Phil was a fighter and so are you, pleas know that our thoughts and love are with you and Phils family.
Mike
Type: Posts; User: Michael Bell
Phil was a fighter and so are you, pleas know that our thoughts and love are with you and Phils family.
Mike
I have to agree with the majority on this Andrew. This site is very important to WG sufferers, we need it, and we need each other. It is a very nice idea to expand the site but we would be swamped...
I spent five and a half months in hospital when this disease got me and another two months watching day time tv. I could not wait to get back to work. I was still using a walking stick and could only...
I have two idiotic cats in the house so not a good idea to have fish.
Mike
I hope you get this flare under control quickly. I know it is hard but try and stay possitive, many people on this site have had this SOB of a disease for decades and are still going strong. Keep on...
I work 12 hour shifts, days one week nights the next. Sleeeping in the day is always a problem for me but I seem to be able to cope on 5 hours sleep so concider myself very lucky.
Mike
my prayers and thoughts are with you both. I hope the power of all the love that people on this thread feel for you both makes a positive difference to you. And yes look after yourself Alysia.
Mike
I have been challenged to do it on facebook so am keeping a low profile. I am always happy to donate to such a good cause but NOT willing to have a cold dousing for anyone.
I think I may be just a...
My skin is also thinning, very easy to take a chunk out and lots of bruises with the smallest knock. I blame it on the pred.
Mike
you are in my prayers, and I hope to hear some good news soon.
Mike
Hello Morningsunshine and welcome. I hope you are responding well to your treatment and things continue to improve for you. You have found the right group here, and the advice and information is...
there is a plant called feverfew which can be used as a tea or as an infusion, which I have used a few times for migrane. It grows as a weed in the UK and I have it in the wild part of my garden. I...
Prayers and hugs:hug1:from the UK as well Lisa, hope your mum is well soon.
saddle nose free but it has been broken a few times and has never looked very pretty.
Mike
So glad you have had a good week. Iwish you and your family many many more.
Mike
So very sorry to hear of your loss. You will be in the thoughts and prayers of everyone on this site.
Mike
We are all so different in the way this disease attacks us, I spent 5.5 months in hospital, suffered kidney, liver, lung, digestive system and heart failier. I was in an induced coma for 10 weeks and...
Not me Geoff, I have two very large and uncontrolable left feet, and arms that only seem to want to imitate the actions of a windmill in a gale.
Mike
I beat Wegs today after completing a 12 hour night shift following a 9.5 hour night shift supervising the students summer ball at the college where I work. It was a great night but I was on my feet...
Hi Julie, I was also suffering from night sweats before diagnosis, sometimes so bad we had to change the sheets. These stopped when I was put on full medication and it is over two years now since...
I work in a college with 750 residential students and 3000ish day students. Scary sometimes and I have picked up a few infections, mostly in the first few months after returning to work. But I made a...
I hope it lasts too, make the most of this good time and store the memories in case you end up back at the new normal. Enjoy.
Mike
I'm a lefty when it comes to my monthly bloods. My right arm just does not want to give( possibly it had a bad scare when I was watching a vampire movie) although it was not too bad when I was in...
so glad it went well for you.
Mike
Hi Alysia, sorry to hear about the stress in your life. I try not to let stress get to me now, and so far I am doing ok with it. I do not know what to tell you,
as it is all personal as is how we...