Back: Navigating Health Conditions and Employment

Hi Everyone,I have been a member on the site for about a year. I dropped out for awhile feeling it could help with my self induced anxiety. I felt I was not moving forward and accepting my health conditions. Currently I have acknowledged with my doctors that I am dealing with the following health conditions and medical diagnosis. Along with this acknowledgment I cannot help but feel my employer P&G plays some responsibility for some of my current health conditions. They paid me one year of severance with medical and said goodbye. Currently I am paying for my medical through Cobra and it has not been easy.Current health diagnosisPsoriatic ArthritisDDD in lower lumbarBFS w cramps and or Myokima Sleep disorderI have psoriasis and it finally turned out to advance into psoriatic arthritis. During my employment at P&G the psoriasis was spreading even though I was using prescribed treatment. I know today the psoriasis seemed to be aggravated by constant job stress along with the continued liquid soap contact to my skin. I found myself covered with liquid Dawn, Ivory, and Joy soaps on my skin daily. I think it was the skin sensitivity to such large amounts of these products. As an employee we were constantly looking for parts to patch equipment together to do our daily job. P&G would subcontract skilled ex-employees back to come in a refurbish parts because we were always running out of usable equipment. I likened it to swimming in soap products and working under constant stress to keep this dated equipment up and running at 85 percent or greater. As an employee you would work 12 hour plus days without a guarantee of a scheduled 10 minute break or your 20 minute lunch break. When I would rotate to cover the shipping dock area as a dock coordinator I was never given a break or scheduled lunch break. With that job you were constantly running to keep up with everything to run the shipping business. To date my skin is 99.9 percent clear and one would have no idea that I suffered from psoriasis. My psoriasis arthritis is being managed with 375mg naproxen daily. I have a topical skin crème that I rarely have to use. My rheumatologist is pleasantly surprised how well everything has cleared up skin wise. It is also his opinion that my work environment most likely caused my health problems.I have DDD with disc damage L5 S1 with a bulge, L4 L5 that the disc is flat and dark without fluid, L2 L3 with some degeneration visible. During this time I was on STDB and began a procedure of disc decompression. At the same time my employer P&G was adding pressure to me to return to work. I was under a tremendous amount of stress and uncertainty of whether I could return. I was unsure of my inconsistent sleeping patterns and the disc decompression procedure and my health as a whole. Knowing the P&G work environment I was also unsure if the company truly understood or cared about my current health. I was left feeling P&G wanted to get everyone back to work because they were so short staffed. It was during all this duress and disc decompression sessions that I first felt the fasciculation’s that started in my calf muscles. The continued stress and pressure of P&G manifested my fasciculation’s into shakes and tremors. These shakes, tremors, fasics, etc. were made worse after my employer finally forced me back to work against my doctor’s approval. I lasted 6 weeks and my tremors worsened and the fasics were throughout my body head to toe. Another letter sent from my doctor stating no shift rotation had P&G giving me a 52 weeks severance. At this time I have lost my job. I take 5mg clonazepam daily and have 50mg tramadol for muscle pain etc. My fasics are constant in my calves and occasionally in my thighs. Rarely do I get them in my upper body. Sometimes they appear in my triceps, shoulders and upper back area. I had also seen another neurologist that heads the movement disorder dept at KU to be told that I suffer from an extreme case of myokemia. I have also followed up with KU neurology to show them an unusual 2-3 inch dent in length running vertical above my right knee cap. I have no weakness and can single eg curl 70 80 lbs in reps of 12 along with seated squats of 250 in reps of 12. The doctor believes it to be fat tissue loss. I told the doctor I feel some sensation in the area but the doctor did not think anything was further needed. During the last couple of years of P&G employment I was also suffering from always being tired and unable to sleep without the use of OTC Benadryl and or Tylenol PM. The work schedule was designed as 7 days on and seven days off. To lower finished product cost a reduction of staff with job cuts by management left the department understaffed by 30 plus employees. This lack of staff basically threw the 7 days on and off out the window. Overtime was beginning to become more and more common which further lead to my sleeping problems. I was then tested in a sleep study and found to have sleep apnea. I was not surprised due to the fact that I was working 12-13 hour shifts and as mentioned asked to work my days off with the continued scheduling of biweekly days and night shift rotations. I know sleep better but still take 5 mg of clonazepam at bedtime. I also dream again which I had not done for some time. So, in a nut shell it has been a long health road to haul. I hope everyone is doing better or have seen some health improvements along the way. Sorry for the history and long update. It’s good to stop in and chat. Anyone registered here from the Kansas area?CheersDwaine :)
 
Hi there, I have had psoriasis my whole life and like you am 99% clear due to a great compound my dermatologist formulated for me. My question to you is, what were your symptoms of the psoriatic arthritis and did you have an elevated sed rate or ANA? I am having shoulder pain and sometimes wrist pain and am beginning to think I may be developing the same. Currently just taking excedrin back and body for it. Thanks,Linda
 
DonJose,my sed rate was always in the normal range. my ANA was 160 Homogeneous. my RA factor was slightly raised but within range. It was not until they performed the Anti-CCP that they concluded it was PA. I was told by the doctor the ant-ccp is a more specific and accurate test for RA. I also displayed minor discoloration of my finger nails. It was like a very strange pitting under the nail in the nail bed its self. Since that time my WBC is around 6.3, RBC is 4.67 which is border line low on range of 4.70 to 6.10, HCT is 40.2 which is also border line low on a scale 42.0 to 52.0, My HgB was low for 6 months and has now moved back into the normal range for past 6-8 months.Current meds 375 mg naproxen twice daily, Skin; triamcinolone acetonide 0.1 as needed. Have not needed since clearing up. use to have facial, hair, inner ear, elbows and right knee along with finger nails. ALL clear except for smaller than dime size on left elbow. All clear on finger nails.Diet changesraisins, craisins, walnuts daily. raisins have kept and raised my RBC back towards the normal range2 table spoons of cold pressed flax seed oil daily. cold pressed better MEGA 3more fruits and veggies, eat red delious apples dailyno dairycherries or cherry fruit extract.2 vitamin e fish oilNote sure what is helping diet wise but I will try anything to make a change for the good. PA for me started in the index finger of my right hand. I have seen flairs in a wrist, hip ankle shoulder and yes the left jaw. It has been fairly inactive for some time. Every once in awhile I will get a little extra discomfort. Mainly I get it in my right hand. I hope and believe I am doing something right in keeping it from flairing up. My Rheumi says he is suprized and happy to see how well the psorisis has cleared and good the arthritis is doing. Got my fingers crossed!Dwaine :)
 
Hi Dwaine, thanks for all the info. I just had a CBC with hematocrit , RBC,WBC etc, done and all was normal. Also my sed rate was normal as was CK. I do have some nail pitting and discoloration, but I have had that on and off for 30 years. I suppose if my shoulder doesn't improve I should see a rheumy and check out the PA possibility. My pain seems more muscular than joint though. I have autoimmune Hashimotos thyroid and I was assuming my aches and pains were from that? My ANA is 1:40 homogenous and my GP said that is a weak positive and likely from the Hashimotos and psoriasis.At any rate, glad you have improved so much. Good job on clearing the psoriasis too. I just saw my dermatologist and he injected a stubborn spot on my elbow with steroids. Poof...all gone. I know it is temporary, bit sure was nice to be rid of it! lol.Linda
 

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