Newly Diagnosed
Newly Diagnosed
MS Ireland is here to provide the support, resources and information you need.
Being Newly Diagnosed with MS
In the past few hours, days, or weeks, your neurologist has told you that you have multiple sclerosis (MS). After what may have been weeks or months of symptoms and tests, you now have a diagnosis. This can bring a mix of emotions—relief, sadness, anger, frustration, or even acceptance. However you feel right now, know that it is completely normal.
The next few weeks will be a time of adjustment. You may have many questions, feel overwhelmed, or even try to block out thoughts of MS altogether. That’s okay. When you’re ready, MS Ireland is here with information, services, and support to help you navigate this new chapter.
Take your time to process the news. Some people choose to tell family and friends straight away, while others prefer to wait. There’s no right or wrong way—do what feels right for you. Allow yourself space to absorb the diagnosis and, when you’re ready, think about the next steps.
When looking for information, go at your own pace. Be selective—reading everything at once can be overwhelming, and not all symptoms will apply to you. Stick to trusted sources, such as recommended books, magazines, and reputable websites.
Your neurologist and MS nurse are key sources of information, especially at this stage. Our MS Ireland team is also here to listen and support you when you feel ready. You can reach out to our MS Information Line or connect with your local Regional Services team. They can offer guidance, answer questions, and speak with you and your loved ones.
Many others have been where you are now. Their experiences can offer reassurance and insight into how life with MS can unfold. You are not alone, and support is available whenever you need it.
Our Information Line is available from 9:30 am to 5:00 pm, Monday to Friday (excluding public holidays) on 0818 233 233.
Starting Off
We know you have lots of questions at the moment. Our staff talk to people newly diagnosed everyday, they have put together these common first questions. Our trained staff can answer your questions - Call the MS Information Line on 0818 233 233 Monday to Friday 9.30am-5pm or email info@ms-society.ie
Give yourself some time to come to terms with the news. Some people tell their family and friends straight away, others wait. Do what is comfortable. But do take time to overcome the initial shock and begin to see how you can move on.
Seek information out at your own pace. Be selective. Reading everything you can find about MS may be upsetting and may of the symptoms will not apply to you. Use trusted websites and recommended books and magazines.
Your neurologist and MS nurse are a central source of information for you, particularly at this time. Our own staff are also ready to listen and talk when you are ready. You can contact our MS Information Line or get in touch with the Regional Services team in your area. They can meet with you and/or your family or partner to talk through any concerns or questions you have.
Unfortunately, many people have gone through what you are going through now. Find comfort from their experiences and learn about the ways they dealt with their diagnoses and life that materialised afterwards.
Our direct and confidential service is open from 9:30am – 5pm, Monday to Friday (excluding public holidays)
0818 233 233
Newly Diagnosed Webinar
In November 2020 MS Ireland held a series of webinars for those newly diagnosed. They covered the topics of being diagnosed, stress management and exercise.
My MS Story
Katie St. Lawrence was diagnosed with Multiple Sclerosis when she was 22 years old. She shares her story of living with MS.
Treating and Managing MS
Information on how to treat and manage life with Multiple Sclerosis