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The information on the Blog Posts reflects my opinions, personal suggestions and is not intended as medical advise. The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. All content, including text, graphics, images and information, contained on or available through this web site is for general information purposes only. PVNS Success makes no representation and assumes no responsibility for the accuracy of information contained on or available through this web site, and such information is subject to change without notice. You are encouraged to confirm any information obtained from or through this web site with other sources, and review all information regarding any medical condition or treatment with your physician.

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NEVER DISREGARD PROFESSIONAL MEDICAL ADVICE OR DELAY SEEKING MEDICAL TREATMENT BECAUSE OF SOMETHING YOU HAVE READ ON OR ACCESSED THROUGH THIS WEB SITE.



Sunday, December 9, 2012

How is Swelling Harming My PVNS Joint?


I found this wonderful article explaining the importance of minimizing swelling. It was written by verycoolrunner at coolrunning.com.au and it goes like this.

One of the main reasons for using ice post-injury is to slow down the metabolic rate of the cells in the area (like a vet putting a lizard in the fridge before surgery, you know...).  By doing that, you can temporarily decrease the cells' requirements for oxygen, and hopefully fewer cells in the area of your injury will suffer damage related to lack of oxygen, in the acute phase of your injury.  (A complete aside, here - the rooms used for heart surgery and the like are also cooled, for the same reason as the lizard going into the fridge - to decrease the metabolic rate, and decrease cell damage as a result.  Neat, huh - but VERY cold for the theatre staff)

The reason that your tissues in the injured area are at risk of damage from lack of oxygen, is due to THE SWELLING, because swelling increases the pressure surrounding the cells in the injured area.  That makes it harder for the blood supply containing oxygen and nutrients to battle (or diffuse) their way into your cells.  Like trying to pump up a bike tyre with a fat guy sitting on the bike - it's a pressure thing, you know? (and thank you to my spouse for that particular analogy).  

The reason that the swelling is there in the first place, is because when you injured yourself (and damaged some of your tissues - you reckless maniac!), the damaged tissues called for their own ambulance - and a fleet of them arrived.  This is the response we know as inflammation, and it involves an increase in blood flow to the area, an increase in the permeability of the walls of your capillaries, so lots of fluid leaks into the space in your tissues surrounding your cells, and often clots there (read - stacks of ambulances parked all over the place), and the cells themselves swell.  The effect this inflammation is intended to have, is to put up a barrier around the injured area (read - police roadblocks), to slow the passage of any bacteria or toxic products that may be in the injured tissue, into the surrounding healthy tissue (read - quarantine).

So the swelling does have a purpose, but it also comes at a cost to the tissues in the "quarantined area" - with all those ambulances parked all over the place, it's hard to get on with things.  Then, when the quarantine period (read - acute inflammatory phase of injury) is over, the tissues have to repair their damaged lives.  This includes rebuilding and remodelling, and this is where your friendly physio will start raving on about collagen fibres in disarray, and scar tissue in abundance.  To avoid this (both the scarring and the raving, I mean), most people set out to minimize the inflammatory response as far as possible, when they get injured.

Now Macattack may get hot and bothered when I type this, and demand to see references (sorry, Macca) - but when I was a student, there was more evidence to suggest that the best way to prevent swelling, was to elevate the affected part, and put a pressure wrap on it.  The wrap increases the pressure from outside the body, and makes it harder for the extra fluid to leak into the tissues etc., as part of the inflammatory response, while the elevation serves to make it an uphill drive all the way for those darned inflammatory ambulances to get into the tissues.  Meanwhile, the rest and ice part of the RICE equation, are meant to decrease the metabolic rate of the cells in the injured area, to hopefully minimize the damage to those cells, and therefore lessen the rebuilding and remodeling that will be required.


I am not a physician and the above is in no way to be taken as medical advise. This is my interpretation of what I have been told by my physicians and from what I have read. Always consult with a professional for case specific accurate information.

Thursday, November 1, 2012

PVNS Tears, Bridges, Journeys

Yoda Jedi Master
I've been using my time doing origami and finding new articles for this site so I haven't written lately. You may ask what does origami have to do with pvns. Origami is a way that I refocus my senses away from the constant burning pain of neuropathy in my back/legs and the insistent dull knee pain of PVNS. I love the textural feel, pliable character and the sounds created when folding the many different types of paper. It may sound weird but it's exciting to take a flat piece of paper and make an art form out of it.

Autoimmune Testing

Finally finished with all of the massive amount of testing for immune deficiency and auto immune disease workup. Fortunately all of the tests came back good and at least for me there isn't any type of connection with those types of diseases and the PVNS. This was important to check out since I've been feeling so poorly and due to the possible recurrence of PVNS at the 6 mo follow-up. Well that was the good news but my brilliant research rheumatologist asked if I wanted her to tell me the truth. I'm thinking, hmmm??? No!!! because it doesn't sound like anything that I want to hear, on the other hand yes!! because that's why I'm here.  Now the problem with hearing the truthful answers to my many questions is that it can be quite difficult to swallow, internalize and digest.

Not Fibromyalgia

My doctor was unconsciously shaking her head as she mulled over my extensive medical history. Reviewing the long list of illness, injury and trauma... she explained how each malady and it's residual effects has effected my body long term. She eventually looked at me and stated in a very serious manner "You have residual effects from previous illness, arthritis, PVNS, a chronic pain syndrome and polyneuropathy that is making you feel so bad...and no you don't have fibromyalgia." "Your pain is severe and has known physical causes which means that you need to trust and work with your pain management doctor."  Now I'm usually the eternal optimist but not today. Today I am crushed knowing that I will never enjoy another day without pain. Some days will be better and some worse but never pain free.

Momentary Despair

This is a day that I wish to forget my weaknesses. Today I will cry a river for my broken spirit. I will curse my knee for giving-way nearly hurdling me down stairs. I will huddle in a corner and hide from bills, worries and responsibilities. Today I will mourn for the activities that my body refuses to participate in. My mind is young but my flesh has aged beyond its years and is foreign to me. With this insight I acknowledge my shame and fears. Before giving in to total despair let me take a closer look at my life.

Memories of No Hope

Today, I also cringe at a road map of scars which has built a bridge of memories. I crawl into my past filled with battles won and lost, times of sadness and great joy.  I look at photos of myself in a wheelchair... remembering the doctor telling me that I must accept this fate. I refused and today I smile for I walk. Today I confidently breathe knowing that only a few short years ago I had was attached to high flow oxygen, an IV providing continuous morphine, a tube inserted into my intestines to provide nourishment and a life expectancy of a week. I have bled and suffered to save strangers lives...for those occasions I am most proud.  This pride and strength allows me to stand tall in the face of all adversity. It doesn't matter how deep your river may be for the importance lies in how well and quickly you are able to build a bridge, cross the river of tears and continue on your journey.


I am not a physician and the above is in no way to be taken as medical advise. This is my interpretation of what I have been told by my physicians and from what I have read. Always consult with a professional for case specific accurate information.




Wednesday, October 3, 2012

Building Resistance to PVNS Tumors



{Correction 02/13/2013): 6 mo f/u MRI 06/2012 showed a false pvns recurrence. It was proven during f/u surgery 12/14/2012that the mri was showing scar tissue and not pvns. After you have surgery the mris become more difficult to read accurately. After the 6 mo f/u mri I had two more mris done showing that the (false) pvns was remaining stable (unchanged) that was the clue that it was scar tissue and not pvns.} The tests that I referred to in this article all came back good. I do not have an over or under active immune system nor anything besides osteoarthritis from age and pvns.

Being a Pioneer

I am well aware that we are all guinea pigs and it doesn’t matter what treatment we choose. On a positive note the more data that is collected increases the chances that a common link could be found. I commend everyone who is willing to try adjuvant treatments because you are the pioneers that may someday make a cure possible. Note please make sure your physicians are sharing your information (positive and negative) with researchers and not just keeping it in their private files. 


MRI Report of  a False PVNS Recurrence

Why did my treatment regimen fail when others (approx. 80%) with the same amount of PVNS, damage and treatment remain in remission? During surgery the joint was visualized arthroscopically then an open complete synovectomy was done. My orthopedic oncologist is a top rated surgeon familiar with pvns. She removed all visible signs and areas that showed on the mri. I followed up with 18 treatments of 200 greys each which would have disabled . My six month follow up mri showed a new area of recurrence. Something is making my body more susceptible to the pvns and until that is corrected I’m afraid it will continue to recur, destroy my joint as it has caused the chondromalacia to worsen in just one year even with surgery. 

The cellular composition of diffuse pvns is exactly the same in each individual so this means that pvns itself has the same strength and destructive properties in everyone. What makes some bodies more susceptible to a recurrence? I have arthritis in both knees and throughout my spine that is well out of proportion to my age and lifestyle. 
I’m working with a research arthritis specialist who is running many tests to see if I have some type of defect that makes me more susceptible to arthritis and or pvns. I am also working with an immunologist who is checking to see if there is a link via the immune system. some of these blood test take a month to get the results so I will post any information that they may provide. For now the doctors are trying to build up my body as much as possible immunologically by addressing my allergies (they have already done allergy testing for which are minimal), with diet (I’m looking into cancer diets), and supplements including Vit D because it was very low and low vitamin has connections to tumor growth. Hopefully along with what they find out from the blood tests I will be in better shape to resist future tumors (recurrence) after my next surgery. 


I am not a physician and the above is in no way to be taken as medical advise. This is my interpretation of what I have been told by my physicians and from what I have read. Always consult with a professional for case specific accurate information.


Wednesday, August 29, 2012

Vitamin D Deficiency and PVNS

(Correction 02/13/2013): 6 mo f/u MRI 06/2012 showed a false pvns recurrence. It was proven during f/u surgery that the mri was showing scar tissue and not pvns. After you have surgery the mris become more difficult to read accurately. After the 6 mo f/u mri I had two more mris done showing that the (false) pvns was remaining stable (unchanged) that was the clue that it was scar tissue and not pvns.

Having pvns I have become hyper aware of any pain or swelling that occurs in any of my joints. I’ve had rapidly recurring pvns in spite of radiation in my left knee with pain that seems out of proportion to the pvns along with my right knee beginning to swelling and be painful. I also started noticing other joints and muscles were aching along with severe fatigue. This resulted in other joints having mris which showed no pvns. I started thinking I was becoming a hypochondriac or at least a bit crazy but that wasn’t the case. 

Funny but not. I live in the sunshine state of Arizona and look pretty good for being 48 because I have always used sunscreen to protect my skin unknowingly blocking the rays that I needed to make vitamin D... resulting in a severe vitamin D deficiency. Keep using your sunscreen, however, be aware you may not be getting enough vit D from the sun and your diet especially if your lactose intolerant like myself, avoid milk and use sunscreen. 

The last few months I have been reading about research done on the cellular mechanisms of pvns. I then started to look further into the cellular mechanisms involved in vit D deficiencies which led me to this and many more related studies.

Low levels of Vitamin D are associated with increased incidence of many cancers. Vitamin D normalizes cell to cell communication, impacts uncontrolled cell growth and allows cells to differentiate into normal cells with a normal life cycle. “Breast cancer patients with suboptimal vitamin D levels were more likely to have tumors with more aggressive tumor profiles and worse prognostic markers” by Nalini Chilkov, L.Ac., O.M.D.

PVNS is not cancer but it is a tumor and I’m just wondering if having a severe vitamin D deficiency has had anything thing to do with the pvns recurring so quickly and aggressively in my knee in spite of surgery and radiation. I have seen many people with multiple joint complaints that turned out not to be pvns related yet not seem to have an explanation so I decided to share this information as food for thought. I will write more on this subject as I 

continue my research.


I am not a physician and the above is in no way to be taken as medical advise. This is my interpretation of what I have been told by my physicians and from what I have read. Always consult with a professional for case specific accurate information.


Friday, August 24, 2012

PVNS Questions to Ask Your Doctor


Questions to Ask at  your PVND Doctors Appointment:

  • What type of experience do you have with PVNS? diffuse, nodular, open/arthro, clinical trials
  • What type of PVNS do I have? diffuse, nodular, mixed, intra-articular, extra-articular
  • When will biopsy be taken, how long for the results and will surgery be done at that time? 
  • How has this disease affected my joint? what damage is the mri showing if any?
  • What are my treatment choices and which is the best treatment for this type of PVNS?
  • Do you prefer open vs arthroscopic surgery and why? How many have you done? Outcomes?
  • Will I be given a nerve block along with general anesthesia?
  • Do you use staples or sutures to close the incision and why?
  • Knee joint: will a continuous passive movement machine be available after surgery? 
  • How long will I be in the hospital?
  • What will I be given for pain management?
  • When will I begin physical therapy and for how long?
  • Will I need crutches or any other equipment after surgery?
  • When will I be able to return to work and normal activities?
  • What are the risks of delaying or opting out of surgery?
  • What will your long term follow up plan for monitoring the PVNS be? Check ups/MRIs
  • Are there any complementary or alternative therapies that I should consider? radiation internal/external, chemo, cryotherapy, homeopathic?
  • What are the risks and possible side effects of each treatment including long term effects?
  • Are there any clinical trials that would be appropriate for me?
  • Do you recommend any herbs or other supplements- such as fish oil or glucosamine?
  • What should I do if my symptom worsen?
  • What can I do to decrease the discomfort?
  • What can I do to preserve my joint?
  • What kind of out-of pocket expenses can I expect; are payment plans available?

Monday, August 13, 2012

PVNS Estimated Time Of Recovery 2

Journal Of My Recovery From Open Synovectomy, Radiation, Manipulation, False Recurrence of PVNS



SUMMARY OF PVNS
Current Status: 04/25/2013
  • Remission since first surgery 12/2011, Partial knee replacement 02/2013, 95% normal, no swelling, pain free
Type of PVNS: 
  • Diffuse PVNS, Bakers Cyst of left knee
Surgeons:
Diagnosis
  • 11/2011 per MRI
Surgeries: 
  • 12/14/2011, open, frontal synovectomy of left knee
  • 04/18/2012, 18 weeks post op. Manipulation Under Anesthesia
  • 12/14/2012 Arthroscopic knee surgery (out pt) for possible recurrent pvns, lateral and medial meniscus repair and to address the catching and pain. PVNS recurrence, per MRI, proven wrong; it was scar tissue, need replacement
  • 02/07/2013 Minimally invasive, quadricep sparing, partial knee replacement; using the Arthrosurface HemiCAP wave system. PVNS remains in remission
MRI: 
  • 11/2011 Initial MRI showing diffuse PVNS in left knee, Bakers Cyst, effusion
  • 06/14/2012, 6 mo. f/u- recurrence (false positive)
  • 09/28/2012, 9 month f/u, pvns stable (false positive) 
  • 12/10/2012, 11 1/2 mo f/u, pvns stable (false positive), Bakers cyst gone
Physical Therapy: 
  • 3 weeks post surgery; started
Adjuvant Treatment:
  • External Radiation Therapy: 7 weeks post op. 18 treatments, 200 greys each.
  • Steroid Injections: 06/28/2012. (unsuccessful)
Detailed Time Line:
November 7th MRI Diagnosis PVNS
November 15 Researching pvns, treatment options, finding surgeon. What will pvns mean to my lifestyle? Making a list of questions for surgeon.
Dec 3 met Dr DeComas, xray taken,  discussed if biopsy confirmed pvns she would switch from arthroscopic to open synovectomy.
Dec 14, 2011, Open front synovectomy left knee, 23rd surgery from other stuff
1 day post op in hospital, worked with PT department on crutch use.  36 hrs post op femoral block wore off. I was taking Tylenol, 10 mg Oxycontin ER every 12 hrs, Oxycodone 5 mg for break thorough pain, and injectable morphine every half hour and I was still crying like a baby. In the middle of the night switched to Dilaudid which controlled the pain but made me nauseated, Reglan & Zofran to control vomiting. pain 6-8. Drain still expelling much fluid.
2 day post op, Johnson Pratt drain pulled in late afternoon.2-3 seconds of intense pain.
3 day post op, discharged from hospital, medication, ice, many pillows useful to secure leg in drive home. Large zip lock bag for nausea. good leg and hip are hurting due to the extra stress.
Day 4 post op, feeling better, pain 4-,5, narcotics, lymph massage, ice, elevate. washed hair in kitchen sink and sponge bath 
Day 6 post op, pain 3-4, take meds prior to getting out of bed in a.m., tempted to use only 1 crutch at home but knee gives out without warning. need to get out of house.
1 wk post op, pain 2-3, 1st regular shower, reduced breakthrough narcotics, bruising is showing now, prefer to use 2 crutches in order to focus on correct strides. Good knee is aching due to the additional stress of compensating for pvns knee.
2 wk post op, pain 2-3,  stabbing pain begins, staples removedunable to drive, use crutches only on outings. narcotics evening only to sleep. crutches in storage, resumed sex 
3 wk post op began physical therapy, beginning to drive short distance
4 wk post op ROM 56 degrees, frustrated with being gimpy, mentally anxious to return to my desk job but physically not ready. 
6 wk post op ROM 70 degrees, pain 2-3, stabbing pain intermittent, family stresses, financial stresses as bills start rolling in. Driving normal distances. Will make decreased monthly payment arrangements until return to work. 
7 wk post op, Radiation Treatment begins, 18 treatments at 200 greys per. 
8 wk post op 2/13/2012, Ready to return to work managing a physicians office, if not for the up coming RTROM 84 degrees, pain spiked  3-4 with increasing activity, good knee continues to hurt due to extra stress. 4 Radiation Treatments done, increasing fatigue, swelling. Rarely take narcotics.
9 wk, 9th RT session, feeling the cumulative effectspain 3-5, slight burning sensation, vice grip feeling, heat at site, darkening of skin, swelling, fatigue is overwhelming. I had to back off on physical therapy. Compression, elevate, Ice, meds. ROM is still at 84%.
10 wk post op, At this point it's a mental game of keeping your attitude in check and not having too many pity parties.
12 wk post op radiation therapy finished. Physical therapist says one more month of pt. focusing on range of motion.
14 wk post op. My best range of motion prior to radiation therapy was 84 degrees. During radiation I lost 10 degrees, 2 weeks after rt stopped I’m at 81degrees. 
16 wk post op, 4 wks post radiation therapy ROM has been stuck at 81 degrees for 2 wks. Prior to RT ROM 84 degrees, lost 10 degrees during RT= 74 degrees, regained 7 degrees the 1st 2 wks post RT. 
18 wk post op, 04/18/2012, Knee manipulation under anesthesia followed up by aggressive physical therapy 4 times a week. Obtained 110° in surgery, had a reaction to morphine requiring iv benedryl. PT following day rom 110° with help 118°. Healing wise put me nearly back to week 2 post oppain 5-6.
19 wk post op, 1 wk post manipulation, ROM 113° with help, pain level 4 with nerve pain feeling like a knife jabbing into my knee, with swelling, 10-12 hrs daily in cpm machine for 4 weeks.
20 wk post op, 2 wk 4 days post manipulation. ROM 113°pain level 3. The nerve pain has stopped and my knee quickly stiffens up if I have it immobile for an hour. It is a very fine line between working it too much or too little. I continue to have problems with swelling. 
25 wk post op, 7 wks post manipulation 6/6/12. Surgeon is pleased with rom @ 113° which means I haven't really lost any rom since manipulation. She is hoping that the rom will continue to increase as the residual pain and swelling decreases  in the next six months, which will make it a year from surgery date. Pain level is 2-3 but decreases with moderate movement. It is a fine line between doing too much vs too little.  I finished physical therapy a couple of weeks ago since I have the motivation to do pt on my own, I  know all of the exercises that I need to do and I have easy access to a gym. My good knee has been hurting for nearly three months but is now constant and hurts nearly as much as pvns knee. Surgeon has ordered mri on pvns knee for  follow up and on the good knee to rule out pvns.
6 month post op follow up MRI 6/14/12. 9 week post manipulation 6/21/12. Per mri new diffuse thickening and rare intratendinous of pvns post surgical. Joint effusion and synovitis noted with additional hypointense focus superior margin which is new, decreased popliteal cyst however multiple foci of hypointensity present diffusely. Residual or recurrent pvns.{Correction 02/13/2013): 6 mo f/u MRI 06/2012 showed a false pvns recurrence. It was proven during f/u surgery  12/14/2012that the mri was showing scar tissue and not pvns. After you have surgery the mris become more difficult to read accurately. After the 6 mo f/u mri I had two more mris done showing that the (false) pvns was remaining stable (unchanged) that was the clue that it was scar tissue and not pvns.}
My good knee continues to be swollen and painful mri showed no pvns but it does show chondromalacia and a small effusion.  In pvns knee constant dull pain level 5-7, diffuse swelling, minor swelling in non pvns knee, continuing exercises 3 time wk, ice, elevate. Range of motion at best 110° due to swelling. Pain may be much increased due to pain pump being reduced by 15%. 
06/03/2012, UTI treated with 4 days of Cipro, very very ill
06/28/2012 Bilateral steroid injections in the knees due to swelling and constant pain. Experienced a Cortisone flare increasing the pain for 2-3 days. Had a mild systemic reaction to the steroids causing severe anxiety, moodiness, flushing of the face, slight difficulty breathing and increased heart rate, necessitating Valium to avoid asthma attack and tachycardia... this lasted  about 4 days.  The symptoms are slowly abating and my knees are feeling much better with very little swelling. Do your research prior to having steroid injections, systemic reactions are rare but can be quite severe and far outweigh the benefits of the shots especially if you are menapausal. I'm unable to have the Cortisone shots again due to the reaction. In the end I only had 6 weeks of good pain control and 8-10 weeks of moderate pain control from the injections. The shots are very expensive and in my case totally not worth the expense and side effects.
07/08/2012,  2nd  UTI treated with 10 days Cipro, flank pain, very very ill
07/23/2012,  3rd UTI treated with Cipro, bad flank, abdominal pain, appointment with urologist 08/01/2012. Wondering if the subsequent infects have anything to do with the steroid injections.
07/30/2012, 1 month post steroid injection, pain level prior to steroid injections 5-7 nearly a month later it is now a 2-3, swelling is very much reduced. ROM estimate 120+. Knee continues to stiffen after being sedentary. Felt comfortable going down an escalator for the first time since surgery. The posterior knee cyst continues to enlarge causing minor discomfort. Knee constantly aches but actual pain is finally dissipating. My body feels very worn out probably due to all of the procedures and recurrent UTIs this past year. I had a dream last night that I had returned to work and I was so happy. Someday :-) The last 8 months has been more then challenging and I see it wearing on everyone around me. The battle becomes most fierst at the end.

08/01/2012, I saw the urologist, flow, nuclear study and cystoscopy all came back normal. Been very ill and with less movement I'm not able to exercise my knee so it is stiffening more, heat is still coming off of it but from what I hear it is normal. Difficult to deal with pvns issues and other illness at the same time.

08/21/2012 appointment with new primary care doctor. Diagnosed high cholesterol, low vitamin D, post menopausal. Wow isn't that all a slap in the face and I actually thought I was in good shape for 48

08/29/2012 neurologist appointment, dx primary peripheral axon loss polyneuropathy, brain mri normal.

09/12/2012, 11 weeks post bilateral steroid injections, ROM normal w/o swellingpain level 4-5 in pvns knee and continue to get that crushing sledgehammer feeling intermittently, pain level 2 in non pvns knee. 


09/20/2012  Two hour appointment with arthritis specialist, 12 vials of blood and very thorough exam

09/28/2012 Nine month f/u mri showing pvns stable, saw PA for Dr DeComas f/u

10/01/2012, 4 month post bilateral knee steroid injections, positive effects totally worn off. Pain 5-7 in pvns knee probably due to tendonopathy and bakers cyst pressing on nerves. Non pvns knee pain level 3. appointment with immunologist today, allergy testing done, immune system checked 11 vials. Increased vit d to 50,000 IU 3x week and given allergy medicine. 

11/04/2012 Returned to physical therapy due to muscle weakness and balance problems from polyneuropathy. Left knee is giving way and locking is making my leg swing way out during strides. Bupivicaine was taken out of pain pump 1 wk ago, now burning back radiating to bilateral legs. Pain 4 in pvns knee, Right knee 2, burning back, legs 6.

11/20/2012 Returned to PCP, cholesterol and blood sugar levels are all within normal levels now since changing diet and increasing activity.

11/29/2012 Pain Pump increase 20%, Bupivicaine put back into pain pump with pump fill. Burning in back and legs has decreased to a 2.

12/10/2012 Follow up mri 11 1/2 mo, showing pvns stable. I can no longer take a normal stride due to catching in my joint which is causing my hip to hurt and the knee pain is increasing. If I bend my knee while sleeping I wake up in pain. Pain is 6-7, Right knee 2,  0% swelling and great ROM

12/14/2012 Arthroscopic knee surgery (out pt) for possible recurrent pvns, lateral and medial meniscus repair and to address the catching and pain. Exactly one year ago to the date I had open synovectomy on the same knee.{Correction 02/13/2013): 6 mo f/u MRI 06/2012 showed a false pvns recurrence. It was proven during f/u surgery 12/14/2012that the mri was showing scar tissue and not pvns. After you have surgery the mris become more difficult to read accurately. After the 6 mo f/u mri I had two more mris done showing that the (false) pvns was remaining stable (unchanged) that was the clue that it was scar tissue and not pvns.} No PVNS, repaired meniscus, cleaned up joint, Patello-femoral joint is bone on bone and I will need a knee replacement. Drove car and began PT day 3, Pain steady 4, is a decrease since meniscus repair. ROM 109 after couple weeks of rehab. Used crutches one day. Could have returned to my desk job at 4 weeks but 6 weeks would have been better.


02/07/2013 Minimally invasive quadricep sparing partial knee replacement using the Arthrosurface HemiCAP wave system. Overnight hospital stay with femoral block. Should have stayed 2 nights due to pain when block wore off. Day one/surgery, no drain, ROM 118, walked in hall with PT,  Day two ROM 90, 10 mg oxcycodone q 4 hours, 2 crutches, evening Pain 9+ sobbing, meds adjusted 20 mg q 4 hours, minimal swelling, pain under control in 6 hrs, Day three 15 mg oxcy q 4-6 hrs,1 crutch,  Day four 10 mg oxcy 2 times,no crutches/ was supposed to start PT, Day five, PT begins, 10 mg oxcy 1 time. 1 week, CPM 6 hrs day 110 degrees, no restrictions. Knee moves smoothly and no longer hurts with every movement.


02/23/2013 Two weeks post partial knee replacementROM 114, Pain 0, Tightness and very mild aches from surgery, drove car to have staples removed on day 11, continue to use the cpm a couple hours each day, Day 12 began PT, Using both legs to ascend and descend stairs, no noticeable swelling, energy remains low but improving everyday, not ready yet to return to work but I'm beginning to look. 

03/21/2013 Six weeks post partial knee replacement. ROM 118. 4 1/2 wks post op was a passenger on crotch rocket = no discomfort. Pain 0-mild aching minimal activity, 3 from mild swelling(walking 3 miles) full returned to activities except jogging and kneeling which doc wants me to wait until 3 mo post op. Energy hasn't returned yet. I would be ready to return to office work at this point if not for other issues. Extremely pleased with this procedure. Knee feels like better then my biological knee. Severe bone on bone nerve pain 0% gone immediately post op. 

07/01/2013 Time to call the surgeon and have her order my 6 month follow up MRI. Keeping my fingers crossed for good results. An update on my PVNS knee; It's been 6 months since my partial knee replacement and I'm doing wonderful. Little to no pain, 2 on the pain scale if slight swelling is present. Range of motion is normal and I don't think about my knee unless I need to kneel down, in which case I am extremely careful and put little pressure on it. My PVNS leg is still a little weak so I'm still careful on the stairs. The quadricep muscle still tightens up and aches, since open synovectomy.  

08/13/2014 Update: I remain nearly three years PVNS Free. MRI in December is now showing extensive chondromalacia (arthritis) in the medial and lateral aspects of my knee, less than a year after the partial replacement was done. This is disappointing since I will require a revision of my partial replacement into a total knee replacement in the near future. I suspect the having the pvns and or the radiation therapy may be playing a role in accelerating cartilage destruction, since I had no signs of arthritis prior to the synovectomy in December of 2011. 

Monday, July 30, 2012

RT...Questions To Ask About PVNS Radiation Therapy



Questions To Ask Your Radiology Oncologist
  1.   Why is radiation a good or poor choice for me?
  2.   How many PVNS patients have you treated?
  3.   What are my chances of recurrance with or without radiation treatment? 
  4.   How does radiation effect the PVNS and healthy cells in my joint? 
  5.   What dose of radiation will you be using and how/why did you select that dose?
  6.   How often and how long will I receive radiation treatment?
  7.   What are the chances that radiation will cause a secondary cancer?
  8.   Will the dose of radiation have any effect on fertility?
  9.   What kind of side effects will I experience during the treatment?  Fatigue, etc
  10.   What is the process for setting me up for radiation and how long will it take?
  11.   Will I need a post surgical MRI or CAT scan?
  12.   What is mapping and will my surgeon be participating it?
  13.   If I have radiation now will I be able to have the same joint radiated in the future?
  14.   What is your follow up care plan?
  15.   Is there anything that I can do to reduce adhesions from forming?
  16.   How much will my treatment cost and do you participate with my insurance?
  17.   What is the best time of day to schedule my appointments to avoid long waits?
  18.   If I experience treatment complications who do I call and who handles it?
  19.   How will my joint be immobilized to prevent movement during treatment?
  20. I am not a physician and the above is in no way to be taken as medical advise. This is my interpretation of what I have been told by my physicians and from what I have read. Always consult with a professional for case specific accurate information.