Newbie Alert
Hi everyone, I'm in my 10th year of battling MND, well I say battling but more like living with, it's a really bad relationship! Anyway, just thought I would say hello.
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Hi Daniel Fudge-Harman 10 years that's a long time in a 'really bad relationship' gives me some hope. Glad you decided to say hello...nice to hear from you👍Initial diagnosis 7-4-2021 'suspected MND' confirmed by 2nd opinion 4th June 2021 ALS. Began with R foot limp and lots of falls. NIV overnight. Generally weak. Mostly terrified. -
Hello Dan - welcome to our of select clubComment
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Hi, yes 10 Years. I thought I could share information and findings over the years and hopefully make some friends along the way!Comment
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Hey Gordan1111 thanks. I always wanted to be part of an elite club but not sure this is the one I was aspiring to!
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Daniel Fudge-Harman A warm welcome to the forum Daniel, or do you go by 'Fudge'? (yumm yumm)
Congrats on reaching 10 years - which form of MND have you? You appear to be still working 👏👏
Love Ellie.Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.
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Hi Daniel and a warm welcome to the forum from me.
Its lovely to hear from you. We are a friendly, supportive team and I'm sure you must have lots of good tips after 10 years.
OK..all I can think about is fudge atm.
Love Debbie xComment
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Hey Daniel Fudge-Harman happy ten years birthday dude. 👍😄😁😂xxBulbar started Jan 2020. Mute and 100% tube fed but mobile and undefeated. Stay Strong 🤗😘🤗😁xxComment
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Hi Daniel,
Well you must have learnt to cope with many changes.Glad you joined the forum.
Best wishes
MaryComment
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Hi Daniel, you're very welcome here - I'm also sure you'll be able to help a lot of people given your experience over ten years.Diagnosed October 2020 - See my blog at https://www.myneurodiary.comComment
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Hi Daniel. 10 years, wow. Great to hear that you reached this sign post. You’ve found a smashing place to share, give and accept support, rant occasionally if if helps, laugh and make friends. Welcome aboard. Lynne xALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my balance.
I'm staying positive and taking each day as it comes.Comment
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Hi Daniel a warm welcome to the forum from me too 🤗 Janette xJanette xComment
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Thanks everyone, appreciate the warm welcome.
Ellie I have slow progressive sporadic MND, so currently have no mobility, can eat and drink normally, speech is starting to get slurry but still working full time running my business which keeps me busy and distracted. I'm currently on a trial in America, and have been for two years. If anyone wants to ask questions then give me a shout. I'm not sure how this forum works or how to reply to individuals but I'm learning.Comment
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Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.
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Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.
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