

Pete Caluori
Forum Replies Created
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Pete Caluori
MemberNovember 16, 2022 at 8:20 am in reply to: Is anyone getting the 4th shot/booster?Hi Folks, I received my 5th booster (Moderna) a few weeks ago. I’ve always had breathing issues my entire life and am deathly afraid of getting Covid, so I’ll take every precaution against it! This latest booster was for the omicron variants. So far no adverse reactions other than a slightly sore arm the day after.
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Pete Caluori
MemberOctober 9, 2022 at 1:35 pm in reply to: Has ALS changed your perception of aging?Dagmar, thanks for mentioning toxins! My particular toxin was CO2. When my wife took me to the doctor, which I have no memory of, the doctor told her to take me to the hospital. It was there after testing my blood they found my CO2 level at close to 200! I now rely on a BiPAP machine to keep the CO2 levels down. I wear the BiPAP 20+ hours a day, only time I take it off is when I eat or talk to someone.
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Good Luck Eric! I’m in the same position, I walked into the hospital at the end of march and was taken home 2 weeks later in a private ambulance and could not walk. Luckily with some help from a physical therapist I can now walk (actually, hobble around) but I tire easily and use a cane because I’m afraid of falling. I was placed on Maine’s Hospice and they had a manual wheelchair and hospital bed waiting for me when I got home. Since my upper body strength has diminished I now have a power wheelchair thanks to the New England chapter of the ALS group! I am now on Maine’s Home Health Care and they have been great!
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Pete Caluori
MemberOctober 1, 2022 at 2:54 pm in reply to: Has ALS changed your perception of aging?I was diagnosed at 63, but what I thought were signs of old age was probably undiagnosed ALS. I spent 14 days in the hospital while being diagnosed and they gave me about 1 month to live; needles to say my wife was devastated. I look at each new day with hope and a new beginning. I was diagnosed in March 2022! when it comes to ALS most doctors know little to nothing about it!
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Though recently diagnosed with ALS, as I think back I’ve probably exhibited signs of ALS for at least 3-4 years. Now, I feel tired after walking with a cane after going a block or two. I recover after sitting down for 15 to 20 minutes, but I can’t sit on a low seat, because then I can’t get up by myself. I keep a positive attitude though and remember what my new normal is like. Think before moving!
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Pete Caluori
MemberSeptember 15, 2022 at 2:33 pm in reply to: Dressing up for hospitals or appointmentsI wear what makes me comfortable!
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Pete Caluori
MemberSeptember 15, 2022 at 2:30 pm in reply to: Swallowing your pride and using a walker/rollatorSwallow your pride and be glad you can still walk!
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Amanda, please don’t let someone who may have been having a bad day spoil your good nature and manners. If you held a door for me I would profusely thank you for your kindness!
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In addition to what everyone else has said, this really needs to be emphasized to allergists. For years I was seeing an allergist and taking all sorts of medicine for it with little to no result. After being diagnosed with ALS, I let my allergist know and he said thinking out loud, “no wonder your lungs sounded clear”
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Pete Caluori
MemberJuly 29, 2022 at 7:49 am in reply to: Summer COVID Updates – – How are YOU doing?I’m sorry to hear that some of you had COVID. Fortunately my wife and I have steered clear of this horrible pandemic. Everywhere we go we wear a mask even to the dismay of others, but with that said we don’t go out much and when we do we take all precautions. We especially avoid crowds and avoid social contact with those we don’t know. We are both fully vaccinated and fully boosted. Personally I’m terrified of getting this horrible disease, because I’ve had breathing issues my entire life!
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Pete Caluori
MemberAugust 31, 2022 at 1:44 pm in reply to: A brand-new sub-forum: Let’s discuss mobility, technology and medical equipmentHi Kris, check if your state has a hospice or home care service that you can use. I was placed on the hospice service in my state and they provided a Hoyer lift for free, but I have never used it. I’m now in Home Care, because the Hospice folks wanted me to croak in 6 months or less!