FDA approval of Xyrem as a medication for the sleep disorder associated with fibromyalgia. The study period was 16 weeks and included four medical exams (of the tender points) by a rheumatologist and four overnight sleep studies.

I had to sign for the "drug" because Xyrem was considered a controlled substance. I also had to assure the clinician (in writing) that I would keep it secured to prevent theft in case my apartment was broken into. So now it was more than a medical problem I was trying to get help for - I could be faced with charges by the DEA for misuse, loss, etc. Clinical trials for drugs are always a federal matter.

As I said, there was no guarantee that I would be receiving the actual drug or placebo. This was a double-blind placebo vs actual drug trial. In a double-blind study, neither the clinician or patient know whether or not the "drug" is the placebo or the actual drug.

Also, there are two parts in the drug testing in the trial.

On your initial visit to the clinic - if you are accepted into the clinical trial you - are given a Palm Pilot. The Palm Pilot beeps indiscriminately signally you that it is time to answer the questionnaires. It can beep once a day or several times a day and you have to take it with you everywhere you go. In the evening you have to send the transmission of the questionnaires to the pharmaceutical company or clinic via the fax modem included with the Palm Pilot.

The "drug" comes sealed in a box with instructions but on plain unlabeled bottles. Each box and bottle have a serial number on them which the clinician records beside your name on your chart. Then you have to sign for the "drug" proving that you have received it. Each time you return to the clinic you are required to bring the "drug" with you in the box and bag you received it plus the Palm Pilot. The clinician checks the bottle to be sure you have followed all instructions and taken the required dosages. If it is the end of the first phase of the trial, you turn in the first package with "drug" and, after close inspection by the clinician, you are given another box with another bottle of the "drug". Still neither you or the clinician knows if it contains the placebo or actual drug. Each visit to the clinic includes a medical exam including blood tests, more questionnaires to fill out or interview with questions. Each visit to the clinic can last between one to two hours.

The four sleep studies included in the Xyrem clinical trial was the main reason I wanted to participate. It is a known fact that there is a sleep disorder associated with fibromyalgia, but due to the cost, most doctors feel that a sleep study is an unnecessary expense that undoubtedly can offer proof of disability. This was documentation I needed for my Social Security Disability claim.

Anyway, at the end of the clinical trial it was discovered that (both times) I was given the placebo. Of the participants who were given the placebo, I was the only one who showed no improvement in sleep. as documented in all four sleep studies. There is no way anyone can bluff their way during sleep monitoring.

The other participants who received the placebo showed improvement giving validation of the placebo effect claim of mind over matter.

I knew I had the placebo both times. Xyrem was used as one of the "date rape" drugs. It did not make me drowsy or disoriented. Many times, in the middle of the night, an hour after taking it, I would walk to CVS and shop. I'm sensitive to meds and haven't been able to drink alcohol in years.

And the results of the sleep study the night of May 18, 2004: Delta stage 3 sleep was 3.8% and stage 4 was 0.8%. Normal for each stage is 10% . I had 2 REM episodes for 18.5 minutes which was 20%, normal is 25%.

I had three other abnormal but worse sleep studies in this trial, all of which I submitted to Social Security in my initial filing for disability in August of 2004. Despite FOUR abnormal sleep studies, I received two denials by the Social Security Administration resulting in homelessness in 2005.

By the way, I was paid a total of $3500.00 for participation.

In 2006, I also had THREE abnormal sleep studies from Metro Hospital in Cleveland and a CPAP was ordered.

Also, in 2006, I participated in another double-blind placebo clinical trial for FDA approval of the drug Milnacipran. I had to leave this trial due to dizziness so severe that I ended up in the emergency room then the Cardiac Ward for three days. It is not known whether or not I had a reaction from the "drug" but I wasn't going to take any more chances. It was discovered by the facility where I was participating in the trial that I was receiving the actual drug. Milnacipran was approved for the treatment of fibromyalgia pain in 2009. Despite the scary side effect, it did relieve my pain. No sleep study was involved by the physical exam, monitoring of the drug and usage of the Palm Pilot to monitor my progress was part of the study. Payment for participation wasn't very lucrative. I received $150.00 for the time I was in the 12 week program.

I was awarded SSDI in August 2007 by an administrative law judge for the myriad of symptoms associated with fibromyalgia - sleep disorder, pain, anxiety, depression; chronic fatigue immune dysfunction syndrome (CFIDS), degenerative discs in my spine, osteoarthritis, etc.

Today on the news there was a segment of another drug approved by the FDA for the treatment of fibromyalgia pain symptoms. I used my "cool camera" to video the segment. I apologize for the sound quality midway and to the end. I must have had my thumb over the mic.

Sunday, March 15, 2009

My CFIDS/Fibromyalgia weekend

Living with the pain & fatigue

Damn I'm exhausted; sore (burning and throbbing sore) and those ETs must have visited me while I was asleep in the recliner for 6 hours - the mind is mush. So here I am slumped over my desk - staring vacantly at the monitor, the key board, the wall, my cigarettes. hand eye coordination is awful.

Thoughts coming to mind - click, change the channel; another thought-click change the channel. Staying focused is problematic but I've had more severe bouts with Fibrofog like the year or so when I couldn't read.

Plenty about that in another post - later.

Another thought just came to mind - whatever mind I still have left. I forgot to eat supper Saturday. I guess I'll fix peanut butter toast and a tall glass of chocolate milk - sounds real good!

I feel bruised; beaten. I have a certificate for a free 40 minute massage from a local massotherapist. Finally I found someone to go to here. I haven't had a deep tissue massage in a year since I moved and I miss going to my massotherapist in North Royalton . Massage did far more for pain relief than the drugs.

This week and all the stressors have taken a toll on my anxiety level leading to all the pain.

Did anyone get the number of the bus that hit me? Oops, forgot; not in Cleveland anymore. Back in my hometown of Toronto, Ohio - there has been no public transportation here since 1972.

I have a truck tho'. Gary bought it when we were living in East Cleveland - got it for $500.00. We got more than our very limited money's spent worth out of it so...

Need $600 + to fix it - Transmission! The walking is killing me. I can't believe - dare I say it? - I miss RTA (urine stained cloth seats, having to stand because of kids sitting in the disability seats, etc).

Despite having a disability RTA ID and bus pass, I'm surprised I was able to get a disability seat.
Heading eastbound on the #6 Euclid. Photo by Cindy Miller - 2007


It's been a rough two days - 2 hours of rest for every 15 minutes of housework. I managed to change the bed linen tho'; took me an hour because I stuck with it! I also had to go upstairs to the apartment and get it ready for the new tenant. The timing - despite that I feel like crap - couldn't have been better. We need the cash!

Just standing to wash the dishes is nearly impossible. My feet are a mess from all the walking I had to do just to get around downtown Cleveland before the state approved my disability cash assistance. I have nerve damage too in my legs.

Once my Medicare is straightened out and I am able to find a competent doctor here, I'm requesting assistance to help with the housework - at least three days a week.

I've managed to keep the house in relative good order. I kicked Gary out of the living room and he is spending most of his time in bed. He was trashing the living room and really breaking down my new couch. He can barely walk and besides, the bedroom is closer to the bathroom for him. I don't care if the bedroom gets trashed from all of his meds all over the place.

People ask me how I managed dealing with my illness while homeless.

I had my safe places to go when I left the shelter every morning. Voinovich Park behind the Rock Hall was one place - no one questioned anyone laying down there. Since I had a food stamp card, I could belly up to the salad bar at the market inside of Reserve Square for one salad, pasta, fruit platter to go. I spent the entire day resting along the shore of Lake Erie.
Voinovich Park, Cleveland. This guy is relaxing in my old spot.
Yep, I took this photo and the one below it - 2007


Another safe place that I spent a great deal of my time was at the Northeast Ohio Coalition for the Homeless where I volunteered.

I researched, wrote for "The Homeless Grapevine Newspaper" -when my mind worked
but they had a couch and there were certainly plenty of times when I had to nap during the day.

Usually I was beat when I got there. The walk wasn't far from Community Women's Shelter on Payne but sometimes that short walk from E. 22nd Street to 3631 Payne Avenue could take me an hour on a bad fatigue day.

I met Gary while homeless. He and four other guys and one of the guy's girlfriend were all living in a camp near I-90. Another place for me to lie down if needed.

For obvious reasons, thank God those days are behind me now. Despite having a big house and property to maintain, at least I don't have a schedule to deal with. It's nice to be able to lie down whenever I please.

And I most definitely will be making an appointment for my free 40 minute massage Monday morning - even if I have to pay for a cab ride to get there.

In the meantime, I am going to drag myself back
(with a heating pad and Tylenol) to my recliner. Time to go back to sleep.

I'll just post this and edit it later when I have more energy and far less pain.




Monday, March 9, 2009

WHO IS Diana Dennis... and why is she writing terrible things?

What she witnessed; what she experienced at the shelter

Diana Dennis was a resident of Community Women's Shelter for approximately 7 months in 2005. Other residents and a few of the staff members (only the ones with compassion) confided in her and she personally observed and noted various civil rights violations against the women who were sheltered there.

Diana Dennis reported her observations to Brian Davis, Executive Director of the Northeast Ohio Coalition for the Homeless who encouraged her to write commentaries about the conditions at the shelter for NEOCH's street newspaper "The Homeless Grapevine".

A Fly on the Wall, a four-part series of published commentary writings by Diana Dennis was about many of her own and other residents' experiences at the shelter.

In writing about her own personal experiences, Diana wrote in the third person for fear of retaliation, something many of the women at the shelter also feared. Often, she did not write about things that only she had witnessed. Some of what staff members told her were not published either - to protect them as well.

Only the first part of the A Fly on the Wall series is posted online in "The Homeless Grapevine" archives. The rest of the series was removed from the archives as part of an agreement in negotiating corrective resolutions between NEOCH and the shelter provider.

One of my duties as a volunteer at the Northeast Ohio Coalition for the Homeless, was to archive past issues of "The Homeless Grapevine". Because of having archived many of the past issues, I found a copy of Diana Dennis' draft of the fourth installment of the A Fly on the Wall series.

Due to the agreement between NEOCH and the shelter provider, I have taken the liberty to omit the name of the Executive Director of the agency that ran Community Women's Shelter.

To read Part One of the A Fly on the Wall series click here.

The following is the rough draft from Part Four of A Fly on the Wall. Diana's personal experiences are in bold italic.

A Fly on the Wall - Final in a series of four commentaries by Diana Dennis. Written December 2005.
Blustery weather with frigid temperatures and wind chill factors of minus 1 degree have beset the City of Cleveland. Nonetheless, the women and children who reside at Community Women's Shelter on Payne Avenue go unprotected from the brutal cold.

Supper is served between 5:30 and 6:30 p.m. Monday through Friday with weekend serving time beginning at 6 p.m. After dinner is served, residents volunteer to clean up after the meal by stacking chairs, wiping down the tables and mopping the floors. The sooner these tasks of cleaning are accomplished, the sooner the residents can re-enter the Community Room dining area to wait for the rooms to be opened at 7 p.m.

Because of the size of the facility, the residents (women and sometimes children) have no other place to stand and wait other than a narrow hallway leading back past the bathroom in Building #1, the small entrance foyer or the outside of the building. Not all residents can fit in the small contained areas and many have to stand outside in the elements-whether it be in rain, hail, thunderstorms with lightning or a blizzard with deadly cold temperature.

Community Women's Shelter is NOT a safe haven for children and if a parent willfully exposed a child to the elements, the parent would likely be charged with child endangerment. In this case, the shelter is negligent by standing firm on its policy of not permitting residents to go to their rooms early as protection for the inclement weather. Common sense or a kind heart doesn't prevail over policy.

Many of the residents (myself included) now suffer from bronchitis and use inhalers to aid in breathing. In speaking with residents who have since left CWS and presently have found housing, the symptoms of respiratory distress left within several days of being away fromthe shelter. Most of us did not have breathing problems prior to entering the shelter.

Most of the time, the temperatures in the dormitory areas are inconsistant with the weather conditions outside. Air conditioning runs when the outside temperature drops into the 40s and the heat runs when the temperature exceeds 70 degrees.

Many women in Building #2 (above Care Alliance) suffer from high blood pressure, respiratory conditions such as asthma and heart conditions. Three rooms in this building lack windows and these women suffer as a result of lack of means to properly ventilate their rooms when the thermostat reading is 83 degrees and the furnace is running. Some have been sent to the ER by ambulance or hospitalized as a result.

Residents do not have enough blankets to keep warm.

Linen (two wash cloths, two towels, two blankets, two sheets and one pillow case are assigned to each resident once a week during linen exchange. The blankets are very thin (summer blankets) and offer very little warmth when the temperature in the dorms falls below 60 degrees, which is often the case.

Policy once again dictates. No personal blankets. Although some women do have their own personal blankets (many of them learned to crochet while at the shelter), some of the women (myself included) had their personal belongings thrown out during a sweep by staff in November.

Many residents returned to their rooms at 7 p.m. only to find clothing, personal bed linen and even important documents gone from their sleeping quarters and thrown into the dumpster. Some residents filed police reports of theft against the shelter. Others tried retrieving their belongings from the dumpster only to be threatened with arrest. A group of women filed grievances and met with the Client Rights Officer, all to no avail.

One woman. who has since left the shelter, was able to get her important documents retrieved by the second-shift program director only to later be threatened by the same manager for bragging to others that she got her paperwork back. The shelter resident was told by the program manager that, because she (supposedly) bragged, she (the manager) would be watching her closely and she (the resident) better not slip up or she would be put out of the shelter.

Various threats of arrests continue at CWS; two instances involved residents in Building #2.

One resident in Building #2 was falsely accused of stealing another resident's socks and was threatened with arrest. She later was apologized to by staff which offered her little solace form the embarrassment and emotional trauma she was put through.

Another woman was having breathing problems due to the excessive temperature from the heat. The thermostat reading was 83 degrees. Because her bunk was beside the baseboard heater causing the bunk to act as a conductor, making the temperature seem higher, she requested to go outside for fresh air.

The male coordinator, working the night shift came out of the main building (#1), ordering her into the Community Room rather than allowing her to return to her room. He did not believe her explanation that she had permission to be outside due to the heat and its affect on her blood pressure.

While trying to explain to the night security officer why she was outside and that now she needed to go to the ER, the security officer accused her of lying and ordered her into the Community Room. An ambulance was called for the resident and hospital records prove that she was put in further distress from the anxiety of this incident-from which she received NO APOLOGY.

The three paragraphs above are about Diana Dennis' personal experience.

So who was Diana Dennis?

I was Diana Dennis and I will go into complete detail about my experience at Community Women's Shelter in a later post.