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We want to hear from you: please tell us about your experience of the online community.

Hi, my name is Cary!

Cary

Fibromyalgia, IBD, arthritis, MCS and plenty more. South Hams based.

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Comments

Dmb1975

Hi Cary,

It’s good to hear from you, I hope today is a good day for you

All the best Darren

Cary

Hi Darren,

Thanks for your message. Not too bad a day today, have managed to visit my elderly parents. Just fed up with myself that I am not able to do more to help them (85 and 91). Where abouts are you? Hope all is well for you too today.

Cary

debbiedo49

I have fibro too. Welcome

Cary

Thanks Debbie. So fed up with myself being so unable to live a proper life and struggling as if it wasn't for this government changing the goal posts I would have been receiving the pension I worked for until I became so ill. How are you doing?

cary

Dmb1975

Hi Cary,

Let’s celebrate the positive, you have been to see your parents which is brilliant, I am sure your parents understand your situation.

If you ever want to chat about anything just drop me a line and I will respond as soon as possible.

I appreciate how difficult life can be I still struggle coming to terms with my life, I am a forty-two year old with Cerebral palsy and associated muscle spasms, I still live at home with parents and they have to do everything for me and I worry that I am a burden.

I am aching a bit but it is nothing I cannot handle.

Have a lovely rest of the day.

Darren

Ami2301

Hi Cory
Welcome to the community! Please let us know if we can do anything to help!

Chloe_Alumni

Hi @Cary and a warm welcome to the community. Please do have a look around and let me know if there is anything that I can do to help

Steve_in_The_City

Hi @Cary I have MCS/IEI. I was declared disabled because of this in 2007, but disabled is a legal term and not a diagnosis. I wondered if you have been diagnosed? I expect you know of mcs-aware. I find it a useful forum. Do you think it may be worthwhile to start a dedicated MCS discussion here on Scope? Hope you are coping well with MCS, as in my experience there is zero help from the NHS.

poppy123456

@Steve_in_The_City this thread is 4 years old and Cary hasn’t been active on the forum for the same length of time.