First Rib Resection For Thoracic Outlet Syndrome? Experience / Recovery?


Oct 8, 2014

Has anyone had this surgery and had a good recovery? If so how long did it take, do you feel normal, and are you restricted at all?

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Cervical Rib - Thoracic Outlet Syndrome And Venogram?

Im looking for some advice,I have been diagnosed with cervical rib on both sides and also thoracic outlet syndrome. I have had loads of tests and been told I have got to have the ribs removed but before they can do anything I have got to have one more test that is a VENOGRAM of the upper limbs, they have told me I will need anorectic and I will be in for the day but I'm still none the wiser of what they are doing other than having the dye. I was hoping someone on here has had it done and could tell me more about this procedure.

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Thoracic Outlet Syndrome :: Cervical And First Rib Removal

I (have) had Thoracic outlet syndrome. It took approx 8 years to figure out what I had. Finally found a doctor I could agree with. He found cervical ribs both right and left. Only had symptoms on my right side. Pretty sure symptoms were brought on by a car accident (whiplash). Anyway.. Had the cervical rib removed and the first rib removed along with the scalene muscle that was in a spasm. It has been 5 weeks and I am still taking pain meds, although I am finally starting to feel some relief. Not ready to quit the pain meds though. Although I'm gonna have to since my dr wants me off them. Wish he could feel this pain. My chest is numb but it is painful underneath. It burns like heck and the muscles, or it may be the fascia that runs from my neck to my chest that is so tight it kills me. I try to do my stretches but it hurts. Mornings are awful. Be prepared to not sleep at first. I am thankful to have found this site. You feel like you are the only one out there who has been through this since it is such a rare anomaly. If you are going to have this surgery prepare yourself for not only the pain but the mental challenge of being in pain for so long. You will have some really down days.

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Endometrial Resection - Recovery Time - Still Bleeding (18 Days)

I had this operation done 18 days ago. To remove the lining from the womb. I am still bleeding. It isn't as heavy as it was before operation. But still like a light to normal period. I suffer with very lower left back pain, this has been worse since I have been bleeding heavy & it is still there. Anyone else had endometrial resection? 

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Laminectomy With Resection Of Synovial Cyst - Experience?

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Uterine Fibroids :: My Recovery Experience

4 days ago I had open abdominal myomectomy resulting in the removal of 22 fibroids i was previously on esmya to reduce the size if them which worked by reducing my womb from 20 weeks to 16 weeks in size.

It took 3hrs I had a epidural also as the anesthetist said it would help reduce blood loss

I'm home now with prescription of tramadol and paracetamol

I have staple like closures feel like Frankenstein bride.

The pain is pretty bad but I'm hopeful I'll be up and better soon.after being suffering for 8years of heavy bleeding iron transfusions pain depression embarrassing accidents.etc

I'll keep you all updated on my recovery..

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Hemorrhoids :: My THD Procedure Recovery Experience Normal?

For approx. 10 years I've been dealing with internal and external haemorrhoids (rhoids) and the occasional prolapse - too embarrassed to seek medical attention I've just tried my hardest, despite the discomfort, to carry on regardless.  After a recent defining moment in the bathroom I decided enough was enough and booked a visit to see my GP, which to my surprise was not as embarrassing as I thought it would be.  Following a digital examination the GP confirmed that the usual solutions would not suffice and a referral to a Consultant was needed - fortunately I have private medical insurance and my appointment came through quickly.

At my first appointment the Consultant completed a digital examination for himself and deduced that my rhoids were “quite large”.  At this stage he suggested a Sigmoidoscopy (lower bowel camera) and ligation (banding) to see if that would help - whilst I was told the procedure is uncomfortable and not painful I opted for sedation on the basis that why would anyone choose to be in any discomfort when they really don’t need to be!?![/color]

Having researched the procedure online I returned to the hospital some 3 weeks later.  I have to say the enema was a surprise in more ways than one – I now understand it’s a necessary requirement, but given the reason it’s being administered is it unreasonable to assume they would be a little more gentle? #Wowzers!  Anyway, I waited around all morning and I was eventually taken to the Operating Room (OR). At this point I have to say Sedation is wonderful - I remember nothing between the fluid being injected in the cannula and subsequently being in the recovery room. Given I had been tinkered with all I can remember at this point is feeling as though I needed to go to the toilet.  I was subsequently transferred back to my room where I remained for a couple of hours in a little discomfort, but I recall being in pain – the Consultant came to say he would see me at my follow-up appointment and I was eventually released by a nurse that said “it looks like you’re coming back to see us” and I spotted THD on her paperwork.

It was about 2-3 weeks when I had a follow-up with my Consultant, which gave me lots of time to read up on what THD was etc. – compared to the rhoidectomy of yesteryear it sounded like an absolute gem of a procedure.  The Consultant asked how I had got on with the ligation and I explained there had been no real change however, he said he didn’t think it would work given the size of the rhoids – so we discussed returning for a THD in 2 weeks’ time. So, there is the background…

I returned to the hospital for my THD last Friday and, given the procedural information I had read on line, I was feeling quite good about it.  Having had another fairly uncomfortable enema (by the hands of the person that delivered the previous one! #Ouch) I was told that I was 2nd on the list and would be seen quite quickly – it was roughly mid-morning when I walked to the OR.  At this point I was given the cannula etc. before the GA was administered.  Quick question:  Is it just me that likes that dizzy lightheaded feeling you get with a GA?  I’ve had a few in my time and I really enjoy it!

]The next thing I remember is waking up in the Recovery Room with an overwhelming feeling that I needed a bowel movement (BM) – I’m talking that real desperate need somebody has when they have a stomach upset.  I recall one nurse saying it’s probably the packing and the other said the consultant did not use any – I was then told somebody was on their way to transfer me to my room but I could have a bed pan if I needed it.  I was quickly returned to my room and I asked if I was able to go to the toilet – I was told I could, but needless to say I actually couldn’t do either of the things one usually does when they visit the lavatory!

After a good hour or so I asked if any pain relief was available as I was really quite uncomfortable.  I was subsequently given codeine, which did help – mainly because I fell asleep if I’m honest!  I was woken by a nurse wanting to take my obs – I said I needed the loo first and the nurse agreed to return within several minutes.  I managed to urinate however, upon returning to the room the nurse had quite a fright as found me lying on the bed looking as white as the pillow case, feeling dizzy and sweating – I was given Oxygen for a while.  I was given more codeine later on and, after more sleep, I eventually saw the Consultant who said that he would see me again in a couple of weeks, but with regard to that day I could stay overnight or go home. Being tired as I was unable to get any decent sleep, I opted to go home at around 18:30. Upon check out I was prescribed Fybogel (to be taken Twice Daily) and Paracetamol (as and when) – due to other ailments I have access to Co Codamol 30/500 and Tramadol hence I was good to go. The journey home was not too bad however, the left side of my rectum was particularly sore hence I sat with all my weight on the right bottom cheek for the duration. When at home I pretty much spent the evening sleeping, thinking about the toilet or trying to go to the toilet!

I woke up several times in the night with the feeling that I needed to go to the toilet, so I eventually got up to watch TV at around 04:30. Feeling the need to go to toilet lasted all day – other than briefly after passing wind or a short while longer after taking a Tramadol.  I eventually went for a very small BM however, it was quite painful to be honest and I wondered if my body was telling me I needed to but my head was telling me not to – I was literally having spasms, such a weird feeling that happened several times throughout the day. The good news was that whilst I still felt rough, I was more mobile and thought THD may just be the best thing since sliced bread.

Pretty much mirrors Day two having woken up at 04:00.  I went downstairs and eventually managed to go to the toilet for a small BM however, it was soooo painful I felt exhausted afterward.  I returned to bed mid-morning for a couple of hours and then remained in the confines of my house for the rest of the day. 

Woke up at a reasonable time and managed to potter around the house all day.  Took a 40 minute drive to take my child to school and back and noticed that the desperate urge to go to the toilet has been replaced with a fullness/weight feeling and there is now an aching on the left side of my rectum.  I managed to do the smallest of BM’s, which, in the main, was probably my body dispelling some of the Fybogel!  In cleaning myself I noticed a small lump on my rectum, which I can only liken to an external rhoid – brilliant, just brilliant! By the afternoon I actually felt like I was in pain until I read about and decided to take a sitz bath – temporarily relieving the pain, until I took more Tramadol

Today. I’m feeling somewhat down about my post THD experience.  It doesn’t seem to be consistent with the majority of literature that says you’ll be running marathons within 48 hours (slight exaggeration, but you know what I mean)!  I’ve got what I think is an external rhoid, the left side of my rectum is uncomfortable, and when I sit down or stand up I can feel pressure - like you do when the rhoids are playing up…not to mention that after I drove my child to school today I felt like I’d received a swift kick up the arse when I got back to the house.  I had a BM this afternoon and it was painful…AGAIN…I ended up elevating my feet on a footstool to making the passing of the BM more comfortable!

Having got all that of my chest, I’m hoping somebody can offer an opinion on the following…[/color]

Could the lump on my rectum be linked to the procedure and shrink over time?  I’m wondering if I’ve not noticed before as I previously had a prolapse?

Could the lump be a new rhoid or hematoma given the constant feeling of requiring the loo and then my associated attempts to go?

Given I’m now at Day 5, should I really have an aching feeling where I think the procedure was completed?

Given I’m still uncomfortable, would you contact the GP or carry on taking the tramadol for now?

I’m off work at the moment, but I will need a sick note in 2 days – is it likely that I’ll be ready to go back at this point?

Many thanks for reading and, where you can, replying with your comment(s).

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Addiction Recovery :: How I Overcame Opiate Withdrawal - Experience

I have taken painkillers off and on for years. I've gone thru withdraws many many times. I finally overcame my addiction by realizing why I started abusing them and research research research...I've tried the Thomas recipe, etc. My biggest issues are anxiety, irritability, and insomnia. Without getting into everything and making whoever is reading this bored, I'll jump right in. This is how I did it, cold turkey. I went to the Dr and told him I had sCiatica. Anyone addicted to opiates I'm sure knows how to Google an ailment, go to the Dr and complain. Tell the Dr you read about the medication gabapentin and want to try it. Tell him that you also have mild anxiety and read that gabapentin. May help with that. If you throw things in like, "I've tried prescription pa in meds And things like Xanax but they just make me loopy so after reading about this medication, I got really excited and would like to try it." Ok, so after you get it, also go to a health food store and get L-tyrosine, Source of Life vitamins and of course, imodium. The best way to do this, the most effect way, is to take about 600-900mg of the gabapentin right before you go to bed on the LAST day that you use opiates. It will help you sleep And feel good the next day. Upon waking, take 1000mg of the L-TYROSINE, your vitamins and your immodium, and another 300 mg of the gabapentin. 2 hrs later take another 300 mg of the gabapentin. It's better absorbed if you drink a glass if orange juice or take an ibuprofen. I should've said that 1st. So take an aleve Or advil With it. That would help with any aches and pains. Halfway thru your day, take another 300mg of the gabapentin and 500mg of the tyrosine. Do this every day for a week. It will get you thru the toughest part. I absolutely swear by this. Of course you're still going to want the drugs and kinda crave then but I promise you, you will feel fine physically and mentally. I read a while back that major depressive disorder sometimes is caused by a gaba deficiency. Major depressive disorder can cause anxiety, aggression, etc. I researched and tried everything. Then I read about these meds And gabapentin Is used for seizures, insomnia, alcohol withdrawal, etc. I have quit cold turkey and thought I was gonna shoot myself in the head because of the physical and emotional hell it caused. Coming off of roxys,oxys, methadone is no easy task. But I swear to you, if you do this, you won't have to suffer. You will feel good. Feel fine. Sleep, eat, take a shower and not feel like it's an overwhelming chore. No sweats. No stomach pain. No anxiety. No aggression. I hope someone reads this, tries it and posts back. Maybe the hell I've been thru will mean something. If I can even just help one person than it was all worth it.

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All of you who have suffered from post tubal ligation syndrome and have had a tubal reversal : Have the side effects of the tubal ligation gone?

I have suffered from post tubal ligation syndrome for many years and I am thinking to have a reversal, but I want to know if it really helps.
 

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Tracheal Resection Due To Stenosis

I have Tracheal Stenosis (narrowing of the windpipe) and I'm hoping to get an operation called a resection wherein the narrowed section of windpipe is removed and then rejoined again....

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Colon Resection Due To The Diverticulosis

I'm just 2 weeks into recovering from a colon resection due to the diverticulosis I had and last night I was getting that horrible pain on my lower left side as if I was having a diverticulitis attack !

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I received a pancreatic resection of my tail in May of last year and have just been diagnosed with a 10 mm cyst in the head.  I'm told all that can be done is manage pain/rest and food.  Energy is lacking.  Has anyone had any luck with B12 shots?

 

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Endometrial Resection - Bleeding After 9 Weeks

I had my the lining of the womb taken away 9 weeks ago. I still have bleeding everyday. It's not heavy but mild to medium. It's everyday.

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Diverticula Surgery :: Undergoing Colon Resection?

Can anyone share their experience of undergoing colon resection? Does it make a difference if you have IBS?

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Bowel Resection With Giant Cyst - Cancer?

Again, haven't been on in ages. Seems I always have an issue, though, every year or so.

This time a large "cyst" was found when I went to the ER for severe "gas" pain back Labor-Day weekend, with CAT scan.

Now I have a young surgeon who has looked at that and blood tests (CgA - high) and MRI and says I need to have all my right colon removed along with the cyst. Just in case it's cancer, basically.

Anyone have a huge cyst outside their bowels and have this kind of surgery? I am scared of cancer, but even if I don't have that I'm scared of what the complications might be from the surgery itself and removing 1/3 of my colon. I'm 44, have a very young son, and a mother already bereaved from losing my sister last year to breast cancer. I start worrying about sepsis, MRSA and "leakage" (poor surgical connections) and blockage. Is it silly to worry about all this?

What bugs me is that the surgeon seems very concerned about cancer, although the 1 marker - CgA - that was high could be high because of my 7-year usage of double Nexium. I also had a "beautiful" colonoscopy the month before the ER visit.

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Diagnosed With 4.6 Thoracic Aortic Aneurysm

I had a 2D echo last week and found 4.6 thoracic aortic aneurysm.

Cardiologist has prescribed blood pressure medicine. Shall I go ahead for surgery or wait till become 5 cm. I am 37 yrs old. I play volleyball every day. Is it ok to continue or stop?

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Diagnosed With Thoracic Aorta Aneurysm

My younger sister aged 50 was diagnosed with TAA of 5.1 cm in January and operated in February due to her small frame. She is recovering well which is encouraging. I have been meaning to go and have a check myself but kept putting it off. I went to my GP 2 weeks ago and he immediately picked up a murmur. Echo followed by a CT scan confirmed I also have an aneurysm but mine is still at 4.27 and I am 55 years old. Clearly we have a genetic disposition but mine is growing more slowly (so far) . I am in shock and still cannot get my head round it. I am fit, practise yoga, follow mainly  a vegetarian diet, don't smoke, hardly drink and do not have high blood pressure. I am now now in 'watchful waiting' and will have another CT scan in 6 months time.  I have been advised to take Beta Blockers and was wondering how patients react to them. I have a professional job in sales and need to keep my energy up. I have off course been considering giving up work but sitting at home waiting for my aneurysm to grow will not help me. I would also like to know if aneurysms always grow and if I need to accept that mine will be bigger by the time I have my next CT?

 

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Degenerative Change Is Present In The Thoracic Spine?

The doctor said the lung tissue is possible (mild) pneumonia. I'm less concerned about that, and I'm being treated with antibiotics. However, I have no idea what "degenerative change is present in the thoracic spine" means. He said nothing about that, but he's an allergy/asthma specialist, so it's not really his field...

Here's what the whole thing says:

"Minimal linear infiltrate is present in the left base. The lungs are otherwise clear. The cardiomediastinal silhouette is normal size and configuration. No pneumothorax or pleural effusion is identified. The pulmonary vascularity is normal. Minimal degenerative change is present in the thoracic spine."

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Scheduled For Thoracic Aortic Aneurysm Surgery Soon

Approximately 8 years ago, doctors discovered a 4.6cm aneurysm in my aorta during routine testing in preparation for an upcoming surgery. Fast forward 8yrs later my aneurysm has increased in size to 5.8cm so everyone in these forums know what that means...its surgery time! I've had echoes and CT Scans every 6 months as this appears to be the wait and watch approach when aneurysms are under 5cm.. My aneurysm was slow growing until the last 18 months. At least 3 CT scans were missed and the echoes didn't clearly show growth. Now, I am terrified out of my mind about having an "open repair". It has been brought to my attention that because of the location of my aneurysm, I am not a candidate for an "endovascular repair". Imagine my disappointment. My anxiety level is at an all time high and I am symptomatic. Chest heaviness and back pain coupled with migraine headaches. Apart of me realizes that these surgeries are done rather routinely now but that still doesn't stop the horrendous fear I have. I have had severe allergic reactions to meds in the past. I'm not a good sleeper generally and now its worst. I have to schedule my surgery by June, to have at least 6 months of recovery time before my family cruise in Dec.. I am a 56yr old female veteran. I used to run least east 3 miles a day and Jazzercise at least 5 days a week until I was told to stop by my cardiologist. I have since gained about 15 lbs in these last 8yrs but other than that, no high cholesterol, high blood pressure or diabetes. My doctors assure me that I am a perfect candidate and shouldn't experience any complications but the idea of my sternum being cut open and just the entire procedure is frightening. What's more concerning is once you have aneurysm in one place, another could eventually show up somewhere else in the future. I've also been told that these repairs can require maintenance in the future! Its all just a little too much but knowing the alternative..carrying around a ticking time bomb, I have to have the surgery. I know people that survived a couple yrs after the surgery, had to have some type of maintenance and never truly recovered and died. My niece fiancé was life alighted to the hospital in mid March with a dissection, he is currently and the road to recovery. I have a lot of family support but of course they are all concerned as well. The saga continues..

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Back Issues :: Thoracic Pain & Trouble Breathing

I have issues with my back & neck, am aware I have degeneration but can't get an MRI done to see if anything else is going on. The pain gets tight in my thoracic area, makes my abdomen (in my esophageal area) cramp up really bad, sometimes my chest gets tight, and I think it's my diaphragm muscles getting tight, then I feel like I'm not able to get the air I need from my lungs. Whole left side has went in pain and went numb. The only thing I know to do is find a way to reduce the pain to stop it but I would love a solution that could help me breathe better in the process. I'm also having trouble breathing when I eat, there's nothing wrong with my lungs or heart. It is my spine doing this. I'm in PT right now but it's not helping.

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When Surgery Is Required? Abdominal (and Thoracic) Aortic Aneurysms?

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