Jump to content

  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.


  • Celiac.com Sponsor (A1):
    Celiac.com Sponsor (A1-M):

  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Summer Job

curlyfries

Recommended Posts

curlyfries Contributor
curlyfries
Posted

I work at a middle school as an instructional assistant, and in another month, I won't have any income for six weeks. Most businesses won't hire someone for only six weeks. Plus the fact that I have fibromyalgia. Last summer I worked at my husband's factory for four weeks. I have never been in so much pain in my life! We've been struggling this past year, so we haven't been able to prepare for it like we had hoped.

Any suggestions?

Lisa

Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


Cheri A Contributor
Cheri A
Posted

Could you nanny for someone with elementary-aged kids? How about tutor someone over the summer?

I know a girl who is lining up families that are willing to pay her to watch their kids once/week for SAH or WAHMs. I'm hiring her to watch my kids once/week while I WAH.

Phyllis28 Apprentice
Phyllis28
Posted

Have you looked into the summer positons available for the local school districts? I know in my district the Pre-K special education programs run most of the summer.

Another idea is to get permanent part time job where the hours increase during the summer and decrease during the school year. Where I live this would include theme parks (Disneyland, California Adventure, Knotts Berry Farm), Blockbuster, food service (not recommended for Celiacs)

curlyfries Contributor
curlyfries
Posted
  • Author

I've thought about tutoring, but it's a crapshoot whether I'd get enough clients to get me thru the summer, but I am considering giving it a try. I didn't know SAH or WAHMs hired nannies.

Our school district has summer school programs, but my school is year-round. Summer school starts before I am done with the school year.

No theme parks nearby, and I did work part-time for 5 years at a pharmacy just to have a job during the breaks. But it became too hard on me physically---all the standing and looking down to count pills (lots of issues with upper back and neck).

Thanks Cheri A and Phyllis28 for replying! I really appreciate your trying to help :P

Lisa

Cheri A Contributor
Cheri A
Posted
I've thought about tutoring, but it's a crapshoot whether I'd get enough clients to get me thru the summer, but I am considering giving it a try. I didn't know SAH or WAHMs hired nannies.

Our school district has summer school programs, but my school is year-round. Summer school starts before I am done with the school year.

Your welcome. Keep us posted about what you try. Maybe you could do some tutoring and some kid-sitting.

My mom is a preschool teacher and she tutors a little during the summer. She also has them break her salary down so that she still gets some pay during the summer.

This will be my first year hiring someone to watch my kids for a day. I'm going out on a limb and trying to be positive that I'll be busy with my WAH job. If I don't, then I'll use the time to clean, cook, shop in peace. :lol:

Phyllis28 Apprentice
Phyllis28
Posted

Your welcome.

I'll toss out another couple of more options that may or may not work for you:

1) Look into transfering to a school with traditional calendar. Summer employment will be much easier to locate.

2) Apply at employement agencies that supply temporary help. These jobs would be mainly clerical (Examples are filling, accounting clerk and secretarial). The first agency that comes to my mind is Kelly Girl. I don't know if they are still in business or in your area. You should be able to find names of your local agencies advertising in the want ads in the paper. They will be advertising for full time postions but you can call and ask if they also place temporary.

curlyfries Contributor
curlyfries
Posted
  • Author
Maybe you could do some tutoring and some kid-sitting.

My mom is a preschool teacher and she tutors a little during the summer. She also has them break her salary down so that she still gets some pay during the summer.

The tutoring and kid-sitting is a possibility. Unfortunately, spreading out the salary is only available to teachers, not assistants, since we are paid hourly.

Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


curlyfries Contributor
curlyfries
Posted
  • Author
Your welcome.

I'll toss out another couple of more options that may or may not work for you:

1) Look into transfering to a school with traditional calendar. Summer employment will be much easier to locate.

2) Apply at employement agencies that supply temporary help. These jobs would be mainly clerical (Examples are filling, accounting clerk and secretarial). The first agency that comes to my mind is Kelly Girl. I don't know if they are still in business or in your area. You should be able to find names of your local agencies advertising in the want ads in the paper. They will be advertising for full time postions but you can call and ask if they also place temporary.

1) I work with hearing-impaired kids. I go where they go.

2) I should try that. Don't know why I didn't think of it! Darn brain fog hasn't lifted completely :P But that's why we're all here---to help each other figure things out :lol:

Sweetfudge Community Regular
Sweetfudge
Posted
Could you nanny for someone with elementary-aged kids? How about tutor someone over the summer?

I know a girl who is lining up families that are willing to pay her to watch their kids once/week for SAH or WAHMs. I'm hiring her to watch my kids once/week while I WAH.

I have to say that I LOVED nannying for a summer. It was a lot of work, but a lot of fun, and very rewarding. I watched some really good kids though. Probably helped :)

BTW, SAH/WAHM = stay at home/work at home mom i'm assuming?? just checkin'

Hope you find something :D

Cheri A Contributor
Cheri A
Posted
I have to say that I LOVED nannying for a summer. It was a lot of work, but a lot of fun, and very rewarding. I watched some really good kids though. Probably helped :)

BTW, SAH/WAHM = stay at home/work at home mom i'm assuming?? just checkin'

Hope you find something :D

Yes, SAH/WAHM = stay at home/work at home mom. :)

GREAT idea about the temporary employment agencies, Phyllis!! Why didn't I think of that too? I did that while I was between jobs and getting ready to move. I loved the time I spent "temping".

amybeth Enthusiast
amybeth
Posted

Summer camps might also be an option....day camps.....in our area, some hire people just to pick up and transport the campers.....

Maybe a local library --- or even newspaper delivery....a lot of the kids who have routes during the school year are away or cannot fulfill their routes during the summer months.

Good luck!

Archived

This topic is now archived and is closed to further replies.

Go to topic listing

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate
  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):



    Celiac.com Sponsors (A17-M):



  • Recent Activity

    1. trents
      - trents replied to EssexMum's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Concerning GP advice

      Welcome to the celiac.com community @EssexMum! First, let me correct some misinformation you have been given. Except in the case of what is known as "refractory" celiac disease, which is very rare, it is not true that the "fingers" will not grow back once a consistently gluten free diet is adopted. Celiac disease is an autoimmune condition whereby the...
    2. Scott Adams
      - Scott Adams replied to Florence Lillian's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      Gluten-Mimicking Proteins that can affect some Celiac individuals.

      Here are some articles on cross-reactivity and celiac disease:
    3. knitty kitty
      - knitty kitty replied to HectorConvector's topic in Related Issues & Disorders
      327

      Terrible Neurological Symptoms

      @HectorConvector, Here are some articles about "dry Beriberi" and neuropathy. I hope you've been able to acquire thiamine hydrochloride or Benfotiamine. I'm concerned. Dry Beriberi Due to Thiamine Deficiency Associated with Peripheral Neuropathy and Wernicke's Encephalopathy Mimicking Guillain-Barré syndrome: A Case Report and Review of the ...
    4. cristiana
      - cristiana replied to EssexMum's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Concerning GP advice

      Good evening @EssexMum You are quite right to be concerned about this situation. Once diagnosed as coeliac, always a coeliac, and the way to heal is through adopting and sticking to a strict gluten diet. That said... I have travelled twice to France since my diagnosis, firstly in May 2013 and again in August 2019. My spoken French isn't bad...
    5. EssexMum
      - EssexMum posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Concerning GP advice

      Hi, I am after some advice re my step daughter and her Coeliac Disease. She is 9 years old and had a very limited diet before being diagnosed (very fussy and very lenient parents), since being diagnosed it has become hard to find places out that will cater for her, but we manage. History: She had been having severe tummy pains on and off every...
  • Celiac.com Sponsor (A19):

  • Member Statistics

    • Total Members
      133,635
    • Most Online (within 30 mins)
      7,748
    DWZ
    Newest Member
    DWZ
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):

  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):

  • Who's Online (See full list)

    • There are no registered users currently online

  • Upcoming Events

  • Posts

    • trents
      Concerning GP advice

      By trents · Posted

      Welcome to the celiac.com community @EssexMum! First, let me correct some misinformation you have been given. Except in the case of what is known as "refractory" celiac disease, which is very rare, it is not true that the "fingers" will not grow back once a consistently gluten free diet is adopted. Celiac disease is an autoimmune condition whereby the ingestion of gluten triggers an inflammatory process that damages the millions of tiny finger-like projections that make up the lining of the small bowel. We call this the "villous lining". Over time, continued ingestion of gluten on a regular basis results in the wearing down of these fingers which greatly reduces the surface area of this very important membrane. It is where essentially all the nutrition from what we eat is absorbed. So, losing this surface area results in inefficiency in nutrient absorption and often to medical problems related to nutrient deficiencies. Again, if a gluten-free diet is consistently observed, the villous lining of the small bowel should rebound. "We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesn't react to the gluten straight away, it will be a build up and then the pains start. " That sounds like unscientific BS to me. But it does sound like your stepdaughter may have a type of celiac disease we know as "silent" celiac disease, meaning, she is asymptomatic or at least the symptoms are not intense enough to usually notice. She is not completely asymptomatic, however, because you stated was experiencing tummy aches off and on. Cristiana gives some good suggestions about ordering "safe" food for your stepdaughter from restaurant menus in Europe. You must realize that as the step parent who only has her part of the time you have no real control over how cooperative her other set of parents are with regard to your stepdaughter's needs to eat gluten free. It sounds like they don't really understand the seriousness of the matter. This is very common in family settings where other members are ignorant about celiac disease and the damage it can do to body systems. So, they don't take it seriously. The best you can do is make suggestions. Perhaps print out some info about celiac disease from the Internet to send them. Being inconsistent with the gluten free diet keeps the inflammation smoldering and delays or inhibits healing of the villous lining. 
    • Scott Adams
      Gluten-Mimicking Proteins that can affect some Celiac individuals.

      By Scott Adams · Posted

      Here are some articles on cross-reactivity and celiac disease:      
    • knitty kitty
      Terrible Neurological Symptoms

      By knitty kitty · Posted

      @HectorConvector, Here are some articles about "dry Beriberi" and neuropathy.  I hope you've been able to acquire thiamine hydrochloride or Benfotiamine.  I'm concerned.   Dry Beriberi Due to Thiamine Deficiency Associated with Peripheral Neuropathy and Wernicke's Encephalopathy Mimicking Guillain-Barré syndrome: A Case Report and Review of the Literature https://pubmed.ncbi.nlm.nih.gov/30862772/ Dry Beriberi Manifesting as Acute Inflammatory Demyelinating Polyneuropathy in a Patient With Decompensated Alcohol-Induced Cirrhosis https://pmc.ncbi.nlm.nih.gov/articles/PMC7707918/ A Rare Case of Thiamine Deficiency Leading to Dry Beriberi, Peripheral Neuropathy, and Torsades De Pointes https://pmc.ncbi.nlm.nih.gov/articles/PMC10723625/
    • cristiana
      Concerning GP advice

      By cristiana · Posted

      Good evening @EssexMum You are quite right to be concerned about this situation.  Once diagnosed as coeliac, always a coeliac, and the way to heal  is through adopting and sticking to a strict gluten diet. That said... I have travelled twice to France since my diagnosis, firstly in May 2013 and again in August 2019.   My spoken French isn't bad, and whilst there I tried my best to explain my needs to chefs and catering staff, and I read labels very carefully when shopping in supermarkets, but both times I came away with worsening gastric symptoms and pain. Interestingly,  after the second holiday, my annual coeliac review took place the following month and although I'd been very careful to avoid gluten all year, thanks to that August holiday my coeliac antibodies were elevated,  Clearly I hadn't been imagining these symptoms and they must have been caused by gluten sneaking in somehow. When I spoke to my gastroenterologist on my return, who is an excellent doctor, he told me with a smile that this was a very common experience in France among his patients, and not to worry too much about it! In fact, before we went away in May 2013, which was just after I had been formally diagnosed, he told me not to even bother trying to adopt a gluten free diet until I returned, knowing what France was like, but I was feeling so awful at that time I ignored his advice and at least tried to make a start with it. (I ought to say - both these visits were some time ago, so perhaps things are a lot better there now.) So what to do?  I would say at least try to explain to catering staff the situation - they should be able to rustle up a plate of cheese, boiled eggs, tuna, salad and fruit, and if things like crackers and gluten-free pot noodle or oats can be packed in the UK, those can be produced at mealtimes.    Of course, most larger supermarkets in France do now cater for coeliacs, but when I was last there the the choice wasn't as wide a range as we have in the UK but I think that is partly because the French like to cook from scratch, whereas our gluten-free aisles have quite a lot of dried or pre-baked goods in them/convenience foods, because I think we as a nation tend to use them more. I would be worth doing a bit of research on the internet before the trip, - the words you want are 'sans gluten'.  I've just googled 'sans gluten Disney Paris" and this came up.  I do hope at least some of this is of help. https://www.tripadvisor.co.uk/Restaurants-g2079053-zfz10992-Disneyland_Paris_Ile_de_France.html  Whatever befalls in France, at least your stepdaughter can resume her usual diet on her return. On a related tack, would you be happy to post any positive findings/tips upon her return - it might be of use to others travelling to Disneyland Paris with children in future? Cristiana
    • EssexMum
      Concerning GP advice

      By EssexMum · Posted

      Hi, I am after some advice re my step daughter and her Coeliac Disease. She is 9 years old and had a very limited diet before being diagnosed (very fussy and very lenient parents), since being diagnosed it has become hard to find places out that will cater for her, but we manage.  History: She had been having severe tummy pains on and off every few months so had a bunch of tests and eventually was diagnosed with celiac disease a number of months ago. We was told that she is at a very high level and should avoid gluten for the rest of her lift, we was told that the gluten she has been eating has damaged the 'fingers' inside her and they will not replenish. We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesnt react to the gluten straight away, it will be a build up and then the pains start. We was advised that by her not reacting straight away, it did not mean it wasnt harming her inside. We was given literature about buying a separate toaster and cutting board etc to avoid cross contamination and have been checking all food labels etc.  Problem: the issue is the novelty seems to have worn off with her Mum and we are now posed with a situation. They are going on holiday to Disneyland Paris for 3 nights and she phoned the hotel who said they cannot cater for gluten free. She phoned the GP and had a conversation and then told my partner that the GP had said it was fine for her to have gluten for the 3-4 days. He questioned it and she said no its fine, she hasnt had it for months so a few days wont hurt and she exposed to it anyway without knowing so it will be fine and shes not ruining her holiday etc.   My partner could see from the online notes that his ex wife had told the doctor that the child does not follow a strict gluten-free diet anyway - not true. At least not with us! My partner requested a call with the same doctor who told him that it is the mums discretion and that the child should be monitored for reactions - he explained that the issue is she doesnt react straight away. The GP said no its all mums discretion and she knows best. We are going to try to speak to the consultant at the hospital, but I just wanted to gauge some thoughts. It just seems bizarre to me that we can go from being told to avoid gluten for the rest of her life and how harmful it is to her body, to now it being ok for her to have it for a few days. Thanks in advance  
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.