Jump to content
The MS PEOPLE UK Forum
Support, help, advice and information for Multiple Sclerosis. Ask questions and share experiences with people affected by MS.
Frecks

can you take injection a day early?

3 posts in this topic Last Reply

Recommended Posts

Frecks

Hi all,

 

hope your weeks are going ok.

 

I'm on Avonex and have my injection every Friday, anyone know if your allowed to take your injection a day early? I know ideally if you want to change days your suppose to do it a day later each week until you get back round to the day you want it on but that's not I want to do. I've seen something on the internet saying you can take it as much as 5 days early not that you would want to of course.

 

The reason I was thinking about doing this was because I'm out tomorrow night and didn't fancy doing injection before or after I went out or delaying it till the Sat. I may just take it early tomorrow morning I suppose.

 

Thanks

 

Kate x

Share this post


Link to post
happyandy

I was told you could go forwards but never back.

 

Andy


If I knew I was going to live so long I would have taken better care of my body

Share this post


Link to post
Frecks

Yeah I think that's the case. I've decided to do it in the morning then I can get any symptoms out the way, fingers crossed. Not been too bad last few weeks

 

Thanks

 

Kate

Share this post


Link to post

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Similar Topics

    • Injection Tracker MSers

      Hi All,   I made a website to help me keep track of my injections in the hope that they'd hurt less due to not injecting in hidden bruised areas (and it does!). I've like to share it with fellow MSers (and others if it's useful to them!).   I made it because there wasn't an app that I could use to take photos of my injection areas and track injection sites, (and add 'landmarks' like blemishes!) and have been using it since August last year and am very pleased with it!   Have a look, I'd love some feedback if you have the time? Injection Tracker for MSers   Thank you,     Jon

      in General Discussion about MS

    • First injection done

      Hi all,   Well the first injection was done yesterday at 2:30pm in the hospital. I thought the pen had malfunctioned as i didnt feel a thing but it worked fine.   My legs started hurting a lot about 4 hours after the injection and by about 8pm were really painful with a few aches down the shoulders and arms but the chills started in about 9ish alternating with hot spells. I did however have a cold and a sore throat before the injection and the nurse said that this could make the symptoms a bit worse so until i inject when i am well i wont get a true reading of side effects. My head is a bit thick this morning but that i think is due to the cold i have. My legs are still a bit achy but if thats all the side effects i get i will be more than happy.

      in General Discussion about MS

    • dismissal, ill health early retirment, disability discrimination?

      any advice really dont know where to turn right now, Hubby has worked for the same company for 17 years, his job has recently changed and there has been several months of conspiracy to get him out, Instead of looking at what adjustments they could make they have been on a mission to prove he cant do the new job with nothing short of lies. The company appears to have followed correct procedure but have lied and fabricated questions to get the answers they require, one of them being can he walk 3 miles. of course he cant but a motorised vehicle had already been discussed with his immediate manager. Its all about the work hours changing and they sold this to him, his consultant and the works doctor as being working 4x12 hour shifts together when the actual hours are mainly 2 on 2 off with the most days together being 3 days and only 2 instances of this in a month! a HUGE difference! Everyhting that could incriminate them is missing from the case management package,( but we do have copies of the majority of them) he had the final stage meeting last week and was given 12 weeks notice, dont actually know what reason it is because he has asked the union rep about going for unfair dismissial and according to him he hasnt been dismissed. According to the case management package he should have been told how to appeal at the meeting and he wasnt, and still dont know ( time is ticking away fro he 14 day deadline) He has said all along that he doesnt want to take early retirement but will be forced into something we cant live on the pension let alone nothing! and being capable of doing a job with the employer that is bound to make adjustments and keep you is very different to getting another job! Hes now been told to apply for IHR although it looks like this should have been done before the final stage meeting came about, I cant see how he can be trying to prove he should have IHR and prove he can work 12 hour shifts at the same time? He was asked to sign a disclaimer at the meeting and offered his notice pay to be paid tax free, he refused they apparantly were quite shocked. From what I can see they wernt actually giving him anything as aits just a different way of paying notice pay. I really think he has more than enough to take this for discrimination I cant believe you can work for an employer and come out of it with nothing but the pension you have paid for and be forced to have no job because of a disability. any help and advice, tired local disability place before he actually lost his job they gave him the phone number of a good laywer and havent been able to contact. he has secondary progressive and in the last 5 months its made him worse than the last 5 years have MS nurse does say its stress, making him worse.

      in General Discussion about MS

    • Injection sites

      Hi,   I injected copaxone yesterday into my left arm. I didn't inject deep. In correct spot I'm pretty sure, you can't go wrong really. My left arm feels dead and I can hardly us it. Have anyone else had this with copaxone or other injections? Also, my thighs aren't great either, with bruising and huge welts. So I am now going to have to use my buttocks and tummy.....3 spots, that's it.   Hope someone knows!   Jen x

      in General Discussion about MS

    • 1st rebif injection today

      Hi all. Thought I would bring you all up to date with me.   Had my rebif training today and did the 1st injection which I might add BLOODY HURT!!   had the injection about 11am once I did it the nurse couldnt get out of my house quick enough lol.   Felt very woozy about 5 minutes later but luckily enough cleaner turned up and took my mind off it. Wen she left I felt instantly shattered plus injection site still hurting. Still feel woozy and tired after an afternoon nap.   Well next next injection on friday.   Vanessa xx

      in General Discussion about MS

About Us

Founded in 2004, MS People UK is a community website and discussion forum by and for people with Multiple Sclerosis as well as for friends, families, supporters and those interested in this disabling condition.

If you’re newly diagnosed or want to ask about possible first symptoms, or if you’ve had Relapse Remit, Secondary or Primary Progressive MS for some time, a welcoming group of fellow MS sufferers is here to chat with you about MS symptoms, diagnosis and treatments.

The atmosphere is friendly whilst being compassionate, supportive and caring. Members also post about a variety of subjects not related to MS, as well as share jokes, talk about their hobbies, have fun, and more.


The MS People Forum is not responsible for advice or information supplied by members. We suggest you seek medical advice before trying anything.
×