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@chloeautumnx 

Last reply

chloeautumnx

New to the MS world...

Hey there. I'm afraid I just stumbled across this site and it looks beneficial. I'm Chloe, age 22 and I was diagnosed with MS two days ago. Although I had my symptoms for a while (optic neuritis, tingling, balance issues, ms hug and numbing to be a few), it was still a huge shock for me. Although I am coping well, it is still daunting to be faced with this. I am a strong person so I won't allow it to affect me too much mentally. I am due to go back to the Neurologist soon and to be assigned with an MS nurse apparently. I hope you are all doing well and hope to speak to you soon!
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@cameron
@cameron
 

Welcome, Chloe! This is a very supportive community and we all learn from each other. An MS diagnosis is a game-changer, but nowadays the big focus is on MS management, i.e. getting on with your life with as little disruption as possible. There's a lot to learn! Your MS nurse will be your first line of information and support, so good luck with that referral. Expect ups and downs emotionally (we've all been there) and let us know how you get on. Big hugs xx

@Stumbler
@Stumbler
 

@chloeautumn , I am sad that you have had to find us, but, given the circumstances, I'm glad you have found us. A diagnosis of MS does answer quite a few questions about events in your earlier life, but it is still a shock. So, now, you just need to be kind to yourself whilst you allow this news to sink in. Use this time, as you are doing, to start learning about this medical condition. MS does not appear to be openly discussed and is regarded as a bit of a taboo subject. But, it's not a terminal condition and, with the advances in medical science, is now a manageable condition. So, you need to see how you can best manage it. I see you have already received some great advice above. And, hopefully, the forum members will be able to continue to support you. Shift.ms came into being to provide support for the younger generation, as it was felt that there was little support available. So, the majority of the membership would be around your age. However, the membership also comprises of people not yet diagnosed through to those of us who have had the condition for too many years. So, sit down, put your feet up and have a look through the forum. It's a pretty informal place so feel free to ask any questions that you may have.