I have a 26 year old daughter with 22q.11. I've learned a lot on this journey. Some things might be helpful to some of you, but due to the nature of 22q.11, and how the syndrome manifests differently in each person, some things might not be. I'm simply hoping that people will become educated about this interesting genetic syndrome.
People with intellectual disabilities are often unaware of their personal hygiene. Teaching hygiene when they're young may be helpful.
All the events happening in the world right now are really confusing for anyone, but imagine how confusing it is for an individual with intellectual disabilities. Our conversations matter. These issues can bring fear and anxiety. It's our jobs as caretakers to explain world events simply and very carefully. Our conversations with others need to be monitored because even though your child may not be the one you're talking to, they may be listening, and are trying to make sense of everything they are seeing on TV and hearing all around them.
It seems fitting to end this season now - when the world awaits the current coronavirus Cliffhanger. May God bless you in your journey, and know that I truly believe that God sends extra angels to protect families with special needs children.
The thinking process can be interesting, and sometimes genuinely doesn't seem to make any sense. You can respond in different ways. That's YOUR choice, and, trust me when I say that can I say that empathetically. Either you can get frustrated, or annoyed or you can find humor in it, OR if you're really feeling patient you can try to follow the train/trail of where the thought began and how it led to the verbal communication. Good luck!
Thinking for two can be EXHAUSTING! I personally believe that it means we're not only amazing, we're also freaking brilliant! Here's why!
A person with 22q11.2 will (most likely) not have the same level of productivity that you have or that you'd like. You may not be okay with that, but they will, and sometimes it causes guilt.
Brooke is 23 years old, has her nursing degree and has a 6 month old baby. The interview got cut short, (my phone rang) but I was pretty much done. I hope something is beneficial to someone.
We all seem to "feel" things spiritual a little differently. Speaking things of a spiritual nature is also very individual. Both may present a challenge for an intellectually disabled person, but it doesn't mean that they don't experience those feelings. Sarah usually experiences them through love.
After people ask me about independent living they usually ask about the possibility of a group home. It's a good question. In the area that I live I have not found group home accommodations, but that may be different in your area. You will also need to take into account the level of disability in these group homes, because if your child is anything like Sarah, they will be extremely aware of these differences.
I get asked this question a lot. The short answer, I believe, is ‘yes' but I haven't figured it out yet, and this podcast episode explains why.
This is a very unplanned, raw interview. We hope this gives your some insights into a sibling's perspective.
Final thoughts about taking care of the caregiver.
This episode got cut off because my husband called. But it's am important episode. ☺️
Happy Valentines Day! Statistics have shown that having a special needs child increases the stress on a marriage. It's important to me to take regular inventory on where our marriage is at, and what we need to do to keep it strong.
It took a long time for me to see the effects that having a disabled child had on our family. Each individual was affected, and coped with the family dynamic differently. Looking back I wish I'd seen each person's difficulties more clearly, however, even those difficulties brought about beautiful characteristics in each member.
A desire to live life isn't any different for an individual with special needs. I'm so glad that we've been able to find ways to make that happen for our daughter.
This subject is hard. Trying to explain to someone why it's hard is...hard!! Don't let people who don't understand your situation make you feel inadequate. This is tricky business. If your state has good accommodations for helping your child get a job, and keep a job, then get them involved.
Jobs are tricky. When looking for employment be certain to communicate limitations and the need for potential accommodations.
This episode is about dating and your special needs child. Things may happen that make you feel uncomfortable, however, overreaction never helps anything or anyone. Remain calm.
This is such an important topic! Everyone suffers when the caregiver gets burnout. They are NOT weak for getting to that point. Honor them by keeping them in your mind and making sure they are cared for. If YOU are the caregiver you NEED to communicate your needs to others.
Sarah experiences trichotilmania. It's gotten better, however, she still pulls out her eyelashes and eyebrows. I don't know if this podcast will be helpful to anyone, but here's some information and experience that we went through.
It's a big decision. Both have advantages and disadvantages.
Stuck in an age, stuck in a pattern, stuck in emotions. None of it is uncommon, and honestly, sometimes it's really hard.
This one is a little longer because PUBERTY feels like an ETERNITY!
After going to a geneticist I learned that that are "flags" that indicate chromosome deletions. It's so interesting! It's worth it to take notice of these things if you have concerns.
Mom Tip- Find a really good ENT specialist because you're probably going to need one.
Figuring out an education plan can be difficult. Make sure you have a good team of professionals, and be so grateful when you do!
Having 5 children helped me realize that something was different about Sarah. I embraced the diagnosis because more information always leads to greater inspiration, and I needed all the information and inspiration I could get.
I've never done a podcast before so please be patient with the learning curve. I'm hoping that my experiences with 22q11.2 will be helpful to someone else dealing with this syndrome, or even another parents special needs journey.