Showing posts with label vomiting. Show all posts
Showing posts with label vomiting. Show all posts

Friday, January 29, 2016

The CVS Bucket Photo Challenge


In the run up to Cyclic Vomiting Syndrome Awareness day we're doing a challenge.
The challenge will be to get as many people as you can to be pictured with a bucket. They can do anything with their bucket. They could do something funny with it, wear it, decorate it, snap a friend, Nurse, Dr or school teacher with it, anything they like. So long as they picture it.
Awareness Day 5th March
We're asking people to make a small donation to the Cyclic Vomiting Syndrome Association too if possible to assist with awareness and research funding.


Wednesday, December 02, 2015

Cyclic Vomiting Syndrome Awareness





Photos of Buckets for CVS Awareness Day 2016

Hello guys and girls,

We are hosting an awareness drive in which we will be asking people to take pictures of buckets.


We need name ideas for the photos with buckets challenge. The challenge will be part of CVS Awareness day on 5th March. We are hoping to get as many people from all around the world involved. 


If you are able to help me promote this event please let me know.


You can do anything you like with your bucket in the photos. You could do something funny with them, wear them, decorate them, snap a friend with them anything you like. We will be posting them in the run up to awareness day so we need a good catchy name for the challenge. I will then design some posters to promote the challenge which you can share all over the place to get others involved IE: schools, shops, churches, workplaces, friends & family etc. I hope you'll all join in and have a bit of fun in the process. 


Just submit your name ideas in the comments section below, this will run for 2 weeks and on 16th Dec we will narrow them down to about 6-8 names. After we narrow them down we can start a vote on the groups, pages and websites in order to decide the final name.


Other places name ideas are being posted are...


CVS Facebook Page


CVS Facebook Posters Page


CVS Facebook Group


Cyclic Vomiting Twitter


**PLEASE ADD YOUR NAME IDEAS IN THE COMMENTS SECTION BELOW**


Monday, September 28, 2015

15 things not to say to someone with a chronic illness or invisible illness

This was not written by me but is from the A Sweet Life Website 15 things not to say to someone with a chronic illness or invisible illness

Invisible illnesses are illnesses that you can’t see just by looking at someone. Things like Type 1 diabetes, Chronic Migraines, Lupus, Postural Orthostatic Tachycardia Syndrome, Fibromyalgia and Cyclic Vomiting Syndrome.  These may not affect your appearance, but they affect how your body functions and feels. Every day. Probably for the rest of your life.
When you say the following things to someone with a chronic illness, you probably don’t mean to hurt their feelings. A lot of the time you are just trying to understand or sympathise. Well, from the perspective of someone who lives with a chronic illness, here are 15 things you should never say to someone with a chronic illness:

1. You don’t look sick

Not everyone “looks like” what is happening to them. You would never say “you don’t look like someone who is going through a terrible divorce” if your stressed out friends still manage to put on a brave face and pull themselves together. Not all illnesses are manifested outwardly. 
  
But you don't look sick - Invisible Illness

 

 

2. You’re too young to be sick

I get this one more than #1. You can get ill or go through any kind of stressful situation no matter your age. Age is completely irrelevant here. Young, unfortunately, does not always equal disease-free. When you tell someone they’re too young to be sick, it just makes them feel even more guilty or embarrassed for having an illness they have no control over when society expects them to be healthy.  And, moreover, just because you have an illness, doesn’t mean you want to be called “sick.”

3. Everyone gets tired

That may be true. And most people are not getting enough sleep and rest. But the difference between someone with chronic illness associated fatigue and an otherwise healthy person is the level of fatigue. If I go out drinking with friends and stay up late, it could take me a week to recover. I have to carefully plan every activity of the day so that I can save energy to do all of them. The best line I’ve heard for this one is: you don’t know what fatigue is until you’ve had to rest after taking a shower. Unless you literally think to yourself“how much energy will that take?” for every single action you take during the day (including brushing teeth, combing hair, standing to do dishes, putting on makeup, cleaning, driving, etc.) then you experience a completely different kind of tired than people with certain chronic illnesses. I’m not saying you aren’t tired. Everyone does get tired. But my kind of tired is not the same as a healthy person’s kind of tired. If I push myself past the amount of energy I have in a given day, the consequences are pretty bad. See the spoon theory for more about this one.

 

4. You’re just having a bad day

I know you are trying to motivate someone and make them feel better when you say this, but it doesn’t come off like that. Personally, only about 10 people in my life see me on my bad days. If I am outside, dressed, and active, that is a good day. So instead of making someone with a chronic illness feel supported and motivated when you say this, it feels like you are brushing off their symptoms. Chronic illnesses are with you for life. You can change your lifestyle and find treatments to help them, and some of them can be “managed,” but for the most part, that person will have to deal with a lot of bad days for many years to come.

5. It must be nice not having to go to work/school

This one. Oh man. If you only knew. Sure, it can feel that way when you take a day to play hooky or a long vacation. But when you are forced not to go to work or school, even when you want to be there, it is a different story. People with chronic illnesses don’t want to fall behind in school and fight with the school district to get the accommodations they need. People with chronic illnesses don’t want to miss work and not be able to generate an income. Everyone wants independence.
Personally, I loved school and hated every day I wasn’t there. It is way more stressful not being in school and knowing all the work you will have to do to make up for it than being there on any given day. And I have loved the jobs I’ve had and been sad about every day I have missed. Believe me, it is not nice having to stay home instead of being productive, just trying to find ways to distract yourself from pain or exhaustion. It’s fun to watch TV for a day or two, but after that, I feel trapped. I guarantee anyone with a chronic illness would gladly trade in their symptoms for a full time job.

6. You need to get more exercise

Exercise is really important and no one is denying that. It helps pretty much any health condition. But it isn’t a cure-all. For someone like me, whose heart rate regularly reaches 120 bpm just from standing still, exercise isn’t always doable. I do “exercise” but it is more like physical therapy exercises than what most people would consider a good work out. But remember, everyone has limitations. For people with chronic illnesses, their physical limitations may make it harder for them to do traditional exercises. And even if they do, it will probably not be a cure for a condition that is caused by something totally different like an immune system that attacks itself or a nervous system that doesn’t regulate itself correctly.

 

7. I wish I had time to take a nap

See numbers 3 and 5, which relate to this one. To someone with a chronic illness, to whom napping is not a luxury but in fact a necessity, hearing someone say this is as much a slap in the face as hearing someone say they wish they could take a break from work or school too. Hearing anyone “wish” they could have a part of a chronic illness just shows how misinformed they are when they say this. Wishing you had more time is pretty much a universal wish. But wishing you had the time that a person with a chronic illness has is not the same. If your wish is granted, you can get more time, but you also have to get the pain, the exhaustion, and the difficulty figuring out how to be productive in society. Remember that next time you have the desire to say this.

Wednesday, August 12, 2015

Our CVS Pinterest Board

My CVS PINTEREST Board

This board is mostly made up of posters I have made myself over the years to raise awareness of CVS. Click on this link CVS Pinterest Board to see our board.
Please share and raise awareness.

CVSA - UK Family Day

CVSA - UK Family Day

 November 21st 2015 

Birmingham Children's Hospital

What happens at a Family Day?

First, the name. We call it a Family Day as it is "family friendly" and children are welcome, but it is open to everyone.
We normally start the day with two, or three, formal presentations by medical experts, both from the UK and abroad, or occasionally sufferers. We have had speakers from the USA, Italy and Spain. If time allows we hold a panel discussion where all the doctors can be questioned about issues affecting all CVS sufferers.

After a break for lunch, we hold a short annual general meeting of the charity. We then hold one-to-one sessions between the doctors and the attendees. We offer 10 or 15 minute personal consultations with each of the speakers and a sufferer or their family. Access to world experts on CVS on such a personal basis is a rare opportunity.

The less obvious side of the day is the chance to meet and chat with other sufferers. For many CVS sufferers they feel isolated, not knowing anyone else with the condition. Meeting others and sharing experiences can be a really important aspect of attending.

We offer a free creche with activities and CRB checked helpers to supervise. If a child is ill or upset, they can be brought into the main room to find the parent or carer, even during the "formal" presentations - family first.

When are they?

We normally hold the meetings on a Saturday during early-mid November.

Where are they held?

In the education centre of Birmingham Children's Hospital. This is as central a location as possible for people to travel to, and has good facilities available.

How much does it cost?

The meeting and creche are entirely free. We do pay for the facilities and often for travel costs of speakers, so we do appreciate any donations to help offset the cost.


Cyclic Vomiting Syndrome Awareness Drive

Cyclic Vomiting Syndrome Awareness Drive

Please share this poster to raise awareness thanks


Doctor – I am still vomiting and I feel nobody understands

Doctor – I am still vomiting and I feel nobody understands 

Lena Togher, Sandra Warren and Dr. David Thompson


This article appeared in the CVSA-UK Autumn 2004 newsletter and was designed to cover some of the basic questions about Cyclic Vomiting Syndrome for the non-specialist reader. It has been set up in the form of a dialogue between a hypothetical patient and an equally hypothetical doctor, to enable some of the very personal issues around the problem to be discussed in a way that should be recognised by and be of help to sufferers and carers.
It should be noted that not all the issues raised in the article will be of equal relevance to all sufferers, nor is it possible to include the specific issues of all sufferers in this necessarily brief article.

The Sufferer

Emma is in her late twenties, she has been working successfully and happily as a manager in a large company and has started a family with one small daughter. At the beginning of the year she woke at night from sleep, feeling very nauseated and began vomiting profusely. She saw her general practitioner after one day of vomiting and was given a course of anti-emetics following which the vomiting slowly resolved over the course of 3-4 days. One month later a similar event occurred whilst she was away from home which led to an emergency admission to a hospital away from home. During seven days in the hospital she received fluids by vein and large doses of anti-sickness medications and a number of investigations were performed to exclude serious causes of vomiting. She was discharged after a week on anti-emetic therapy but no explanation for the vomiting was identified. She has now had several further attacks in the months following the hospital admission, and has found herself in a consultation with her doctor, Dr. Medic. She is naturally very concerned, and feels totally alone with her problem so she raises the following questions.


The Consultation

Emma: Doctor, I have now had several episodes of uncontrollable vomiting and I am very concerned because no-one has really been able to tell me what it is that is the matter. So what is it that I have got, and is it very serious?

Friday, July 24, 2015

About our other CVS social media sites

My name is Angie and I'm a Cyclic Vomiting Syndrome (CVS) sufferer. I've had the rare illness CVS since I was 14 years old I was diagnosed in 2008 at the age of 31. I was sitting at home one day thinking what I can do to help people with CVS even when I'm stuck at home unwell. The answer came via my computer as it's sometimes the only way for me to reach the outside world. 
I started a Facebook group in 2012 called ‘Cyclic Vomiting Syndrome (CVS) Support Group’ with the intention of using it for supporting people with CVS and adding CVS information to raisawareness. The group really took off and soon we had Thousands of members from all over the world. The members love the group and are so happy to find people who can relate to what they or their loved one has. We talk about all kinds of subjects like symptoms, medication, feelings, medical staff, hospital visitsraising awareness and lots more. We also offer support to each other when times are rough which has proved valuable to many members. I have made some amazing friends from within the group which have become more like family to me. We share stories of sadness and joy and we help one and other daily it’s amazing. I also started a Facebook sister page in 2012 called ‘Cyclic Vomiting Syndrome’ which has over 2000 likes from people worldwide.