Chronic Costochondritis - Cortisone Injections Are Helpful?
Aug 25, 2015
I was diagnosed with costochondritis when I was 14 and have had it for five years now.
I can manage the pain when it isn't flaring up but for the last few months it has been very bad to the point where I can't sleep. My job is quite physically demanding sometimes which causes the flare ups.
I recently went to my gp and requested x-rays as I haven't had any taken since I was diagnosed. Last year I had a bone scan but nothing showed up.
Last week the doctor said that I also have mild thoracic scoliosis curving to the left which may give a reason for the costochondritis, finally!
I have decided that the time has come to get cortisone injections as other medications/treatments don't relieve the pain. I will be seeing a specialist in a month's time.
Has anyone else had the injections? Did they help you? What was the whole procedure like for you?
View 1 Replies
Advertisement
Anyone have experience with cortisone injection for costochondritis - positive or negative - benefits or side effectS?
View 7 Replies
I am due to have cortisone injections on 7th November but am feeling a bit anxious about it.
View 2 Replies
I had cortisone injections in both knees 5 days ago and both of my feet are really swollen. Is this a normal side effect of injections in knees?
View 1 Replies
I am thinking about having cortisone injections in my feet for arthritis pain and I've heard 1 good and 1 bad report about the success of it. Can anyone who's had it let me know how it went.
View 9 Replies
I'm just doing some research at present regarding Cortisone/steroid injections into the shoulder joint within a 12 month period.
How many injections in a year is classed as too many without any noticeable improvement in the symptoms?
Injections both in clinic and in theatre as part of an MUA or EUA.
View 5 Replies
Has anyone found that these injections make you put on weight. I have had a fair few and due for some more next week. In the beginning I had a spine injection and then in the leg - I am on Pazital and Lyrica but a lose dose. But looking back, the injections have been the best as I walk quite a bit.
I know the UK have a maximum - but can't remember how many. I last had the injections about 3 years ago, 4 in one thigh and 3 in the other. I suppose it depends on the strength too but I haven't ever been told the strength.
View 37 Replies
I went to a dermatologist today and i was told my face had a good deal of acne. I have my acne or my forehead and a lot around my jawline area that are cystlike. I have a few of them and those are cystic pimples. The dermatologist recommended me to do acne surgery ... extraction she mentioned and i kinda did not want to do this b/c i had a bad experience with a an esthetician many years ago plucking my face. The difference was that was in a salon and not a dermatologist. I remembered when i did it, i had holes and my acne was really bad right after it so I said I didn't want to do it.
However i asked if i could get cortisone shots done in my jawline where i have cystic pimples that doesn't seem to go away. Dermatologist did the cortisone injections and it was not painful at all. There were 3 of them done when i checked by bill. Anyways i came back home and then i saw i still had the cystic pimples there... I made the mistake of actually thinking these shots destroyed the cystic pimple on the spot... found out recently it takes a few days or close to 1 week for it to flatten.
Well I got prescribed epiduo for my acne and also solodyn as an antibiotic. I'm told to follow the same regimen i have but use epiduo at night and take solodyn once a day.
My question is should i even start the epiduo cream now after i got the cortisone injections? Should i wait a few days first till it flattens a bit and then use it? I'm worried using it might make it worst. I called the office and one of the reps there said it didn't matter you could start now but im thinking i shouldn't use this product on the area of my face yet right after the injections? Should i put anything on these spots where i got the injections? Because im thinking all i should do is wash my face like normal and put aloe vera gel on it or nothing at all and don't put any acne cream on it till few days later?
How long did it take for the cystic pimple to get smaller after the injection? Does it flatten fully or does it not? How soon can you do it again on the same spot if it didn't work? I assume if it doesn't flatten in 1 week, then it didn't work? I read online that ppl mention 2-3 days it should flatten and the cystic pimple should be gone...
View 11 Replies
Flying after anesthetic for cortisone injections to the coccyx?
I was told by my surgeon that I could have my cortisone injections ( under general anesthetic ) to my coccyx before taking a 8 hour flight in 8 weeks time. He said he would get me in. 4 weeks later no letter. Rang his office and was told he's away until mid April and there was no way I could have it done before I flew in 4 weeks as I was having a general and you CANNOT fly for 6 weeks after a general!! So confused as to why the surgeon would say it's ok but receptionist is adamant I can't have it!
Can I have a general anesthetic and fly 4 weeks later? Any info would be much appreciated. I have googled it but I'm finding that I should be able too!
View 1 Replies
I've had this nasty problem for almost 5 years now. I was in a severe vehicle collision where I fractured my L1 vertebrae, and then about 6 months later, I started getting this nagging pain in my left sit bone and down my leg.
I was misdiagnosed for the first 3 years of it. At first they thought I had piriformis syndrome ( which is most doctor's first diagnosis since it sends pain down the sciatic nerve. I did 6 months of rigorous physio/chiro/needling to attempt to fix the pain, but nothing helped.
Then they thought it was a bulging disc radiating pain down my back from the injury.
All the while, my pain was getting worse and worse. Taking more and more pain medication. Getting heavy into the opiates. Then after losing my career in the military, and after a year of wasting time. I finally got in to see a spinal specialist. one who teaches around the world and after 5 minutes of asking questions and a couple of manipulations, he diagnosed my with Ischial Tuberosity bursitis.
While I was happy to finally KNOW what it was. It hasn't been fixed. I get cortisone injections every six months, and unfortunately the relief is is not the best. I am taking a Fentanyl patch for consistent pain relief.
It sucks that a pain in my butt is a constant in my daily life. It's depressing and it makes it so i can't live like a normal person....doing normal things....movies, dinners, socializing, driving... etc.
All I do, is try to keep on moving......moving....trying to stay flexible...doing my stretches....trying to keep in decent shape and health.
If anyone wants to chat about their issues with Ischial Bursitis, I'd be glad to. Or if anyone wants to know about treatments etc....ask away.
View 6 Replies
I had bulging disc over two years ago and i was sent for mri scan a while later i got cortisone injection into L5 disc worked ok and lasted for a few years,two months ago it returned and is very painful the doctors gave painkillers and said to exercise couldn't stand up never mind exercise,,i'm confused on why they are asking me to see a spine specialist which is taking months and why don't they just do the injection like they did a few years ago ,anyone any answers?
View 3 Replies
My husband has been suffering with a pain in his right arm for a few months now. He saw the doctor and he diagnosed it as tennis elbow, he did do a lot of fence painting in the summer, the doc has suggested a cortisone injection in the elbow, just wondering if anyone has had one and are they of any benefit as I've read some horror stories where the pain has been twice as bad afterwards?
View 8 Replies
As we were chatting about teeth earlier on the spectacles thread I thought I would start one specifically about ME and teeth.
I think I have mentioned this before, but when I saw my dentist a while ago and told him that I had been diagnosed with ME he informed me that if ever I needed to have a local anaesthetic injection he would give me one which doesn't contain adrenaline ....... because anything with adrenaline is a complete no no for ME sufferers.
One of the theories about the cause of ME as some of us know, is that for some reason we are unable to 'switch' off adrenaline as a 'normal' person would and as a result we just drain all our energy, and the only way to regain it is by resting. I am convinced that there has to be an awful lot of truth in this theory.
Several months before I was diagnosed with ME I had extensive reconstructive work done on my upper teeth (my generation didn't have fluoride toothpaste and many of us subsequently have soft teeth), and I often wonder if the dozen or so adrenaline injections triggered something. Also, I had a lot of amalgam fillings removed, and I wonder if the lead from these was released into my system during the drilling.
Who knows - but hopefully one day we will find out what causes this wretched illness :?
So folks ..... no injections which contain adrenaline.
View 19 Replies
I have CS in my neck and am in constant chronic (pain for the past three years). I am sick of being in pain.
My first visit to the NHS pain clinic was interesting, as the consultant informed me that I need to have Facet Joint Injections into the top part of my neck, which he plans to do in April !
I asked the consultant if there are any potential dangers from this procedure and he informed me that me that nothing can go wrong !
I got home ran a web search on Facet Joint Injections and am really horrified to read that there are rare - but very serious potential dangers from this procedure ... I feel that the NHS consultant has not explained the potential dangers to me.
View 21 Replies
Was referred to a neurosurgeon to see a physiatrist which then referred me to 2 other drs - a neurotherapist and a neuropsychologist. also prescribed nortriptyline. i guess i shouldn't have said i was a little depressed. but man isn't feeling that way probably normal after a car accident, then chiari diagnosis, then possibly brain surgery, and finally after being told i may never again get to play the sport i love which is hockey because of all this? been to 3 neurosurgeons - 1st two say surgery is an option and come back when you're ready basically. 3rd one referred me to physiatrist and said basically surgery will be an option down the road. 26mm herniation with a CSF blockage (i had a cine study with 2nd neurosurgeon). jw if anybody else has been down this road. feels like im taking steps backward instead of forward...
View 4 Replies
Good advice here on the subject of cervical spondylosis, apart from the wearing of a support collar maybe. I have found wearing a soft collar at night very helpful in preventing an attack of neck pain turning into a horrible headache by the time morning comes. And very occasionally, it's useful even in the day for severe flare-ups. But I completely agree that neither collars nor corsets should be worn for prolonged periods. My problem started nearly 30 years ago after a car accident, and I'm able to deal with it by the collar at night, Dihydrocodeine, and occasionally voltarol.
I'm sure it's important to keep as active as possible, but families (and GPs) need to understand that it can be a significantly disabling condition for a minority of us. It has stopped me working, and limits my ability to paint, which I love to do. If diagnosed with it, take all the physio and other help you can get as early as possible, and ensure you are not written off by the medics - badger them until you get help that works for you.
View 27 Replies
I'm started bending forward due to AS, my neck has also bent slightly rightwards. Will back brace assist in keeping my posture.
View 1 Replies
Just wanted to share my experience, the weekend before Easter I had to go home from work on the Thursday with Flu like symtoms, I returned to work the following Wednesday, still feeling under the whether, coughing but thought to myself that I have a long weekend to come so I would rest and recover. After the Easter break I returned to work still not up to par and still coughing but also had a pain in my lower rib cage as if someone had sharply elbowed me. These symptoms continued onto the weekend and on the Saturday became worse, I had to pick my daughter up and the cold wind hit my lungs and it took my breath away. On returning to the car I couldn't fill my lungs up the pain was so excruciating, after the car warmed up the pain subsided enough to enable me to drive home. On returning home the situation became worse and I waited for my husband to come home and he had to take me to accident and emergency where I was admitted straight away. They had to administer morphine for the pain to enable me to breath more easily, it was as if I were being stabbed with a thousand knives. The doctor, after blood tests and x-ray diagnosed pleurisy and I went home with Ibuprofen, codeine and paracetamol which I took to the maximum daily dosage!
1 week later I was at my own GP who gave me another sick note, I saw him again the following week and after examination he said that the pleurisy had gone but I had had a double whammy as I was also suffering with costochondritis and it could take a while, just to rest and keep taking the tablets.
It is now 28th April and the symptoms on some days have now subsided enough to the enable me to do very light duties and on other days I can't do much at all. The doctor hasn't really given me much indication as to how much I should or shouldn't be doing, feeling very frustrated, the mind is willing but the body isn't. He said that, "many people don't realise that more people die in a year from influenza than meningitis and I had to be patient". Being a full time working Mum who is usually house proud and very busy, is now living with a basket full of ironing and dust that I can write my name in. My employer has been very understanding and great about it all but not sure how long they will be patient and my work will no doubt be building up there too.
View 2 Replies
I have had Tietze's/costochondritis for 6 years now and it has affected my life drastically. Not sure if it began with a bacterial infection (like one doctor said) or a slight ribcage injury. My symptoms or more like 'gasping for air' and just about passing out because i can't breathe as well as a feeling of 'swelling in the ribcage area'. The pain is around mid-section and wraps around so very difficult to sleep on side. It has affected my quality of life because i have become reclusive and don't do anything that involves a crowd because i don't want to get bumped or elbowed in the ribs. The last time someone hugged me (which was three years ago) i had to go to ER and get a steroid shot and dose pack because ribcage area was so inflamed. I am a thin person so that may have something to do with it--not sure because i saw where someone said that doctor told them they would get better if they lost weight?? When i go to a doctor (and i have been to many from rheumatologist to neurologist) they do not have answers for me as to why this will not go away. I have been told everything from vitamin deficiency to chronic inflammatory problem to 'they don't know what it is or what to do for me'. I am very frustrated at this time because I get roadblocks everywhere i go for help. Any suggestions?
View 4 Replies
i have suffered with teitze for the last 12 years but for the last 8 weeks i feel like a thudding in the left side of my chest but more recently it feels like my heart is jumping out my chest and it takes breath away. I find this very scary as you wonder what will happen next,it disappeared for 4 days this week but appeared again now and has been happening most of the day
View 1 Replies
I've had a bad costo flare up for the past 5 months since my dad passed away but lately if I do heavy cardio (my heart is fine) I get the standard pain in the sternum but one rib is up higher and I can feel slight tingly pain in area even brushing my fingers lightly against my chest. Not even pushing. Has anyone else experience this. It's a weird kind of baggy pain and tingling in chest. I can also feel bumps along the intercostal muscles in my ribs that are pea sized.
View 3 Replies
