Lovely Holiday

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blueonthetyne
Jul 05, 2015 6:41 am

Well, I'm home again after a lovely holiday.

The British weather certainly looked after us with nearly unbroken sunshine and it was hot every day. I managed to bury a few demons and swim and sunbathe on the beach. I was a bit nervous at first, but in the end, you realize that nobody really cares and you are no different from anybody else. The Comfizz waistbands with black swim shorts are great, even though when wet the bag popped out now and again, but it only added to the fun. I did watch what I was eating and took a "what goes in must come out" attitude while on the beach, but that's a small price to pay to be running and laughing around with my granddaughter on the beach. I still have another week off work and I'm looking at the back garden thinking, how am I going to attack that grass.

Thank you all again for your support during my bad time gone.

What a difference a week makes.

mild_mannered_super_hero
Jul 07, 2015 11:50 am
sounds like you had a great time.!!
bababoo
Jul 08, 2015 7:46 am

Great to hear that you had a good holiday and buried a few demons. Now that you've done it once, you will do it time and time again... well done you!!! Hope you are feeling refreshed and raring to go. Take care, Blue, and sending best wishes to Mrs. Blue.

Posted by: ejbetty

Geekyjen,

Thanks for the reply.  I will be seeing my doctor on Friday and mention Entyvio.  I did not remain paralyzed for more than 2 days, but it was terrible and I was so scared.  The doctors just used alot of xanax and other drugs like that to UN paralyze my joints that were being attacked by the remicade.  Turns out I have been diagnosed with LUPUS. It is attacking my nervous system.  I had ulcerative colitis in 1996 and they had to remove my colon.  Had a J pouch for 10 years, until it started failing.  I then got a permanent iliosomy, and I suffer from severe chronic diareha, and I dehydrate frequently.  I recently had a proctectomy, and that is when the new autoimmune disorder, Lupus, appeared.  I have had two hospital stays now because of the blisters and the paralyzing incident.  I will be dealing with this forever now.  I have just been working on acceptance.

I love this website because of wonderful people like you!

 

Betty

blueonthetyne
Jul 08, 2015 9:54 am

Hi bababoo, thanks. Still not sure what's going on. They are holding off on treatment until they can work out if it's her blood with the cancer or the donor from the transplant. Should know next week. One thing is that this time around I'm in good health, so that will be a help. The Freeman is one of the top hospitals in the country for blood cancers, so it's a case of letting them do their best. Take care and hope you and yours are coping as well.

Rosiesmom
Jul 08, 2015 7:36 pm

Hi, Rosiesmom here. It sounds like you had a great holiday. It helps to stoke the fire of self-confidence. If I might ask, do you live in Newcastle? I thought with your name that perhaps you live in or around the area. I just spent some time in Durham; my sister lives in Penshaw. Good luck with the future testing and care.

 

Getting Support in the Ostomy Community with LeeAnne Hayden | Hollister

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blueonthetyne
Jul 09, 2015 5:31 pm

Hi RosiesMom, I'm RosiesGrandad, ha ha. Yes, I do live in Newcastle. Did you get to see the city of Newcastle while you were here? County Durham is very beautiful, wild at times in the winter months but always a pleasure to visit. My origins are in the south of England. Did you see any of that while you were here? My next challenge is to travel again and I will. The last holiday was a great help and I managed to stay in charge quite easily of my little friend and stay one step ahead. I was quite ill for many years with Crohn's and it's a new lease on life to be well.