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

Stopped Smoking

GF Lover

Recommended Posts

IrishHeart Veteran
IrishHeart
Posted

Photography and being out in the fresh air is good.

(having suffered intense jaw pain, I soooo get that.)

We're photographers in this house, too. It's a great way to lose yourself in the creative process.

okay, here's another idea:

You need a massage!

Go get one!!

It will relax your muscles and detox the tissues. :)

and you will sleep well.

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

Celiac.com Sponsor (A8-M):


ravenwoodglass Mentor
ravenwoodglass
Posted

Acupuncture can be very helpful with quiting smoking. If you have a practioner near you maybe give them a call. I went to a naturopath for a short time that would do both acupuncture and massage. There are also pressure points that you can massage yourself with acupressure that can help.

I hope you will pick up that camera again. I know the feeling and the mourning when you lose a large body or your work. I lost every painting I had ever done when I was in my 20's. It was devestating and I didn't pick up a paintbrush for many, many years. When I did start to paint again I realized it really was quite theraputic.

When you put those photos on your computer do make sure you do a back up of them right away if they are ones you like. I learned that one the hard way too. I still mourn the loss of a set of photos of a praying mantis that was very cooperative. Even let me move it from front porch to back yard on a stick and didn't mind close ups.

Keep going. The withdrawl from the nicotine will be over before too long. It will likely still be hard but you've come this far and you can go all the way.

GF Lover Rising Star
GF Lover
Posted
  • Author

:(

I have rash squares where the adhesive pads were and she had also put a strip of tape over them. When she ripped it off I actually screamed.

When I like millions of others, was diagnosed with fibro, it was for pain from pressure on my skin. I haven't been able to use a bar of soap in the shower in years. It was so excruciatingly painful when she ripped. The top of my chest is now just all rash and feels bruised.

Then we went to the golf course, these hugh horse flys were out in droves. They were at least 1 1/2" long, I've never seen them so big. I told hubs "this isn't working for me", and it was so hot again.

I think that's enough complaining for one day.

Good news is, still smoke free :D

IrishHeart Veteran
IrishHeart
Posted

It is my deepest hope that you will see that sensitive skin sensation go away. I had it. I wanted to die rather than put up with that sh*t. Misery for years.

I heard the word fibro, too from doctors who guessed what it could be going on inside me.

I was ON FIRE from head to toe and I could barely stand the water in the shower or towel drying off. Hurt to be rubbed.

Wearing clothes hurt. Laying down in bed hurt. Sitting hurt.

Now, I am in intense physical therapy and have deep massages. :) Why? The high histamine response inside me is dying down. My muscles, tissues and tendons are not so severely compromised as they once were. I am gaining ground every month. I could not open a jar or lift my arms over my head. I could not tie my own shoes. In fact, shoes HURT, so I went barefoot. I had to be dressed when it was bad. Hubs joked about my bra: I know how to take these things off, but putting them on is tricky!

Many of us had this painful skin/muscle issue. (Love2Travel, included. I know she will not mind me saying that)

It can go away. You may discover you do not even have fibromyalgia at all. My GI doc calls it "a secondary" response to the gluten. The MT I work with suggests a gluten-free diet to her fibro patients to see what happens. They ALL have no pain now. Coincidence? I think not. :)

Put a COLD cloth on your chest. Try some lotion on it. I know it hurts, believe me.

Sorry, kiddo. :(

Hope today is a better day.

GF Lover Rising Star
GF Lover
Posted
  • Author

Your making me cry but it's a good cry. This has been the first time in my life that I have not felt so alone. So few people in my life understand how painful things can get. I know that it's gonna keep getting better. I have already had some improvement in some of my back muscles. I have always felt that fibro is another catchall, just like IBS.

I think trying to increase my activities has put too much of a strain on me. The cig cravings are subsiding so I can relax about that. Since all of me hurts, I'm gonna continue to gingerly lay on the couch and be content to let Hubs and my son wait on me.

You give me so much hope Irish, I can never thank you enough.

I've got ice on my chest and seeing I'm gonna try and nap for awhile. I know tomorrow will be a better day and can't wait :)

IrishHeart Veteran
IrishHeart
Posted

Do NOT try to over- exercise until your muscles have healed some more!! I made this mistake so many times.

I will tell you what my doc said to me:

Slow and steady wins the race.

Yeah, I don't like that either, but it is what it is.

We have to be patient with tissue and muscle repair.

I want to share something else with you. This young woman came on the sit e a few weeks ago. At 34, she had spent 4 years in pain, unable to pick up her own child. I saw her post. She was trying so hard to get a DX, but to no avail She knew it was gluten.

She just wrote me an email this morning as I had asked her to keep me posted. 16 days gluten-free and her life has turned around. She no longer needs her pain meds and is not in agony every day. Now, I am crying!

Stay the course and take it slow. Your body is going through major changes--between no gluten and quitting smoking, it's wondering what the sam hill is going on. :)

IrishHeart Veteran
IrishHeart
Posted

You need to laugh your head off right now, so look at this:

when you get to the site, there are about 13 pages, so keep scrolling.

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

Celiac.com Sponsor (A8-M):


  • 4 weeks later...
Judyin Philly Enthusiast
Judyin Philly
Posted

way to go G F Lover

haven't been on the forum in a couple years but I did quit smoking a year and 7 months ago

just wanted to post a congrats so I can get alerts and keep tabs on you

  • 2 weeks later...
nomoregluten Newbie
nomoregluten
Posted

hang in there! it's hard but you can do it! Quit 6 years ago when i went on a family hike and i was the only one who couldnt make it to the top of the mountain.

GF Lover Rising Star
GF Lover
Posted
  • Author

hang in there! it's hard but you can do it! Quit 6 years ago when i went on a family hike and i was the only one who couldnt make it to the top of the mountain.

Thanks. It's been a few weeks now and have not had one cig. I'm super proud of myself. Thanks for checking on me

:D :D

msmini14 Enthusiast
msmini14
Posted

I want to say congrats to all the people out there that have been able to kick this unhealthy habit.

I finally stopped smoking in March of 2009 and have not had one since! I smoked for 14 years straight at an average of 1 pack a day.

Quitting was soooo hard but I did it. And like others have said, "If you can stop eating gluten, you can stop smoking".

During my quit I told myself "I only feel this way because I smoked and not because I quit."

It is easy to say, I feel horrible because I stopped smoking but in reality you feel this way because you started to smoke.

Good luck to you and remember it is a long process but you can do it =)

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):

  • Member Statistics

    • Total Members
      133,643
    • Most Online (within 30 mins)
      7,748
    MariSmit
    Newest Member
    MariSmit
    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

    • Jmartes71
      Second chance

      By Jmartes71 · Posted

      Thats the thing, diagnosed in 1994 before foods eliminated celiac by biopsy colonoscopy at Kaiser in Santa Clara  now condo's but it has to be somewhere in medical land.1999 got married, moved, changed doctor's was with former for 25 years told him I waz celiac and that.Fast forward to last year.i googled celiac specialist and what popped up was a former well known heard of hospital. I thought I would get answers to be put through unnecessary colonoscopy KNOWING im glutenfree and she wasn't listening to me for help rather than screening me for celiac! Im already diagnosed seeking medical help.I did all the appointments ask from her and when I wanted my records se t to my pcp, thats when the with holding my records when I repeatedly messaged, it was down played the seriousness and I was labeled unruly when I asked why am I going through all this when its the celiac name that IS what my issue and All my ailments surrounding it related. I am dea6eoth the autoimmune part though my blood work is supposedly fabulous. Im sibo positive,HLA-DQ2 positive, dealing with skin, eye and now ms.I was employed as a bus driver making good money, I loved it for the few years my body let me do until I was yet again fired.i went to seek medical help because my body isn't well just to be made a disability chaser. Im exhausted,glutenfree, no lawyer will help and disability is in limbo thanks to the lax on my health from the fabulous none celiac Google bay area dr snd team. Its not right.
    • 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
×
×
  • 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.