On October 25, 2018 in screaming pain I summoned my husband out of bed. I was crying and in the worse pain possible. I told him we need to go to Little Co. of Mary that something is wrong with me. We got to the hospital and oddly enough it was not packed. I was taken to Triage with my blood pressure at 200/ 125. That’s high – too high. They asked me all sorts of questions and next thing I know – I am being wheeled down for a Cat Scan.
Well to my crazy surprise – I had a 8 MM Kidney stone LODGED in me. It would not move. It was considered in the medical field to be QUITE big.. Er doc had me admitted to Observation Floor. Finally they were shooting me up with medication that worked for the pain. On Friday, a Urologist on call came to see me and I liked him immediately. He decided to take me to surgery that night at 6PM sharp to put a stent in me. This was to help with urine flow and that horrible pain. They did not want to go in and blast the stone because of it’s location and the fact that it was lodged.
Saturday afternoon I was discharged. I was happy to be going home. I see Dr. Tomasic this Friday , Nov. 9th, the urologist. Hopefully he will have more answers. Truth be told, I have NOT felt well for several months. Very tired and now I know why. I am diabetic and that was another reason for admitting me. All of it was too dangerous.
Last night I ended up with my head in the toilet. Ok, so I am being over dramatic. Truth is, for some reason I was very ill. Everything inside of me came up. My left side hurt like a dickens. I called Little Co. of Mary ER but they were swamped. I passed.
I ended up taking a Trazodone which relaxed me and I fell to sleep. I have been under a lot of stress recently. Had an argument with my daughter. I have been fighting for years with my health It has not been good.
I do need to find out what happened last night and I hope it was only stress. Why on earth would my left side hurt so much? This too shall pass.
I had sat down and wrote to this foundation. I was very kind and considerate. I explained to them that I had been on Fentanyl patch since 2005 (50MCG) and have not heard from them. I guess they were not interested in my story. I’m not addicted to the medication and chose not to go to a higher dose.
I also shared with them about my brother John who had been addicted to Meth for years and then got addicted to Vicodin. Again, they were not interested.
Rummler’s and Mendell families have lost their loved ones to overdoses. I feel so sorry for them because I lost my brother John who I will write about soon. I understand the loss. Having said this- there is a group of people out there who DO NOT ABUSE their opioid medications. We are the collateral damage in this war on opioids.
Thank God for Greg Gutfeld of the FIVE on Fox. He has come out in support of us. He has also interviewed JOHN HEUBUSCH, Executive Director of the Ronald Reagan Presidential Foundation who suffers from RSD.
Again, people who overdose turn to other drugs and do often mix alcohol with their meds. They turn to harder drugs. It’s not their fault as they have an addiction but please do not take it out on us who do not abuse!
I find it terribly sad that there is a war going on out there, and chronic pain patients seem to be the collateral damage.
As this fight continues, more and more people are committing suicide as they can no longer stand their pain. Are these people being tapered down on their medication? Just how far has the DEA gone or CDC?
It seems doctors cannot be trusted all of a sudden? Horse manure. I had a wonderful Internist who prescribed my medication but the DEA was getting too involved and my doctor got scared. I do not blame her. I have utmost respect for physicians- they go to school for years to become a doctor. All of a sudden they do not know what they are doing?
For me, it worked out great as I was referred to a wonderful pain management doctor but for many others – they are not so lucky. They are turning to suicide. Just had another one in Redondo Beach. This man was hurt in an construction accident, and had been on leave for over a year due to extreme pain. I have no idea if he was tapered down or doctor refused to give him a higher dose. Clearly the man was in pain and suffering. He killed his wife- son and himself. So so sad. This could have been avoided possibly.
We had a law enforcement officer in Montana commit suicide. She was a patient of Dr. Forest Tennant whose office was ripped apart by the DEA. Suicides are happening more frequently now. We NEED to stop this and take a good hard look at what we are doing to the very people who are legit – in chronic pain.
This is NO laughing matter. I am begging the main stream media to look into this and help us out here. We need someone on our side. We have been caught in the middle, in this War on Opioids. After reading the story about the Waz family, it literally broke my heart. It could have been avoided. Someone dropped the ball here.
We in the Chronic Illness/Pain community need Pres. Donald Trump to sit down with us. We need guidance today as we are losing patients to suicide due to medications being taken away or tapered way down.
The people I know via Twitter are a great group of people working hard to change how the public view us. We are NOT drug addicts. We take our medications as prescribed and do not abuse. I use Twitter because it commands a lot of attention and we do know publications are hearing us as they have written about us and the opioid crisis.
The DEA cannot keep using these Nazi like tactics – storming in to doctors offices and ransacking them. Dr. Forest Tennant is one such doctor in Covina, CA. Please read this article. What happened to Dr. Tennant is happening to a lot of doctors – GOOD doctors. Not your pill mill docs.
Thankfully we have a good following of therapist, doctors on Twitter who are on our side and doing what they can. Thomas Klein MD actually went to Washington DC on our behalf. These are the people we need – doctors. Where are all the doctors? I will tell you many have been treated terribly by the DEA. What happened to doctor-patient privilege? What happened to doctors knowing their patients? My own doctor was upset over the DEA. She told me in May of 2017 she was referring me to a pain mgmt doctor in Torrance. That was fine with me but it wasn’t because I was a bad patient or abusing. She knew I would be taken care of by a wonderful physician who specialized in chronic pain. I cannot say enough about Dr. Bradley. His bio is one that I found so impressive. He worked with wounded soldiers. Also worked at Walter Reed. That’s pretty darn impressive.
This is my life now. I cannot get down and dirty in the trenches but I can still write and make my voice be heard. RSD is very painful – so many have no idea. They don’t understand. I will sit down when not too tired and write to Pres. Trump. I can at least try. We’ll see.
Got up this morning and I was in severe pain. I was due to change my pain patch tomorrow morning. Decided to take some break through pain medication that my pain mgmt doctor gave to me back in November 2017. I try not to take it but sometimes I just have to.
My hands were hurting so bad and I fear my carpal tunnel is getting worse as well as Osteoarthritis in hands. Legs were burning. It just was not a good day today at all. I think my body was also reacting still to what has been going on since Christopher passed away. Day of services I was on my feet for many hours. I was in extreme pain that day but I kept it to myself and got through the day. It was difficult but I did it.
I think I will talk with Tom and see what he thinks about me going in to see about my carpal tunnel. Probably time.
I have waited for a month and a half for this appointment on April 5th. I will find out about needle biopsy on right breast. It has been dogging me since last May. I have had two ultrasounds but they could NOT guarantee I did not have cancer. They could not rule it out. Thank Goodness I have a great Internist. She wants the biopsy done. I have pain in right breast where they found the mass. I am scared to death. Our grandmother had Breast Cancer and I was exposed to chemicals where I use to work.
Update: My appointment with surgeon went well. She looked at my images from mammograms and decided that the radiologist was correct. Nothing to worry about now. Just keep going in for my 6 month check ups and she did not feel I had cancer. So there you go. I am happy!
I never shared this but back in May 2017 I walked in for my routine visit with my Internist and she announced that the DEA was sending her alerts on every medication (Opioid) she wrote. I was shocked. She told me she would be sending me to a Pain Mgmt Specialist who she felt would be good for me. I was not happy as it always seemed easier to go to the drs office – pick up my script once a month.
I made the appointment with Dr. Bradley. He spent 30 mins with Tom and I and we both liked him a lot. I read his bio before going, and was impressed. He spent 18 years in the Army and had worked with wounded soldiers. He knew about pain. He ordered a MRI of my back (lumbar) as he wanted a good image of it. He told me I was the classic case. I had surgery at L5 S1 in 2008 after having a Discogram. Dr. Bradley stated that after a few years you do start to have problems. He was right. I also had Degenerative Disc Disease which Dr. Rogers (Surgeon who did my surgery) told me I already had. Of course I also had the painful RSD which is neurological.
We tried the epidurals but I got violently sick- blood sugar spiked on me and I ended up in Urgent Care on IV’s for dehydration. I was a mess. They got my sugars down before I left there.
Next time I saw Dr. Bradley we decided together to just stay on the Fentanyl as it seemed to work for me for now. I was also given a low dose break through pain med which I have only taken a few thus far… It’s hard but I do not want to go any higher. It tough – really tough. I know they will help me if I really want it. I am blessed to have a great team of doctors. I really am.
Every month I go to see Dr. Bradley – we talk and I get my prescription. Not a big deal.
It will be 6 months since my last mammo. Am waiting for the approval for my ultrasound on right breast which they are watching. I recently got a letter it was time to be checked again. I spoke to my Internist this week, and if it is still a “Probably Benign ” diagnosis (which means they still cannot rule out Cancer) she still wants me to see surgeon for a biopsy.
There have been three gals from the office I worked in for 16 yrs who developed Breast Cancer. The company closed down in 1998. It was an Oil/Petro Chemical Company that manufactured products for cars. We were exposed to many chemicals namely Toluene and Benzene. Tom, my husband was upset 6 months ago when they told me I had the mass and they did not do a biopsy. They flat out told me the kind that I had – is one they worry about.
I have to be re-checked now… All these years I have been clean – no problems until 6 months ago. I was on Estrogen for years after a Hysterectomy in 1993, and exposed to the chemicals. I will keep this updated.
January 31, 2018 – I am seeing a surgeon on April 5th to have consultation. Needle biopsy and removal of mass was suggested by my Primary care doctor due to family history of Breast Cancer. As I have stated I am not in panic mode but I do have a lot of anxiety over this. Is it just a coincidence that a few girls I worked with got Breast cancer? Perhaps. Better to be safe then sorry in light of our history. If the chemicals were part of the problem – it’s “spilled milk” and even if I could – I would not seek to sue anyone. The owner is deceased and was a man I truly respected and liked. I would not even go there.
For a few days, my left leg was swelling up – deep red in color with blisters on shin. I kept thinking it would go down. My sister-in-law pleaded with me to go in and be checked. I finally did!
I went to the ER and the attending physician wanted to admit me but was also concerned that I might pick up a nastier infection in the hospital. The diagnosis of my leg was Cellulitis which can be deadly and go into sepsis which I already knew. They did an ultrasound to rule out a blood clot just in case. It was negative. They took a lot of blood and gave me medication for the pain. My husband came up to the hospital later as I was more worried about leaving our animals. Luckily he was off duty and around.
I was in the hospital for about 12 hrs. This was my 4th bout with Cellulitis. The first two times I got it- I was in the hospital for days on an IV drip. Today they want you out. I was given Keflex and Bactrim and finally finished it today. My leg still has some redness and it is concerning. It’s not going away fast enough for me. I requested a home health nurse to come out and take a look at it but hasn’t happened yet. I do not want to be in public places where people are sick as I cannot take a chance.
Being a diabetic makes this all more serious. People don’t seem to understand that but it is true. From my knee to my ankle- my leg was so swollen it was horrible. It was rock hard from the fluid and hurt like the dickens. Normally when I got cellulitis it was a single red streak going up my leg but boy this time – it was red all over. You cannot mess with this stuff. It can be deadly and you can’t let it go as I did this time. Very angry at myself.
10-27-17 Just an update. Home Health from LCMH has been coming out checking my leg. I have CVI (Chronic Venous Insufficiency) along with Chronic Stasis Dermatitis. We are trying to keep my leg clean and moisturized so bacteria cannot get into. This has been by far the worse case I have had. I am frustrated. The Cellulitis cleared up with the medication but I am not out of the woods. I want to get back to my old self and it’s just not happening fast.